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多发性骨髓瘤(MM)中α干扰素(IFN-α)维持治疗与IFN-α联合化疗的比较。希腊骨髓瘤研究组。

Maintenance therapy with interferon-alpha (IFN-alpha) versus IFN-alpha plus chemotherapy in multiple myeloma (MM). The Greek Myeloma Study Group.

作者信息

Zervas K, Pouli A, Perifanis V, Papanastasiou K, Chatziyianni M, Mitsouli C, Maniatis A

机构信息

Department of Haematology, Theagenion' Anticancer Hospital, Thessaloniki, Greece.

出版信息

Eur J Haematol. 1996 Aug;57(2):142-8. doi: 10.1111/j.1600-0609.1996.tb01352.x.

Abstract

Results of studies using IFN-alpha treatment for maintaining remission and prolonging survival in multiple myeloma (MM) are in conflict and trials seeking optimum use for this biological response modifier are continuing. Between 1989 and 1993 a prospective randomized multicentre trial was undertaken to evaluate the role of the combination of IFN-alpha with chemotherapy (CT) in maintenance treatment of MM. For remission induction, in patients 65 yr or younger, we used VAD (group A) and for the remaining Melphalan and Prednisone (MP) (group B). For maintenance, patients were randomized to receive IFN-alpha 3 x 10(6) i.u. s.c. t.i.w. (group I) or alternating monthly cycles of IFN-alpha and CT. The CT cycles were also alternated (VAD, MP, CP) in an effort to prevent the development of multidrug resistance. Median survival of the two maintenance groups from randomization (36 months for group I and 31 months for group II, p = 0.3) as well as response duration (13 months in group I and 15 months in group II, p = 0.95) were similar. Toxicities were more pronounced both with VAD induction and in the combination maintenance arm. The addition of chemotherapy to the IFN maintenance regimen in MM did not have an advantage over IFN alone.

摘要

使用干扰素-α治疗多发性骨髓瘤(MM)以维持缓解和延长生存期的研究结果存在矛盾,探寻这种生物反应调节剂最佳用法的试验仍在继续。1989年至1993年间,开展了一项前瞻性随机多中心试验,以评估干扰素-α联合化疗(CT)在MM维持治疗中的作用。对于缓解诱导,65岁及以下患者使用VAD方案(A组),其余患者使用美法仑和泼尼松(MP)方案(B组)。对于维持治疗,患者被随机分为接受皮下注射干扰素-α 3×10⁶国际单位,每周三次(I组),或干扰素-α与CT交替每月一次的周期治疗。CT周期也交替使用(VAD、MP、CP),以防止多药耐药的发生。两个维持治疗组从随机分组起的中位生存期(I组为36个月,II组为31个月,p = 0.3)以及缓解持续时间(I组为13个月,II组为15个月,p = 0.95)相似。VAD诱导治疗以及联合维持治疗组的毒性更为明显。MM患者在干扰素维持治疗方案中添加化疗并不比单独使用干扰素更具优势。

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