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多发性骨髓瘤的初始治疗:多药化疗并不优于美法仑-泼尼松。瑞典西部骨髓瘤研究组。

Initial treatment in multiple myeloma: no advantage of multidrug chemotherapy over melphalan-prednisone. The Myeloma Group of Western Sweden.

作者信息

Hjorth M, Hellquist L, Holmberg E, Magnusson B, Rödjer S, Westin J

机构信息

Department of Medicine, Lidköping Hospital, Sweden.

出版信息

Br J Haematol. 1990 Feb;74(2):185-91. doi: 10.1111/j.1365-2141.1990.tb02564.x.

Abstract

From October 1983 until December 1986, 164 patients with multiple myeloma stage II-III were included in a prospective randomized multi-centre study comparing melphalan-prednisone (MP) with multidrug chemotherapy (MDC). The patients comprised 77% of all newly diagnosed myeloma stage II-III cases reported from 18 hospitals covering the entire Health Care Region of Western Sweden (1.5 million inhabitants). Patients randomized to MP (29 stage II and 55 stage III patients) were given oral melphalan and prednisone every 6 weeks. For patients randomized to MDC, stage II patients (n = 25) were given VMCP every 4 weeks and stage III patients (n = 53) VBAP and VMCP alternately every 4 weeks. For stage II patients, the response rate for MP compared to VMCP was 69 versus 56% and the median survival 46 versus 33 months. For stage III the response rate for MP compared to VBAP/VMCP was 58 versus 57% and the median survival 26 versus 24 months. No statistically significant differences were seen. The time to response and remission duration were also similar in both treatment arms. The dose intensity index (cumulative given/planned dose of myelosuppressive drugs) was greater than or equal to 0.8 in 89% of the MP patients and 81% of the MDC patients. Patients with index values less than 0.8 had the same response rate as patients with index greater than or equal to 0.8. This study has not demonstrated any advantage of MDC over traditional MP in multiple myeloma stage II-III.

摘要

从1983年10月至1986年12月,164例II - III期多发性骨髓瘤患者被纳入一项前瞻性随机多中心研究,比较美法仑 - 泼尼松(MP)与多药化疗(MDC)。这些患者占瑞典西部整个医疗保健区域(150万居民)18家医院报告的所有新诊断的II - III期骨髓瘤病例的77%。随机分配至MP组(29例II期和55例III期患者)的患者每6周接受一次口服美法仑和泼尼松治疗。对于随机分配至MDC组的患者,II期患者(n = 25)每4周接受一次VMCP治疗,III期患者(n = 53)每4周交替接受VBAP和VMCP治疗。对于II期患者,MP组与VMCP组的缓解率分别为69%和56%,中位生存期分别为46个月和33个月。对于III期患者,MP组与VBAP/VMCP组的缓解率分别为58%和57%,中位生存期分别为26个月和24个月。未观察到统计学上的显著差异。两个治疗组的缓解时间和缓解持续时间也相似。剂量强度指数(骨髓抑制药物的累积给药量/计划给药量)在89%的MP组患者和81%的MDC组患者中大于或等于0.8。指数值小于0.8的患者与指数大于或等于0.8的患者缓解率相同。本研究未证明MDC在II - III期多发性骨髓瘤中优于传统的MP。

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