| Literature DB >> 20697840 |
Ramzi Jeddi1, Hèlà Ghédira, Yosr Ben Abdennebi, Karima Kacem, Ramzi Ben Amor, Lamia Aissaoui, Walid Bouterâa, Raihane Ben Lakhal, Hèla Ben Abid, Samia Menif, Zaher Belhadjali, Balkis Meddeb.
Abstract
Reports on childhood APL from developing countries are scarce. We treated 65 APL with two consecutive trials combining ATRA and chemotherapy. Twenty (30.7%) were aged less than 20 years including 11 girls and 9 boys, with a median age of 12 years. Fever at presentation (P=0.002) and variant APL (P=0.044) were more frequent in children, while there were no significant difference between children and adults for WBC count, Sanz's score distribution and additional cytogenetic abnormalities. The CR rate was 95% (19/20) in children and 80% (36/45) in adults (P=0.13). Differentiation syndrome (DS) was less often observed in children (1/20) than in adults (13/45) (P=0.031). Two children relapsed and died during salvage therapy, and 2 died in CR from infection and from cardiac failure attributed to anthracyclines, while other children remained alive in CR. With a median follow-up of 4 years, 4-year EFS was 75% in children and 71.1% in adults (P=0.57), while 4-year OS was 75% in children vs. 73.3% in adults (P=0.72). Our results suggest that, even in the absence of optimal socio-economic condition, ATRA combined with anthracycline-based chemotherapy gives adequate results in childhood APL, as in adults.Entities:
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Year: 2010 PMID: 20697840 DOI: 10.1007/s12032-010-9642-9
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064