Taxol and Herceptin for small node negative breast cancer
Hi everyone,
Just wondering if they are still treating small under 1 cm node negitive HER2positive breast cancer with Taxol and Herceptin. Taxol and Herceptin for 12 weeks and then Herceptin for the remaining year every third week? Sending warm sunny thoughts to everyone!!!
Comments
-
Yes! i had this treatment and it worked out well very minimal side effects from the taxol and was definately dueable i worked throughout, also i didnt not loose any hair i used the penguin cold caps and lost no hair on my head did loose hair everywhere else and my eyebrows thinned considereable and after three weeks post my last taxol still no hair on my legs:)
-
I don't think there is any study that has released results for the treatment. There are some studies underway of Taxol and Herceptin for Stage I, but the ones I've seen were just getting started 2 years ago and I expect it would take longer before they would have preliminary results.
-
what is the penquin cap? I am facing AC-TH chemo, would really like to have TCH but doubt my oncologist would go for it. I am er/pr (-) and Her2+ Not looking forward to losing my hair, it is down to the middle of my back and I get lots of comliments on itl..getting it cut very short tomorrow in anticipation of the loss. Also, not looking forward to the possible heart damage from the AC around of chemo
thanks
-
Tdsmgb the penguin cap is a cooling cap to save ur hair check out the thread call penguin cold cap users past and present or click on my name n see where I have posted to find it that way there are lots of us who have kept our hair through Chemo tch has great results not positive about ac but the woman will answer u if u post there lots of woman do tch with her2 positive especially if ur node negative but there are lots with node positive too who have done tch b/c of the heart issue possibility with ac and with herceptin keeping my hair meant so much! Let me know if u have more questions!
-
This is the treatment I am currently on. It was recommended by two out of three of the oncologists I interviewed before beginning treatment.
-
Fluffqueen...thats great! How are you feeling? How is the treatment going for you?
-
I did the taxol for 12 weeks and the herceptin for a year every 3 weeks. I finished the herceptin a year ago in March and I am now past 2 years NED. Compared to a lot of chemos this is easy to do. If I had not been HER2++ I would just have done rads and no chemo, but the HER2 meant needing herceptin and they did not do herceptin without chemo so the taxol weekly was the one most easily tolerated. Hope this helps. Annette
-
update on my care: finished the E/C chemo (adriamycin was in short supply), it was tough, but predictable. The week of chemo spent in bed or bedridden, the following week, high energy and got everything done for 2wks in 1. The Taxol/ Herceptin regiment, for me, a lot harder to tolerate. The Taxol at 100% strength, I cannt tolerate. Have had it reduced to 75% for treatment 2 & 3, back up to 100% for #4, could not tolerate it. I have severe neuropathy, the numbness doesn't leave on 100%. Had it reduced again to 75% for #5 and #6 we tried it at 7/8 strength. Have had some neuropathy, but it is tolerable. I have reflexology and that helps. I ballroom dance and have not stopped, it is hard at times, my balance is affected. I have #7 this coming Monday. Cannot wait for the weekly Taxol to be over! No taste buds, still, it has been 4 months without taste buds and my mouth always has a sickly sweet flavor to it and my saliva is very thick. My hair loss began on day 14 of the E/C chemo and is coming back in on the Taxol. I eat only 1 meal a day as I am not hungry, but the weight gain hasn't come off. Gained 10 lbs on the E/C and on the 1st Herceptin treatment, I gained another 8 lbs. Have lost those 8, but have had to buy clothes 2 sizes larger than I normally wear. My liver panel is all over the place too, have been sent to a liver specialist. Had a full body scan before the E/C chemo was started and no cancer was found. I am also anemic, which my oncologist knows about but is not concerned, the liver specialist is tho. I am concerned as my glucose is high, no one is concerned about that either. Father and his mother were adult onset diabetics, my Drs. know this and are not concerned.
