首页> 外文期刊>Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology >Intermediate-dose methotrexate and intravenous 6-mercaptopurine chemotherapy for children with acute lymphoblastic leukemia who did not respond to initial induction therapy.
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Intermediate-dose methotrexate and intravenous 6-mercaptopurine chemotherapy for children with acute lymphoblastic leukemia who did not respond to initial induction therapy.

机译:对初次诱导治疗无反应的急性淋巴细胞白血病中剂量甲氨蝶呤和6-巯基嘌呤静脉内化疗。

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PURPOSE: To determine the complete remission rate of children with acute lymphoblastic leukemia (ALL) who were not induced into remission by initial therapy, when subsequently treated with intermediate-dose methotrexate and intravenous 6-mercaptopurine. PATIENTS AND METHODS: Children with B-precursor ALL who did not achieve initial remission after 4 or 6 weeks of standard three- or four-drug induction chemotherapy were entered on study. Therapy consisted of three doses at weekly intervals of methotrexate 1,000 mg/m2 over 24 hours followed by 6-mercaptopurine 1,000 mg/m2 over 8 hours 20 minutes. Patients achieving a partial remission could receive two additional weekly courses of methotrexate and 6-mercaptopurine. Initially, patients received weekly intrathecal chemotherapy, but the study was amended to include intrathecal therapy only at week 1. RESULTS: Nineteen patients were entered on study. All were evaluable for toxicity and response. There were seven complete remissions, four partial remissions, six patients with no response, and two children with progressive disease, for an overall complete remission rate of 37%. One patient was removed from the study after the second course of methotrexate and 6-mercaptopurine because of renal failure. Two patients had neurologic toxicity resulting in a study amendment. No patients subsequently experienced neurologic toxicity. CONCLUSIONS: Intermediate-dose intravenous methotrexate and intravenous 6-mercaptopurine can induce remission in some patients with ALL who experience initial induction failure. Features predicting complete remission, however, could not be identified.
机译:目的:确定随后通过中剂量甲氨蝶呤和静脉内6-巯基嘌呤治疗的初始治疗未引起缓解的急性淋巴细胞白血病(ALL)儿童的完全缓解率。患者与方法:研究对象是在标准的三药或四药诱导化疗4或6周后未达到初始缓解的B前体ALL儿童。治疗包括在24小时内每周三剂甲氨蝶呤1,000 mg / m2,然后在8小时20分钟内使用6-巯基嘌呤1,000 mg / m2。达到部分缓解的患者可以每周接受两次氨甲蝶呤和6-巯基嘌呤疗程。最初,患者每周接受鞘内化疗,但该研究仅在第1周进行了鞘内治疗。结果:有19名患者进入研究。所有这些都可以评估毒性和反应性。有7例完全缓解,4例部分缓解,6例无反应的患者和2例进行性疾病的儿童,总体完全缓解率为37%。甲氨蝶呤和6-巯基嘌呤的第二疗程结束后,由于肾功能衰竭,一名患者退出研究。两名患者具有神经毒性,导致研究修订。随后没有患者经历神经系统毒性。结论:中剂量静脉甲氨蝶呤和6-巯基嘌呤静脉注射可诱导部分ALL患者的缓解,这些患者最初会出现诱导失败。但是,无法确定预测完全缓解的特征。

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