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α-2干扰素/美法仑/泼尼松用于既往未经治疗的多发性骨髓瘤患者:一项I-II期试验

Alpha-2-interferon/melphalan/prednisone in previously untreated patients with multiple myeloma: a phase I-II trial.

作者信息

Cooper M R, Fefer A, Thompson J, Case D C, Kempf R, Sacher R, Neefe J, Bickers J, Scarffe J H, Spiegel R

出版信息

Cancer Treat Rep. 1986 Apr;70(4):473-6.

PMID:3698041
Abstract

Alpha-2-interferon (IFN) has demonstrable activity in advanced, relapsing, or refractory multiple myeloma. Because of the in vitro synergism between the IFNs and cytotoxic agents, we conducted a trial of 30 previously untreated patients with multiple myeloma utilizing various doses of alpha-2-IFN in combination with standard oral doses of melphalan and prednisone. The combination was well-tolerated without unusual or unexpected toxic effects. The limiting toxicity included dose-related myelosuppression, and alpha-2-IFN induced flu-like symptoms and fatigue. Response was seen in at least as many patients as would be expected with melphalan and prednisone alone. The maximal tolerated dose for a phase II-III trial was 5.0 X 10(6) IU/m2 of alpha-2-IFN in combination with standard doses of melphalan and prednisone. Future trials should utilize this dose of alpha-2-IFN with dose de-escalation according to tolerance.

摘要

α-2干扰素(IFN)在晚期、复发性或难治性多发性骨髓瘤中具有明显活性。由于IFN与细胞毒性药物之间存在体外协同作用,我们对30例既往未接受治疗的多发性骨髓瘤患者进行了一项试验,使用不同剂量的α-2-IFN联合标准口服剂量的美法仑和泼尼松。该联合方案耐受性良好,未出现异常或意外的毒性作用。剂量限制性毒性包括与剂量相关的骨髓抑制,以及α-2-IFN诱导的流感样症状和疲劳。观察到的反应患者数量至少与单独使用美法仑和泼尼松时预期的数量相同。II-III期试验的最大耐受剂量是α-2-IFN 5.0×10(6) IU/m2联合标准剂量的美法仑和泼尼松。未来的试验应使用该剂量的α-2-IFN,并根据耐受性降低剂量。

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