HonCode

Go Back   HER2 Support Group Forums > her2group
Register Gallery FAQ Members List Calendar Today's Posts

Reply
 
Thread Tools Display Modes
Old 03-28-2007, 07:57 PM   #1
Esther
Senior Member
 
Esther's Avatar
 
Join Date: Sep 2005
Location: Riverside, CA
Posts: 484
Unhappy Not so good news for me.....

I was sitting in bed watching TV and minding my own business on Mon morning, when I got a call from my Neurosurgeon at Cedars-Sinai. And he starts off by saying the radiation oncologist is there with him....

Well, he was calling to say that after reviewing the MRI taken post surgery about 3 weeks ago, they spotted a tiny 1mm new lesion in my brain stem. They wanted me to come in and consult with the radiation onc on Tuesday.

The options they gave me were Gamma Knife, Modified Linear Accelerator Radiosurgery, WBR. MLAR is given in multiple sessions and is the treatment of choice for delicate areas while minimizing effects on healthy tissue around it. So that is option I chose.

I went in this morning and had an MRI, CAT scan, and was custom fitted for the frame for the treatments. I will have 5 treatments in total beginning next week on Wed. and Fri, then Mon/Wed/Fri of the following week. They got all excited about the Lapatinib option, and said if that wasn't in the picture, they would be recommending WBR, which for me would be my absolute last choice.

I am scheduled to have the MUGA and EKG this Fri, then see my onc on Wed morning next week. I AM getting the lapatinib. My sister and brother have said if insurance does not cover the cost, they are prepared to cover the approx. 42K per year that Lapatinib will cost. So I will be starting the Lapatinib within the next couple of weeks, one way or another.

This is one more unforeseen hurdle to get over....knocked me down for a bit, but I'm re-grouping and doing what I have to do to power through this. Now I'm sincerely hoping that the fact that I've been such a complete responder to Herceptin, may be an indication that I will respond to the Lapatinib as well....One can only hope!!!!
Esther is offline   Reply With Quote
Old 03-28-2007, 08:28 PM   #2
eric
Senior Member
 
Join Date: Sep 2005
Posts: 589
Esther,

I'm really sorry about your surprise news. It stinks that you have to deal with this but,as you mentioned, the lapatnib might be a silver lining. My wife seemed to respond well to herceptin and the onc feels she's a perfect fit for lapatnib so I would expect you to be as well.

Eric
eric is offline   Reply With Quote
Old 03-28-2007, 08:42 PM   #3
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
Wow - such intense news to get. I am inspired by your strength and determination to power through!

I am having my brain MRI on Friday. So far all we know of is a spot on my cervical spine... around C1 or 2. The MRI will tell us the size. Hopefully nothing shows up in the brain. Have had headaches everyday for the last 3 weeks, but living in central Texas, everyone including my onc, has had the crazy allergy headaches non stop for weeks.

I learned so much from your post, thanks for sharing. I am sorry that you are facing this hurdle.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 03-28-2007, 08:53 PM   #4
PatS
Senior Member
 
Join Date: Sep 2005
Location: Maine
Posts: 97
Hi Esther,

I'm sorry to hear the latest news. It's good news about being able to get lapatinib though. The last time I saw my onc. she said she had two patients with brain mets who had been through different meds with no response but have responded to lapatinib.

Take care,
Pat
PatS is offline   Reply With Quote
Old 03-28-2007, 09:28 PM   #5
Lolly
Senior Member
 
Lolly's Avatar
 
Join Date: Aug 2001
Location: Oregon
Posts: 1,756
Esther, I'm so sorry you were hit with this news so unexpectedly. But it seems you and your team have a pretty good handle on things. I wonder if the lapatanib will have any synergy with the MLAR? That might be a good thing. Best wishes for next Wednesday, I'll be thinking of you while I'm in Chemo

<3 Lolly
__________________
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.
Lolly is offline   Reply With Quote
Old 03-28-2007, 10:04 PM   #6
StephN
Senior Member
 
StephN's Avatar
 
Join Date: Nov 2004
Location: Misty woods of WA State
Posts: 4,128
Unhappy

Oh BLAST it! Cancer sure CAN get into our business!
Just when you thought that the brain stuff was under control for a while.

