Boccadoro M, Marmont F, Tribalto M, Avvisati G, Andriani A, Barbui T, Cantonetti M, Carotenuto M, Comotti B, Dammacco F
Dipartimento di Medicina ed Oncologia sperimentale, Cattedra di Ematologia, Torino, Italy.
J Clin Oncol. 1991 Mar;9(3):444-8. doi: 10.1200/JCO.1991.9.3.444.
The efficacy of alternating vincristine, melphalan (M), cyclophosphamide, prednisone/vincristine, carmustine, doxorubicin, and prednisone (VMCP/VBAP) polychemotherapy was compared with the M and prednisone (MP) regimen as induction treatment in multiple myeloma (MM). Three hundred four MM patients entered this study between March 1983 and July 1986; the analysis was performed in December 1989. The treatment groups did not show significant differences with respect to major prognostic factors. Median overall survival was 33.8 months. In the VMCP/VBAP and MP arms, after 12 induction chemotherapy cycles, 59.0% and 47.3% (P less than .068) of the patients achieved an M component reduction greater than 50%. No significant difference was observed in the two treatment arms in terms of remission duration (21.3 v 19.6 months, P less than .66) and survival (31.6 v 37.0 months, P less than .28). Patients younger than 65 years did not show any advantage from the alternating polychemotherapy. At diagnosis, the plasma cell labeling index (LI) and serum beta-2 microglobulin (beta 2-m) were evaluated in 173 and 183 patients, respectively. A significantly reduced survival was observed for patients with LI greater than or equal to 2% (16.4 months) or beta 2-m greater than or equal to 6 mg/L (20.4 months). Even in these poor-risk subgroups, VMCP/VBAP was not superior to MP.
将长春新碱、美法仑(M)、环磷酰胺、泼尼松/长春新碱、卡莫司汀、阿霉素和泼尼松(VMCP/VBAP)联合化疗作为诱导治疗方案,与美法仑和泼尼松(MP)方案治疗多发性骨髓瘤(MM)的疗效进行了比较。1983年3月至1986年7月期间,304例MM患者进入本研究;1989年12月进行分析。治疗组在主要预后因素方面无显著差异。总生存期中位数为33.8个月。在VMCP/VBAP组和MP组中,经过12个诱导化疗周期后,分别有59.0%和47.3%(P<0.068)的患者M成分减少超过50%。在缓解持续时间(21.3对19.6个月,P<0.66)和生存率(31.6对37.0个月,P<0.28)方面,两组治疗方案无显著差异。65岁以下的患者未显示出交替联合化疗有任何优势。诊断时,分别对173例和183例患者评估了浆细胞标记指数(LI)和血清β2微球蛋白(β2-m)。LI大于或等于2%(16.4个月)或β2-m大于或等于6mg/L(20.4个月)的患者生存率显著降低。即使在这些高危亚组中,VMCP/VBAP也不优于MP。