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Old 11-28-2010, 08:58 AM   #21
michka
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Posts: 858
Re: Bad MRI.Liver Met

Lori, thank you so much for explaining your case. Please forgive me because I feel like asking hundreds of questions: was the met that came back in the same place as the first one you had taken out with Cyoablation. Is that why you had a more aggressive procedure? In the same place?
I am interested in this procedure because it is not too heavy. Please share the answers of your interventional radiologist when you come back!
I have the feeling I am not going fast enough. It is the week end and nothing is happening. Except the tumor growing. I want to zap it out!
Love to all. Michka
__________________
08.2006 3 cm IDC Stage 2-3, HER2 3+ ER+90% PR 20%
FEC, Taxol+ Herceptin, Mastectomy, Radiation, Herceptin 1 year followed by Tykerb 1 year,Aromasin /Faslodex

12.2010 Mets to liver,Herceptin+Tykerb
03.2011 Liver resection ER+70% PR-
04.2011 Herceptin+Navelbine+750mg Tykerb
06.2011 Liver ned, Met to sternum. Added Zometa 09.2011 Cyberknife for sternum
11.2011 Pet clear. Stop Navelbine, continuing on Hercpetin+Tykerb+Aromasin
02.2012 Mets to lungs, nodes, liver
04.2012 TDM1, Ned in 07.2012
04.2015 Stop TDM1/Kadcyla, still Ned, liver problems
04.2016 Liver mets. Back on Kadcyla
08.2016 Kadcyla stopped working. mets to liver lungs bones
09.2016 Biopsy to liver. no more HER2, still ER+
09.2016 CMF Afinitor/Aromasin/ Xgeva.Met to eye muscle Cyberknife
01.2017 Gemzar/Carboplatin/ Ibrance/Faslodex then Taxotere
02.2017 30 micro mets to brain breathing getting worse and worse
04.2017 Liquid biopsy/CTC indicates HER2 again. Start Herceptin with Halaven
06.2017 all tumors shrunk 60% . more micro mets to brain (1mm mets) no symptoms
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Old 11-28-2010, 11:16 AM   #22
Lien
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Re: Bad MRI.Liver Met

Hi Michka,

The weekend is almost over, so you will be taking action soon. It is hard to wait, but a few more days won't do you any harm.

Please take a little time to find out what's the best plan of action for you. There are several options and you need to be certain that you are getting exactly what you need. If need be, you can get a second opinion. I'm not suggesting waiting for months, just don't rush into anything you might later regret.

When we are faced with danger we want to regain control over the rollercoaster we find ourselves in. But there are different kinds of control.

Hang in there. You have a very good chance of getting this under control, and scary as it is now, you will adjust to the new normal.

We will be here to help you through all this.

Hugs

Jacqueline
__________________
Diagnosed age 44, January 2004, 0.7 cm IDC & DCIS. Stage 1, grade 3, ER/PR pos. HER2 pos. clear margins, no nodes. SNB. 35 rads. On Zoladex and Armidex since Dec. 2004. Stopped Zoladex/Arimidex sept 2009 Still taking mistletoe shots (CAM therapy) Doing fine.
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Old 11-29-2010, 06:09 AM   #23
Lori R
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Re: Bad MRI.Liver Met

Michka,
I am so pleased that you are asking lots and lots of questions!!! My only request is that when you meet with your Dr. you share his/her responses on the board as well. Thus, we can create quite the body of knowledge regarding liver mets.

My liver met has returned twice to the "generally" same location in my liver, the left lobe. To date, it does not appear to have scattered into multiple mets.

Below is the article I located comparing/contrasting resection to cryoablation. (sorry...I had to copy the entire thing to this post as I don't know how to insert a document) It is very scientific and might be a good discussion point if your Oncologist is very numbers oriented. There were graphs in the article that did not copy. If you are interested, you can locate this article on the Web for an easier read.

I will keep you posted following my appointment with the interventional radiologist.

Cryoablation and liver resection for noncolorectal liver metastases
John D. Goering, M.D., David M. Mahvi, M.D., John E. Niederhuber, M.D.,
Deb Chicks, R.N., Layton F. Rikkers, M.D.*
University of Wisconsin-Madison, Department of Surgery Division of General Surgery, H4/710 Clinical Science Center, 600 Highland Avenue,
Madison, WI 53792 USA
Manuscript received December 17, 2001; revised manuscript January 5, 2002
Abstract
Background:
Liver resection for noncolorectal liver metastases has merit for selected primary tumor types. The role of cryosurgical tumor
ablation within this cohort of patients has not been evaluated. This is a single institutional review of treatment outcomes using cryosurgical
ablation and conventional resection techniques for noncolorectal liver metastases.

Methods:
The medical records of 42 patients undergoing 48 hepatic tumor ablative procedures from February 1991 through May 2001 at
a single institution were retrospectively reviewed. Overall survival and local hepatic tumor recurrence-free survival were analyzed for
different surgical procedures and primary tumor types.

Results:
Overall survival rates at 1, 3, and 5 years are 82%, 55%, and 39%, respectively (median survival, 45 months). Local hepatic tumor
recurrence-free survival rates for resection only (
n  25) and cryosurgery with or without resection (n  23), at 3 years are 24% and 19%,
respectively. The survival rates at 5 years are 40% and 37%, for resection only and cryosurgery with or without resection, respectively.

Conclusion:
Cryosurgical hepatic tumor ablation for metastatic noncolorectal primary tumors results in survival and local hepatic tumor
recurrence rates similar to resection alone. The combination of cryosurgery and resection extends the cohort of patients with surgically
treatable disease. © 2002 Excerpta Medica, Inc. All rights reserved.

Keywords:
Cryoablation; Hepatic metastases; Liver resection

Hepatic resection for colorectal metastases has gained acceptance
as a potentially curative therapy with five-year
survival rates from 20% to 50% [1– 8]. However, the majority
of patients with metastatic disease to the liver are not
surgical candidates because of the number or distribution of
metastases or the presence of extrahepatic disease. Because
of the success of liver resection for metastatic colon cancer,
resective therapies have been applied to noncolorectal liver
metastases. Several series have reported improved survival
rates for patients undergoing curative or palliative liver
resections for noncolorectal metastatic disease [9 –11].
However, these studies have included only those patients
deemed suitable for conventional hepatic resection and have
generally excluded patients with bilobar or anatomically
unresectable disease.
Ablative therapies, such as cryosurgery and radiofrequency
ablation, are alternative options for complete hepatic
tumor ablation. Cryoablation alone or in combination
with hepatic resection increases the number of patients with
colorectal metastases who can be treated surgically [12–16].
Patients amenable to cryoablation, either alone or in combination
with resection, include those with bilobar disease,
or underlying liver dysfunction [12,17]. Cryoblation in
combination with hepatic resection is an aggressive surgical
approach and should be utilized only if survival is enhanced
and operative morbidity and mortality are low. The purpose
of this single institutional study is to assess survival and
local hepatic recurrence following hepatic resection and
cryosurgical ablation of noncolorectal liver metastases.
Methods
The medical records of all patients who underwent hepatic
resection or cryosurgical ablation of noncolorectal
liver metastases at the University of Wisconsin Hospital
from February 1991 through May 2001 were retrospectively
reviewed. Patients undergoing hepatic resection for direct
* Corresponding author. Tel.: 1-608-265-8854; fax: 1-608-263-
7652.
E-mail address:
rikkers@surgery.wisc.edu
The American Journal of Surgery 183 (2002) 384–389
0002-9610/02/$ – see front matter © 2002 Excerpta Medica, Inc. All rights reserved.
PII: S0002-9610(02)00806-1

