Durie Brian G M, Jacobson Joth, Barlogie Bart, Crowley John
Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
J Clin Oncol. 2004 May 15;22(10):1857-63. doi: 10.1200/JCO.2004.05.111. Epub 2004 Apr 26.
Four Southwest Oncology Group (SWOG) standard-dose chemotherapy protocols for multiple myeloma (MM) initiated between 1982 and 1992 were evaluated. The purpose was to clarify the predictive value of specific levels of myeloma-associated monoclonal protein reduction and time to first progression using mature data sets.
Study data on 1,555 eligible previously untreated patients with MM enrolled onto SWOG phase III trials 8229, 8624, 9028, and 9210 were used in these analyses. Six-month and 12-month landmark analyses were performed to evaluate the outcome for patients in each response category.
The overall and event-free survivals for the four protocols combined were 33 months and 18 months, respectively. Using 6- and 12-month landmarks, the median survivals of 30 to 35 months were not different for responders (> or = 50% and > or = 75% regression) versus nonresponders in patients without disease progression before the landmarks. Conversely, at the 6- and 12-month landmarks, the median survivals for patients who had experienced disease progression were 13 and 15 months, respectively, versus a 34-month median for patients who did not experience progression. Using the Cox survival model, with response and progression considered as time-dependent covariates, survival duration was influenced more by the occurrence of progression than by the occurrence of response.
The magnitude of response, as a single variable, does not predict survival duration. Patients with response and stable disease have equivalent outcome. Only patients with progressive disease have a poorer outcome. The best indicator of survival is time to first progression.
评估1982年至1992年间启动的四项西南肿瘤协作组(SWOG)针对多发性骨髓瘤(MM)的标准剂量化疗方案。目的是利用成熟数据集阐明骨髓瘤相关单克隆蛋白特定水平降低及首次进展时间的预测价值。
这些分析使用了纳入SWOG 8229、8624、9028和9210号III期试验的1555例符合条件的既往未治疗MM患者的研究数据。进行了6个月和12个月的标志性分析,以评估各反应类别患者的结局。
四项方案合并后的总生存期和无事件生存期分别为33个月和18个月。使用6个月和12个月的标志性时间点,在标志性时间点前无疾病进展的患者中,反应者(≥50%和≥75%缓解)与无反应者的中位生存期为30至35个月,无差异。相反,在6个月和12个月的标志性时间点,经历疾病进展的患者的中位生存期分别为13个月和15个月,而未经历进展的患者的中位生存期为34个月。使用Cox生存模型,将反应和进展视为时间依赖性协变量,生存持续时间受进展发生的影响大于受反应发生的影响。
作为单一变量,反应程度不能预测生存持续时间。有反应和疾病稳定的患者结局相当。只有疾病进展的患者结局较差。生存的最佳指标是首次进展时间。