Key result
Different progression-free survival definitions fail as surrogates for overall survival in preoperative cancer therapy.
Why the study?
Progression-free survival is an often-used endpoint in preoperative therapy trials, but optimal definition is difficult due to timing differences in surgery and incomplete resection handling.
Answers are grounded in this paper and cite their sources.
Progression-free survival can fail as a surrogate for overall survival in preoperative cancer therapy trials, and overall survival should remain the primary endpoint.
OBJECTIVE: Progression-free survival is an often-used endpoint in clinical trials comparing preoperative therapy and surgery-first therapy. Because the surgery date is always later in the preoperative arm than in the surgery-first arm, it is difficult to define progression-free survival optimally. We evaluated three progression-free survival definitions that used different methods to handle incomplete resection. METHODS: The three definitions specify the event date of incomplete resection (IR) as follows: 'IR = event' method, date of surgery; 'IR not event' method, date of radiological or clinical progression after incomplete resection; landmark method, landmark time. According to these definitions, the theoretical strengths and weaknesses of the three definitions are investigated. Three patterns of progression-free survival and overall survival were estimated using the data of the Japan Clinical Oncology Group studies. RESULTS: Theoretically, 'IR = event' inflates alpha error while 'IR not event' method and landmark method reduce the statistical power under the alternative hypothesis. In JCOG9907, hazard ratios for the three definitions were: 'IR = event', 0.80 (95% confidence interval, 0.59-1.07; P = 0.13); 'IR not event', 0.81 (95% confidence interval, 0.60-1.09; P = 0.16); landmark, 0.80 (95% confidence interval, 0.59-1.07; P = 0.15). No P value of any methods corresponded with the positive result for overall survival (P = 0.03). In the preoperative arms of the four studies, maximum differences in median and percentage of 1 year progression-free survival among the three definitions were 0-6.4 months and 1.2-5.2%. CONCLUSIONS: Progression-free survival sometimes fails as a surrogate of overall survival, and differences among results obtained with various progression-free survival definitions can be large. Overall survival should be used as primary endpoint in studies evaluating preoperative therapy.
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Nakamura et al. (2012) studied Cancer. Definitions of progression-free survival vs. Overall survival was evaluated on Progression-free survival ('IR = event' method) (HR 0.80, 95% CI 0.59-1.07, p=0.13). Different definitions of progression-free survival in preoperative cancer therapy yielded hazard ratios of 0.80 to 0.81 (P≥0.13), failing to surrogate the positive overall survival result (P=0.03).
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