T1A (4mm), HER2+, No clear cut treatment plan
I was diagnosed with IDC - very small tumor (4mm) - and DCIS. Had lumpectomy mid-July with clear margins & no nodes affected. Path report indicates ER+/PR+/HER2+. I am a healthy 44-year old.
From what I have been told, my situation is somewhat unique as most small tumors are not HER2+ so there is not a lot of data to base a treatment plan on. The NCCN guidelines indicate no adjuvant therapy, radiation & tamoxefin only. But there is controversy about this and some research indicates that treatment should be given.
1st opinion strictly followed guidelines. Got 2nd opinion yesterday and they originally indicated 4-cycle TCH, Herceptin for a year. Asked about Herceptin alone and initial response was it is not typically done. Then 2nd doctor came in & said that there are many choices: TCH, Herceptin alone, Navelbine + Herceptin, or just radiation.
I don't want to be dealing with this again - I don't want to look back in 5-10 years and wish I had made a different decision. I am so confused and want to know what others in this situation have heard/done.
Comments
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Hi there...I was diagnosed in May 2008. I had a small 8mm tumor. I had a lumpectomy with no node involvement. My tumor was ER positive and Her 2 positive. I followed a trial at that time through Dana Farber and Sloan Kettering which many on this site have done. It is for small (under 1 cm, node negative Her positive tumors) I received Taxol and Herceptin for 12 weeks straight and then finished the Herceptin every three weeks for the remainder of the year. This treatment was very manageable. I believe that this is now a standard of care for similar tumors. Hope
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My tumors were larger, grade 3 and aggressive so I wasn't in the same boat but my suggestion would be to go with the most aggressive treatment and then you won't have any regrets.
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Hi, JSandstrom. Whatever direction you are leaning, you might ask to see the studies on which the recommended protocol is based. Some patients would be unlikely to agree to a treatment that isn't derived from a protocol that produced the best available results, unless it was in an advanced situation. Having said that, I asked for a second year of Herceptin, even though that protocol is linked to a study that is not yet complete. But that's on top of, not instead of, a complete course of chemo and Herceptin.
You can look these protocols up online, and some of them are linked to this website and others like it.
I hope this helps; there is nothing easy about early stage treatment decisions.
Cathy
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The problem is that there have been few or no studies with tumors this small so there really is no recommended protocol (at least that is what I have been told & been able to find on line). Most studies & guidelines are based on > 5mm.
I am afraid to go overboard and be completely aggressive (I also worry about the toxins that I would be putting into my body) but I also don't want any regrets either.
Jennifer
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There is actually a great retrospective study from MD Anderson on Her2 gals that were <1cm at dx. This study made it crystal clear that all tumors Her2 positive should do chemo, the relapse rate was high somewhere over 25 percent for the <1cm after no treatment.
I would highly suggest forging ahead with treatment.
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5mm to 1cm is the gray area. Dr. Winer at Dana Farber is doing that trial right now using Taxol only with Herceptin. There are standards on >1cm. <5mm the standard is as you said - not much if anything.
Some have pointed out that some of the aggressive prognostic factors like HER2 status and perhaps tumor grade, possible LVI (?), etc would cause one who is aggressive to lean more towards chemo.
For what it is worth, my wife had a 7mm DCIS with "suspicion of invasion", Grade 3, "possible" LVI, HER2+++, and 0/13 nodes. Sounded pretty manageable. Our decision at that time was similar, what treatment to do. That decision was made for us when an isolated 3cm met on the liver was also found. So much for Stage 1a, welcome to Stave IV.
Moral of the story, don't be fooled by the 'size' of a tumor being 'only' 4mm... other factors should be involved and treatment should be as aggressive (in my opinion) as you are willing to bear. (and the staging should be as complete as possible to rule out all possible other areas).
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My tumor was originally sized at .7mm - after the mastectomy, they said it looked more like .9cm - but they weren't sure (since the biopsy removed a lot and left a lot of scar tissue). My onc was shocked that it was Her2+ since it was "only" a Stage 1, Grade 1 tumor - so he sent it out to an independent lab for a second FISH test and it came back even more highly Her2+. So without a second's hesitation he said I needed Herceptin for a year - but to reduce toxicity to the heart - he put me on 4 months of Navelbine (every two weeks given with Herceptin).........it was very manageable; I didn't go bald (got a bit thinner) and had very minor digestion issues that lasted only a few hours.
Ask your onc if he's absolutely sure your tumor is Her2+.........get a second pathology lab to test the tumor if necessary - then if it really is, go for the Herceptin - if the onc won't give it to you without any chemo then ask if he can give you Navelbine. Good luck with your difficult decisions!
