Still worried about timing of things
I still have my concerns regarding timing of things due to the fact a lot doesn't seem to match with people here.
My wife wrapprd neoadjuvant chemo on 12/23/2016. Her surgery was a month later 1/24/2017. The pre surgery scans showed no activity but the pathology came back with more nodes involved than originally thought and main tumor shrank and was swiss cheesed 40%. She also had an unclean deep margin of less than 1 mm. She bounced back from surgery very quickly with no complications.
From there nothing happened aside from weekly tissue expansion until radiation started on 4/10/2017. Two and a half months later.
We are told she won't start hormone therapy until two weeks after radiation ends. The MO stated that studies have shown that mixing the hormones and radiation have messed with the effects of treatment.
I've brought up these timing concerns and the fact that of being on hormones during radiation. None of the doctors seem worried about my concerns which I take as a good sign that I'm just freaking out however I just dont see anyone else here on that same path.
I also don't know if we should ask about more chemo, or what the best plan of attack is. I'm no doctor so I don't know for sure and it's the Cleveland Clinic so I assume they know what they are doing. She even had her case put in front of the tumor board and they all agreed on treatment. I guess I'm just worried.
Bueller...Bueller....anyone?
Comments
-
Hi Tom, I'm in the UK but my diagnosis & treatment seems to have followed a v similar path to your wife's and I didn't start my hormone therapy until after radiotherapy had finished. Hope she is doing OK.
-
I started Rads a week after last adjuvant Taxol (4 DD A/C neoadjuvant and 12 weekly Taxol). A week after starting Rads (2 weeks after last Taxol) I started Femara (was still under copyright. So not available as generic letrozole).
My Chemo Dr wanted me on it ASAP and my Rads Dr had no problem with getting on it. BUT we are each unique as are our Drs.
-
The treatment path sounds about right to me. I had 4 TAC before surgery and had the surgery two weeks after the 4th TAC. Then a month later I was given the option of taking the final 2 TAC which I did. Following that, I did 30 rads about two weeks after the last TAC. After rads I began the anti-hormonal treatment. All told, it took about 6 months to get all treatments completed and start the anti-hormonals.
-
Hi Tom,
My treatment plan was very similar to your wife's. I was also concerned about the wait periods between each step, but it seems to have worked out well so far for me. It was hard, but I had to put my trust in my doctors and hope they were doing what was best. It was a long process.
-
Try not to worry. I was "late" on almost everything and my MO said no worries to all of it, and I had grade 3. Got to sx 2 months after dx due to needing ps and bs both present. Had 4 drains in for 5 weeks instead of the average of up to 2 weeks. A couple weeks later the skin area above my right tissue expander became infected. 7 days of Amoxacilan did nothing so I was admitted to the hospital for 5 days of IV abx. Had a picc line placed and sent home for another week of self adminstered IV abx. Once all was clear, MO does the pre-chemo standard tests she does and finds I'm severely anemic. So 3 days of IV iron infusions. Sx was 8/6. Started chemo 11/3, exactly on the line of the most effectiveness of chemo, but what can you do. You have to be well before you undergo chemo. So all is going ok on schedule thereafter all the delays until on 2/27 I go to pay my BC insurance premiums through Covered CA exchanged and it's been cancelled. What?? Long story short, with a lot of back and forth for almost a month they had mistakenly changed my income to 0 and threw me on Medi-Cal. So my last chemo was about a month late. I had started rads when a week in I had both lungs partially collapse and so I was in the hospital for 3 days and the following I felt some chest pain so no rads for a couple days there--- a total of a week behind in rad schedule. So I had a longer than average active tx time line, starting 8/6/15 with bmx w/tissue expander placements to final rads completed mid-June 2016. I asked my MO how long do I have before needing to get on Tamox and she said up to a year but of course sooner if you can do it. I gave myself a month off to recover more from chemo and rads before popping the pill.
So the moral of the story is if you can't stick to the "schedule" it doesn't mean you are doomed. Plenty of things happen that interferes with getting tx and people wind up being fine.
-
One thing to add that might give you a bit of reassurance, is that my doctor told me that the chemo drugs are active in your system for about 12 months after your final one.
-
Hi Tom,
Yep, It all sounds right to me.
Her tumor type is a slower growing, indolent type, then some other types of BCs, and yes chemo does remain in the tissues for a time. It is quite normal to expect things to move quickly, but healing from surgery and being off antiestrogens at time of rads is standard.
Also having more nodes at time of surgery is extremely common, as scans often do not pick them up unless they are quite large. I myself had 12 positive nodes, 2 were actually extraencapsulated and none of my nodes were detected on my PET scan.
She had a good response to her chemo which is extremely favorable.
Finally, rads does a good job of mopping up any residual cells. I also did not have clear margins either ( within 1 mm too) and am fine now approaching 12 years.
Sounds like you are a great support to your wife. Please reassure her she will ok!
-
I was given tamoxifen to start post chemo but pre surgery and rads.
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