Magnitude of advantage in tumor response contributes to a better correlation between treatment effects on overall survival and progression-free survival: a literature-based meta-analysis of clinical trials in patients with metastatic colorectal cancer
Autor: | Mamoru Narukawa, Masayuki Kaneko, Yosuke Yoshida |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Oncology medicine.medical_specialty Colorectal cancer Subgroup analysis law.invention 03 medical and health sciences 0302 clinical medicine Randomized controlled trial law Internal medicine Antineoplastic Combined Chemotherapy Protocols Humans Medicine Progression-free survival Proportional Hazards Models Randomized Controlled Trials as Topic business.industry Surrogate endpoint Hazard ratio Hematology General Medicine medicine.disease Progression-Free Survival Clinical trial Treatment Outcome 030104 developmental biology 030220 oncology & carcinogenesis Meta-analysis Surgery Colorectal Neoplasms business |
Zdroj: | International Journal of Clinical Oncology. 25:851-860 |
ISSN: | 1437-7772 1341-9625 |
DOI: | 10.1007/s10147-020-01619-8 |
Popis: | Although it is suggested that the endpoints originated from the concept of tumor shrinkage dynamics, such as early tumor shrinkage and depth of response, are strongly associated with overall survival (OS) in patients with metastatic colorectal cancer (mCRC), they are yet to be validated as a single surrogate endpoint of OS by themselves. This study aimed to investigate the impact of advantage in tumor response on the correlation between treatment effects on progression-free survival (PFS) and OS in mCRC patients. Based on an electronic search, we identified randomized controlled trials of first-line therapy for mCRC. The impact of advantage in objective response rate (ORR) on the correlation between treatment effects on PFS and OS was evaluated based on Spearman correlation coefficients (rs). Forty-seven trials with a total of 24,018 patients were identified. The hazard ratio for PFS showed a relatively higher correlation with that for OS (rs = 0.63) when the trials were limited to those that demonstrated a larger difference in ORR, compared to the case for trials that demonstrated a smaller difference (rs = 0.32). This tendency was also observed in the subgroup analysis stratified by the types of treatment agents (targeted or non-targeted). The magnitude of advantage in tumor response was suggested to contribute to a better prediction of OS benefit based on PFS in patients with mCRC. The accuracy of OS estimation in mCRC is expected to be improved by considering the degree of tumor shrinkage in conjunction with PFS. |
Databáze: | OpenAIRE |
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