P.S. Edited to add: is there any chance you could have your tumor sent out for Oncotype DX? Mine was (before the results of FISH were know)..........it might help you in your decision making.
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It is only my humble opinion, but I can't imagine having a Her2 component and not going with an aggressive treatment plan, one that includes Herceptin. Her2 is like rocket fuel to a cancer cell. It is worth finding out the degree of Her2 in both your idc component and your dcis; as Sundiego points out, these cells don't roll like the others do.
I had a barely1.6 cm breast tumor, and a 2cm lymph node. Her2.
Sympathetic hug,
Cathy
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Go for Herceptin and chemo. HER2 is nothing to fool around with. Another way of looking at it perhaps--if you are trying to avoid the toxins now, you can do that but with HER2 being so aggressivie--you could possibly develop mets later and then you will really have to be treated wit very agressively, much more than the protocol you are looking at now. Good luck, this is a very difficult part of the process but once you have decided which is the best treatment for you, things will settle down and you can begin treatment. And before you know it, treatment will be finished.
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Check out these *links on Dr. Susan Love's site:
I have early stage disease. Can I use Herceptin?
http://www.dslrf.org/breastcancer/content.asp?L2=3&L3=7&SID=132&CID=585&PID=22&CATID=20My tumor is HER2-positive. What chemotherapy should I receive?
http://www.dslrf.org/breastcancer/content.asp?L2=3&L3=7&SID=132&CID=584&PID=22&CATID=20Additional links on Dr. Love's site regarding HER2 positive issues:
http://www.dslrf.org/breastcancer/content.asp?L2=3&L3=7&SID=132&PID=22&CATID=20------------------------------------------------------
*NOTE: for some reason the links don't work when you click on them so you'll have to copy and paste.
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mmm5 meant to say recurrence rates are high even for tumors< 1 cm.
Please see this link for statistics (from bluedasher):
http://community.breastcancer.org/forum/80/topic/742119?page=1#post_1556180
I read a subgroup analysis that indicated even very small Her2+ tumors <0.5 cm have high similar recurrence rates as tumors that at 0.5 cm to 1.0 cm. No way would I go without at least a mild chemo + herceptin (such as taxol + herceptin)
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Link to MD Anderson press release discussing a stude re: early-stage breast cancer patients with HER2 positive tumors one centimeter or smaller are at significant risk of recurrence of their disease.
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Thank you all for the great feedback. I will certainly take all of this into consideration after my 3rd opinion on Monday.
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I followed the middle link that Iago posted from Susan Love's site and IMO it is very out of date and especially is not good advice for someone who is stage I. Before Herceptin, Adriamcyn had a treatment advantage over the other chemotherapies for HER2+ tumors. But now we have Herceptin. Therapy with Herceptin plus a Taxane is about as effective as therapy with Adriamycin and Herceptin (there was no statistical difference between AC-TH and TCH arms in the BCIRG 006 study). Using a therapy with Adriamcyn and Herceptin greatly increases the risk of heart problems (over 2% of the women in the AC-TH arm had a grade 3 or grade 4 CHF develop). Both AC-TH and TCH were much more effective at preventing recurrence than AC-T (an Adriamycin therapy without Herceptin).
Susan Love doesn't seem to be keeping her website up to date - the first page only mentions earlier studies but doesn't include BCIRG 006.
They only recently started testing lighter therapies for Stage I HER2+ tumors. There are trials under way for 4 cycles of TCH vs 6 cycles (which is what BCIRG 006 tested) and using Taxol plus Herceptin. There are also some studies of Herceptin only for elderly women for whom chemo would be too great a risk. They all started fairly recently so none have published results and it may take several more years before they do.
I did TCH because it was a therapy that had been tested and shown good results with less side effects and long term risks than the other tested therapy AC-TH. I think that Taxol or Taxotere plus Herceptin would have also been a good choice for Stage I because the Carboplatin adds its share of side effects.
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I am in the same boat, 4mm Her2+. I am ER- and PR slightly positive. 1st opinion at local hospital said it is not the national standard to treat with chemo and herceptin but if I wanted them to, they would. 2nd opinion at bigger hospital said he doesn't care about the size of the tumor, he wants to treat the biology of it, recommended chemo and herceptin. 3rd opinion at a larger cancer institute said no chemo and herceptin because there are not enough studies to support the benefits on a tumor so small. Came down to I did not want to regret not being as aggressive as possible. This might be my only chance to have it cured. It is a very hard decision. I am waiting for the second of 6 rounds TCH. If you want to PM me feel free. I certainly understand the horror of making this decision. It comes down to you needing to do what is best for you and what you can live with. Unfortunately no one is making that decsion for us.
