| Literature DB >> 20673585 |
Meral Beksac1, Ridvan Ali, Tulay Ozcelik, Muhit Ozcan, Osman Ozcebe, Mahmut Bayik, Semra Paydas, Yahya Buyukasik, Osman Ilhan, Fahir Ozkalemkas, Gunhan Gurman, Akin Uysal, Hamdi Akan, Ender Akcaglayan Soydan, Ahmet Tunali.
Abstract
This prospective multicenter phase III clinical trial was designed to assess efficacy and safety of G-CSF as an adjunct to de novo AML remission induction therapy (www.clinicaltrials.gov. NCT00820976). Patients' characteristics were similar in both arms. G-CSF improved severity and duration of leukopenia. Three-year OS were similar (25.6 ± 5.1% vs. 31.8 ± 5.6%) in both arms except for patients with myeloblastic features. Significant factors for better survival were the use of G-CSF (p=0.049), female sex (p=0.05) and single induction cycle (p<0.001) in multivariate analysis. Female patients performed better than male patients. Better survival obtained among female AML patients needs to be validated within the context of cytogenetic analysis.Entities:
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Year: 2010 PMID: 20673585 DOI: 10.1016/j.leukres.2010.07.005
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156