tumor extension to the liver from an adjacent primary tumor
were excluded. Curative procedures were de
fined as (1)
resections in which all gross tumor was removed with histological
proof of negative margins or (2) intraoperative
ultrasound evidence of complete iceball coverage of hepatic
tumor or (3) in the case of ovarian cancer, 90% or more
concurrent extra-hepatic tumor debulking.
Patient records were reviewed and analyzed for the following
factors: (1) demographics, (2) primary tumor type;
(3) synchronous or metachronous presentation; (4) unilobar
or bilobar disease; (5) number of hepatic lesions; (6) curative
or palliative resection; (7) resection or cryosurgical
tumor ablation; and (8) extent of hepatic resection. Outcome
measures included: local liver recurrence-free survival, disease-
free survival, and overall survival. Subgroup analysis
compared outcome measures between different surgical
procedures (resection and cryosurgery) and different tumor
group primaries.
Intraoperative ultrasound was performed using a dedicated
high-frequency 7.0 MHz T-shaped transducer to delineate
all hepatic lesions. In patients undergoing a combined
procedure, the resection was done
first, followed by
cryoablation of the remaining lesions. Cryoablation was
performed under intraoperative ultrasound guidance to con-

fi
rm the location of all lesions and their relationship to
major biliary and vascular structures. An 18-gauge, Te
floncoated
needle was inserted into the tumor followed by a
cryoprobe using the Seldinger technique. Selection of probe
size was determined based on the required iceball size that
would be necessary to create a 1 cm margin around the
tumor. Multiple cryoprobes were placed in larger lesions
when necessary to achieve a 1 cm margin. Either liquid
nitrogen or argon gas units (Cryomedical Sciences, Inc.,
Rockford, Md., and EndoCare, Inc., Irvine, CA) were used
in this series. Cryogen was infused through the probes,
creating a temperature below 160
°C at the tip. Two 10-min
freeze cycles with an intervening 5-min thaw were completed
for each lesion [12].
Survival rates were estimated with the Kaplan-Meier
estimator. Differences in survival rates between groups
were tested for with the log-rank test. For disease-free
survival and local hepatic recurrence-free survival, the end
point event was recurrence or death. Differences between
study groups were tested for with t-tests. A 5% critical level
was used to determine statistical signi
ficance. All analyses
were performed with SAS statistical software (SAS Institute
Inc., Cary, NC).

Results
Patient and tumor characteristics
Forty-eight hepatic tumor ablations (resection and/or
cryosurgery) were completed in 42 patients (6 patients had
2 operative procedures due to local recurrence of liver
tumor). Twenty-
five patients underwent resection only, 16
received cryoablation only and in 7 patients a combination
of resection and cryoablation was utilized (Table 1). The
median age of the patients was 48 years (range 2
77 years).
Twenty
five female and 17 male patients were treated.
Tables 1 and 2 summarize the characteristics of the metastases,
the treatment administered, and the types of tumors.
In total, there were 32 resections and 23 cryoablations
(Table 1). Twenty of the liver resections were lobar or
greater. Only 4 of the 48 procedures were not potentially
curative. Tumor types were grouped by anatomic association
in a manner similar to that proposed in an earlier study
[11] (Table 2).
Of the patients with neuroendocrine tumors, one patient
with a nonfunctional islet cell tumor, one with a carcinoid
primary, and the patient with a gastrinoma underwent two
operative procedures, the second one for local liver recurrence.
Three patients underwent resection and/or cryosurgical
ablation of hepatic tumors for palliation of endocrinetype
symptoms.
Of the patients with genitourinary tumors, one patient

Table 1
Characteristics of metastases and therapy
Resection only Cryoablation only Both resection
and cryoablation
Total
Number of metastases (mean and range) 1.72 (1
10) 3.19 (130) 6.43 (112) 2.9 (130)
Presentation
Synchronous 6 2 5 13
Metachronous 19 14 2 35
Location of metastases
Right lobe 11 11 2 24
Left lobe 8 3 0 11
Bilobar 6 2 5 13
Extent of resection
Wedge 9 3 12
Lobectomy 12 3 15
Ext. Lobectomy 4 1 5
385
J.D. Goering et al. / The American Journal of Surgery 183 (2002) 384–389

with ovarian cancer and one individual with testicular cancer
also underwent two operative procedures. All ovarian
cancer patients had preoperative chemotherapy and prior
tumor debulking. In addition, 5 of the 7 ovarian cancer
patients had concomitant extrahepatic tumor debulking at
the time of hepatic tumor ablation. Both testicular cancer
patients had undergone prior chemotherapy without evidence
of extrahepatic disease at the time of hepatic tumor
ablation. One of the renal cancer patients was a 2-year old
boy with bilateral Wilm
s tumor, the remaining two individuals
were adults with renal cell carcinoma.
Fourteen patients had soft tissue tumors. The primary
sites of the sarcomas were visceral (
n  3), retroperitoneal
(
n  1), ovarian (n  2), uterine (n  1), and extremity (n


2). Leiomyosarcoma made up 45% of the histologic
subtypes. One melanoma patient presented 5 years after eye
enucleation for ocular melanoma.

Outcomes
There was one operative mortality (2%). The median
follow-up time is 48 months. The overall 1-, 3-, and 5-year
survival rates are 82%, 55%, and 39%, respectively, with a
median overall survival of 45 months (Fig. 1). The 1- and
3-year disease-free survival rates are 41% and 19%, respectively.
The 1- and 3-year local hepatic tumor recurrence-free
survival rates are 43% and 21%, respectively (Fig. 2).
Overall survival rates for the resection-only group (
n 

25) at 1-, 3-, and 5-years are 79%, 49%, and 40%, respectively.
In comparison, survival rates for the cryoablationonly
and combined treatment groups (
n  23) at 1-, 3-, and
5 years are 86%, 62%, and 37%, respectively (Fig. 3). The
difference in survival based on treatment is not statistically
signi
ficant (p  0.57). Local hepatic tumor recurrence-free
survival rates at 3 years for resection only and cryoablation
alone or combined with resection are 24% and 19%, respectively
(Fig. 4).
Survival rates for patients with neuroendocrine, genitourinary,
and soft tissue tumors at 3 years are 91%, 52%, and
34% (
p  0.26), respectively (Fig. 5). (Local hepatic tumor