My dx was stage 1B, but am being treated as if I were stage 4 as my tumor grade was a 3. No lymph node involvement, cancer was invasive, but have clear margins after 2 surgeries. I am er- / pr- but am Her2+. I had a partial mastectomy against my own better judgement, was talked into that proceedure by 3 Drs and my husband. Radiation will begin after Taxol is completed. That will be the std 6 wks daily and the Herceptin continues every 3wks til end of March 2012. Long process and then the 2 yr wait begins. I have been told that I have a 90% chance of recurrence in the 1st 2 years. I hope they are wrong. Tying to stay possitive is not an easy task, but am living day to day and sometimes hour to hour or min by min.
-
Teri - I don't know who told you that you have a 90% chance of recurrence, but that is bullshit. I was told 23% and having chemo/herceptin would halve it. Maybe you mistunderstood what they said. I don't think you are being treated like you are Stage IV - all HER2 +ve bc is treated in the same way if it is bigger than 1cm. My tumour was smaller than yours and I had TCH. I scored the highest score for everything that makes up the grade.
Sue
-
Was told that because of the tumor grade and the type of receptor I have that the treatment recommended is for stage 4. Looked it up online too, and the protocol that I am on is for stage 4. It is the the gold standard for grade 3, hormone neg and her2 possitive, but also same treatment for stage 4 bc only the herceptin is an added drug. No tamoxafin for me. As far as the 90% recurrence, they do not know if it has invaded the blood, if so the 90% stands as a chance of recurrence. 2-5 yr survival is 50%. I hope they are wrong, as it is not in lymph nodes and I truely believe it did not have time to travel w/in the blood. Just want to this to be over done with, want the radiation to be here and gone too. So far diag to time in treatment has been 5 months and it is getting really old! The support here at the chemo ctr, is not good, they are way over booked and overwhelmed w/cancer patients. My network of friends who have gone thru this those who have not, has been remarkable. I wouldn't be getting thru this w/o them. I
My Drs all thought for sure that it would be in my nodes, the only Dr who said it wasn't was the radiologist. It is what is is, I am trying to make the best of this situation, but it is already getting old, wearing the wigs, and I have 9 so far, too many to choose from. The process is much longer than any of my friends had to go thru. I know this is not curable as I was not insitu but still feel like for all the inconvoence and annoyances this bc has caused, I will survive, I have to, way too many ppp in my life that I need to piss-off! Thanks for responds Sue, btw love your nickname
-
Teri - maybe the hormone negative bit has an impact, but please don't think you are being treated as if you are stage iv - lots of us have the exact same treatment and are stage 1 like you. Yes, they may use the same drugs, but they are used for all stages. I'll see if I can find out any more positive recurrence rates - I'm good at googling
Sue
-
tdsgmb,
I still believe that the % risk of recurrence you got is wrong. I am Stage 3, Grade 3, ER+ and highly HER2 positive. I had 7 tumors in my armpit. I got the risk of recurrence at 20 % without any AI's, if I take any form (Femara, Aromasin) it will lower the risk to 10 %.
They don't know if any of the cancerous cell traveled with my blood either.
-
tdsmgb,
I believe you may have misundestood your chance of reccurence. I have almost the exact diagnosis and have seen 3 oncologists (2 in San Antonio and 1 in Austin). They have all given me the same recommendation: TCH - 6 treatments with 1 year of Heceptin and they have all put my recurrence rate between 5% and 10%. I had a BMX with reconstruction on 2/28/11 and the detailed path found 3 additional small tumors in the left breast and 1 in the right (I only had the right breast removed as a preventative measure). There was no node involvement but all the tumors were invasive. Pet Scan showed no mets. I consider myself very lucky that I decided on the BMX. Chemo was delayed about a month because I have had incision problems with the reconstruction, but it looks like I'll be ready to go the first week in June. I have been reading about the weight gain. Does anyone know what causes that during chemo?
