| Literature DB >> 25170123 |
Frédéric Millot1, Joelle Guilhot1, André Baruchel2, Arnaud Petit3, Yves Bertrand4, Françoise Mazingue5, Patrick Lutz6, Cecile Vérité7, Christian Berthou8, Claire Galambrun9, Nicolas Sirvent10, Karima Yakouben11, Claudine Schmitt12, Virginie Gandemer13, Yves Reguerre14, Gérard Couillault15, Françoise Mechinaud16, Jean-Michel Cayuela17.
Abstract
Studies in adults have shown that an early molecular response to imatinib predicts clinical outcome in chronic myeloid leukemia (CML). We investigated the impact of the BCR-ABL1 transcript level measured 3 months after starting imatinib in a cohort of 40 children with CML. Children with a BCR-ABL1/ABL ratio higher than 10% at 3 months after the start of imatinib had a larger spleen size and a higher white blood cell count compared with those with BCR-ABL1/ABL ≤10%. Children with BCR-ABL1/ABL ≤10% 3 months after starting imatinib had higher rates of complete cytogenetic response and major molecular response at 12 months compared with those with BCR-ABL1/ABL >10%. With a median follow-up of 71 months (range, 22-96 months), BCR-ABL1/ABL ≤10% correlated with better progression-free survival. Thus, early molecular response at 3 months predicts outcome in children treated with imatinib for CML. This trial was registered at www.clinicaltrials.gov as #NCT00845221.Entities:
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Year: 2014 PMID: 25170123 DOI: 10.1182/blood-2014-05-578567
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113