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米托蒽醌、泼尼松龙氮芥和长春新碱用于老年侵袭性非霍奇金淋巴瘤患者

Mitoxantrone, prednimustine, and vincristine for elderly patients with aggressive non-Hodgkin's lymphoma.

作者信息

Yau J C, Germond C, Gluck S, Cripps C, Verma S, Burns B F, Koski T M, Lister D C, Goss G D

机构信息

Ottawa Regional Cancer Centre, Ontario, Canada.

出版信息

Am J Hematol. 1998 Oct;59(2):156-60. doi: 10.1002/(sici)1096-8652(199810)59:2<156::aid-ajh9>3.0.co;2-x.

Abstract

Elderly patients with intermediate- or high-grade non-Hodgkin's lymphoma have a worse outcome than those who are younger than 60 years. It has been shown that aggressive combination chemotherapy is poorly tolerated in older patients resulting in a subsequent decrease in dose intensity. A phase II trial was conducted with mitoxantrone, prednimustine, and vincristine (NSO) in this group of patients. NSO consists of mitoxantrone 12 mg/M2 intravenously on day one, vincristine 1.4 mg/M2 intravenously on day 1 (maximum dose of two mg), and prednimustine 100 mg/M2 orally once a day for four days. NSO was repeated every 21 days. Thirty-six patients were able to be evaluated. There were 18 males and 18 females with the median age of 71 (range 60-85). NSO was well tolerated and nonhematological toxicities were uncommon. More than 80% of the patients received 90% or greater of the intended dose. The complete response rate was 60.6% and partial response was 21.8%. At 60 months the Kaplan-Meier estimate of progression-free survival was 47.9% (standard error 8.6%) and actual survival was 40.6% (standard error 8.8%). There were no differences in outcome between those with performance status (PS) of zero or one and those with PS > 1. NSO is well tolerated by elderly patients including those with PS > 1. These results compare favorably with other combinations in elderly patients with aggressive non-Hodgkin's lymphoma.

摘要

中高危非霍奇金淋巴瘤老年患者的预后比60岁以下患者差。研究表明,老年患者对积极的联合化疗耐受性差,导致后续剂量强度降低。对这组患者进行了米托蒽醌、泼尼松氮芥和长春新碱(NSO)的II期试验。NSO方案包括第1天静脉注射米托蒽醌12mg/M²,第1天静脉注射长春新碱1.4mg/M²(最大剂量2mg),泼尼松氮芥100mg/M²口服,每日1次,共4天。每21天重复一次NSO方案。36例患者能够进行评估。其中男性18例,女性18例,中位年龄71岁(范围60 - 85岁)。NSO耐受性良好,非血液学毒性不常见。超过80%的患者接受了90%或更高的预期剂量。完全缓解率为60.6%,部分缓解率为21.8%。60个月时,无进展生存的Kaplan-Meier估计值为47.9%(标准误8.6%),实际生存率为40.6%(标准误8.8%)。体能状态(PS)为0或1的患者与PS>1的患者在预后方面无差异。包括PS>1的患者在内,老年患者对NSO耐受性良好。这些结果与老年侵袭性非霍奇金淋巴瘤患者的其他联合方案相比更具优势。

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