 |
06-28-2010, 03:32 AM
|
#1
|
|
Senior Member
Join Date: Mar 2006
Posts: 4,783
|
ASCo report--the more things change, the more things change
A Swedish study looked at primary tumors and biopsied their metastases to see if ER, PR status changed
I dubbed it the"the more things change....the more things change" study
ERstatus changed + to - 27% of the time, from - to + 8% of the time
PRstatus changed + to - 38%of the time, from - to + 5 % of the time
They plotted out the survival curves (prognoses) of all four combinations of
primary vs met an found
+ primary assoctd w + met did best
- primary assoctd w +met did second best
+ primary assoctd w - met did next to worst(had 1.5 tp 2 times the risk of dying at any one point of time)
- primary assoctd wit - met did the worst
Another study showed the rates of concordance between primary tumor and mets (including her2) were
14.5% had a change of ER statys
49%had a change of PR status
14% had a change of her2 status
overall the treatments of 12%of those patients developing metatasis should have changed after biopsy
The above study looked at liver mets
her2 discordance was 3.5% + to -, __% -to +(hope the talk is on the virtual meeting as I missed that %)
I hope this encourages doctors, patients and insurance companies to come together and make biopsying mets an integral part of treatment.
It doesn't help if you have a smart bomb if the target has changed!
|
|
|
06-28-2010, 12:23 PM
|
#2
|
|
Senior Member
Join Date: Oct 2005
Posts: 3,519
|
Re: ASCo report--the more things change, the more things change
I would agree to a degree... but keep in mind that not all mets are able to be biopsied.
Also, as my docs have confirmed, the biopsied sample may not tell you everything about the met. Within any given tumor, there may be areas with differing cells. Part of a tumor can show ER+ and a different part can show ER-.
My first recurrence was able to be biopsied. It showed what looked like the cancer had switched from ER+ to ER-. At that point we discontinued Aromasin. Last summer, once we kept seeing brain mets, etc., my doc decided it was worth adding back in the Aromasin to see if there was a chance that we were ignoring an important potential target and if the biopsy a few years before was partially misleading. Aromasin being the only change we enacted at that time seemed to gain us some footing and stability. Once we saw the tiniest new spot on the adrenal back in March, we switched again, this time back to Tamoxifen. TMs have continued to drop, scans have continued to show clear in the brain, and we will MRI the adrenal spot next month to see what it is doing, hopefully shrinking.
My point being that yes! biopsying mets is a tremendously important piece of information, but it is not always possible and it can still only yield a part of the whole picture... sadly, if depended on too heavily, it might also mislead and may send you down the wrong path, too.
__________________
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."
Last edited by hutchibk; 06-28-2010 at 12:25 PM..
|
|
|
06-28-2010, 12:38 PM
|
#3
|
|
Senior Member
Join Date: Mar 2006
Posts: 4,783
|
Re: ASCo report--the more things change, the more things change
It seems to me it is better than NOT biopsying.
FYI when they look at circulating tumor cells in metastatic bc patients, they find all kinds of combinations floating around, not just those the patients are being treated for ie, triple negative CTCs in her2+ Stage IV patients being treated with herceptin
|
|
|
06-28-2010, 12:55 PM
|
#4
|
|
Senior Member
Join Date: Oct 2005
Posts: 3,519
|
Re: ASCo report--the more things change, the more things change
If it can be biopsied, of course, it is one more piece of info that can be tremendously integral to the whole picture.
I am not arguing your post, I am adding more info to the bigger picture.
__________________
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."
|
|
|
06-28-2010, 03:16 PM
|
#5
|
|
Senior Member
Join Date: Sep 2005
Posts: 556
|
Re: ASCo report--the more things change, the more things change
Lani,
Just want to find out if doing biopsy of CTCs is a proven method and whether oncologists will agree to do that.
As Brenda mentioned I have mediastinal mets and I would like them to see if anything changed but my onc. wouldn't do that because it is an invasive procedure.
Julie
__________________
Diagnosed in Sept 2004 while pregnant with the second child. Stage 3b, tumor 4.5cm, 4 auxillary and supraclav node positive. Her2+++ FISH 9.4 and er-,pr-.
Had dose dense neoadjuvant AC,Taxol then mastectomy,radiation+xeloda+Herceptin.
|
|
|
06-29-2010, 01:46 PM
|
#6
|
|
Senior Member
Join Date: Mar 2006
Posts: 4,783
|
Re: ASCo report--the more things change, the more things change
Julie, ctcs do not need to be biopsied. They just take a small tube worth of blood from you like any other blood test. No they are not proven to represent mets and often have different characteristics (ER, PR her2 Status) than either the primary or the met.
I believe there is something called a mediastinoscope, sort of like a laparascope for abdominal procedures or an arthroscope for joint procedures. Depending on where your mediastinal nodes are and how big they are, perhaps they could be biopsied by this minimally invasive procedure. I believe it is done by thoracic surgeons.
Oncologists are medically trained and not surgically trained. To many of them a bone marrow biopsy is too big of an invasive procedure (it is minimally invasive as well and has an ill-deserved reputation, probably because oncologists don't like ANY invasive procedure (that is why they went into medicine and not surgery!)
I know little about mediastinoscopy, other than that it can be done. Can you ask for /refer yourself to / have your radiation oncologist**
refer you to a thoracic surgeon just to find out if it would be appropriate. You can cite the ASCO talk I referenced about the percentage of cases in which treatment might be changed depending on the results.
**they seem to interface more easily with the surgeons it seems.
Good luck!
|
|
|
Posting Rules
|
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts
HTML code is Off
|
|
|
All times are GMT -7. The time now is 04:47 AM.
|