Table 2
Types of tumors
Resection
only
Cryoablation
only
Both
resection
and
cryoablation
Total
Neuroendocrine
Islet Cell
Nonfunctional 1 2 3 6
Gastrinoma 1 1 0 2
Carcinoid 2 2 1 5
Genitourinary
Ovarian 2 6 0 8
Renal 2 1 0 3
Testicular 1 1 1 3
Uterine 0 1 0 1
Cervix 1 0 0 1
Soft tissue
Sarcoma 9 0 1 10
Breast 2 1 0 3
Melanoma 2 0 0 2
Gastrointestinal
Esophageal 1 0 0 1
Cloacogenic 0 0 1 1
Pancreatic 0 1 0 1
Head/neck
Adenocystic 1 0 0 1
Fig. 1. Overall survival for all patients.
Fig. 2. Overall hepatic recurrence-free survival for all patients.
386
J.D. Goering et al. / The American Journal of Surgery 183 (2002) 384389

recurrence-free survival rates at 3 years for neuroendocrine,
genitourinary, and soft tissue tumors are 32%, 19%, and
20%, respectively (Fig. 6).) Among the ovarian cancer patients,
3 of 7 patients died within 19 months of surgery. The
remaining 4 patients, with 1 patient undergoing 2 ablative
procedures, are alive with hepatic recurrent disease occurring
1, 4, 7, 9, and 12 months after surgery. The two patients
with cervical and uterine primary tumors died with recurrent
disease at 6 and 4 months postoperatively. One testicular
cancer patient had a 44-month survival, whereas the other is
alive without disease 76 months after resection. The patient
with bilateral Wilm
s tumor is alive without disease almost
5 years after hepatic resection for a metachronous lesion. In
addition, 1 renal cancer patient is alive without disease 3
years after resection, although the other renal cancer patient
died one year after resection.
Five of 9 patients with sarcoma primaries died within 3
years of surgery. The remaining 4 patients are alive with
recurrent liver disease occurring between 4 and 60 months
post-treatment. Both patients with melanoma died within 4
months after undergoing liver resection. Two of 3 patients
with metastatic breast cancer are alive without disease although
one underwent resection only 1 month ago.
There were only three patients with gastrointestinal primary
tumors, (esophageal adenocarcinoma, pancreatic adenocarcinoma,
and cloacogenic carcinoma) and two recurred
within
five months. Two died within seven months and one
(cloacogenic carcinoma) remains alive with disease. One
patient with adenocystic carcinoma metastases from a submandibular
gland primary tumor underwent a wedge resection
and concomitant extrahepatic tumor debulking. Hepatic
tumor recurrence developed 11 months postoperatively.

Fig. 3. Overall survival by procedure. (circles
 resection only; plus signs


cryoablation with or without resection; P  0.57).
Fig. 4. Hepatic recurrence-free survival by procedure. (circles
 resection
only; plus signs
 cryoablation with or without resection).
Fig. 5. Survival by tumor class. (plus signs
 genitournary; circles 

neuroendocrine; squares
 soft tissue; P  0.26).
Fig. 6. Hepatic recurrence-free survival by tumor class. (plus signs


genitourinary; circles
 neuroendocrine; squares  soft tissue)
387
J.D. Goering et al. / The American Journal of Surgery 183 (2002) 384389

Discussion
This report suggests that cryoablation alone or combined
with surgical resection results in similar survival rates when
compared to resection alone in selected patients with noncolorectal
liver metastases. Liver resection for metastatic
colorectal carcinoma is now accepted as a potentially curative
modality [3
6]. All colorectal carcinoma patients with
anatomically resectable disease isolated to the liver are
candidates for resection. In addition, several series have
shown that cryoablation alone or in combination with hepatic
resection for colorectal hepatic metastases increases
the number of patients amenable to surgical treatment [12

16]. The outcome for patients who undergo liver resection
for isolated hepatic metastases from noncolorectal primary
tumors is less clear due to the smaller patient populations
that have been studied. Results from this series and others
[9
11] suggest that surgical therapy for carefully selected
patients with isolated hepatic metastatic disease from noncolorectal
primaries improves survival. In addition, results
of this study suggest that cryosurgical ablation may increase
the number of patients amenable to surgical therapy with
liver metastases from noncolorectal primary tumors.
The overall 5-year survival rate of 39% (median survival
of 45 months) in this series is similar to that reported by the
Gustave Roussy Institute [10] (36%) and Memorial Sloan-
Kettering Cancer Center (MSKCC) [11] (37%). These series
are not directly comparable, however, because of the
heterogeneity of the patient populations. For example, the
MSKCC study did not include patients with neuroendocrine
tumors who tend to have a survival advantage due to more
indolent tumor biology. The present investigation, in contrast
to the other reports, includes treatment with both liver
resection and cryoablation.
Patients with neuroendocrine primary tumors demonstrated
the best outcome with a 3-year survival rate of 91%,
which compares favorably to previous series reporting a
4-year survival rate of 73% [18] and a 5-year survival rate
of 73% [19]. These investigations have not only demonstrated
a probable survival bene
fit following resection of
neuroendocrine hepatic metastases, but also signi
ficant palliation
from the associated endocrine syndromes. In one
study, patients deemed unresectable by conventional resection
techniques had a 5-year survival rate of only 29% [19].
In the present series, 9 of 13 cases with neuroendocrine
metastases required cryosurgery to ablate all disease. Thus,
in this group of patients, the addition of cryosurgical ablation
may improve survival and provide more effective palliation
than was previously possible by hepatic resection
alone.
Patients with genitourinary tumors had a 52% 3-year
survival rate. The MSKCC series, which demonstrated a
60% 5-year survival rate for patients with genitourinary
metastases, included mainly patients with testicular, adrenal
and renal cell cancers, which have previously been shown to
have prolonged survival [20
22]. In contrast, ovarian cancer
was the predominant tumor type in the genitourinary
group in the present series, which may account for the
poorer survival rate in this group of patients. In an earlier
study, there were no 5-year survivors with hepatic metastases
from ovarian, endometrial and cervical primary tumors,
suggesting a worse prognosis for these tumors when they
metastasize [9]. Looking more closely at our series, we
found a trend toward improved survival outcomes for renal
and testicular cancer primaries, consistent with other small
series [10,23,24].
Patients with soft tissue tumors had a 34% 3-year survival
rate. Other series have reported 5-year survival rates of
approximately 20% after resection of liver metastases secondary
to sarcomas [10,11,25]. The two melanoma patients
in our series had limited survival. Two of 4 patients in the
MSKCC series with melanoma survived longer than 5 years
after hepatic resection [11]. Two of 3 patients with metastatic
breast cancer are alive without disease. Others have
reported 5-year survival rates of approximately 20% after
liver resection for metastatic breast cancer with one study
demonstrating median survival of 38 months [10,26
29].
Hepatic resection for noncolorectal gastrointestinal adenocarcinomas
has generally resulted in limited survival
[30]. One exception may be metastatic gastric adenocarcinoma
where long-term survivors have been reported after
liver resection in Japan [31]. These results have not been
duplicated in a Western series. None of our 3 patients were
long-term survivors. Hepatic resection for patients with
these tumor types should be con
fined to clinical trials.

