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Association of candidate surrogate endpoints with overall survival in advanced biliary tract cancer

Castet, F.
Fabregat-Franco, C.
Bridgewater, J.
Kim, J. W.
Rimini, M.
La Casta, A.
Lamarca, A.
Kang, M.
Salani, F.
Castillo, A.
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Abstract
BACKGROUND & AIMS: Surrogate endpoints are increasingly used in biliary tract cancer (BTC) trials. While this may expedite drug approval and decrease costs, surrogate endpoints may not always correlate with an overall survival (OS) advantage. We aimed to explore the association of progression-free survival (PFS), objective response rate (ORR) and disease control rate (DCR) with OS at the trial- and patient-level. METHODS: For the trial-level analysis, we performed a systematic review of Pubmed/MEDLINE, Embase, Cochrane, clinicaltrials.gov and conference proceedings for phase II-III trials in advanced BTC. We used a weighted linear regression to measure the correlation of OS with PFS, ORR and DCR. For the patient-level analysis, we analyzed patients included in five randomized trials and three real-world datasets. The protocol is registered with PROSPERO, CRD42023398279. RESULTS: For the trial-level analysis, we included 41 studies, involving 88 treatment arms and 7,817 patients. The coefficient of determination (R(2)) of the model was 0.71 (95% CI 0.56-0.86) for PFS, 0.01 (0-0.08) for ORR and 0.39 (0.14-0.64) for DCR. Predefined subgroup analysis showed consistent results. For the patient-level analysis, we included a total of 2,506 patients, 783 in randomized trials (first-line 512, second-line 271) and 1,723 in routine clinical care (first-line chemotherapy 773, first-line chemotherapy-durvalumab 628, second-line chemotherapy 322). Across the distinct datasets, the correlation coefficient ranged from 0.73 to 0.86 for PFS. A responder analysis found no association between response and survival. CONCLUSION: PFS shows a moderate correlation with OS both at the trial- and patient-level, while ORR and DCR show a low correlation. Whilst PFS is currently the best candidate surrogate marker for OS, our results highlight the need for novel endpoints in this field. IMPACT AND IMPLICATIONS: The use of validated surrogate endpoints in biliary tract cancer trials may decrease costs and improve study feasibility, particularly with agents that only target small subsets of patients or in trials that incorporate a crossover design. A formal statistical validation of surrogacy requires patient-level and trial-level data. This is the first comprehensive analysis to incorporate novel agents (including immunotherapies and targeted agents), include patient-level data and rigorously and homogeneously extract appropriate measures of treatment effect for endpoint correlation. These results show a moderate correlation for progression-free survival both at the trial- and patient-level and a low correlation for disease control rate and response rate. This information will aid clinicians in appropriately interpreting contemporary clinical trials and guide clinical researchers and trial sponsors involved in clinical trial design. Furthermore, it has important implications for the regulatory approval process and may aid agencies in appropriately evaluating novel drugs.
Affiliation
Upper Gastrointestinal and Endocrine Tumor Unit, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron University Hospital, Barcelona, Spain. Catalan Institute of Oncology (ICO), L'Hospitalet de Llobregat, Barcelona, Spain. Department of Medical Oncology, University College London Cancer Institute, London, United Kingdom. Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea. Department of Oncology, Vita-Salute San Raffaele University, IRCCS San Raffaele Scientific Institute Hospital, Milan, Italy. Department of Medical Oncology, UGC Oncología Guipúzcoa, País Vasco, Spain. Department of Medical Oncology - Onco Health Institute, Instituto de Investigaciones Sanitarias FJD, Fundación Jiménez Díaz University Hospital, Madrid, Spain; Department of Medical Oncology, The Christie NHS Foundation, Manchester, Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom. Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy and Sant'Anna School of Advanced Studies, Pisa, Italy. Department of Medical Oncology, Asturias Central University Hospital, ISPA, Oviedo, Spain. Cancer Research UK & UCL Cancer Centre, University College of London, London, United Kingdom. Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea. Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (Milan), Italy; Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano (Milan), Italy. Department of Medical Oncology Hospital Universitario 12 de Octubre, Madrid, Spain. Biblioteca, Docència, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain. Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain. Cholangiocarcinoma Foundation, Herriman, UT, United States; Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom. Upper Gastrointestinal and Endocrine Tumor Unit, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron University Hospital, Barcelona, Spain. Electronic address: tmacarulla@vhio.net.
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2025
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Article
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Castet F, Fabregat-Franco C, Bridgewater J, Kim JW, Rimini M, La Casta A, et al. Association of candidate surrogate endpoints with overall survival in advanced biliary tract cancer. Journal of hepatology. 2025 Nov;83(5):1102-15. PubMed PMID: 40473034. Epub 2025/06/06. eng.
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