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Old 02-23-2009, 03:57 PM   #1
Jean
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a Question on herceptin...

Does anyone know or heard from their onc. or has anyone read written material on the viability of herceptin afer a patient completes the year of herceptin treatment?

Thank you,
Jean
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Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006
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Old 02-23-2009, 04:24 PM   #2
hutchibk
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You know, I hope Maryanne in TX sees this and answers. I think her doc is a real forward thinker who might have given her a clue about this...
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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."
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Old 02-23-2009, 04:49 PM   #3
Laurel
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Jean,

Are you asking whether there may be an option for us adjuvant patients to continue Herceptin for another year or more?

My onc. had said that she is expecting trials to begin where patients like us can continue Herceptin for 2 years. I will ask her about this when I see her in mid-March.
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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 02-23-2009, 04:49 PM   #4
SoCalGal
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had to log in just to comment on the avatar Hutch...who is that?
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1996 cancer WTF?! 1.3 cm lumpectomy Er/Pr neg. Her2+ (20nodes NEGATIVE) did CMF + rads. NED.
2002 recurrence. Bilateral mastectomy w/TFL autologous recon. Then ACx2. Skin lymphatic rash. Taxotere w/Herceptin x4. Herceptin/Xeloda. Finally stops spreading.
2003 - Back to surgery, remove skin mets, and will have surgery one week later when pathology can confirm margins.
‘03 latisimus dorsi flap to remove skin mets. CLEAN MARGINS. Continue single agent Herceptin thru 4/04. NED.
‘04 '05 & 06 tiny recurrences - scar line. surgery to cut out. NED each time.
1/2006 Rads again, to scar line. NED.