Summary
Cryosurgical hepatic tumor ablation for noncolorectal
primary tumors is a reasonable alternative for some patients
who are unresectable by conventional means because of
anatomic location of metastases. Overall survival and local
hepatic recurrence-free survival rates were similar whether
patients were treated with cryoablation or with conventional
hepatic resection. Thus, cryosurgical ablation allows surgical
management of a greater number of patients with liver
metastases from a variety of tumors. Selection of patients
for this treatment option requires careful preoperative and
intraoperative assessment to exclude extrahepatic tumor and
diffuse hepatic disease. Hepatic resection and/or cryosurgical
ablation for metastases from neuroendocrine, renal, adrenal,
Wilm
s, and testicular liver tumors appears to provide
a survival advantage when compared to nonoperative management
of these patients. In addition, careful selection of
patients with hepatic metastases from sarcomas, and from
ovarian, breast, and melanoma primary tumors may yield a
20%
five-year survival rate after hepatic ablative procedures.
Surgical treatment for metastatic noncolorectal gastrointestinal
adenocarcinomas cannot be supported at the
present time.

388
J.D. Goering et al. / The American Journal of Surgery 183 (2002) 384389

__________________
2007
Oct - Diagnosed - Stage IV
5 c.m. IDC - Left Side er/pr- Her2+++
Node + 2/14 - Single Liver Met
Double Mastectomy
Nov - Begin T+H
2008
Feb-Complete 6 cycles- T&H- NED
March - Continue - Herceptin Only
April - Rads for 6 weeks
2009
Continue Herceptin - Continue NED
April - Recurrance- 3 cm. Liver Met
May - Cryosurgery
June - November - Abraxane + Herceptin
Aug - PET/CT - CTC = 0 Back to NED
2010
January - Continue NED
July - Recurrance - 3 cm Liver Met CTC=1
August - Cryosurgery #2
August - November Navelbine
November - Back to NED - End Navelbine
2011
Feb - Recur - 4 cm Liver Met - Same Left Lobe
March Surgery it is -Couldn't get a clean margin
July - Confirmed continued liver involvement
August - Begin Herceptin + Tykerb
October - Mixed results from H+T
Add Abraxane + H + T - Nov - April
2012
January PET Scan - It's working!!
April - Back to NED
July - Recurrance
August - Begin TDM-1 Trial (Taxol + TDM-1)
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Old 11-29-2010, 07:45 AM   #24
michka
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Posts: 858
Re: Bad MRI.Liver Met

Thank you Lori! I printed it out. The survival rates are so low. My only hope is that since all kinds of cancers are mixed, we may pull out better. And the article is from 2002. I did not find any more recent article myself.
What it shows however is that Cryosurgery is a good option.
I am waiting by the phone for the surgeon to call since this morning. I figure they consider I am no longer an urgency.
Tomorrow I am going for a spine MRI and I also have to go for a brain MRI to check if there is no other met.
Love. Michka
__________________
08.2006 3 cm IDC Stage 2-3, HER2 3+ ER+90% PR 20%
FEC, Taxol+ Herceptin, Mastectomy, Radiation, Herceptin 1 year followed by Tykerb 1 year,Aromasin /Faslodex

12.2010 Mets to liver,Herceptin+Tykerb
03.2011 Liver resection ER+70% PR-
04.2011 Herceptin+Navelbine+750mg Tykerb
06.2011 Liver ned, Met to sternum. Added Zometa 09.2011 Cyberknife for sternum
11.2011 Pet clear. Stop Navelbine, continuing on Hercpetin+Tykerb+Aromasin
02.2012 Mets to lungs, nodes, liver
04.2012 TDM1, Ned in 07.2012
04.2015 Stop TDM1/Kadcyla, still Ned, liver problems
04.2016 Liver mets. Back on Kadcyla
08.2016 Kadcyla stopped working. mets to liver lungs bones
09.2016 Biopsy to liver. no more HER2, still ER+
09.2016 CMF Afinitor/Aromasin/ Xgeva.Met to eye muscle Cyberknife
01.2017 Gemzar/Carboplatin/ Ibrance/Faslodex then Taxotere
02.2017 30 micro mets to brain breathing getting worse and worse
04.2017 Liquid biopsy/CTC indicates HER2 again. Start Herceptin with Halaven
06.2017 all tumors shrunk 60% . more micro mets to brain (1mm mets) no symptoms
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Old 11-29-2010, 09:05 AM   #25
schoolteacher
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Posts: 1,486
Re: Bad MRI.Liver Met

Michka,

This is the first chance I have been able to get on the board sinceThanksgiving. Please let us know what is happening. You are in my prayers. You were one of the first people to respond when I first posted on the board, so you have a special place in my heart.

Amelia
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Old 11-29-2010, 12:02 PM   #26
KDR
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Posts: 1,580
Re: Bad MRI.Liver Met

I am always concerned when I see numbers. Of course, for someone with liver mets., these numbers hit me hard...am I to assume that I may have a 39% chance of being alive in five years? I never had any surgery, and the chemo has already decreased my tumors by 50-75% over the course of three months. One of my oncos has said that liver tumors generally "melt" away. The wife of my ob-gyn had colon cancer with mets to liver (which shriveled it up to nothing) and it regenerated. That was 10 years ago. The below information makes me feel unsettled, while I do appreciate it. Then again, I've never been good at reading these types of summaries. Any input from longtime liver mets survivors?

Results:
Overall survival rates at 1, 3, and 5 years are 82%, 55%, and 39%, respectively (median survival, 45 months). Local hepatic tumor
recurrence-free survival rates for resection only (
n  25) and cryosurgery with or without resection (n  23), at 3 years are 24% and 19%,
respectively. The survival rates at 5 years are 40% and 37%, for resection only and cryosurgery with or without resection, respectively.

