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Old 11-30-2007, 09:14 AM   #1
Erin
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Uh-oh! New test results have me worried

Hi Ladies,

I am a bit freaked out and looking for information. In June I had a CT with contract done which was unremarkable (Whew!) Then, last week I had a high resolution CT done to try to diagnose the cause a persistent cough I have had since just before my dx. Well, when I got the test results ( I always get a copy of them directly from the imaging center - I have an HMO, and it takes weeks to get back to me about results) what popped up was a "7mm spiculated lesion with central cavity"....Yikes, this can't be good! On top of that, I got "the call" from the pulmonologist nurse today "the doctor wants to see you tomorrow to discuss your test results" (my HMO only moves that fastwhen it's bad news) :-(

First, let me thank anyone who is poised to write "don't worry, it is probably nothing, I am sure you will be OK". I truly appreciate the support and well wishes, but what I am looking for here is information. From my research so far (yes, the internet, but only legit sites) the "spiculated" part of the information is the most troubling. Some research work out of Sloan-Kettering quoted the stat of 84 to 90% of spiculated lesions are malignant. Interestingly, most of the articles say a lesion like this has a slightly higher statistical chance of being a new primary lung cancer (?) than mets from my bc (??).

So, has anyone out there got any personal info for me on something like this? I assume from my bc history that they will want to do further tests to find out what it really is. What are the most logical next steps going to be?.... a PET scan? (or is that just going to confirm the info they already know?) .... a bronchoscopy? A needle biopsy? The pulmonologist I am seeing is new to me and my onc, who I trust with my life, is on vacation! I go in today and I want to be prepared.

Help!
__________________
Age 50, premenopausal
Dx 1/2/07 DCIS/IDC
Lumpectomy 1/4/07 1.1cm tumor
SNB 3 nodes clear
Stage 1, Grade 2, HER2+++ (FISH 6.8)
ER + / PR +
TCH, 6 rounds, finished 6/1/07!!!
Herceptin to continue for 1 year
36 rads finished 8/22/07
Port out 8/27/07
Switched to Herceptin weekly for joint pain
Ooph 11/13/07
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Old 11-30-2007, 10:59 AM   #2
Becky
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Dear Erin

I am sorry about having to have additional tests. They might do a PET/CT as it may be able to see lesions smaller than 7mm. In the case of mets, there tends to be more than one nodule. In the case of a new primary, there tends to be just one nodule. You are right about "spiculated" as that tends to be not a good thing.

If I were you, I would push for biopsy unless your doc thinks otherwise. Also, call your onc and fax your report to him and ask what he thinks and how you should proceed.
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Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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Old 11-30-2007, 09:04 PM   #3
Joan M
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I understand what you're going through

Erin,

I relate to you and understand your anxiety because I had the same experience.

I too had a CT scan of the chest, which showed a 9 mm spiculated nodule in the apex of my left lung (the scan was a routine scan of the chest, abdomen and pelvis). A single nodule is known as a solitary pulmonary nodule or SPN.

The good news is that if it is a bc met, it's small and can be removed by minimally invasive surgery, as was the case with my nodule, which has been shown to give a good survival benefit.

Here's what I suggest from my experience, and also some information that might be helpful to you in making decisions about this.

You should have a PET/CT scan. However, at 7 mm, the nodule may not "light up" on PET (it's borderline). The guideline for PET imaging is about 1 cm to give an accurate reading, but smaller nodules have been shown to light up depending on how strong the signal is, and of course if they light up they shouldn't be ignored.

So what this means is that it may or may not light up even if it is a bc met. If it doesn't light up, you have the option of getting a biopsy or waiting out the nodule to see whether it gets bigger, and if it does grow to have another PET/CT scan. The reason for waiting is because it's hard to get an accurate biopsy of a nodule that is less than 1 cm.

I went through this. I had two thorasic surgeons, two oncologist, and one pulmonoligist say that it was not possible to get a good reading on a biospy from a nodule less than 1 cm. But a third surgeon said to try for the biopsy and I did. All three surgeons "swore" I had lung cancer ("the position of the nodule, the look of it," etc.).

The results of the biopsy showed an adenocarcinoma. As it turns out, both lung cancer and breast cancer are adenocarcinomas, and the doctor could not get enough biopsy tissue for a differential diagnosis. However, this was important because the treatment for each diagnosis is different. If it had been lung cancer (and I'm a former smoker), the surgery would have been a lobectomy. But for a lung metastasis, the treatment is a wedge resection, which is taking a slice of pie taken from the lung.

My onc suggested that the lab compare my original bc slides with the biopsy, and the result was that the lab thought it looked close to my bc. But, of course, this was just their gross observation after the fact. It was still inconclusive.

I decided on a wedge resection via VATS (video-assisted throsic surgery) because I wanted the nodule out.

At 9 mm, if the nodule had been lung cancer it would have been "tiny, tiny, tiny," as all three thorasic surgeons said. In the lung cancer world, the nodule would have been stage I, and I probably would not have had any other treatment (chemo or radiation).

This leads back to your cough. In my opinion, a 7 mm nodule would not be the cause of your cough. The nodule's not big enough. That's what's so devastating about lung cancer: by the time you have symptoms, the tumor is large, much bigger than 7 mm.

However, if your nodule turns out to be either lung cancer or a bc met, you could say it was good to have been found so small.

