Influence ofSLCO1B1polymorphism on maintenance therapy for childhood leukemia
Autor: | Ai Yoshimi, Atsushi Iwabuchi, Masahiro Tsuchida, Emiko Noguchi, Kazutoshi Koike, Hideto Takahashi, Keisuke Kato, Nobutaka Kiyokawa, Enbo Ma, Hiroko Fukushima, Makoto Saito, Takashi Fukushima, Ryoko Suzuki, Chie Kobayashi, Aiko Sakai, Ryoko Nakajima-Yamaguchi, Ryo Sumazaki, Tomohei Nakao |
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Rok vydání: | 2015 |
Předmět: |
Oncology
medicine.medical_specialty Childhood leukemia biology business.industry medicine.disease Leukemia Maintenance therapy Internal medicine Methylenetetrahydrofolate reductase Pediatrics Perinatology and Child Health Immunology medicine biology.protein ITPA business SLCO1B1 Childhood Acute Lymphoblastic Leukemia Dose Modification |
Zdroj: | Pediatrics International. 57:572-577 |
ISSN: | 1328-8067 |
DOI: | 10.1111/ped.12682 |
Popis: | Background Management of the adverse effects of chemotherapy is essential to improve outcome of children with leukemia. Some genetic polymorphisms can predict treatment-related toxicity, and be used individually in dose modification of 6-mercaptopurine (6-MP) and methotrexate (MTX) in maintenance therapy for childhood acute lymphoblastic leukemia (ALL). We investigated associations between clinical course and candidate gene polymorphisms less evaluated in Japanese patients. Methods Fifty-three children who received maintenance chemotherapy were enrolled in this study. The scheduled dose of oral 6-MP was 40 mg/m2 daily and that of oral MTX was 25 mg/m2 weekly. The doses were adjusted according to white blood cell count (target range, 2.5–3.5 × 109/L) and aspartate aminotransferase and alanine aminotransferase level ( C than in the patients with wild homozygous genotype. The other analyzed polymorphisms were not associated with toxicity, 6-MP, or MTX dose. Conclusions Polymorphism of SLCO1B1 c.521 T > C could be a strong predictor of 6-MP dose reduction in maintenance chemotherapy in childhood ALL. |
Databáze: | OpenAIRE |
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