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My tumor was 7mm. My onc said that there are no "nice" HER2+ cancers. I did TCH x6 plus the year of herceptin without a question in my mind as to whether I was doing the right thing or not. I agree with what mommichelle said: this may be your only chance to have it cured. My thouhts are, if it comes back, at least it won't be because of something I didn't do.
In most cases if the tumor is 5mm-1 cm, chemo and herceptin is usually recommended (I think the ASCO guidelines use the word "considered") but I think that most doctors treat it unless there is a reason for not being healthy enough for it. With yours being 4mm, that to me is too close to the 5mm cut off. If it was 2mm or maybe even 3mm, I might think differently.
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Can someone help me????
I'm so confused. My first HER2 reading came after my biopsy. It came back from the lab and the fish test as equivocal (meaning I was in the gray area - not negative and not positive) but almost at a positive reading. After my lumpectomy, my path reports and fish came back as HER2- My onc said she went over the results with pathologist and said I was negative. I was gearing up for 8 rounds of AC and T
Today I get a phone call from the onc and she said that after further review they have decided to go with the original HER2+ result. She is sending my node path for the fish test.
What do I do? I am being treated at the Newton Wellsley Brest Center a good sized, recognized breast cancer center. I felt extremely confident with surgery and everything up to this point, but I don't know what to do now.
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Dear jag
I recommend treating as Her2+ and get chemo + herceptin. It turns out that Herceptin significantly reduces risk of recurrence about 50% for tumors that ever tested her2+, regardless of method or degree. The details are shown in the abstract of the study below. If you are not familiar with clinical studies, let me know and I will explain the rationale in detail
In this study - all classes of tumors that showed evidence of Her positivity (IHC 1+, 2+ 3+ and FISH+) benefited significantly from Herceptin, including tumors that scored IHC 1+ or 2+ and did notsubsequently test positive by FISH testing. From Journal of Clinical Oncology, 2007 ASCO Annual Meeting Proceedings (Post Meeting Edition). Vol 25, No 18S (June 20 Supplement), 2007: 511AbstractBenefit from adjuvant trastuzumab may not be confined to patients with IHC 3+ and/or FISH-positive tumors: Central testing results from NSABP B-31S. Pal, C. Kim...others511Background: Trastuzumab is a humanized monoclonal antibody targeted to HER2 protein and currently indicated for Her2 positive breast cancer defined by overexpression of Her2 protein (3+ IHC staining by HercepTest) or Her2 gene amplification (Her2/CEP17 ratio over 2 by PathVysion FISH assay). These criteria were determined for advanced disease but have not been formally tested in the adjuvant setting. We examined these tests' ability to predict benefit from adjuvant trastuzumab in NSABP B-31. METHODS: All available tumor tissue blocks from the B-31 trial were sujected to HercepTest and PathVysion assay as defined in the B-31 protocol. Formal statistical test of interaction between HER2 levels measured by these two tests and benefit from trastuzumab was performed. RESULTS: 207 or 1795 cases (11.5%) showed gene amplificiation as as determined by PathVysion, and 255 of 1662 (15.3%) showed overepression as determined by HercepTest. 161 of 1662 (9.7%) had neither gene amplificiation nor overexpression There was a consistent benefit from trastuzumab in every subset defined by IHC or FISH. No statistical interaction was found between DFS benefit from trastuzumab and level of protein (p = 0.26) or Her 2 gene copy number (p= 0.60). Benefit was observed in patients with tumors that were negative for FISH and had less than 3+ staining intensity on IHC by HercepTest (RR= 0.36, p = 0.32). CONCLUSION: Current definition of HER2 overexpression/gene amplificiation based on data from adjvanced disease may need to modified for the adjuvant setting.In all categories of Her2+, regardless of degree or how measured, relative risk with Herceptin was less than half of what it was without. And all results were highly statistically significant, meaning results were likely not due to random chance. -
I have no horse in this race...but I have a question. A lot of DCIS is technically HER2+, I wonder if with the tiny tiny tumors, the HER2 has not had a chance to shift? This is based on nothing but my own conjecture after reading the microinvasion thread.
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jag- I had a similar situation to yours. IHC from biopsy came back equivocal, FISH from biopsy came back highly positive but I asked them to retest on the lumpectomy tumor which came back negative. To make a long story short, the conclusion was that my tumor was heterogeneous and for the most part was HER2- but there were sections of the tumor that were HER2+.
The tumor was grade 1 and my oncotype came back 19 (low intermediate) so with all of that information in hand my onc decided to treat with Taxotere/Cytoxan x 4 plus the herceptin for a year. For me the TC was very manageable and I have no side effects as of yet from herceptin which I've been on for 3 months. My veins were good so with this regimen, I'm doing this without a port and I have no problems. Also, I used penguin cold caps so I didn't lose my hair with the TC.