Another thing. A CT scan can see nodules much smaller than a PET/CT. Sounds surprising, right? A CT scan can see a nodule that's as small as 2 mm. But a PET can't see it.

Here's the difference. A CT scan is looking at the morphology of the nodule. That is the form of the nodule (like the size, whether is spiculated, whether it's opague, etc.), but a PET measures metabolic activity. Cancer cells involve a lot of glucose metabolism, much more so than normal cells, and that's what a PET scan measures -- metabolic activity.

With a PET/CT there's a radioactive tracer for the PET (a shot in the vein), but no tracer for the CT part (that is, no intravenous dye in the arm), so the picture isn't perfect on the CT part of the scan, and the scan is just used for attenuation purposes, giving a picture of all your organs to give perspective to the PET part, which is just measuring a signal.

I've been there and I understand how anxious you must be. I was very upset.

You should first start by getting a PET/CT, to see whether the nodule is PET positive.

My prayers are with you. Please let me know if I can help in anyway.
__________________
Diagnosed stage 2b in July 2003 (2.3 cm, HER2+, ER-/PR-, 7+ nodes). Treated with mastectomy (with immediate DIEP flap reconstruction), AC + T/Herceptin (off label). Cancer advanced to lung in Jan. 2007 (1 cm nodule). Started Herceptin every 3 weeks. Lung wedge resection April 2007. Cancer recurred in lung April 2008. RFA of lung in August 2008. 2nd annual brain MRI in Oct. 2008 discovered 2.6 cm cystic tumor in left frontal lobe. Craniotomy Oct. 2008 (ER-/PR-/HER2-) followed by targeted radiation (IMRT). Coughing up blood Feb. 2009. Thoractomy July 2009 to cut out fungal ball of common soil fungus (aspergillus) that grew in the RFA cavity (most likely inhaled while gardening). No cancer, only fungus. Removal of tiny melanoma from upper left arm, plus sentinel lymph node biopsy in Feb. 2016. Guardant Health liquid biopsy in Feb. 2016 showed mutations in 4 subtypes of TP53. Repeat of Guardant Health biopsy in Jana. 2021 showed 3 TP53 mutations, BRCA1 mutation and CHEK2 mutation. Invitae genetic testing showed negative for all of these. Living with MBC since 2007. Stopped Herceptin Hylecta (injection) treatment in March 2020. Recent 2021 annual CT of chest, abdomen and pelvis and annual brain MRI showed NED. Praying for NED forever!!
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Old 12-01-2007, 10:49 AM   #4
murph
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I am new to this forum(bare with me) I have IDC/DCIS 4 primary sites/all Her2+++ER/Pr+. I am told due to no node involvemnet and largest size being 1.5cm I am stage 1. Had a Ct scan w contrast in aug/07 due to left abd. pain. Scan showed possible nodule on left adrenal gland along with multiple sub-cm hypodense lesions in both lobes of liver. I am scheduled for PET/CT nxt. wk. How likely are these connected to my bc? Are there many of you out there with her2+++ with stage 1 no node that have had mets/ thank you in advance
Pam
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Old 12-01-2007, 10:57 AM   #5
murph
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sorry, here is my signature
dx1/24/07 biopsy (annual mammo/I felt small lump)
2/19/07 bi-lat mastectomy (bc in left only/ large calcifications in rt.)
no reconstruction---yet
4 multiple primaries/all connected to 4 DCIS (comedo 30%)dont know what that means
all 4 Her2+++ High grade/Grade 3
all ER pos/ one primary ER/PR pos
40 yrs old
4 AC followed by 12 wks of Taxol along with weekly 30 min. Herceptin
now on 3 wks Herceptin 1 yr
10/01/07 oopharectomy followed by Femora
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Old 12-01-2007, 05:13 PM   #6
Lolly
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Hi Pam, welcome to Her2 Support
You should start a new thread so some of our members who have progressed from Stage I to Stage IV can respond. So sorry for your worry, and hopefully the PET/CT will clarify what you're dealing with.

<3 Lolly
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Sept.'99 - Dx.Stage IIIB, IDC ER/PR-, HER2+++ by IHC, confirmed '04 by FISH. Left MRM, AC x's 4, Taxol x's 4, 33 Rads, finishing Tx May 2000. Jan.'01 - local/regional recurrence, Stage IV. Herceptin/Navelbine weekly till NED August 2001, then maintenance Herceptin. Right Mast. April 2002. Local/Regional recurrence April '04, Herceptin plus/minus chemo until May '07. Gemzar added from Feb.'07-April '07; Tykerb/Abraxane until August '07, back on Herceptin plus Taxotere and Xeloda Sept. '07. Stopped T/X Nov. '07, stopped Herceptin Dec. '07, started Avastin/Taxol/Carboplatin Dec. '07. Progression in chest skin, stopped TAC March '03, started radiation.

Herceptin has served as the "Backbone" of my treatment strategy for over 6 years, giving me great quality of life. In 2005, I was privileged to participate in the University of Washington/Seattle HER2 Vaccine Trial.
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Old 12-01-2007, 07:32 PM   #7
Sheila
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Pam
I was diagnosed stage 1 in 2002, and in 2003 I was Stage IV...as you can see from my signature, I have been in treatment since, but with good response. Also Chrisy went from a 0 to a IV in no time....I hope she will respond.
__________________
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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 12-04-2007, 12:47 PM   #8
Becky
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Erin

Any news on what is going on with you? My thoughts are with you.
__________________
Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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