__________________
World Trade Center Survivor (56th Floor/North Tower): 14 years and still just like yesterday.
Graves Disease, became Euthyroid via Radioactive Iodine, June 2001.
Thyroid Eye Disease. 2003. Decompression surgery in 2009; eyelid lowering surgery in 2010.
Diagnosed: June 2010, liver mets. ER-/PR+10%; HER2+++.
July 2010: Begin Taxol/Herceptin. Eliminate sugar from diet. No surgery or radiation.
January 2011: NED
April 2011: Progression in liver only. Other previous affected areas eradicated. Stop Taxol/Herceptin after 32 infusions.
May 2011: Brain MRI: clear.
May 2011: Begin Tykerb daily, Xeloda twice per day for one week on, one week off, and Herceptin.
November 2011: Progression in liver. All other tumors remain eradicated.
December 2011: BEGIN TRIAL #09-093 Taxol, MCC-DM1 (T-DM1), Perjeta.
Trial requires scans every six weeks, bloodwork and infusions weekly.
Brain MRI: clear.
January 2012: NED. Liver mets, good riddance!
March 2012: NED. Developed SMA (rare blood clot) in intestinal artery and loss of sight in right eye due to optical nerve neuropathy. Resolved when Taxol removed this month.
Continue Protocol of T-DM1 weekly and Perjeta every 3 weeks.
May 2012: NED.
June 2012: Brain MRI: clear.
June-December 2012: NED.
December 2012: TRIAL CONCLUDED; ENTER TRIAL EXTENSION #09-037. CT, Brain MRI, bone scan: clear. NED.
January-March 2013: NED.
June 2013: Brain MRI: clear. CEA upticking; CT shows new met on liver.
July 3, 2013: DISASTER STRIKES during liver ablation: sloppy surgeon cuts intercostal artery and I bleed out, lose 3.5 liters of blood, have major hemothorax, and collapsed lung requiring emergency resuscitative thoracotomy, lung surgery, rib rearrangement and cutting deep connective tissue, transfusion. Ablation incomplete. This life-saving procedure would end up causing me unforgiving pain with every movement I make, permanently, otherwise known as forever.
July 26, 2013: Try Navelbine/Herceptin. Body too weak after surgery and transfusion. Fever. CEA: Normal.
August 16, 2016: second dose Navelbine/Herceptin; CEA: Normal. Will skip doses. Watching and waiting.
September 2013: NED, Herceptin only. CEA: Normal. Started Arimidex.
October-November 2013: NED. Herceptin and Arimidex. CEA, CA125, 15-3: Normal.
December 2013: Something brewing. PET lights up on little spot on liver; CEA upward trend, just outside normal. PET and triphasic liver scan confirm Little Met. Restart Perjeta with Herceptin, stay on Arimidex. Genomic sequencing completed for future treatments, if necessary.
January 2014: Ablate Little Met on the 6th. Happy New Year.
March 2014: Brain MRI: clear. PET/CT reveal liver mets return; new lung mets. This is not funny.
March 2014: BEGIN TRIAL #10-005 A(11)-Temsirolimus plus Neratinib.
April 2014: Genomic testing indicated they could work, they did not. Very strange drug combo for me, felt weird.
April 2014: Started Navelbine and Herceptin. Needed something tried and true, but had significant progression.
June 2014: Doxil and Herceptin.
July 2014: Progression. Got nothing out of it. Brain: NED.
July 2014: Add integrative medical hematologist-oncologist to my team. Begin supplements. These are tumor-busting, immune system boosters. Add glutathione, lysine and taurine IV infusions every three weeks.
July 2014: Begin Gemzar, Herceptin & Perjeta. Happy.
August 2014: ECHO perfect.
January 2015: Begin weekly Vitamin D Analog infusions. 25 mcg. via port.
February 2015: CT: stable.
April 2015: Gem working, but not 100%. Looking into immunotherapy. Finally, treatments for the 21st century!
April 2015: Penn Medicine. Dendritic cell immunotherapy.
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Old 11-29-2010, 12:46 PM   #27
DianneS
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Re: Bad MRI.Liver Met

Hi Michka,

I don't write on this board very much but I saw your post and wanted to respond.

I'm so sorry you are having to deal with all of this, but take heart in the posts from women who have been there and are still doing fine.

I am very much an advocate for complimentary alternative medicine or CAM. Perhaps you have this in France? There are oncs here in Canada and I know in the States as well, who will work alongside doctors (naturopaths) who are knowledgeable with herbs and supplements to treat cancer or to stay cancer free. These herbs/supplements can be very potent along with chemo/drugs to help the body. For example, milk thistle is just one herb that can help the liver regenerate and can detoxify it. Naturopaths know what herbs work synergetically with chemo, if that is what you and your doctors decide will work best for you. Also, many herbs and supplements help to heal the body naturally and keep the immune system strong. Chemo tends to trash the immune system. I can give you the phone number of my oncologist naturopath, who works with oncologists in Canada and the US and has people coming from all over to see him. He can either work with you or refer you to an oncologist/naturopath who could help. I'm not saying you should replace the doctors you have now, just suggesting some additional help. Please let me know if you want more info. You can PM me and I will send you this doctor's name and phone number.

All the best,
Dianne
__________________
Three years and 5 months NED
Dx: Aug 2008 right breast IDC with 50% of tumor DCIS, Stage II or IIA, tumor size: 2.1 cm
Grade 3
8/9 Richardson/Bloom test
ER+ weakly positive
Alred Score: 4 (suggesting I would strongly benefit from hormone therapy)
PR-,
HER2 positive +++
No vascular invasion
No lymph nodes involved
Surgery: Sept. 9, 2008 -Modified radical mastectomy, right breast. I chose to have a simple mastectomy on the left. Began Taxotere/Carboplatin/Herceptin November, 2008. Finished T/C March 2009. Finished #16 Herceptin Sept. 09. AI's and Tamoxifen made me sick. Began natural Tamoxifen which is Quercetin, I3C and a combo of other supplements. I am also a DES Daughter. There is now a link between DES exposure in utero and breast cancer!
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Old 11-29-2010, 01:44 PM   #28
michka
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Re: Bad MRI.Liver Met

Karen, I too would like to know long term survivors. I can only think of AndyBB. it would help me. Dianne I have to figure out in French what is "milk thistle".
I take Omega3 fish oil and curcuma and very low dose aspirin. I try to keep vitamin D at a correct level although it keeps droping. It didn't help obviously. I kow, I am not in positive thinking mood. In fact, I am still cying. Michka
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08.2006 3 cm IDC Stage 2-3, HER2 3+ ER+90% PR 20%
FEC, Taxol+ Herceptin, Mastectomy, Radiation, Herceptin 1 year followed by Tykerb 1 year,Aromasin /Faslodex

12.2010 Mets to liver,Herceptin+Tykerb
03.2011 Liver resection ER+70% PR-
04.2011 Herceptin+Navelbine+750mg Tykerb
06.2011 Liver ned, Met to sternum. Added Zometa 09.2011 Cyberknife for sternum
11.2011 Pet clear. Stop Navelbine, continuing on Hercpetin+Tykerb+Aromasin
02.2012 Mets to lungs, nodes, liver
04.2012 TDM1, Ned in 07.2012
04.2015 Stop TDM1/Kadcyla, still Ned, liver problems
04.2016 Liver mets. Back on Kadcyla
08.2016 Kadcyla stopped working. mets to liver lungs bones
09.2016 Biopsy to liver. no more HER2, still ER+
09.2016 CMF Afinitor/Aromasin/ Xgeva.Met to eye muscle Cyberknife
01.2017 Gemzar/Carboplatin/ Ibrance/Faslodex then Taxotere
02.2017 30 micro mets to brain breathing getting worse and worse
04.2017 Liquid biopsy/CTC indicates HER2 again. Start Herceptin with Halaven
06.2017 all tumors shrunk 60% . more micro mets to brain (1mm mets) no symptoms
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Old 11-29-2010, 05:54 PM   #29
Laurel
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Re: Bad MRI.Liver Met

Michka,

I was away from the site for a few days and was so very saddened to hear of your newest battle. You will, of course, battle on with renewed vigor, because life is so precious. StephN had liver mets. Send her a PM and ask what she did while she underwent treatment. She's had great success with a long NED run of many years.
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Smile On!
Laurel


Dx'd w/multifocal DCIS/IDS 3/08
7mm invasive component
Partial mast. 5/08
Stage 1b, ER 80%, PR 90%, HER-2 6.9 on FISH
0/5 nodes
4 AC, 4 TH finished 9/08
Herceptin every 3 weeks. Finished 7/09
Tamoxifen 10/08. Switched to Femara 8/09
Bilat SPM w/reconstruction 10/08
Clinical Trial w/Clondronate 12/08
Stopped Clondronate--too hard on my gizzard!
Switched back to Tamoxifen due to tendon pain from Femara

15 Years NED
I think I just might hang around awhile....

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Old 11-29-2010, 05:55 PM   #30
chrisy
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Re: Bad MRI.Liver Met

Michka and Karen,

Michka, it's ok to cry - this diagnosis is overwhelming for sure. It is also useful to get as much information as you can regarding various treatment options to help you choose your path.

