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Progression-Free Survival Early Assessment Is a Robust Surrogate Endpoint of Overall Survival in Immunotherapy Trials of Hepatocellular Carcinoma
- Source :
- Cancers, Cancers, Vol 13, Iss 90, p 90 (2021), Volume 13, Issue 1
- Publication Year :
- 2020
- Publisher :
- MDPI, 2020.
-
Abstract
- Background: Radiology-based outcomes, such as progression-free survival (PFS) and objective response rate (ORR), are used as surrogate endpoints in oncology trials. We aimed to assess the surrogacy relationship of PFS with overall survival (OS) in clinical trials of systemic therapies targeting advanced hepatocellular carcinoma (HCC) by novel meta-regression methods. Methods: A search of databases (PubMed, American Society of Clinical Oncology (ASCO), and European Society for Medical Oncology (ESMO) Meeting Libraries, Clinicaltrials.gov) for trials of systemic therapies for advanced HCC reporting both OS and PFS was performed. Individual patient data were extracted from PFS and OS Kaplan&ndash<br />Meier curves. Summary median PFS and OS data were obtained from random-effect model. The surrogate relationships of median PFS, first quartile (Q1), third quartile (Q3), and restricted mean survival time (RMST) for OS were evaluated by the coefficient of determination R2. Heterogeneity was explored by meta-regression. Results: We identified 49 trials, 11 assessing immune-checkpoint inhibitors (ICIs) and 38 multikinase inhibitors (MKIs). Overall, the correlation between median PFS and median OS was weak (R2 = 0.20. 95% Confidence Intervals [CI]-0.02<br />0.42). Surrogacy robustness varied between treatment classes and PFS endpoints. In ICI trials only, the correlations between Q1-PFS and Q1-OS and between 12-month PFS-RMST and 12-month OS-RMST were high (R2 = 0.89, 95%CI 0.78&ndash<br />0.98, and 0.80, 95% CI 0.63&ndash<br />0.96, respectively). Interaction p-values obtained by meta-regression confirmed the robustness of results. Conclusions: In trials of systemic therapies for advanced HCC, the surrogate relationship of PFS with OS is highly variable depending on treatment class (ICI or MKI) and evaluation time-point. In ICI trials, Q1-PFS and 12-month PFS-RMST are robust surrogate endpoints for OS.
- Subjects :
- Oncology
Cancer Research
medicine.medical_specialty
medicine.medical_treatment
overall survival
lcsh:RC254-282
Article
Settore MED/01 - Statistica Medica
03 medical and health sciences
0302 clinical medicine
Internal medicine
surrogate endpoint
medicine
Overall survival
030212 general & internal medicine
Progression-free survival
neoplasms
Settore MED/12 - Gastroenterologia
business.industry
Surrogate endpoint
Immunotherapy
hepatocellular carcinoma
medicine.disease
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Confidence interval
Clinical trial
Quartile
030220 oncology & carcinogenesis
Hepatocellular carcinoma
surrogate endpoints
immunotherapy
Settore SECS-S/01 - Statistica
business
progression-free survival
Subjects
Details
- Language :
- English
- ISSN :
- 20726694
- Volume :
- 13
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Cancers
- Accession number :
- edsair.doi.dedup.....f80c68187b2a81bef805676b613cd892