3/07 Heartbreaking news - mets! lungs.sternum. Try Tykerb/Xeloda. Tykerb/Carbo/Gemzar. Switch Oncs.
12/07 Herceptin.Tykerb. Markers go stable.
2/8/08 gamma knife 13mm stupid brain met.
3/08 Herceptin/tykerb/avastin/zometa.
3/09 brain NED. Lungs STABLE.
4/09 attack sternum (10 daysPHOTONS.5 days ELECTRONS)
9/09 MARKERS normal!
3/10 PET/CT=manubrium intensely metabolically active but stable. NEDhead.
Wash out 5/10 for tdm1 but 6/10 CT STABLE, PET improving. Markers normal. Brain NED. Resume just Herceptin plus ZOMETA
Dec 2010 Brain NED, lungs/sternum stable. markers normal.
MAR 2011 stop Herceptin/allergy! Go back on Tykerb and switch to Xgeva.
May-Aug 2011 Tykerb Herceptin Xgeva.
Sept 2011 Tykerb, Herceptin, Zometa, Avastin.
April 2012 sketchy drug trial in NYC. 6 weeks later I’m NED!
OCT 2012 PET/CT shows a bunch of freakin’ progression. Back to LA and Herceptin.avastin.zometa.
12/20/12 add in PERJETA!
March 2013 – 5 YEARS POST continue HAPZ
APRIL 2013 - 6 yrs stage 4. "FAILED" PETscan on 4/2/13
May 2013: rePetted - improvement in lungs, left adrenal stable, right 6th rib inactive, (must be PERJETA avastin) sternum and L1 fruckin'worsen. Drop zometa. ADD Xgeva. Doc says get rads consultant for L1 and possible biopsy of L1. I say, no thanks, doc. Lets see what xgeva brings to the table first. It's summer.
June-August 2013HAPX Herceptin Avastin Perjeta xgeva.
Sept - now - on chemo hold for calming tummy we hope. Markers stable for 2 months.
Nov 2013 - Herceptin-Perjeta-Avastin-Xgeva (collageneous colitis, which explains tummy probs, added Entocort)
December '13 BRAIN MRI ned in da head.
Jan 2014: CONTINUING on HAPX…
FEB 2014 PetCT clinical “impression”: 1. newbie nodule - SUV 1.5 right apical nodule, mildly hypermetabolic “suggestive” of worsening neoplastic lesion. 2. moderate worsening of the sternum – SUV 5.6 from 3.8
3. increasing sclerosis & decreasing activity of L1 met “suggests” mild healing. (SUV 9.4 v 12.1 in May ‘13)
4. scattered lung nodules, up to 5mm in size = stable, no increased activity
5. other small scattered sclerotic lesions, one in right iliac and one in thoracic vertebral body similar in appearance to L1 without PET activity and not clearly pathologic
APRIL 2014 - 6 YRS POST GAMMA ZAP, 7 YRS MBC & 18 YEARS FROM ORIGINAL DX!
October 2014: hold avastin, continue HPX
Feb 2015 Cancer you lost. NEDHEAD 7 years post gamma zap miracle, 8 years ST4, +19 yrs original diagnosis.
Continue HPX. Adding back Avastin
Nov 2015 pet/ct is mixed result. L1 SUV is worse. Continue Herceptin/avastin/xgeva. Might revisit Perjeta for L1. Meantime going for rads consult for L1
December 2015 - brain stable. Continue Herceptin, Perjeta, Avastin and xgeva.
Jan 2016: 5 days, 20 grays, Rads to L1 and continue on HAPX. I’m trying to "save" TDM1 for next line. Hope the rads work to quiet L1. Sciatic pain extraordinaire :((
Markers drop post rads.
2/24/16 HAP plus X - markers are down
SCIATIC PAIN DEAL BREAKER.
3/23/16 Laminectomy w/coflex implant L4/5. NO MORE SCIATIC PAIN!!! Healing.
APRIL 2016 - 9 YRS MBC
July 2016 - continue HAP plus Xgeva.
DEC 2016 - PETCT: mets to sternum, lungs, L1 still about the same in size and PET activity. Markers not bad. Not making changes if I don't need to. Herceptin/Perjeta/Avastin/Xgeva
APRIL 2017 10 YEARS MBC
December 2017 - Progression - gonna switch it up
FEB 2018 - Kadcyla 3 cycles ---->progression :(
MAY30th - bronchoscopy, w/foundation1 - her2 enriched
Aug 27, 2018 - start clinical trial ZW25
JAN 2019 - ZW25 seems to be keeping me stable
APRIL 2019 - ONE DOZEN YEARS LIVING METASTATIC
MAY 2019 - progression back on herceptin add xeloda
JUNE 2019 - "6 mos average survival" LMD & CNS new single brain met - one zap during 5 days true beam SBRT to cord met
10/30/19 - stable brain and cord. progression lungs and bones. washing out. applying for ds8201a w nivolumab. hope they take me.
12/27/19 - begin ds8401a w nivolumab. after 2nd cycle nodes melt away. after 3rd cycle chest scan shows Improvement, brain MRI shows improvement, resolved areas & nothing new. switch to plain ENHERTU. after 4th cycle, PETscan shows mostly resolved or improved results. Markers near normal. I'm stunned but grateful.
10/26/20 - June 2021 Tucatinib/xeloda/herceptin - stable ish.
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Old 02-23-2009, 05:52 PM   #5
Mary Anne in TX
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Hi! I did take close to 2 years of Herceptin alone. My onc and I both thought that I needed it. He had to fight for me over and over with my insurance co. they finally told me no more. I did have to pay a part of it, but I still believe that I needed every single bit I got! I'd still be on it, if I could. The battles were worth it! ma
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MA in TX.
Grateful for each and every day....

Diag. 12/05 at age 60
Stage II, Grade 3, 4.5 cm primary tumor
ER/PR- Her2 +3 strongly positive
Her2 by FISH 7.7 amplified
vascular invasion
Ki67 20% borderline
Jan - March '06 Taxotere/Adriamycin X 3 to try to shrink tumor - it grew
April '06 Rt Modified Radical Mas, 7 of 9 nodes positive
April - Aug. '06 Herceptin/Taxol/Carboplatin X 8 (dose dense)
Sept - Dec. '06 Navelbine/Herceptin x 8 (dose dense)
Radiation & Herceptin Jan. 22 - March 1, 2007
Finished Herceptin Dec. 10 '08! One extra year.
Port removed August, 2012.
8 1/2 years since diagnosis! 5 1/2 Years NED!
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Old 02-23-2009, 06:48 PM   #6
karen z
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Good question- I haven't come across anything and my doc has never brought up.
karen
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Old 02-23-2009, 08:54 PM   #7
Jean
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Hi Laurel,
My question is after our treatment of one year (which is what is now protocol) for most stage 1 Her2 patients, how long does the therapeutic value of herceptin last? How long is it expected to last?
Does anyone have written assesments on this?


I was interested in length of time that the herceptin has in our systems. Is it months? a year? two years?
Or even if the dr. have any information on this.
Or any studies?

