Stage I Breast Cancer
Anybody out there have anything supportive to say? Any information about Arimidex?
Comments
-
I was also stage 1 and I refused any anti-hormonal medication. I did the surgeries and radiation and also had a hysterectomy & oomphectomy. Many of the women on the boards will tell you to try it before you decide not to do it. It's a very personal decision. How comfortable do you feel about not doing it? To me, the reduction in the risk was not worth it. Have your onc run your information through the on line risk calculator and that may help you make your decision.
Good Luck -
Also, another approach is to try it, and if you have bad side effects you can stop.
I don't know any reason you cannot stop if the side effects are bad. For reasons unknown, some gals have little or no problems, others have a lot of problems.
So do the checking ADK suggested, so you know what you are risking.
Gentle hugs, Shirlann -
I agree with Shirlann - try it and if you have bad side effects stop.
Are you worried that your cancer will re-occur? Although Stage I has a smaller chance of that it does happen. Hormonal treatments offer protection against that.
You are deciding that you won't like it before you've even tried it. -
With osteopenia, a mother with osteoporosis, and bc treatment with Arimidex, you'd be a candidate for yet another drug that might help with the thinning bones--a bisphosphonate like Fosamax.
-
Can you consider tamoxafin? Although the AIs are the new gold standard for postmenopausal women, Tamoxafin is also quite effective in preventing recurrance. In your case, tamox has the added benefit of working to preserve bone mass.
I am also a stage 1. I am currently on tamox and plan to take it 2-3yrs and then finish out the 5yrs with an AI, thus hopefully minimizing the SEs of both (possible uterine changes with tamox/ vs bone/cardiovascular issues with the AIs). I am premeno at 49, taking zolodex and hoping to go into menopause naturally soon, or possibly have an oopherectomy.
I have been on tamox for about 9 mths with no major complaints. We have more heart/blood pressure issues in our family hx, so I am more afraid of the AIs than the tamox.
Good luck with your decision.
Julie -
I had Stage 1 and thought it would be treated with lumpectomy followed by radiation and tamixifen. As it turned out, bilateral mastectomy was indicated. Follwing this, they told me I don't even need tamoxifen because my tumor was only 1 cm and I have no more breast tissue to contend with. Having the bil mast actually opened other doors for me.
-
Hummm. A question to ask is whether since you were on HRT when you developed the cancer if they consider you to be pre-menopausal.
Certainly your hormone levels WERE higher when you were on HRT, but since you've probably stopped that do they categorize you as menopausal. -
Tamoxifen has been around for about 25 - 30 yrs. All of its effects are well documented. It blocks the receptor cells. Arimidex reduces estrogen in body.
Why not consider Tamoxifen? What was the percent of receptors of your tumor? If very low maybe you could get a second opinion on taking any hormone treatment.
I really am shocked that your doc is giving you Arimidex when you have osteopenia. Arimidex is new on the market -- long term benefits and side effects are not fully known yet.
My onc told me that Tamoxifen has been shown to increase bone density.
Reducing the estrogen in your body - with Arimidex - just doesn't sound good for osteopenia bones. Or osteoarthritis.
I'ld get a second opinion. And check your path report for the receptor percent. -
I always try to remind myself that my doctor is obligated to share ALL POSSIBLE side effects with me, whether they are considered likely, less likely, rare, or extremely rare. (I'm a bit of a side-effect freak-outer!) You may actually experience few or even none of the listed side effects.
Of course, a drug that could exacerbate an existing medical condition is another story, and it sounds like you need more information and assurance that this is the right choice for you. I'm all for second opinions, at any stage of treatment. Alternatively, you could go back to your onc with some of the info you've amassed here and on the internet and have a straight talk about ALL the options and which is best for your sitation. That might be enough to allay your worries and help you make a choice you feel good about. If not, start dialing Doctor #2! -
Hi,
I was stage 1 at diagnosis also last July. I chose the lump/radiation and then had a hyst/ooph because of my ER/PR+. I worry myself about side effects of medications, because I have become ALLERGIC to everything, just shortly after stopping radiation last Jan. Its been baffling for my docs. My hyst/ooph had to be done withOUT pain meds. OUCH x's 200!! I became allergic to EVERYTHING, environmental and medicine wise. Its NOT been fun. I AM however on the advice of Johns Hopkins going to TRY to take the AI therapy. It is TRUE that a stage 1 grade 1 can be highly treatable and a stage 3 or 4 can be worse, but the opposite is also true. Just my opinion, and I am also a firm believer in 2 and even 3rd opinions. Have had them and I dont regret it..
Blessings,
Peachy -
I have been on Arimidex for almost 3 years and have had absolutely no problems. I am 73 years old.
-
I am just starting this journey as I was recently diagnosed with stage 1. I too am highly allergic or at least hyper sensitive to most medicine. It usually takes about 1/2 of everything to do the job for me. I plan on sharing this with the oncologists and other docs. I am even debating the radiation but hope to have the mammosite instead. This input really helps.
-
I have had stage 1 breast cancer. Lumpectomy and 31 radiation treatments. I am now on Arimidex. Have been for approx 7 months. Was having no side effects until about the last 3 weeks ago. Muscle pain, joint pain and all around tireness and weakness. Nothing seems to help. I feel like I have been run over by a truck. Has anybody else had problems later on like this? I know it has to be the arimdex as the only other thing I am on is blood pressure medicine (which I had to change since being on arimidex as it had to then be doubled) and my doctor says the blood pressure meds can't/won't do that.
-
I felt the same way about arimidex; I'm grade 1, stage 1.
I asked how safe arimidex was for someone with osteoarthritis, osteoporosis, and osteopenia.
I'm on tamoxifen for 2 years; we'll revisit after that.
Please note, though, in addition to grade (non-aggressive), and stage 1 - I had huge margins around my lump and almost no DCIS, so all my doctors believe that my chance of recurrence is lower than the statistics given by AdjuventOnline.
-
I've had stage 1 cancer twice, the second one was found a year after I stopped my AIs. (I think it had been there for some time, if not the whole time as the first, but kept in check by the AIs and the oopherectomy.)
I am back on AIs. Had problems with Tamoxifen. Bad pain with Arimidex. Did well with Femara. Now on Aromasin. For as long as I need to be.
I think what's driving me to consider another 5 years on meds is the concept of "dormant" cancer cells. While we may have removed darn near all the breast tissue (some actually can stay behind and become cancerous, or cancer comes back in the scar tissue, whatever), and we may not have had any visible cancer in our nodes, I still believe we need something systemic for treatment. Breast cancer cells may well have gotten into our bloodstream, waiting for the day for conditions to be right for substantial cell division and tumor growth. My belief is that the anti-hormonals help destroy conditions for these dormant cells to thrive.
While we can get some basic prediction for recurrence with tumor testing now, it's not a given. We still don't know why some people recur/get mets regardless of stage and node status, while others never will.
So, for me, time will tell. I may decide to stop AIs early. I can't predict. All I can say is that I was feeling mighty confident in my survival, and then another primary reared its head. That shook me up a bit. My individual statistics on Adjuvant are still excellent for living a long life without cancer. I'm just not ready yet to take that as the gospel. I have learned, during 6+ years of cancer and living how to keep up my quality of life in a manner that supports my value system, and still incorporate a systemic cancer treatment.
My two cents only.
Anne
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