Xeloda
Hi Everyone!!! I'm 45 and was diagnosed with triple negative in February stage 2 grade 3. Mylump was 2.5 then doubled to 4.0 cms In two weeks. I was positive for the palb2 gene. I had chemo ac/and taxol which ended June 11 and had double mascectomy with partial reconstruction on July 23. Removing the lump at surgery it was 1.2 cms - (12mm) stage 1 grade 3. Pathology report stated the primary tumor is pT1c and pno- i have nothing in my lymph nodes. After hearing the pathology report I was very upset I had a residual lump after chemo. At my follow up visit with my oncologist we briefly celebrated being cancer free and thenshe briefly mentioned xeloda gave me a study done on it in Japan. She said it was up to me and we would discuss it more at our next visit. My oncologist did not push but mentioned it and gave the confusing study. She said she would be watching me like a hawk either way
Reading the study in Japan was very confusing and upsetting so I went to my other doctor/surgeon and asked to help read this. He said it was a study in Japan that was done in the 90s that showed only 8 percent increase in survival. He mentioned the study represents one ethnic group in Japan which each ethnic group has different survival rates with Asians having the highest survival rates of all ethnic groups and only half the people finished the study. I have serious lung issues which the chemo knocked out my lungs and my joints in my legs so I have to way the side effects very carefully as my immune system was compromised even before chemo. I went in Facebook groups asking this same question and I was told there were no further studies and only a new recent study is under way in America. I have yet to find anyone with a success story taking xeloda so want to know about side effects and if anyone is taking or found success with xeloda. I don't not feel comfortable at all taking xeloda with not much proof of any success with long termside effects that are unknown. I do understand fighting this thing with all that I have but I want to make sure it's worth putting my body through this when i can not find any proof. . I did not blink twice at a strong treatment of chemo nor had to think twice about a double mascectomy. This xeloda though seems to be giving a great deal of unsureness.Thank you in advance.
Comments
-
My understanding is the CREATE-X study is more recent and the study was stopped early, as it showed improvement in survival especially for TNBC. I know there is some debate of how asian women react to the drug compared to caucasian or any other race. I don't think its been used in the US for very long in early stage, so it would be hard to find long term success stories. Maybe 2 years or less? I admit I do feel like a bit of a guinea pig with this treatment.
My path after mastectomy showed 7 mm residual, making me ypT1b. I have a pretty conservative oncologist and even he recommended Xeloda for any residual. He was willing to go the 6 rounds rather than the standard 8. But I am trying for 8, as long as I can tolerate it.
It's not a walk in the park for me but I am managing. The side effects started hitting me harder on round 4. I am now finishing my round 5 off week. As for side effects, my feet hurt for 7-9 days of the 21 day cycle, my fatigue is worse than IV chemo, loose stools with stomach cramps here and there, body aches. Other than those bad days it's just annoying for me to take pills but life goes on as normal. My blood work taken during those worse days show I am slightly anemic and/or deficient in B12. I was very anemic during AC but bounced back during taxol.
I was willing to give it a try. Since rads are not recommended and I don't qualify for most trials (most want residual to be 1 cm or more and/or positive nodes).
-
Hi Jennifer I hope these weeks go by fast for you and Godspeed!!!! Yes the create X was the trial that took place in Japan an older study recently published in the New England journal of medicine. I tried to look up studies to show different ethnic groups and could not find any but only found this mention of studies that were not positive? I was trying to find out and long term side effects and find that difficult to find.
-
I took Xeloda from Oct 2017 to April, 8 rounds in total...2 weeks on, 1 week off. My dose had to be reduced at about Round 3-4 because my feet were getting quite sore. I found it overall to be fairly manageable. I was fatigued but how much of that was Xeloda and how much was the cumulative effect of being sick and months of harsh treatment, who knows. The biggest side effects were sore feet for me. I kept my feet and hands moisturized with a cream with a high urea content but they still got pretty tender. I also would have an upset gut on the second week.
It took a few months after I finished to start feeling more myself. Good luck with your decision
-
I am on my 2nd day of my 2nd cycle of xeloda with 6 more to go at some point. So far my symptoms are not that bad, I have seem to have indigestion at night and have no desire to eat even on the week off. My sleep tends to get less and less as the cycle goes on. I am watching my feet and hands carefully but so far so good but it's early still.
I had my BMX in July and had 90% of my tumor still in tact, the chemo only killed 10%, which was 4 cm to begin with.
-
Thanks everyone for your input and the article I most appreciate it. My oncologist was on the same page and felt the residual cancer was small enough that she herself would not take it and would be comfortable with me on passing this by. I wanted to focus on getting back to myself and getting stronger. I just had my implant surgery all went well and very happy. A few days later I got sick from my kids who were only sick for 3 days and I was knocked out for two weeks with the flu. It made me realize how my immune system still has not recovered. Doing much better now. This month is one year from diagnosis - I remember it like yesterday. God bless and Godspeed everyone hugs to all!!!
-
Hello
I to hook Xeloda. I had already done my 2 rounds of IV chemo the Red Devil and Taxol. This was brought to me as an extra precaution. I had to take 5 pills in the morning and 5 pills at night 14 days on 7 days off. I barely got through almost to the first weeks. This med made me more sick than the other 2 meds above. I lost 10llbs in 9 days. I was super constipated which it says you will be the other way around. I was super miserable. It made my nurapethy worse in my feet. So for me I had to stop it and pray that what I've already have done has been enough.
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