HonCode

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

Reply
 
Thread Tools Display Modes
Old 09-27-2011, 10:19 AM   #1
Lani
Senior Member
 
Join Date: Mar 2006
Posts: 4,778
Thumbs up long remission possible in advanced breast cancer in a subgroup of her2+ patients

ECCO-ESMO: Long Remission Possible in Advanced Breast Cancer


This report is part of a 12-month Clinical Context series.

September 26, 2011

STOCKHOLM -- A small proportion of metastatic breast cancer patients can achieve complete remission that lasts with trastuzumab (Herceptin) plus chemotherapy, researchers said here.
In a two-center study, almost 10% of HER2-positive metastatic breast cancer patients achieved a "durable complete remission," defined as being disease-free for at least three years, according to Giuseppe Gullo, MD, of St. Vincent's University Hospital in Dublin.

He reported the findings during a scientific session here at the European Multidisciplinary Cancer Congress, formerly known as the joint congress of the European Cancer Organization and European Society for Medical Oncology (ECCO-ESMO).

"It's not a statistical analysis," Gullo cautioned, "but durable complete remission is more frequently connected to being diagnosed in the sixth decade, being ER-negative, and having liver-only disease metastases."

Gullo explained that durable complete remission after treatment with trastuzumab and chemotherapy for HER2-positive metastatic breast cancer has been reported anecdotally in the literature, but there are a lack of data on its long-term outcomes.

There are also scant data on the optimal duration of maintenance trastuzumab after complete remission.

So he and his colleagues conducted a retrospective review of 120 patients who were treated between May 2000 and April 2011 with the combination therapy at two institutions, St. Vincent's University Hospital in Dublin and Humanitas Cancer Center in Milan.

The primary goal was to assess the long-term outcome of patients achieving durable complete response; secondary aims included exploration of the clinical features associated with this type of response.

Durable complete remission was defined by RECIST 1.1 criteria lasting at least 36 months.

Gullo and colleagues found that 11 patients, or 9% of the total population, achieved this level of remission during a median of 6.5 years of follow-up. Median age was 59 and the median duration of trastuzumab was 63 months.

Gullo cautioned that the research team did not perform a statistical analysis, but numerically, durable complete remission was linked with ER- or PR-negative disease or if they were diagnosed in their 60s.

Also, a larger proportion of those with durable complete remission had liver-only metastases compared with those who didn't have durable remission (55% versus 18%).

Three patients relapsed on maintenance trastuzumab -- at 49, 53, and 94 months, respectively.

Five patients discontinued maintenance trastuzumab, and only one of those had ipsilateral breast relapse 52 months after stopping the therapy, Gullo said.

He added that four patients are still on maintenance trastuzumab, and nine patients are still alive and in complete remission. Seven of them never relapsed.

Among those seven, the median age is 60, 71% are ER- and PR-negative, 57% have liver-only metastatic disease, and all had first-line chemotherapy plus trastuzumab -- four had docetaxel/carboplatin, two had a single-agent taxane, and one had capecitabine.

Gullo said the data suggest that in some cases of durable complete remission, maintenance trastuzumab can be safely discontinued with a very low risk of subsequent relapse.

"In our experience, discontinuation of maintenance trastuzumab was not associated with increased disease relapse," he said, again cautioning the lack of statistical analysis. "We can't answer the question about optimal duration, but discontinuation does not appear to be associated with relapse."

However, Martine Piccart-Gebhart, MD, PhD, of the Jules Bordet Institute in Brussels, said the study is "too small to suggest the discontinuation of trastuzumab after 36 months," a sentiment echoed by many in attendance at the session.

Piccart-Gebhart also noted that although seeing the characteristics that may be tied to durable complete remission, the study was "far too small to draw conclusions about clinical subgroups most likely to achieve long-term remission."

Still, she said, Gullo's is the first report on the long-term use of trastuzumab in the advanced setting, and it "points to the existence" of HER2-positive tumors that are "truly addicted to HER2," as they show long-lasting remission under the therapy.

Gullo said there's a need for further study of molecular and cytogenetic profiles of these tumors in order to better target which patients may be more likely to achieve durable complete remission on trastuzumab plus chemotherapy.

The researchers reported no conflicts of interest.



Primary source: European Multidisciplinary Cancer Congress
Source reference:
Gullo G, et al "Long-term outcome of HER2-positive metastatic breast cancer patients achieving durable complete remission after trastuzumab-containing chemotherapy" ECCO-ESMO 2011; Abstract 5000.
Lani is offline   Reply With Quote
Old 09-27-2011, 06:20 PM   #2
KristinSchwick
Senior Member
 
KristinSchwick's Avatar
 
Join Date: Jun 2011
Location: Iowa
Posts: 231
Re: long remission possible in advanced breast cancer in a subgroup of her2+ patients

What a great word of hope for those of us who have been sooooo unlucky with our stage IV battles. 10% can have long term remission- what a huge improvement from like 0. I bet in a few years it will be more like 25%.
__________________
[B]Kristin
Aug 2010: diagnosed stage 3b, 4 mo. after birth of son. 29 yrs old and breastfeeding, ER/PR-, Her-2+ started Neoadjuvant therapy: 4x FEC, 10x abraxane & Herceptin
Feb 2011: L mx with recon. Path. showed only DCIS but 4/10+ nodes.
March 2011: 6 wks rads.
Mother passed, lower back pain.
Late May 2011: Bone mets but organs clear; Tykerb, Xeloda, Xgeva. Stopped Herceptin. Implant infected: removed implant.
October 2011: Bone progression; Gemzar and Carboplatin & restarted Herceptin.
Jan 2012: Progression, re-classified as ER+; Tykerb, Herceptin, Zoladex & Femara. Anti-E is working!
May 2012: ovaries out, markers stable but elevated. Cont. Herceptin, Tykerb, Xgeva & Femara.
Dec 2012: aromasin
Jan 2013: faslodex, herceptin, tykerb
Jun: Kadcyla
Aug: Rads to hip, then Perjeta, Herceptin & Taxotere
Nov 2013: Perjeta, Herceptin, Halaven
Early 2014: Affinitor, Aromasin, Perjeta, Herceptin.
June 2014: Estradiol, Perjeta, Herceptin
Aug 14: Tamoxofin, H & P
http://kristin-notdying-blog.blogspot.com/
KristinSchwick 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 12:53 AM.


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