I have a question since 1mm is SO small and most MRI machines make 2mm cuts. Is it one of the new 3 Tesla magnets?? We have one now at the U of W, but I have continued using the "old" MRI machine from last year for consistency of imaging.

These newer machines can catch the mets in a smaller size and hopefully give a better chance of knocking them into oblivion. Have at it and let us know how it goes.
Your family knows you are a good investment - they must be great people to offer to pitch in like that.
__________________
"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.
StephN is offline   Reply With Quote
Old 03-28-2007, 11:03 PM   #7
Soccermom
Senior Member
 
Soccermom's Avatar
 
Join Date: Jun 2006
Location: Bradenton,FL
Posts: 977
Esther,
Wishing you calm in the face of this news. Stephs comment about "blasting it into oblivion" sounds like a great one to me. Hope your treatment does EXACTLY that!
Hugs,Marcia
Soccermom is offline   Reply With Quote
Old 03-29-2007, 04:57 AM   #8
Sandy H
Senior Member
 
Sandy H's Avatar
 
Join Date: Feb 2005
Location: Norridgewock, Maine
Posts: 778
Esther am sorry to hear your not so good news! It seems this is the season for a few on this board. I will say a few prayers for you especially as I am doing my bone scan today. Sending you a big hug, Sandy
__________________
Dx. 03/01, Rt. IBC
AC/Taxatere
Rt. MRM-with graft Lt. simple
5 rads-skin mets
Herceptin, taxol, carboplatin (taxol seem to be the magic drug)
Navelbine & xeloda (did not work)
topical miltex for skin mets
Tykerb/xeloda
thoracentesis x 2 left lung fluid shows cancer cells
Port removal (4 years) with power port replacement
Doxil
Updated 05-07 Scans show no bone or organ involvement we shall see!




I shall not pass this way again. Any good I can do or any kindness that I can show let me not defer or neglect it for I shall not pass this way again.
Sandy H is offline   Reply With Quote
Old 03-31-2007, 07:44 AM   #9
HavahJ
Senior Member
 
Join Date: Dec 2005
Posts: 98
Oh Esther

I don't come on here often anymore but right away saw your post. You're the only person I know here! I feel so bad about your met. Is the drug you're doing tykerb? I'm supppose to start that soon. It does cross the blood-brain barrier (tykerb that is). You sure are a hanger-onner! I admire you and this sounds like a lickable one. You've managed worse. Hope it goes quick. HavahJ - Jan
HavahJ is offline   Reply With Quote
Old 03-31-2007, 01:42 PM   #10
Sheila
Senior Member
 
Sheila's Avatar
 
Join Date: Aug 2003
Location: Morris, IL
Posts: 3,507
Esther

Seems like this little mets get a mind of their own....but know that you will show them whose boss of the brain...hoping that the Tykerb will work perfect.
Thinking of you and saying prayers
__________________
"Be kinder than necessary, for everyone you meet
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
Sheila is offline   Reply With Quote
Old 04-02-2007, 12:07 PM   #11
Vicki
Senior Member
 
Join Date: Jun 2006
Posts: 44
Smile Esther, keep that beautiful smile going!

Hi Esther,

I'm sorry to hear about this darn bump in the road, so consider it "spring cleaning" and you have the latest, new cleaning agent, lapatinib, to clean house. I'm thinking of you from here in O.C. I'm also going to send this link of yours to my friend in L.A. who is dealing with the same thing and will find your posting valuable to her, as well.

Be well and hang in there.

XO,

Vicki Z
Vicki is offline   Reply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


All times are GMT -7. The time now is 08:33 AM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2024, vBulletin Solutions, Inc.
Copyright HER2 Support Group 2007 - 2021
free webpage hit counter