For me, it was not particularly useful to get hung up on statistics. First, most statistics particularly in that area are either old, not particularly Her2 specific, or small studies. Second and most important, statistics are just that. They are not predictive about how a particular individual will do.

I'm not trying to gloss over the seriousness of the issue - it's a deadly disease. But if even a small % can beat it or survive long term I say "why not me???" Why not us???

There are several long term liver mets survivors on this board. Besides AndiBB, don't forget StephN who is very active here. Others, who are not so actively posting here anymore (because they are doing great!) are Kim in CA who had resection and mamacze who had lung and liver mets resolve with chemo/herceptin. I also have met one of the original Herceptin trial patients who had extensive liver mets and has been in remission like forever.

You just need to get the best advice possible, choose what you think is the most promising treatment option, and see how it goes. Expect to live. People often warn about having "false hope". But there's also "false despair". Do not lose heart.
Chris
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Chris in Scotts Valley
June 2002 extensive hi grade DCIS (pre-cancer-stage 0, clean sentinal node) Mastectomy/implant - no chemo, rads. "cured?"
9/2004 Diag: Stage IV extensive liver mets (!) ER/PR- Her2+++
10/04-3/05 Weekly Taxol/Carboplatin/Herceptin , complete response!
04/05 - 4/07 Herception every 3 wks, Continue NED
04/07 - recurrence to liver - 2 spots, starting tykerb/avastin trial
06/07 8/07 10/07 Scans show stable, continue on Tykerb/Avastin
01/08 Progression in liver
02/08 Begin (TDM1) trial
08/08 NED! It's Working! Continue on TDM1
02/09 Continue NED
02/10 Continue NED. 5/10 9/10 Scans NED 10/10 Scans NED
12/10 Scans not clear....4/11 Scans suggest progression 6/11 progression confirmed in liver
07/11 - 11/11 Herceptin/Xeloda -not working:(
12/11 Begin MM302 Phase I trial - bust:(
03/12 3rd times the charm? AKT trial

5/12 Scan shows reduction! 7/12 More reduction!!!!
8/12 Whoops...progression...trying for Perjeta/Herceptin (plus some more nasty chemo!)
9/12 Start Perjeta/Herceptin, chemo on hold due to infection/wound in leg, added on cycle 2 &3
11/12 Poops! progression in liver, Stop Perjeta/Taxo/Herc
11/12 Navelbine/Herce[ptin - try for a 3 cycles, no go.
2/13 Gemzar/Carbo/Herceptin - no go.
3/13 TACE procedure
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Old 11-29-2010, 09:07 PM   #31
DianneS
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Re: Bad MRI.Liver Met

Michka,

I live in Canada and everything is in French as well as English.

Milk thistle translated is:

'extrait de graines de chardon-Marie (80% de silymarine) 20:1 E.P. 250 mg = 5000 mg.

Of course before you begin supplements you will want to check with your doctor.

Can you find out if there are doctors there in France who also believe in using supplements along with drugs? I find that a lot of oncologists have no training in nutrition (so important when fighting cancer) and they have little if any knowledge of vitamins. Vitamin D is VERY important to keep at a normal level, from what I know now. I assume you're having blood tests to monitor it? I take about 2000 mg a day of Vitamin D. They can also administer it by injection.

My heart goes out to you. If positive thoughts are worth anything (and I think they are!) you are getting a lot of that from this thread. I think I recall that France is #1 in healthcare, so I believe you are in good hands.

Also, information is power and will help with anxiety. Don't be afraid to ask questions! If I can help in any way please let me know,

Dianne
__________________
Three years and 5 months NED
Dx: Aug 2008 right breast IDC with 50% of tumor DCIS, Stage II or IIA, tumor size: 2.1 cm
Grade 3
8/9 Richardson/Bloom test
ER+ weakly positive
Alred Score: 4 (suggesting I would strongly benefit from hormone therapy)
PR-,
HER2 positive +++
No vascular invasion
No lymph nodes involved
Surgery: Sept. 9, 2008 -Modified radical mastectomy, right breast. I chose to have a simple mastectomy on the left. Began Taxotere/Carboplatin/Herceptin November, 2008. Finished T/C March 2009. Finished #16 Herceptin Sept. 09. AI's and Tamoxifen made me sick. Began natural Tamoxifen which is Quercetin, I3C and a combo of other supplements. I am also a DES Daughter. There is now a link between DES exposure in utero and breast cancer!
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Old 11-30-2010, 08:51 PM   #32
mamacze
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Thumbs up

Dear Michka,
I haven't logged on in many months; but I am glad I checked in tonight. I feel heart sick over your "kick in the gut" news of mets to your liver. It seems so overwhelming; the side effects take their toll and if that isn't enough, you have to quickly get up to speed medically so you can have an intelligent conversation in the short apptment you have with your oncologist.

How is the pain from your neurophysiology and your joint pain? Has that subsided?

More important, how is your heart and soul holding up? Can you strengthen your spirit while you take on yet another treatment option?
I too have dealt with mets to the liver and all 4 lobes of my lungs. I am almost 7 years NED. It has been a long journey with many moments of anguish and heartache; and gut wrenching worry about my children.
Like you, I absorbed as much knowledge as I could believing knowledge is power. I made major changes to my spirituality, diet, got 2 second opinions then researched and joined a clinical trial.
If I can offer even a small drop of support; please feel free to PM me. Stay strong, continue absorbing knowledge and please stay with us and keep us posted on your progress.
Godspeed and blessings to you.
Love Kim from CT
__________________
2001 - Stage 0, lumpectomy, radiation, tamoxifen

2004 - Stage 4, mets to 4 lobes of lungs and liver, lumpectomy, er/pr -, her2 neu+++, Herceptin and Navelbine then Herceptin only.

2005 - Breast Ca vaccinations with the Tumor Vaccine Group in Seattle

2011 - Still Herceptin only and NED


2011, June - STOPPED Herceptin and kicked up my heels!

2012, February - 1 small tumor came back to haunt me in my lungs - back on Herceptin only, tumor stable.


