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Higher dose imatinib for children with de novo chronic phase chronic myelogenous leukemia: a report from the Children's Oncology Group.


ABSTRACT: To determine the efficacy of imatinib in children with newly diagnosed chronic phase (CP) chronic myelogenous leukemia (CML).This was an open label, multi-center phase II clinical trial. Courses were defined as consecutive 28-day intervals. Oral imatinib was administered daily at 340 mg/m² without interruption in the absence of toxicity.Fifty-one children received 978 28-day courses of imatinib. The most common toxicities encountered were hematologic. Forty-one patients (80%) achieved a complete hematologic response by the end of course 2. Nineteen children (38%) obtained a complete cytogenetic response (CCyR) at the end of course 3. Overall, 72% achieved CCyR at a median time of 5.6 months. The rate of complete molecular response (>3 log reduction) was 27%. Progression-free and overall survival at 3 years were 72%? ± 6.4% and 92%? ± 3.9%, respectively.Daily oral imatinib at a dose of 340 mg/m² is well tolerated in children. In addition, imatinib therapy is effective in inducing a high percent of hematologic, cytogenetic and molecular responses, comparable to adults with CML. (This study was registered at ClinicalTrials.gov under identifier NCT00030394.).

SUBMITTER: Champagne MA 

PROVIDER: S-EPMC5157124 | biostudies-literature | 2011 Jul

REPOSITORIES: biostudies-literature

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Higher dose imatinib for children with de novo chronic phase chronic myelogenous leukemia: a report from the Children's Oncology Group.

Champagne Martin A MA   Fu Cecilia H CH   Chang Myron M   Chen Helen H   Gerbing Robert B RB   Alonzo Todd A TA   Cooley Linda D LD   Heerema Nyla A NA   Oehler Vivian V   Wood Charlotte C   French Mary Ellen ME   Arceci Robert J RJ   Smith Franklin O FO   Bernstein Mark L ML  

Pediatric blood & cancer 20110404 1


<h4>Purpose</h4>To determine the efficacy of imatinib in children with newly diagnosed chronic phase (CP) chronic myelogenous leukemia (CML).<h4>Methods</h4>This was an open label, multi-center phase II clinical trial. Courses were defined as consecutive 28-day intervals. Oral imatinib was administered daily at 340 mg/m² without interruption in the absence of toxicity.<h4>Results</h4>Fifty-one children received 978 28-day courses of imatinib. The most common toxicities encountered were hematolog  ...[more]

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