Like bluedasher - I was shocked at how outdated Dr. Susan Love's site is.
JSandstrom- Although I did not have a very small tumor I still agree with the posting on this thread that you should treat the HER2+ part of it. In the past, tumors that small were not even detectable so hopefully now that they are detecting the tumors earlier there will be more treatment information available.
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DRIM- I have 1/4 nodes involved and I'm being treated with AC first. I looked into the cold caps but wasn't sure I could handle how much work they are especially if they didn't work for me. Can you please give me some more info on them? My doc doesn't want to do an oncotype because of the one node being involved, she said the score wouldn't matter at this point?????
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Jag - I think your onc is right about the oncotype. They do have test results for node positive but between the node and the HER2+ I'm not even sure insurance would pay for that test. With the 1 positive node I can understand your onc wanting a more aggressive treatment, however as bluedasher pointed out, the combination of AC and H increases the risk of heart problems. If you are definitely going to get herceptin you might want to talk that over with your onc.
As far as the caps, you can check out the thread - Cold Cap Users, Past and Present to Save Hair. It seems to work with all breast cancer therapies - some better than others. It depends on the individual as well. Thickness of hair and liver condition are other factors as well. It definitely is a bunch of work for sure.
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My tumor was less than 1 cm, SNB neg and no nodes involved. I got two opinions and both felt with HER 2+ the chances of recurrence were very high. My suggested treatment was 6 of TCH which I am about to do my fifth and then 9 months of herceptin. Both oncologists told me without chemo, they could be sure it would return and then they could only treat me not cure me. I opted to take the aggressive approach. Although my side effects have been tough, I, like you, don't want to look back in 5 years and say why didn't I do chemotherapy. Of course, it is a personal decision and one you should make with a lot of research and I feel, two opinions.
Isabel
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I had an area of micro-invasion of 1.2 mm, er-, node neg, but HER2 positive. I knew I was in a gray area and thought that there would be some discussion as to a course of action, but my MD Anderson oncologist said that the best results will be with AC-TH treatment. It took days for me to accept the risks involved with the adriamycin. But I finally decided that I would rather not slowly die from cancer recurrences. I researched and found a good article stating the risk factors for cardio-toxicity and I realized that I am in a low risk group ( age, good heart function, and less than 400mg/meter squared cumulative dose.) Studies show that if one stays below that dose, there is less than 3% risk of heart problems. So, I am trusting statistics. I'm still worried, but I am at peace with the regimen.
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I am in the same boat but I have 2 tumors 4mm or <, her2 pos. having sentinal node biopsy Tuesday. From what I understand there is a big conference out west somewhere this week on how to treat this controversial groupl
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Dr. Love doesn't appear to be keeping her web site answers on Herceptin up to date - for example the answer on what type of chemo therapy. And she doesn't have anything addressing the particular issue of Stage I.
MD Anderson released a retrospective study in December 2008 that looked at outcomes for node-negative tumors less than 1 cm no chemo and no Herceptin. For HER2+ tumors, they found 5 year recurrence free survival was 77% and 5-year distant recurrence free survival was 86%. For comparison, those numbers were 95% and 97.5% for hormone+, HER2- and 85% and 96% for tripple negative. So the HER2+ group had about 23% risk of recurrence and 14% risk of Stage IV metatstic recurrence.
It is that sort of data that is changing the view on whether chemo should be given for HER2+ Stage Ia and Ib tumors. Even if the NCCN guidelines haven't been changed to reflect that yet, there is a lot of thought that chemo should be given for all invasive HER2+ tumors, even the very small ones. Then the question becomes which chemo.
BCIRG 006 tested AC-TH and TCH vs AC-T for HER2+ patients. For node negative (which would have included larger Stage 1c and II tumors so our Stage Ia and 1b numbers should be better), disease free 5-year survival was 93% for AC-TH, 90% for TCH and 85% for AC-T. That is quite an improvement from the 77% MD Anderson found with no chemo.While AC-TH chemo had slightly better (but not significant) results, it also carries a much greater risk of heart damage and a small risk of leukemia. Those risks, IMO, outweigh any slight improvement in disease free survival especially for Stage I.
A "lighter" chemo plus Herceptin such as Taxol or Navelbine plus Herceptin may be enough for Stage I but the studies on this were only started a few years ago and last I checked they hadn't released results yet.
Diane, The San Antonio Breast Cancer Symposium was Dec 6-10. That's where a lot of research is presented. Sometimes they have interim results of studies.
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