Lenalidomide Combined to Azacitidine in Intermediate-2 or High Risk MDS With Del 5q
Status:
Completed
Trial end date:
2016-07-25
Target enrollment:
Participant gender:
Summary
Higher risk MDS with del(5q) carry very poor prognosis, but show some response to azacitidine
and Lenalidomide as single agents . The combination of Lenalidomide and Azacytidine is
currently tested in non del 5q MDS patients. Preliminary results have been recently presented
at ASH meeting (Sekeres et al, 2007).
Overall, the combination of Lenalidomide and Azacitidine is well-tolerated and early results
suggest some efficacy in advanced MDS without del 5q.
In this trial, we will combine Lenalidomide to Azacytidine in higher risk MDS with del (5q).
Patients will receive azacitidine( 75mg/m2/day for 5 days every 28 days) combined to
escalating doses of lenalidomide (starting at relatively low dose).
For patients in hematological CR, PR, HI or marrow CR after cycle 2 or 4, it is mandatory to
continue on Azacitidine + Lenalidomide as long as there is no unacceptable toxicity or overt
progression, with the schedule that yielded response.
In patient still responding after 52 weeks, the drug will continue to be supplied, and follow
up until death will be continued in all patients.