2015, November - tumor on lungs removed (Segmentectomy), back on Herceptin only
Received U of W vaccine clinical "booster" Vaccine


2022 On Herceptin and NED continues - WOOT WOOT!
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Old 12-01-2010, 06:51 AM   #33
KDR
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Re: Bad MRI.Liver Met

Kim,
Your post made my day. I hope I am lucky enough, along with all of those here, to follow in your path.
__________________
World Trade Center Survivor (56th Floor/North Tower): 14 years and still just like yesterday.
Graves Disease, became Euthyroid via Radioactive Iodine, June 2001.
Thyroid Eye Disease. 2003. Decompression surgery in 2009; eyelid lowering surgery in 2010.
Diagnosed: June 2010, liver mets. ER-/PR+10%; HER2+++.
July 2010: Begin Taxol/Herceptin. Eliminate sugar from diet. No surgery or radiation.
January 2011: NED
April 2011: Progression in liver only. Other previous affected areas eradicated. Stop Taxol/Herceptin after 32 infusions.
May 2011: Brain MRI: clear.
May 2011: Begin Tykerb daily, Xeloda twice per day for one week on, one week off, and Herceptin.
November 2011: Progression in liver. All other tumors remain eradicated.
December 2011: BEGIN TRIAL #09-093 Taxol, MCC-DM1 (T-DM1), Perjeta.
Trial requires scans every six weeks, bloodwork and infusions weekly.
Brain MRI: clear.
January 2012: NED. Liver mets, good riddance!
March 2012: NED. Developed SMA (rare blood clot) in intestinal artery and loss of sight in right eye due to optical nerve neuropathy. Resolved when Taxol removed this month.
Continue Protocol of T-DM1 weekly and Perjeta every 3 weeks.
May 2012: NED.
June 2012: Brain MRI: clear.
June-December 2012: NED.
December 2012: TRIAL CONCLUDED; ENTER TRIAL EXTENSION #09-037. CT, Brain MRI, bone scan: clear. NED.
January-March 2013: NED.
June 2013: Brain MRI: clear. CEA upticking; CT shows new met on liver.
July 3, 2013: DISASTER STRIKES during liver ablation: sloppy surgeon cuts intercostal artery and I bleed out, lose 3.5 liters of blood, have major hemothorax, and collapsed lung requiring emergency resuscitative thoracotomy, lung surgery, rib rearrangement and cutting deep connective tissue, transfusion. Ablation incomplete. This life-saving procedure would end up causing me unforgiving pain with every movement I make, permanently, otherwise known as forever.
July 26, 2013: Try Navelbine/Herceptin. Body too weak after surgery and transfusion. Fever. CEA: Normal.
August 16, 2016: second dose Navelbine/Herceptin; CEA: Normal. Will skip doses. Watching and waiting.
September 2013: NED, Herceptin only. CEA: Normal. Started Arimidex.
October-November 2013: NED. Herceptin and Arimidex. CEA, CA125, 15-3: Normal.
December 2013: Something brewing. PET lights up on little spot on liver; CEA upward trend, just outside normal. PET and triphasic liver scan confirm Little Met. Restart Perjeta with Herceptin, stay on Arimidex. Genomic sequencing completed for future treatments, if necessary.
January 2014: Ablate Little Met on the 6th. Happy New Year.
March 2014: Brain MRI: clear. PET/CT reveal liver mets return; new lung mets. This is not funny.
March 2014: BEGIN TRIAL #10-005 A(11)-Temsirolimus plus Neratinib.
April 2014: Genomic testing indicated they could work, they did not. Very strange drug combo for me, felt weird.
April 2014: Started Navelbine and Herceptin. Needed something tried and true, but had significant progression.
June 2014: Doxil and Herceptin.
July 2014: Progression. Got nothing out of it. Brain: NED.
July 2014: Add integrative medical hematologist-oncologist to my team. Begin supplements. These are tumor-busting, immune system boosters. Add glutathione, lysine and taurine IV infusions every three weeks.
July 2014: Begin Gemzar, Herceptin & Perjeta. Happy.
August 2014: ECHO perfect.
January 2015: Begin weekly Vitamin D Analog infusions. 25 mcg. via port.
February 2015: CT: stable.
April 2015: Gem working, but not 100%. Looking into immunotherapy. Finally, treatments for the 21st century!
April 2015: Penn Medicine. Dendritic cell immunotherapy.
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Old 12-01-2010, 12:31 PM   #34
michka
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Re: Bad MRI.Liver Met

Thank you Kim for posting just fo me and giving me hope. You went through so much and pulled through. You are right about the mindset. For the moment I just cannot go up the hill anymore. But I have been calling and running around trying to find the right way to get rid of the beast in my liver. It is not easy because by the time you get an appointment all the hospitals then tell you that they close the operation rooms around December 15th and will operate in January.
I went to the American Hospital in Paris where there is a surgeon who is very specialized in laparascopy. He accepted to take me in Friday! It is a very expensive and luxurious hospital but I am lucky I have some savings. I do not want to wait until January! Now I am afraid of the operation. I had a horrible breast reconstruction operation that ended up by a massive hemorrhage. I know things can't go bad all the time....I have to see things more positively. I have only one met, it is resecable. This surgeon is so difficult to have and he made a place for me.
Does anybody have a recommendation about the biopsy of the tumor? HER2,ER,PR, KI67 what else should I check?
Forgive my English. Love to all. Michka
__________________
08.2006 3 cm IDC Stage 2-3, HER2 3+ ER+90% PR 20%
FEC, Taxol+ Herceptin, Mastectomy, Radiation, Herceptin 1 year followed by Tykerb 1 year,Aromasin /Faslodex

12.2010 Mets to liver,Herceptin+Tykerb
03.2011 Liver resection ER+70% PR-
04.2011 Herceptin+Navelbine+750mg Tykerb
06.2011 Liver ned, Met to sternum. Added Zometa 09.2011 Cyberknife for sternum
11.2011 Pet clear. Stop Navelbine, continuing on Hercpetin+Tykerb+Aromasin
02.2012 Mets to lungs, nodes, liver
04.2012 TDM1, Ned in 07.2012
04.2015 Stop TDM1/Kadcyla, still Ned, liver problems
04.2016 Liver mets. Back on Kadcyla
08.2016 Kadcyla stopped working. mets to liver lungs bones
09.2016 Biopsy to liver. no more HER2, still ER+
09.2016 CMF Afinitor/Aromasin/ Xgeva.Met to eye muscle Cyberknife
01.2017 Gemzar/Carboplatin/ Ibrance/Faslodex then Taxotere
02.2017 30 micro mets to brain breathing getting worse and worse
04.2017 Liquid biopsy/CTC indicates HER2 again. Start Herceptin with Halaven
06.2017 all tumors shrunk 60% . more micro mets to brain (1mm mets) no symptoms
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Old 12-01-2010, 02:15 PM   #35
StephN
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Wink Re: Bad MRI.Liver Met

WONDERFUL NEWS! I know you have turned over every rock to come up with this solution at the American Hospital.

Now you can concentrate on that date and be thankful that it is one met that is in an operable position in your liver.

I will send very best thoughts and prayers your way on Friday. Best wishes.
__________________
"When I hear music, I fear no danger. I am invulnerable. I see no foe. I am related to the earliest times, and to the latest." H.D. Thoreau
Live in the moment.

