Progression-free survival as a surrogate endpoint of overall survival in patients with metastatic colorectal cancer

被引:13
|
作者
Cicero, Giuseppe [1 ]
De Luca, Rossella [1 ]
Dieli, Francesco [2 ]
机构
[1] Univ Palermo, Dept Surg Oncol & Oral Sci, Sect Med Oncol, Palermo, Italy
[2] Univ Palermo, Cent Lab Adv Diag & Biomed Res CLADIBIOR, Palermo, Italy
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
关键词
colorectal neoplasm; overall survival; progression-free survival; surrogate endpoint liver metastates; avastin; egorafenib; TUMOR RESPONSE; CHEMOTHERAPY; BEVACIZUMAB; ONCOLOGY; THERAPY; BREAST; TRIALS;
D O I
10.2147/OTT.S151276
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: In many clinical trials designed to assess the efficacy of anticancer treatments, overall survival (OS) is often used as a primary endpoint despite its several points of weakness. Methods: This study evaluated the role of progression-free survival (PFS) in the first three lines of treatment as a potential surrogate endpoint of OS in patients with metastatic colorectal cancer (MCRC). One hundred and twenty patients with MCRC were enrolled in this study. The median PFS of the first-, second-, and third-lines of treatment and the OS were evaluated. The correlation between the time to progression and the OS was analyzed. The median PFS of the three lines of treatment were 8.5, 5, and 3 months, respectively. Results: The median OS was 32.4 months. A modest correlation was found between the PFS to the first-line treatment with Folfox-avastin and OS. Similar data were obtained with the second-line treatment. however, no correlation was found between the PFS and OS during the third-line treatment. The regression analysis revealed that PFS is predictive of OS. Conclusion: In brief, the PFS of the first- and second-lines of treatment could be a good candidate as a surrogate endpoint of OS in patients with MCRC.
引用
收藏
页码:3059 / 3063
页数:5
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