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异环磷酰胺用于既往未经治疗的播散性神经母细胞瘤。欧洲神经母细胞瘤研究组3A研究结果

Ifosfamide in previously untreated disseminated neuroblastoma. Results of Study 3A of the European Neuroblastoma Study Group.

作者信息

Kellie S J, De Kraker J, Lilleyman J S, Bowman A, Pritchard J

机构信息

Department of Haematology/Oncology, Hospitals for Sick Children, London, U.K.

出版信息

Eur J Cancer Clin Oncol. 1988 May;24(5):903-8. doi: 10.1016/0277-5379(88)90200-3.

Abstract

A prospective study of the effectiveness of ifosfamide as a single agent in the management of previously untreated patients with Evans stage IV neuroblastoma was undertaken. Eighteen children aged more than 1 year were treated with ifosfamide (IFX) 3 g/m2 daily for 2 days immediately after diagnosis and 3 weeks later. Treatment was continued with combination chemotherapy using vincristine, cyclophosphamide, cisplatinum and etoposide (OPEC) or a variant. Mesna (2-mercaptoethane sulphonate) was given to all patients during IFX treatment to prevent urotoxicity. Eight of the 18 patients (44%) responded to IFX. Nine had greater than 66% reduction in baseline tumor volume. Of 15 evaluable patients with raised pre-treatment urinary catecholamine excretion, six (40%) achieved greater than 50% reduction in pretreatment levels. Two of 10 patients evaluable for bone marrow response had complete clearance. Toxicity was mild in all patients. Upon completing 'first line' therapy, only four patients (22%) achieved a good partial remission (GPR) or complete response (CR). Median survival was 11 months. There was a lower rate of attaining GPR and shortened median survival in patients receiving phase II IFX before OPEC or variant, compared to patients with similar pre-treatment characteristics treated with OPEC from diagnosis in an earlier study.

摘要

开展了一项前瞻性研究,评估异环磷酰胺作为单一药物治疗既往未经治疗的埃文斯IV期神经母细胞瘤患者的有效性。18名年龄超过1岁的儿童在诊断后立即接受异环磷酰胺(IFX)治疗,剂量为3 g/m²,每日1次,共2天,3周后重复。后续继续采用长春新碱、环磷酰胺、顺铂和依托泊苷联合化疗(OPEC方案)或其变体方案进行治疗。在IFX治疗期间,所有患者均给予美司钠(2-巯基乙烷磺酸钠)以预防尿路毒性。18名患者中有8名(44%)对IFX有反应。9名患者的基线肿瘤体积缩小超过66%。在15名治疗前尿儿茶酚胺排泄量升高的可评估患者中,6名(40%)患者的治疗前水平降低超过50%。10名可评估骨髓反应的患者中有2名完全清除。所有患者的毒性均较轻。完成“一线”治疗后,只有4名患者(22%)达到良好部分缓解(GPR)或完全缓解(CR)。中位生存期为11个月。与早期研究中从诊断开始就接受OPEC治疗的具有相似治疗前特征的患者相比,在接受OPEC或其变体方案之前接受II期IFX治疗的患者达到GPR的比例较低,中位生存期缩短。

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