-
Renee,
I think the steroids and the other meds can cause you to gain weight while on chemo. I had DD AC and then Taxol (and Herceptin) and I didn't gain any weight at all. After chemo I weight pretty much the same as before, a couple of Lb up and down every week.
-
T eri - I found this table - will look for more. Yes, being hormone receptor negative does have an impact, but the survival is way better than you were told.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705275/table/t4/
Sue
-
steroids and lack of stamina and energy have played a huge part in my weight gain.
-
thanks Sue, makes me feel a whole lot better
-
rgd1959, I asked me onc for the tch protocol and he said no, it was not, in his opinion the recommended treatment for my cancer. A friend of mine, she was on it, but her bc was not the same as mine either
-
intwoplaces, what is Als and femara, aromasin?
-
It is my understanding that Stage IV is treated with a completely different philosophy than early stages. Early stage the are very aggressive assuming they can cure. Stage IV they treat as a manageable disease hoping to slow, stop or remission growth also considering quality of life. Many times stage IV is NOT treated as aggressively as earlier stages. As the cancer becomes resistant to treatment then more aggressive treatment follow.
Teri my point is you should be treated more aggressively than stage IV… and it's a good thing you are. I also think you misunderstood your recurrence risk. I would ask your onc for the numbers again. The reason they are treating you so aggressively with chemo is chemo, Herceptin and radiation are the only guns they can use on you. After the year of Herceptin you're done with treatment. Hormone positives have another 4 years of treatment with a drug. Yes they want to hit you hard so it kills what ever might have escaped, if anything at all.
-
Teri - I'm glad you came back and saw the table. AI's are aromatose inhibitors (eg Arimidex) given to post menopausal women who were hormone receptor positive - you won't be given anything like that as you are negative. You might see some people having Tamoxifen - that is for pre menopausal women who are hormone receptor positive.
Stay strong - you'll get through it.
Sue
-
Teri, if you haven't misunderstood your oncologists, then you need to find some other ones to talk to because it seems like they are giving you very incorrect information. HER2- tumors are almost always grade 2 or 3 because the are aggressive, but the chemo you are getting is very effective.
Retrospective studies of women with node negative tumors less than 1 cm (i.e. stage 1a or 1b) who didn't have chemo at all, found 5-year recurrence free survival of 77%. That means that recurrence occured for about 23%. That is why chemo is a good choice for all stages of HER2+.The reserach was done by MD Anderson and the results were presented at the 2008 San Antonio conference.
There also were some recent small retrospective sudies on women with Stage I HER2+ who had chemo and Herceptin that found no recurrences. So, it seems that chemo may have taken our chance of recurrence down from 23% to less than 1% - a far cry from the 90% that you were told.
The research on chemos until recently has focused on stage II and higher so they don't have different chemos for stage I, though there is currently some research underway to see if something like just Taxol and Herceptin would be effective for Stage I Her2+. That is why us Stage I folks often get the same chemo as Stage II through IV. I think TCH which is about the same effectiveness as AC-TH but less long term side effects is generally a better choice for early stage.
-
Blue Dasher...I did the small no node Taxol and Herceptin trial for 12 weeks started in July of 08. I was wondering where I could find the results of the small retrospective study you were talking about above...Thanks and hoping that you are well!
-
There were two small studies mentioned on this board a while ago. I've bumped the thread that has the links to them just in case the link I put here doesn't work:
http://community.breastcancer.org/forum/80/topic/763528?page=1
The title of the thread is:
Chance of recurrence small node neg her2+ treated with herceptin
-
The following link has the poster session slides that go with the first abstract and have a bit more information:
The presentation is Abstract 228 Author Heather McArthur about 2/3 of the way down the page. This is the larger study which had about 150 who got Herceptin and 100 who didn't.The downside is that the median follow-up was just under 2 years for the Herceptin group. The group had 32 with 3 years and a few with 4 years of follow-up. Herceptin hasn't been given to Stage I women for long enough to have 5 year DFS numbers.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team