Home         Forums  

Go Back   Marrowforums > Treatments > Drugs and Drug Treatments
Register FAQ Search Today's Posts Mark Forums Read

Drugs and Drug Treatments ATG, Cyclosporine, Revlimid, Vidaza, Dacogen, ...

Reply
 
Thread Tools Search this Thread
  #1  
Old Fri Sep 14, 2012, 04:58 PM
VickiB VickiB is offline
Member
 
Join Date: Dec 2011
Location: Omaha, Nebraska
Posts: 9
Revlimid

After 8 rounds of Vidaza, will start Revlimid along with Prednisone and an antibiotic . I am worried about the side effects of Revlimid. I had very little problem with Vidaza, but evidently it quit working. I am a 72 year old Female diagnosed last Dec with Intermediate Risk 2. Thanks
Reply With Quote
  #2  
Old Sat Sep 15, 2012, 05:52 AM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Revlimid

Hi Vicki,
Hopefully you won't have any adverse reactions when you take Revlimid. Prednisone will eventually decrease adverse effects from the bonemarrow like low counts initially. What dose will you be taking?

Here is a list of adverse reactions in MDS patients:
Low platelets 62%
Low neutrophils (a kind of wbc) 59%
Diarrhea 49%
Itching 42%
Rash 36%
Fatigue 31%
Constipation 24%
Nausea 24%

Kind regards
Birgitta-A
73 yo, dx MDS Interm-1 2006. Started Thalidomide (similar to Revlimid) 50 mg/day + Prednisone June 2010 but could not tolerate more than 4 caps Thalidomide á 50 mg/week due to low WBC. Still responding after 27 months but HGB and platelets are slowly decreasing.
Reply With Quote
  #3  
Old Sun Sep 16, 2012, 05:35 PM
celebrations celebrations is offline
Member
 
Join Date: Jun 2007
Posts: 34
Dear Vicky,
are you 5q-, since you start a Revlimid therapy?

I also tried Revlimid (in a trial, because I am not 5q- and Revlimid for non-5q- has not yet been approved in Germany).

Unfortunately my doc stopped me after 6 weeks. My leukocytes had dropped under 1, so I was expected to have serious infections. After breaking up with Revlimid my wbc took 8 months to normalize. And I was very lucky not to have any inflammation or sth.

Beside the decrease of the whites I did not have any of the side-effects on the Revlimid leaflet.

Don't be afraid, the doctors will take care of you and look after your counts very thoroughly. Try it, it will probably help you for a while.

Bergit
__________________
female, 54, MDS-RCMD, trisomy 8, dx 2006, response to EPO and therafter VPA only for a couple of months, transfusion-dependent twice a month, watch&wait for SCT somewhen in the future with my brother as a donor
Reply With Quote
  #4  
Old Mon Sep 17, 2012, 01:27 PM
VickiB VickiB is offline
Member
 
Join Date: Dec 2011
Location: Omaha, Nebraska
Posts: 9
I am taking 5 mg of Revlimid for 21 days. Then doc will up it to 10 and lower Prednisone ( now 30 mg daily) by half. Thanks for the posts.
Reply With Quote
  #5  
Old Mon Sep 17, 2012, 02:28 PM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Revlimid

Hi Vicki,
Prednisone dose is often 30mg/day initially - then it is tapered due to adverse long term effects. I asked my doctor if I could continue with 5mg/day because that drug can increase HGB together with Revlimid or Thalidomide in patients with other bone marrow cancers like Myelofibrosis and Myeloma.