MY STORY SO FAR ~~~~
Found suspicious lump 9/2000
Lumpectomy, then node dissection and port placement
Stage IIB, 8 pos nodes of 18, Grade 3, ER & PR -
Adriamycin 12 weekly, taxotere 4 rounds
36 rads - very little burning
3 mos after rads liver full of tumors, Stage IV Jan 2002, one spot on sternum
Weekly Taxol, Navelbine, Herceptin for 27 rounds to NED!
2003 & 2004 no active disease - 3 weekly Herceptin + Zometa
Jan 2005 two mets to brain - Gamma Knife on Jan 18
All clear until treated cerebellum spot showing activity on Jan 2006 brain MRI & brain PET
Brain surgery on Feb 9, 2006 - no cancer, 100% radiation necrosis - tumor was still dying
Continue as NED while on Herceptin & quarterly Zometa
Fall-2006 - off Zometa - watching one small brain spot (scar?)
2007 - spot/scar in brain stable - finished anticoagulation therapy for clot along my port-a-catheter - 3 angioplasties to unblock vena cava
2008 - Brain and body still NED! Port removed and scans in Dec.
Dec 2008 - stop Herceptin - Vaccine Trial at U of W begun in Oct. of 2011
STILL NED everywhere in Feb 2014 - on wing & prayer
7/14 - Started twice yearly Zometa for my bones
Jan. 2015 checkup still shows NED
2015 Neuropathy in feet - otherwise all OK - still NED.
Same news for 2016 and all of 2017.
Nov of 2017 - had small skin cancer removed from my face. Will have Zometa end of Jan. 2018.
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Old 12-01-2010, 06:13 PM   #36
Sheila
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Re: Bad MRI.Liver Met

Michka
So sorry to read of this newest development, but there are so many amazing role models here...Chris, Steph etc who have beaten back liver mets and won....you are in my prayers...stay strong...so glad you are getting in soon to have this dealt with!
__________________
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is fighting some kind of battle."



Hugs & Blessings
Sheila
Diagnosed at age 49.99999 2/21/2002 via Mammography (Calcifications)
Core Biopsy 2/22/02
L. Mastectomy 2/25/2002
Stage 1, 0.7cm IDC, Node Neg from 19 nodes Her2+++ ER PR Neg
6/2003 Reconstruction W/ Tissue Expander, Silicone Implant
9/2003 Stage IV with Mets to Supraclavicular nodes
9/2003 Began Herceptin every 3 weeks
3/2006 Xeloda 2500mg/Herceptin for recurrence to neck nodes
3/2007 Added back the Xeloda with Herceptin for continued mets to nodes
5/2007 Taken Off Xeloda, no longer working
6/14/07 Taxol/Herceptin/Avastin
3/26 - 5/28/08 Taxol Holiday Whopeeeeeeeee
5/29 2008 Back on Taxol w Herceptin q 2 weeks
4/2009 Progression on Taxol & Paralyzed L Vocal Cord from Nodes Pressing on Nerve
5/2009 Begin Rx with Navelbine/Herceptin
11/09 Progression on Navelbine
Fought for and started Tykerb/Herceptin...nodes are melting!!!!!
2/2010 Back to Avastin/Herceptin
5/2010 Switched to Metronomic Chemo with Herceptin...Cytoxan and Methotrexate
Pericardial Window Surgery to Drain Pericardial Effusion
7/2010 Back to walking a mile a day...YEAH!!!!
9/2010 Nodes are back with a vengence in neck
Qualified for TDM-1 EAP
10/6/10 Begin my miracle drug, TDM-1
Mixed response, shrinking internal nodes, progression skin mets after 3 treatments
12/6/10 Started Halaven (Eribulen) /Herceptin excellent results in 2 treatments
2/2011 I CELEBRATE my 9 YEAR MARK!!!!!!!!!!!!!
7/5/11 begin Gemzar /Herceptin for node progression
2/8/2012 Gemzar stopped, Continue Herceptin
2/20/2012 Begin Tomo Radiation to Neck Nodes
2/21/2012 I CELEBRATE 10 YEARS
5/12/2012 BeganTaxotere/ Herceptin is my next miracle for new node progression
6/28/12 Stopped Taxotere due to pregression, Started Perjeta/Herceptin
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Old 12-01-2010, 08:02 PM   #37
Bill
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Re: Bad MRI.Liver Met

Michka, you are in my thoughts and prayers. I know that you are stronger than what you may think. I'm so glad that you have gotten some really good advice and support from your sisters here. I wish I was there right now to give you a big hug. You're going to be okay. You just hang in there and keep doing what you are doing- research, ask questions, get several opinions, and plot the best course of action. Stay positive, and even as you deal with this new battle, try to take a little time out each and every day to get away from it. Maybe light a candle, listen to some soothing music, and try to relax and feel all of our warm thoughts and prayers surrounding you. Love, Bill
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Old 12-05-2010, 07:40 AM   #38
Lori R
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Re: Bad MRI.Liver Met

Michka,
I am back with news from the follow up visit with the interventional radiologist.

But...first of all....I am so, so sorry that the post regarding resection vs. cryoablation may have introduced some frightening #s. I didn't realize how much I IGNORE those statistics, because we are all proving them wrong. I have personally struggled with the decision of whether to continue to freeze the met or pursue a resection., thus the reason for the article.

So...here are some encouraging words from my radiologist....yours will be much better because when my tumor returns it somehow gets to 3 cm. very quickly. You are in a fantastic position with a single 18mm met!!!! The met is very small which is good. Do demand a biopsy. Since the Drs. will be poking around in there anyhow, it is important to confirm exactly what they are dealing with. Even though I've had 3 mets, the Drs. double check it each time.

My original tumor was in the left lobe of the liver, it returned the first time (again in the left lobe) and we froze it. The radiologist used a single probe to freeze a reasonable margin. When it surfaced again (the most recent time), it surfaced next to the earlier tumor. So, the radiologist believes there was a portion of the tumor that wasn't frozen. The 2nd time he used 2 probes and froze an extensive margin.

He was optimistic that between chemo and herceptin, the cancer is not spreading. I was concerned that I would be too optimistic. But...in his words!! There is reason to be optimistic.

I did express concern that if it surfaces a 3rd time, in the left lobe of the liver and no where else....am I missing an opportunity to be done with this. He thought that was a very reasonable question and is going to talk to my Onc. about a potential liver resection. The radiolgoist does not perform this procedure, I would have to locate a surgeon. If this is the course of action, I will be back to this site to locate the best laproscopic liver surgeon in the U.S. I am not comfortable that there is someone experienced enough in Denver.

Michka, with such a small, single met there is reason to be very very optimisitic. Although it sounds quite expensive, it is critical to receive the best care possible with the most experienced Drs.

Have you finalized the decision to go with the resection? It sounded like you have.

I will be thinking and praying for you, so if you see this post, please let me know that date so we can check in on you.

Lots of love sister.....Lori
__________________
2007
Oct - Diagnosed - Stage IV
5 c.m. IDC - Left Side er/pr- Her2+++
Node + 2/14 - Single Liver Met
Double Mastectomy
Nov - Begin T+H
2008
Feb-Complete 6 cycles- T&H- NED
March - Continue - Herceptin Only
April - Rads for 6 weeks
2009
Continue Herceptin - Continue NED
April - Recurrance- 3 cm. Liver Met
May - Cryosurgery
June - November - Abraxane + Herceptin
Aug - PET/CT - CTC = 0 Back to NED
2010
January - Continue NED
July - Recurrance - 3 cm Liver Met CTC=1
August - Cryosurgery #2
August - November Navelbine
November - Back to NED - End Navelbine
2011
Feb - Recur - 4 cm Liver Met - Same Left Lobe
March Surgery it is -Couldn't get a clean margin
July - Confirmed continued liver involvement
August - Begin Herceptin + Tykerb
October - Mixed results from H+T
Add Abraxane + H + T - Nov - April
2012
January PET Scan - It's working!!
April - Back to NED
July - Recurrance
August - Begin TDM-1 Trial (Taxol + TDM-1)
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