Thanks all,
Jean
__________________
Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006

Last edited by Jean; 02-25-2009 at 09:50 AM..
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Old 02-24-2009, 05:00 PM   #8
Laurel
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Jean,

I think I read somewhere that Herceptin has a half-life of approx. 28 days. Perhaps its work has been accomplished in binding the majority (hopefully) of circulating Her2 + ca. cells over the year it is administered? This is an interesting post. I'll have to try poking around to see if I can find anything. Lani?
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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 02-24-2009, 07:50 PM   #9
StephN
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Wink

Hi Jean -
Before taking my two Herceptin Holidays, I have had this discussion with my med onc. The answer is that this drug has a long serum half life and takes an average of 18 - 20 weeks to clear your system.

I also recall in the early days of using Herceptin it was thought to have a much shorter half life and thus the three-week protocol was not ready for prime time until more studies came in to show that this was viable for patients.

Cut to the chase - I can feel comfortable taking a 12 week break and know that the drug is still working in my body - in both the intracellular and extracellular domains.

Hope this helps.

P.S. Laurel - I love your quizzical kitty. Is it a Burmese?
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"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 02-25-2009, 07:56 AM   #10
Paris
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Hi Jean, Do you mean how long herceptin suppresses the Her2 oncogene? I'd be very interested to know that. The most I've found in that regard is that the more aggressive subtypes Her2 bc and triple negative bc tend to recur earlier and then drop off as opposed to er breast cancer which maintains a steadier rate of recurrence.
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Diagnosed 11/06 IDC left breast Stage 1, High Grade w/extensive High Grade DCIS. Right breast extensive hyperplasia w/calcifications.
ER-/PR- HER2+++
Bi-lateral masectomy 12/15/06 w/expanders
SNB Node Negative
Chemo Taxotere, Cytoxan 2/07-4/07
Herceptin Started 5/07
Exchange surgery 6/15/07
Herceptin stopped after 12 rounds due to herceptin induced cardiomyopathy
On heart meds 'til?
Age 40 at diagnosis
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Old 02-25-2009, 07:57 AM   #11
Hopeful
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Jean,

My recollection is that it takes about 18 weeks to fully "clear" the body of Herceptin after treatment ends. (My onc said to me, "Don't tell me I never gave you anything!")

Insofar as the lasting effects of the drug, no one really knows. I recall two papers that came out in 2007 that did a cost/benefit analysis of Herceptin from an insurance perspective (one was a Medscape article). I have them somewhere, but not ready to hand. In that paper, they used an assumption that Herceptin would provide 3 years of protection, and did comment that they thought it was an "outside" estimate. Of course, these folks are bean-counters and not scientists, but that is what I can recall seeing.

Hopeful
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Old 02-25-2009, 08:46 AM   #12
Jean
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Paris,
Yes, you are correct...how long to fully clear the body.

Hopeful, interesting that we cannot find any aritcles on this?

Steph, thank you for confirming the length of time, yes that helps.

Here is a thought ladies: Paris writes,
"more aggressive subtypes Her2 bc and triple negative bc tend to recur earlier and then drop off as opposed to er breast cancer which maintains a steadier rate of recurrence. "

What are your thoughts for a triple neg...(sorry I mean triple positive)...who is er positive, that combo subtype. I am wondering if certain subtypes are being followed to examine the benefit of herceptin on a maintenance program?

Does this sound strange?
Has anyone discussed this topic or seen any articles, trials, etc. for those types?

Just thinking out loud...Thank you all for your replies.

jean
__________________
Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006

Last edited by Jean; 02-25-2009 at 09:50 AM..
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Old 02-25-2009, 09:13 AM   #13
Debbie L.
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Jean, I didn't understand what you were asking at first (and I'm still not entirely sure that I understand).

I'm hearing two questions here. If Herceptin is being given to control mets, then half-life has relevance. But I don't think that's what you're asking.

If Herceptin is given adjuvantly, it is my understanding that it's like chemo - the goal is to eradicate completely any stray cancer cells and "cure" the person of the cancer, during that time of administration. Of course the rub is that there's no way to know who those cured people are. But the theory as I understand it is that those who are not cured will recur at some point and then the game shifts to control rather than total eradication which may be possible with adjuvant treatment (which is not to say that there won't appear to be total eradication for long periods of time).

So half-life of Herceptin for adjuvant treatment isn't relevant. What IS relevant, and we do not know the answer yet, is how long to give Herceptin for best results. A small trial with a very short duration (six weeks?) appeared to do as well as the more-studied one-year duration (but it was not a head-to-head as far as chemo regimen, etc, and it was a small trial). But still, the results were as impressive as the one-year results were. Now there's at least one active trial looking at duration - one year vs. two years. I don't think we have any results yet, though.

