| Literature DB >> 22303898 |
Maurizio Miano1, Angela Pistorio, Maria C Putti, Carlo Dufour, Chiara Messina, Elena Barisone, Ottavio Ziino, Rosanna Parasole, Matteo Luciani, Luca Lo Nigro, Giulio De Rossi, Stefania Varotto, Nicoletta Bertorello, Fara Petruzziello, Michaela Calvillo, Concetta Micalizzi.
Abstract
Clofarabine is a promising new chemotherapeutic agent that is active in the treatment of pediatric acute leukemia. Forty children (16 with acute myeloid leukemia [AML], 24 with acute lymphoblastic leukemia [ALL]), aged 1-20 years (median 7.6 years) with relapsed or refractory ALL or AML were treated because of resistance to first-line treatment (n =5), or for first (n =22), second (n =11) or third relapse (n =2). They received clofarabine (40 mg/m(2)/day) associated with etoposide (100 mg/m(2)/day) and cyclophosphamide (440 mg/m(2)/day) administered as one or two induction cycles (5 days of chemotherapy) in an attempt to reach complete remission (CR) or CR without platelet recovery (CRp). This was followed by 1-3 consolidation cycles (4 days of chemotherapy) for a maximum of four cycles. Seven (44%) out of 16 and 10 (42%) out of 24 evaluable children with AML and ALL, respectively, responded to treatment. The most common adverse events were infections and gastrointestinal and hepatic toxicity. Thirteen (76%) out of 17 responders underwent hematopoietic stem cell transplant. The 24-month overall survival was 25%, while it was 59% among patients who responded to the first induction cycle. Our study suggests that this drug regimen is well tolerated and can be effective in heavily pretreated pediatric patients with relapsed or refractory acute leukemia.Entities:
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Year: 2012 PMID: 22303898 DOI: 10.3109/10428194.2012.663915
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022