Westin J
Department of Medicine, University of Lund, Sweden.
Semin Oncol. 1991 Oct;18(5 Suppl 7):37-40.
Over the course of a 2-year period (September 1987 to September 1989) a total of 432 patients with multiple myeloma were registered in a study comprising 39 Swedish and one Italian clinics. Six of these were university hospitals, the others were county (community) hospitals. A total of 308 patients fulfilled the eligibility criteria of the protocol, and were started on traditional intermittent melphalan-prednisone therapy. Response, defined as a reduction in the concentration of the M-component in serum or urine, was observed in 58% of patients, and a clearly defined plateau phase was noted in 38% of the cases. Of the patients who achieved a plateau phase, 120 individuals (with a median age of 71 years) were at this point randomized between no further therapy and continuous interferon-alfa-2b at a dose of 5 x 10(6) IU subcutaneously three times per week. At relapse the interferon therapy was discontinued, and melphalan-prednisone restarted. Only preliminary data and interim results are at this point available. The final evaluation of the study will be performed after June 1, 1991. The treatment arms are comparable with regard to age, stage according to Durie-Salmon, renal function, immunoglobulin class, and type of response to the cytostatic therapy (rapid versus slow). A median number of six courses of melphalan-prednisone were administered before randomization. For those patients in whom pretreatment serum beta-2-microglobulin was analyzed, no difference in the median values between the treatment arms was found. The median observation time from randomization is 20 months. At the time of this analysis, 85 had relapsed: 33 of 59 (56%) in the interferon arm, and 52 of 61 (85%) in the no therapy arm. An interim analysis of the duration of the plateau phase (from the time of randomization) was performed in October 1990, showing a highly significant difference between the two treatment arms (P less than .001). The median duration of plateau was 59 weeks in the interferon arm, and 26 weeks in the no therapy arm. To date there have been 34 deaths, 13 in the interferon arm and 21 in the no therapy arm. All patients in the no therapy arm died from multiple myeloma (n = 19), or from another cause, but with the myeloma in an uncontrolled, progressive state (n = 2). In the interferon arm, only 10 patients died from progressive myeloma, and four of these either did not start interferon therapy at all (n = 1), or discontinued therapy early (n = 3).(ABSTRACT TRUNCATED AT 400 WORDS)
在1987年9月至1989年9月的两年期间,共有432例多发性骨髓瘤患者登记参与了一项研究,该研究涵盖39家瑞典诊所和1家意大利诊所。其中6家为大学医院,其他为郡(社区)医院。共有308例患者符合方案的入选标准,并开始接受传统的间歇美法仑 - 泼尼松治疗。58%的患者出现反应,定义为血清或尿液中M成分浓度降低,38%的病例出现明确的平台期。在达到平台期的患者中,120人(中位年龄71岁)此时被随机分为不再接受进一步治疗组和连续接受干扰素 - α2b治疗组,剂量为5×10⁶IU皮下注射,每周三次。复发时停止干扰素治疗,重新开始美法仑 - 泼尼松治疗。目前仅可获得初步数据和中期结果。该研究的最终评估将在1991年6月1日后进行。在年龄、根据Durie - Salmon分期、肾功能、免疫球蛋白类别以及对细胞毒性治疗的反应类型(快速与缓慢)方面,各治疗组具有可比性。随机分组前,美法仑 - 泼尼松的中位疗程数为六个疗程。对于那些分析了治疗前血清β2 - 微球蛋白的患者,各治疗组之间的中位数值无差异。随机分组后的中位观察时间为20个月。在此次分析时,85例患者复发:干扰素治疗组59例中有33例(56%)复发,未治疗组61例中有52例(85%)复发。1990年10月对平台期持续时间(从随机分组时起)进行了中期分析,结果显示两个治疗组之间存在高度显著差异(P<0.001)。干扰素治疗组的平台期中位持续时间为59周,未治疗组为26周。迄今为止,已有34例死亡,干扰素治疗组13例,未治疗组21例。未治疗组的所有患者均死于多发性骨髓瘤(n = 19),或死于其他原因,但骨髓瘤处于未控制的进展状态(n = 2)。在干扰素治疗组中,只有10例患者死于进展性骨髓瘤,其中4例根本未开始干扰素治疗(n = 1),或早期停止治疗(n = 3)。(摘要截短为400字)