Osterborg A, Björkholm M, Björeman M, Brenning G, Carlson K, Celsing F, Gahrton G, Grimfors G, Gyllenhammar H, Hast R
Department of Oncology (Radiumhemmet), Karolinska Hospital, Stockholm.
Blood. 1993 Mar 15;81(6):1428-34.
Three hundred thirty-five previously untreated patients with multiple myeloma in clinical stages II and III entered a randomized trial comparing intermittent oral melphalan and prednisone (MP) therapy (n = 171) with MP in combination with natural (leukocyte-derived) alpha-interferon (MP/IFN) (n = 164). The treatment groups were comparable with regard to major prognostic factors. The response frequency was 42% in the MP group and 68% in the MP/IFN group (P < .0001). Eighty-five percent of IgA myelomas and 71% of Bence-Jones myelomas responded to MP/IFN compared with 48% and 27%, respectively, to MP treatment (P = .001). There was no difference in the overall survival between the two treatment groups. However, the survival of 72 patients with IgA or Bence-Jones myeloma randomized to receive MP/IFN was significantly longer (median 32 months) than that of 71 patients treated with MP (median 17 months) (p < .05). No statistically significant difference in response frequency (60% v 46%) or survival was found for patients with IgG myeloma. Hematologic toxicity, WHO grades III and IV, was higher in the MP/IFN group (48%) than in the MP group (33%) (P < .05) during the induction treatment period. Flulike syndrome was observed in 68% of patients receiving MP/IFN. The results show that MP/IFN is a well-tolerated treatment regimen, superior to MP for remission induction, and it improves significantly the overall survival for patients with IgA and Bence-Jones myelomas.
335例临床分期为II期和III期的未经治疗的多发性骨髓瘤患者进入一项随机试验,该试验比较了间歇性口服美法仑和泼尼松(MP)疗法(n = 171)与MP联合天然(白细胞衍生)α干扰素(MP/IFN)疗法(n = 164)。治疗组在主要预后因素方面具有可比性。MP组的缓解频率为42%,MP/IFN组为68%(P <.0001)。85%的IgA骨髓瘤和71%的本周氏蛋白骨髓瘤对MP/IFN有反应,而MP治疗的相应比例分别为48%和27%(P =.001)。两个治疗组的总生存期没有差异。然而,随机接受MP/IFN治疗的72例IgA或本周氏蛋白骨髓瘤患者的生存期(中位数32个月)明显长于接受MP治疗的71例患者(中位数17个月)(p <.05)。对于IgG骨髓瘤患者,在缓解频率(60%对46%)或生存期方面未发现统计学上的显著差异。在诱导治疗期间,MP/IFN组的血液学毒性(WHO III级和IV级)高于MP组(48%对33%)(P <.05)。在接受MP/IFN治疗的患者中,68%观察到流感样综合征。结果表明,MP/IFN是一种耐受性良好的治疗方案,在诱导缓解方面优于MP,并且能显著提高IgA和本周氏蛋白骨髓瘤患者的总生存期。