Can you say more about your question? I'm still not clear. (And triple negative can't BE positive for ER and would not get Herceptin because HER2 is one of the negatives also.)

Again, being somewhat unsure what you're asking, I'm not sure if what I'm saying is even on-topic. I think that there is increasing interest (research) about triple positives (ERPR+ and HER2+) because there appear to be a subset (probably the highly ERPR+'s) in there who do very well and do not seem to have the typical HER2+ worse-prognosis. In addition, they need to figure out the best way to combine Herceptin (or other anti-HER2 treatment) with hormonal treatment for those who are less ERPR+ and/or are in the worse-prognosis group. But it seems like we're just beginning to hear these questions. I hope that all the adjuvant Herceptin trials that have already reported will begin sorting thru such details and at least clarifying what questions we should be asking.

Phew. Sorry - once I get started asking questions it's hard to reign the thoughts back in.

Debbie Laxague
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Old 02-25-2009, 10:10 AM   #14
Jean
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Hi Debbie,
You are on topic...
I aplogize I made a typo error and meant to type positive, (type way too fast)...haste does make waste.

Anyways, getting back to topic.
My thoughts of late have been on duration of herceptin and subtypes. What trials or studies are being done for the subtypes in regards to length of treatment, do we have any results thus far?

I was hoping that some information or data had been released and one of us had viewed it or had some knowledge in regards to adjuvent herceptin trials and offering details.

Just seems there is nothing reported on trials that would place the data in sub groups...as to length of time,
seems one lump sum of duration is what we now have,
I just thought at this point in time we may be hearing more data about subtypes.

I was also curious to the viabilty (length of time) do you think that the herceptin range would change due to subtypes, ( I know this may seem like a strange question Debbie) but it is something my thoughts had hit on.
As we know herceptin works for some not all, what if anything does subtypes play into that? Or does it equate at all?

Last but not least yes, I did not know what length of duration herceptin remained in our systems for
both the adjuvent setting and those patients who have spread of diesease, only knew that for some continued treatment of herceptin will work to remain NED.


Once again thanks,
Jean
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Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006
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Old 02-25-2009, 10:36 AM   #15
Debbie L.
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Interesting discussion! And even when we're not sure we're talking about the same thing, it turns out that we are.

I agree with you, Jean. It seemed like a big deal to figure out HER2 but now we see that might be just the tip of the iceberg.

And now I understand, and agree with, your question about duration related to subtypes. The biggest part of that question to me is to ask whether it might it be important that hormonal treatment for triple positives be accompanied by some sort of Herceptin (or other anti-HER2) for the duration of the hormone treatment? There have been suggestions that treating HER2 might reverse or control resistance to hormonal treatment. Perhaps it would turn out to be not even the same Herceptin dose/interval as is used for adjuvant treatment. Or maybe one of the other, newer, targeted treatments would be a better match. I know there are studies looking at hormonals+targeted agents of various kinds, in metastatic disease (and not just HER2+ disease).

Again, the adjuvant Herceptin trials were not designed to look at all these nuances (at least I don't think that they were). But they did track these things (ERPR positivity, etc) so even a retrospective look back at these subtypes will be of some use. It could at least clarify what the questions ARE that need to be asked. I hope that we start hearing these results soon.

Debbie Laxague
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Old 02-25-2009, 11:20 PM   #16
Jean
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Debbie had to chuckle....when I read...

"And even when we're not sure we're talking about the same thing, it turns out that we are. "

There is so much to be uncovered and discovered!
I appreciate your reply.

Best Wishes,
Jean

__________________
Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006
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Old 02-26-2009, 12:41 PM   #17
Savta
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Join Date: Nov 2008
Posts: 103
Just a thought on the Herceptin one year vs. two years....My oncologist also told me she would have no problem giving me an additional six months of Herceptin, after the initial year, but that I would have to finance it since the insurance would not cover it. But she also said she wouldn't recommend it, as studies done with Herceptin for nine weeks (I think in Finland?) showed results just as good as the one year plan, but that the accepted protocol is one year. Furthermore, there are studies going on giving Herceptin for two years, and the biggest proof that there don't seem to be any adavantage, is that the pharmecutical companies are not yelling from the rooftops how much better it is. They are interested in selling as much as they can, therefore, if there was any hint of an advantage, they'd be the first to announce it.
Seeing as Herceptin is a fairly new drug, we're all hoping we're on the right track.
Best of health to us all.
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