Ontology highlight
ABSTRACT: Purpose
Bosutinib is approved for adults with chronic myeloid leukemia (CML): 400 mg once daily in newly diagnosed (ND); 500 mg once daily in resistant/intolerant (R/I) patients. Bosutinib has a different tolerability profile than other tyrosine kinase inhibitors (TKIs) and potentially less impact on growth (preclinical data). The primary objective of this first-in-child trial was to determine the recommended phase II dose (RP2D) for pediatric R/I and ND patients.Patients and methods
In the phase I part of this international, open-label trial (ClinicalTrials.gov identifier: NCT04258943), children age 1-18 years with R/I (per European LeukemiaNet 2013) Ph+ CML were enrolled using a 6 + 4 design, testing 300, 350, and 400 mg/m2 once daily with food. The RP2D was the dose resulting in 0/6 or 1/10 dose-limiting toxicities (DLTs) during the first cycle and achieving adult target AUC levels for the respective indication. As ND participants were only enrolled in phase II, the ND RP2D was selected based on data from R/I patients.Results
Thirty patients were enrolled; 27 were evaluable for DLT: six at 300 mg/m2, 11 at 350 mg/m2 (one DLT), and 10 at 400 mg/m2 (one DLT). The mean AUCs at 300 mg/m2, 350 mg/m2, and 400 mg/m2 were 2.20 μg h/mL, 2.52 μg h/mL, and 2.66 μg h/mL, respectively. The most common adverse event was diarrhea (93%; ≥grade 3: 11%). Seven patients stopped because of intolerance and eight because of insufficient response. Complete cytogenetic and major molecular response to bosutinib appeared comparable with other published phase I/II trials with second-generation TKIs in children.Conclusion
Bosutinib was safe and effective. The pediatric RP2D was 400 mg/m2 once daily (max 600 mg/d) with food in R/I patients and 300 mg/m2 once daily (max 500 mg/d) with food in ND patients, which achieved targeted exposures as per adult experience.
SUBMITTER: Brivio E
PROVIDER: S-EPMC10906575 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature
Brivio Erica E Pennesi Edoardo E Willemse Marieke E ME Huitema Alwin D R ADR Jiang Yilin Y van Tinteren Harm D R HDR van der Velden Vincent H J VHJ Beverloo Berna H BH den Boer Monique L ML Rammeloo Lukas A J LAJ Hudson Chad C Heerema Nyla N Kowalski Karey K Zhao Huadong H Kuttschreuter Luke L Bautista Sirvent Francisco J FJ Bukowinski Andrew A Rizzari Carmelo C Pollard Jessica J Murillo-Sanjuán Laura L Kutny Matthew M Zarnegar-Lumley Sara S Redell Michele M Cooper Stacy S Bertrand Yves Y Petit Arnaud A Krystal Julie J Metzler Markus M Lancaster Donna D Bourquin Jean-Pierre JP Motwani Jayashree J van der Sluis Inge M IM Locatelli Franco F Roth Michael E ME Hijiya Nobuko N Zwaan Christian M CM
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20231130 7
<h4>Purpose</h4>Bosutinib is approved for adults with chronic myeloid leukemia (CML): 400 mg once daily in newly diagnosed (ND); 500 mg once daily in resistant/intolerant (R/I) patients. Bosutinib has a different tolerability profile than other tyrosine kinase inhibitors (TKIs) and potentially less impact on growth (preclinical data). The primary objective of this first-in-child trial was to determine the recommended phase II dose (RP2D) for pediatric R/I and ND patients.<h4>Patients and methods ...[more]