FLEND (nelarabine, fludarabine, and etoposide) for relapsed T-cell acute lymphoblastic leukemia in children: a report from Japan Children’s Cancer Group

被引:0
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作者
Tadashi Kumamoto
Hiroaki Goto
Chitose Ogawa
Toshinori Hori
Takao Deguchi
Takuya Araki
Akiko M. Saito
Atsushi Manabe
Keizo Horibe
Hidemi Toyoda
机构
[1] National Cancer Center Hospital,Department of Pediatric Oncology
[2] Kanagawa Children’s Medical Center,Department of Hematology and Oncology, Children’s Cancer Center
[3] Aich Medical University Hospital,Department of Pediatrics
[4] National Center for Child Health and Development,Division of Cancer Immunodiagnostics, Children’s Cancer Center
[5] Gunma University Graduate School of Medicine,Department of Clinical Pharmacology and Therapeutics
[6] National Hospital Organization Nagoya Medical Center,Clinical Research Center
[7] Hokkaido University Graduate School of Medicine,Department of Pediatrics
[8] Mie University Graduate School of Medicine,Department of Pediatrics
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FLEND; T-ALL; Nelarabine; Fludarabine; Etoposide;
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摘要
Nelarabine is a key drug for T-cell acute lymphoblastic leukemia (T-ALL). Fludarabine and etoposide might have synergistic effect with nelarabine by inhibiting ribonucleotide reductase and by preparing cell cycle for G1/S phase, respectively. We had started phase 1/2 multicenter clinical trial of combination chemotherapy consisted of nelarabine, fludarabine, and etoposide (FLEND therapy) for children with relapsed/refractory T-ALL which has been conducted since October 2011. Although we could not complete this trial because of recruitment difficulties, we treated five children with first-relapsed T-ALL which were enrolled in the phase 1 dose escalation study of fludarabine and etoposide with nelarabine. No dose-limiting toxicity occurred, and frequent grade 3–4 toxicity was hematological toxicity and febrile neutropenia, as expected. There was no neurotoxicity. All 2 patients who received the target dose of FLEND, in which nelarabine (650 mg/m2), fludarabine (30 mg/m2), and etoposide (100 mg/m2) were administered for 5 consecutive days, were induced to complete remission. We concluded that FLEND might be safe and one of the promising combination chemotherapies to relapsed/refractory T-ALL.
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页码:720 / 724
页数:4
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