Hello,
Does anyone here have experience with cyclophosphamide (Cytoxan, Endoxan), thalidomide, and dexamethasone (CTD) for multiple myeloma?
Would be interested in thoughts / experiences in relation to this treatment regimen.
Thanks very much,
Lex
Forums
Re: Cyclophosphamide, thalidomide, and dexamethasone (CTD)
With that mix of myeloma therapies, you are likely in Europe, correct?
Although my dad has been on Velcade (bortezomib) instead of thalidomide (we are in Canada), he is taking cyclophosphamide and dexamethasone. My dad has experienced little in the way of cyclophosphamide side effects (no hair loss). Dexamethasone has been tough to deal with at times, especially the emotional changes, such as anger and depression (which are already compounded when one is battling cancer).
Although my dad has been on Velcade (bortezomib) instead of thalidomide (we are in Canada), he is taking cyclophosphamide and dexamethasone. My dad has experienced little in the way of cyclophosphamide side effects (no hair loss). Dexamethasone has been tough to deal with at times, especially the emotional changes, such as anger and depression (which are already compounded when one is battling cancer).
-

Little Monkey - Name: Little Monkey
- Who do you know with myeloma?: Father-stage 1 multiple myeloma
- When were you/they diagnosed?: March/April of 2015
2 posts
• Page 1 of 1
Return to Treatments & Side Effects
