Analysis of response-related endpoints in trials of first-line medical treatment of metastatic colorectal cancer

被引:5
|
作者
Colloca, Giuseppe A. [1 ]
Venturino, Antonella [1 ]
Guarneri, Domenico [1 ]
机构
[1] Osped Civile Sanremo, Dept Oncol, Via G Borea 56, I-18038 Imperia, Italy
关键词
Overall response rate; Disease control rate; Early tumor shrinkage; Prognosis; Overall survival; EARLY TUMOR SHRINKAGE; BEVACIZUMAB PLUS MFOLFOX6; RANDOMIZED PHASE-III; COMPUTED-TOMOGRAPHY; LIVER METASTASES; CHEMOTHERAPY; SURVIVAL; CETUXIMAB; PANITUMUMAB; OXALIPLATIN;
D O I
10.1007/s10147-019-01504-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Tumor radiologic response after systemic chemotherapy has been used as endpoint of trials of patients with metastatic colorectal cancer (mCRC), which can report the best overall response rate (ORR) and the disease control rate (DCR) by RECIST criteria as well as the early tumor shrinkage (ETS). The present study perform a trial-level analysis to verify whether such response-related endpoints are predictive of overall survival (OS). Methods After a systematic search, randomized clinical trials (RCTs) were selected each time they evaluated the three response endpoints and progression-free survival (PFS). Two arms per trial were selected, and the correlation between the difference in each endpoint and the difference in OS was calculated. The analysis then evaluated the effects of treatment on Delta ORR, or Delta DCR, Delta ETS, Delta PFS, and on Delta OS, using separate linear regressions for each of them, and the proportion of variability explained (R-trial(2)) on OS for each of the four endpoints was calculated. Results The systematic review of the literature led to the selection of 12 RCTs, 7 phase-3 and 5 phase-2. ETS reported a different performance in the entire sample compared to phase-3 trials (R-trial(2)=0.172 vs. 0.842), differently from DCR (R-trial(2)=0.541 vs. 0.816) and ORR (R-trial(2)=0.349 vs. 0.740). Surprisingly, PFS predicted OS with a weak correlation, which was not significant in the subgroup of phase-3 studies (R-trial(2)=0.455 vs. 0.466). Conclusion The results of the present trial-level analysis report a good performance of two response-related endpoints, DCR and ETS, and suggest that they could be differently used depending on the setting of disease and the type of medical treatment.
引用
收藏
页码:1406 / 1411
页数:6
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