Home         Forums  

Go Back   Marrowforums > Bone Marrow Failure Diseases > MDS
Register FAQ Search Today's Posts Mark Forums Read

MDS Myelodysplastic syndromes

Reply
 
Thread Tools Search this Thread
  #1  
Old Wed Aug 17, 2011, 11:48 AM
Neel Neel is offline
Member
 
Join Date: Dec 2010
Location: delhi india
Posts: 73
thalidomide working ?

My father has been taking thalidomide 100 mg for last 4 months (since 22 april, 2011). he was transfusion dependent when he started thalidomide, required both platelet and blood. After arnd 15 days of start of thalidomide , his counts stablized , there wasnt any marked improvement, but the counts were stable and remained so till today i.e. 17/8/11, i.e. Hb moved slowly till 11, Platelet rose staidly till 40000, then came back to 30000 and remained between 30000-40000, TLC arnd 2000-2400. Howeve todays report shows Hb and TLC as same i.e 10 and 2400 resp, however his platelet count has taken a beating i.e. 18000. Any inputs and what to do ?


Moreover he stopped taking thalidomide for arnd 1 week i.e. 3-8-11 till 10-8-11 due to extreme weakness caused by it. However he started it since 10-8-11.

Is the fall due to discontinuation of thalidomide ?

Has thalidomide stopped working ?

Will thalidomide show its effect later ?

regards,

neel
__________________
Father age 64 diagnosed with MDS RAEB-2, with 15%-18% blasts in October 2010. Only had blood and platelet transfusions. Ayurvedic treatment which showed result for arnd 5 months. Started Tahlidomide 100 mg started on 22 nd April 2011. Revolade 50 mg started on 2 nd april 2012.
Reply With Quote
  #2  
Old Wed Aug 17, 2011, 03:49 PM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Thalidomide

Hi Neel,
Too bad that your father is so weak! Many patients that can't tolerate Thalidomide 100mg/day get lower doses with good or better effect. I am taking 29mg/day (4 caps á 50mg/week) since July 2010 with positive effect - my WBCs decreased when I took 50mg/day.

As I have suggested before I think a low dose of Prednisone could increase your father's counts - especially the platelets. You know the platelets can fluctuate much. If they decrease from 30000 to 18000 they can increase next time. Do avoid everything that can decrease platelets like all types of pain killers.

I don't know if the lower counts depend on discontinuation of Thalidomide. The median response (50% of the responses) is 9 months so 4 months is a short response. There are a few patients who have responded several years - one study mentioned 6 years.

It is true that some patients respond several months after Thalidomide is stopped but I think it is better to cotinue with a lower dose.
Birgitta-A
72 yo, dx MDS Interm-1 2006, received 142 units of PRBCs, Thalidomide + Prednisone since June 2010 with positive effect, don't need iron chelation any longer, take one Neupogen injection/week instead of 2 for my low WBCs, last counts HGB 130, WBCs 4.8 and platelets 95.
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
Thalidomide side affects leading to lack of focus or concentration fuadfaruk Drugs and Drug Treatments 2 Thu May 18, 2017 02:31 PM
MDS, angiodysplasia and thalidomide Paolo D. Drugs and Drug Treatments 5 Tue Jul 10, 2012 05:29 PM
thalidomide therapy Ita MDS 3 Fri May 4, 2012 02:58 PM
thalidomide and weakness Neel Drugs and Drug Treatments 1 Thu Jul 7, 2011 12:48 PM
Thalidomide best for recently dx patients that only have anemia Birgitta-A Drugs and Drug Treatments 0 Sat Jun 6, 2009 01:53 PM


All times are GMT -4. The time now is 02:41 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