Hope you will have a good response to Revlimid!
Kind regards
Birgitta-A
Reply With Quote
  #6  
Old Sun Oct 7, 2012, 04:22 PM
VickiB VickiB is offline
Member
 
Join Date: Dec 2011
Location: Omaha, Nebraska
Posts: 9
Had to have a blood transfusion Fri. Hemoglobin down to 8. I still don't feel well- shortness of breath, exhaustion. Hope to feel better soon. Have tolerated the Revlimid well otherwise. Last one today, then a week off.
Reply With Quote
  #7  
Old Mon Oct 8, 2012, 05:27 PM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Revlimid

Hi Vicki,
Very good that you tolerated Revlimid ! Now we hope that you will respond so your HGB will start to increase.
Kind regards
Birgitta-A
Reply With Quote
  #8  
Old Thu Nov 1, 2012, 01:00 PM
VickiB VickiB is offline
Member
 
Join Date: Dec 2011
Location: Omaha, Nebraska
Posts: 9
Since I last wrote, I have had two more blood transfusions and 3 platelet transfusions. The doctor took me off Revlamid last Fri. I see him again next week, but wonder what's next. I don't feel much better even after the transfusions. I am feeling rather discouraged. If Vidaza and Revlamid don't work, then what?
Reply With Quote
  #9  
Old Thu Nov 1, 2012, 01:56 PM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
Quote:
Originally Posted by VickiB View Post
Since I last wrote, I have had two more blood transfusions and 3 platelet transfusions. The doctor took me off Revlamid last Fri. I see him again next week, but wonder what's next. I don't feel much better even after the transfusions. I am feeling rather discouraged. If Vidaza and Revlamid don't work, then what?
Vicki,

I'm sorry you are still transfusion dependent and had to go off Revlimid. Did the doctor say if you're giving up on Revlimid or just interrupting its schedule?

Another drug often considered is decitabine (trade name Dacogen), which some patients respond to.
Reply With Quote
  #10  
Old Thu Nov 1, 2012, 04:47 PM
DanL DanL is offline
Member
 
Join Date: Dec 2010
Location: Denver, CO
Posts: 590
Vicki,

In addition to Dacogen, which Neil references, there are a couple of drugs that are both in clinical trials, but are showing pretty good results for MDS patients where Vidaza has been discontinued. The first one is Sapacitabine, and the other is Rigosertib (trade name Estybon). I believe both of these are in phase III trials currently.

There are several other drug options that people on this forum are trying.
You may want to discuss all options with your doctor to see if any of these paths are right for your situation.
__________________
MDS RCMD w/grade 2-3 fibrosis. Allo-MUD Feb 26, 2014. Relapsed August 2014. Free and clear of MDS since November 2014 after treatment with Vidaza and Rituxan. Experiencing autoimmune attack on CNS thought to be GVHD, some gut, skin and ocular cGVHD. Neuropathy over 80% of body.
Reply With Quote
  #11  
Old Sat Nov 3, 2012, 12:33 PM
VickiB VickiB is offline
Member
 
Join Date: Dec 2011
Location: Omaha, Nebraska
Posts: 9
The doctor didn't say if I would go back on Revlamid. I'm sure he'll tell me next Wed. Thanks for the names of the other drugs.
Reply With Quote
  #12  
Old Mon Jan 7, 2013, 03:55 PM
TammyB TammyB is offline
Member
 
Join Date: Jan 2013
Location: Winnipeg
Posts: 11
Hi Vicki,
I had some similar issues with the Revlimid. It started out poorly with my body not liking the drug. After some tweeking to the dosage and adding some Prednisone, my body tolerated it for about a year and was in remission. We lowered the dose, due to side effects and once we did I was out of showing dysplastic cells again. I have started it again on a higher dosage 5 months ago, and am waiting on BM Biopsy results. Just thought I would share my Revlimid story with you. Take care.
__________________
Tammy, age 50; Diagnosed MDS Deletion 5Q- in 2008;
Currently on Lenalidomide.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
Time between Revlimid use and SCT? bailie MDS 0 Tue Jul 1, 2014 12:37 AM
Chromosomes and Revlimid Birgitta-A MDS 2 Sun May 19, 2013 07:42 AM
Revlimid dosing Birgitta-A Drugs and Drug Treatments 0 Tue Aug 9, 2011 05:18 AM
Long Term Effects of Revlimid? FZ_MM_free Drugs and Drug Treatments 0 Mon Jun 6, 2011 02:43 PM
Revlimid side effects Rosemary Drugs and Drug Treatments 4 Mon Apr 25, 2011 01:05 PM


All times are GMT -4. The time now is 03:52 AM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org