Gregory W M, Richards M A, Malpas J S
Imperial Cancer Research Fund Clinical Oncology Unit, Guy's Hospital, London, England.
J Clin Oncol. 1992 Feb;10(2):334-42. doi: 10.1200/JCO.1992.10.2.334.
A meta-analysis was performed to compare survival after treatment with melphalan and prednisolone (M + P) with that after combination chemotherapy (CCT) in patients with multiple myeloma.
Meta-analysis was performed on 18 published trials comprising 3,814 patients comparing M + P with CCT. Two-year survival percentages with observed and expected deaths at 2 years were calculated for each trial, and the overview methodology was applied to these figures.
Overall results from the 18 trials suggest that there is no difference in efficacy between the two treatments. This finding, however, masks a highly significant correlation between 2-year survival rates for M + P-treated patients in individual studies and the difference between the M + P and CCT 2-year survival rates for that study (r = .69; P = .0008). In separate overviews, those studies with a high M + P 2-year survival rate showed a survival difference in favor of M + P (P = .02), whereas those with a low rate suggested a difference in favor of CCT (P V .07). Comparison of the 2-year survival rates in the M + P treatment arms of each of the studies with available data showed an inverse correlation between survival and the proportion of patients with either poor performance status (P less than .001) or immunoglobulin A (IgA) M band (P = .02).
These results imply that M + P is superior for patients with an intrinsically good prognosis and inferior for those patients with a poor prognosis. If reliable prognostic factors can be established for this disease, they could be used to select therapy for individual patients.
进行一项荟萃分析,比较美法仑与泼尼松(M + P)治疗多发性骨髓瘤患者后的生存率与联合化疗(CCT)后的生存率。
对18项已发表的试验进行荟萃分析,这些试验共纳入3814例患者,比较M + P与CCT。计算每项试验的两年生存率以及两年时观察到的和预期的死亡人数,并将汇总方法应用于这些数据。
18项试验的总体结果表明,两种治疗方法的疗效没有差异。然而,这一发现掩盖了个别研究中接受M + P治疗患者的两年生存率与该研究中M + P和CCT两年生存率差异之间的高度显著相关性(r = 0.69;P = 0.0008)。在单独的汇总分析中,M + P两年生存率高的研究显示生存差异有利于M + P(P = 0.02),而生存率低的研究则表明差异有利于CCT(P < 0.07)。对每项研究中M + P治疗组有可用数据的两年生存率进行比较,结果显示生存率与功能状态差(P < 0.001)或免疫球蛋白A(IgA)M带(P = 0.02)患者的比例呈负相关。
这些结果表明,M + P对预后本质良好的患者更优,而对预后不良的患者较差。如果能为这种疾病建立可靠的预后因素,就可用于为个体患者选择治疗方法。