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依托泊苷单药治疗复发的晚期淋巴瘤:一项II期研究。

Etoposide as a single agent in relapsed advanced lymphomas. A phase II study.

作者信息

Taylor R E, McElwain T J, Barrett A, Peckham M J

出版信息

Cancer Chemother Pharmacol. 1982;7(2-3):175-7. doi: 10.1007/BF00254543.

Abstract

Twenty-three patients with relapsed lymphomas resistant to standard chemotherapy, 13 with Hodgkin's disease and 10 with non-Hodgkin's lymphomas, were treated with etoposide 120 mg/m2 i.v. daily for 5 days or orally for 7-10 days, repeated 3-weekly. This is a higher dose than has been used previously to treat these tumours. Objective responses were seen in eight of 13 (61%) patients with Hodgkin's disease (three CR, five PR) and in three of 10 (30%) patients with non-Hodgkin's lymphomas (three PR). The response rates for Hodgkin's disease are higher than those previously reported and are probably due to the greater dose of drug than has been previously employed. The dose-limiting toxicity was haematological, with gastro-intestinal toxicity occurring in the minority of patients only. It is concluded that etoposide has significant activity particularly in Hodgkin's disease. Its use in drug combinations should now be assessed.

摘要

23例对标准化疗耐药的复发性淋巴瘤患者,其中13例为霍奇金病,10例为非霍奇金淋巴瘤,接受了依托泊苷治疗,静脉注射剂量为120mg/m²,每日1次,共5天;或口服给药,持续7 - 10天,每3周重复一次。这一剂量高于此前用于治疗这些肿瘤的剂量。13例霍奇金病患者中有8例(61%)出现客观缓解(3例完全缓解,5例部分缓解),10例非霍奇金淋巴瘤患者中有3例(30%)出现客观缓解(均为部分缓解)。霍奇金病的缓解率高于此前报道的,这可能是由于使用的药物剂量比之前更大。剂量限制性毒性为血液学毒性,只有少数患者出现胃肠道毒性。结论是依托泊苷具有显著活性,尤其在霍奇金病中。现在应该评估其在联合用药中的应用。

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