Pan Birmingham gynaecological cancer centre, City Hospital, UK.
Gynecol Oncol. 2012 May;125(2):493-9. doi: 10.1016/j.ygyno.2011.12.420. Epub 2011 Dec 8.
Although overall survival is the ultimate goal of cancer therapy, many clinical and health economic decisions are taken when only progression free survival (PFS) data are available. This study evaluates the relationship between PFS and post progression survival (i.e. the time between disease progression and death) to estimate how many months a new drug for ovarian cancer might add to overall survival if the number of months the drug added to PFS (relative to a standard drug) was already known.
A literature search was conducted over Medline for randomised controlled trials published between January 1990 and July 2010 that evaluated the effect of a drug treatment in comparison to alternative drug treatment in patients with either advanced stage primary or recurrent ovarian cancer. A systematic review of progression free and post progression survival (PPS) was performed. The relationship between PFS and PPS was evaluated by a graphical method and standard statistical tests.
Thirty-seven trials involving 15,850 patients met the inclusion criteria. The review found that increases in median PFS generally lead to little change in post-progression survival. Percentage gains in PFS are generally associated with no percentage gains or with very slight percentage gains or losses in post-progression survival
If the effect of a new drug treatment for ovarian cancer is to extend median PFS by x months, then it is reasonable to estimate that the treatment will also extend median overall survival by x months. This information will be useful for individual and collective decision making.
虽然总生存是癌症治疗的终极目标,但在只有无进展生存(PFS)数据可用的情况下,许多临床和卫生经济决策已经做出。本研究评估了 PFS 与进展后生存(即疾病进展和死亡之间的时间)之间的关系,以估计如果已知新药相对于标准药物增加 PFS 的月数(相对于标准药物),则新药可能会增加多少个月的卵巢癌总生存时间。
对 1990 年 1 月至 2010 年 7 月期间发表的随机对照试验进行了 Medline 文献检索,这些试验评估了药物治疗与晚期原发性或复发性卵巢癌患者替代药物治疗的效果。对 PFS 和进展后生存(PPS)进行了系统回顾。通过图形方法和标准统计检验评估了 PFS 和 PPS 之间的关系。
符合纳入标准的 37 项试验涉及 15850 名患者。综述发现,PFS 中位数的增加通常导致进展后生存的变化很小。PFS 的百分比增加通常与进展后生存的百分比没有增加或只有非常轻微的增加或减少相关。
如果新的卵巢癌药物治疗的效果将 PFS 中位数延长 x 个月,那么可以合理地估计该治疗也将延长 PFS 中位数 x 个月。这些信息将对个体和集体决策有用。