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挽救性治疗用奈拉滨、依托泊苷和环磷酰胺治疗复发/难治性小儿 T 细胞淋巴母细胞白血病和淋巴瘤。

Salvage therapy with nelarabine, etoposide, and cyclophosphamide in relapsed/refractory paediatric T-cell lymphoblastic leukaemia and lymphoma.

机构信息

Division of Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

出版信息

Br J Haematol. 2010 Aug;150(3):345-51. doi: 10.1111/j.1365-2141.2010.08236.x. Epub 2010 May 26.

DOI:10.1111/j.1365-2141.2010.08236.x
PMID:20528871
Abstract

A combination of 5 d of nelarabine (AraG) with 5 d of etoposide (VP) and cyclophosphamide (CPM) and prophylactic intrathecal chemotherapy was used as salvage therapy in seven children with refractory or relapsed T-cell leukaemia or lymphoma. The most common side effects attributable to the AraG included Grade 2 and 3 sensory and motor neuropathy and musculoskeletal pain. Haematological toxicity was greater for the combination than AraG alone, although median time to neutrophil and platelet recovery was consistent with other salvage therapies. All patients had some response to the combined therapy and five of the seven went into complete remission after one or two courses of AraG/VP/CPM. Our experience supports the safety of giving AraG as salvage therapy in synchrony with etoposide and cyclophosphamide, although neurological toxicity must be closely monitored.

摘要

在 7 例难治性或复发性 T 细胞白血病或淋巴瘤患儿中,采用阿糖胞苷(AraG)联合依托泊苷(VP)和环磷酰胺(CPM)5 天,并预防性鞘内化疗作为挽救治疗。AraG 最常见的不良反应为 2-3 级感觉和运动神经病及肌肉骨骼疼痛。与AraG 单药治疗相比,联合治疗的血液学毒性更大,但中性粒细胞和血小板恢复的中位时间与其他挽救治疗一致。所有患者对联合治疗均有一定反应,7 例患者中有 5 例在接受一至两个 AraG/VP/CPM 疗程后完全缓解。我们的经验支持AraG 与依托泊苷和环磷酰胺同步作为挽救治疗的安全性,尽管必须密切监测神经毒性。

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