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异环磷酰胺、米托蒽醌和依托泊苷(VIM)作为非霍奇金淋巴瘤低毒性挽救疗法。

Ifosfamide, mitoxantrone and etoposide (VIM) as salvage therapy of low toxicity in non-Hodgkin's lymphoma.

作者信息

Hopfinger G, Heinz R, Koller E, Schneider B, Pittermann E

机构信息

3rd Medical Department, Hanusch Hospital, Vienna, Austria.

出版信息

Eur J Haematol. 1995 Oct;55(4):223-7. doi: 10.1111/j.1600-0609.1995.tb00261.x.

Abstract

Patients with non-Hodgkin's lymphoma (NHL) who fail to respond to first-line treatment or relapse after having shown complete or partial remission have a poor prognosis, especially in high-grade NHL. Several salvage regimens show considerable toxicity and a poor long-term outcome. In this retrospective study we analyzed data of 55 patients (34 men and 21 women) with a median age of 66 years (range: 18-89). The combination chemotherapy (VIM) consisted of VP-16 (etoposide) 65 mg/m2, ifosfamide 650 mg/m2 and mitoxantrone 3 mg/m2 and was administered on 3 consecutive days along with mesna as uroprotection. Patients were treated for refractory disease or relapse and did not qualify for high-dose chemotherapy and ABMT. Stages according to the An Arbor classification were: stage I/16, II/4, III/8 and IV/37 patients. Thirty-three patients suffered from high-grade and 22 from low-grade NHL. Toxicity (WHO recommendations) was very mild. High-grade NHL showed a better response rate (18/33, 46%) than low-grade NHL (7/22, 36%). Overall response was 41% (12 CR and 11 PR) with a median duration of 36 months (range: 6-57 months). The combination therapy investigated exhibits mild toxicity even in extensively pretreated or elderly patients. The overall response rate of 41% might be improved by increased dosage and growth factor support.

摘要

非霍奇金淋巴瘤(NHL)患者若对一线治疗无反应或在完全或部分缓解后复发,预后较差,尤其是在高级别NHL中。几种挽救方案显示出相当大的毒性和较差的长期疗效。在这项回顾性研究中,我们分析了55例患者(34例男性和21例女性)的数据,中位年龄为66岁(范围:18 - 89岁)。联合化疗(VIM)由VP - 16(依托泊苷)65 mg/m²、异环磷酰胺650 mg/m²和米托蒽醌3 mg/m²组成,连续3天给药,并使用美司钠作为尿路保护剂。患者接受难治性疾病或复发的治疗,不符合大剂量化疗和自体骨髓移植的条件。根据Ann Arbor分期,I/II期16例、II期4例、III期8例、IV期37例患者。33例患者患有高级别NHL,22例患有低级别NHL。毒性(根据世界卫生组织建议)非常轻微。高级别NHL的缓解率(18/33,46%)高于低级别NHL(7/22,36%)。总体缓解率为41%(12例完全缓解和11例部分缓解),中位缓解持续时间为36个月(范围:6 - 57个月)。所研究的联合治疗即使在经过广泛预处理的患者或老年患者中也表现出轻微毒性。通过增加剂量和生长因子支持,41%的总体缓解率可能会提高。

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