Durvalumab-Based First-Line Chemoimmunotherapy in Advanced Biliary Tract Cancer: Real-World Outcomes and Prognostic Factors—A Turkish Oncology Group Study

dc.contributor.author Efil, S.C.
dc.contributor.author Kus, F.
dc.contributor.author Köylü, B.
dc.contributor.author Durukan, B.M.
dc.contributor.author Bayram, S.
dc.contributor.author Guzel, H.G.
dc.contributor.author Şendur, M.A.N.
dc.date.accessioned 2026-01-25T16:24:56Z
dc.date.available 2026-01-25T16:24:56Z
dc.date.issued 2026
dc.description.abstract Background: Durvalumab combined with gemcitabine–cisplatin (GC) has become the standard first-line treatment for advanced biliary tract cancer (BTC) following the TOPAZ-1 trial. However, real-world effectiveness, safety, and prognostic determinants, particularly in underrepresented populations, remain insufficiently defined. The aim of this study was to evaluate the real-world outcomes of first-line durvalumab plus chemotherapy and identify independent prognostic factors in patients with advanced BTC. Methods: This multicenter retrospective cohort study included patients with unresectable or metastatic BTC treated with first-line durvalumab plus chemotherapy across 21 tertiary oncology centers in Türkiye. Clinical characteristics, laboratory parameters, biomarker data, and treatment details were collected. The primary endpoint was overall survival (OS), while secondary endpoints included progression-free survival (PFS), objective response rate (ORR), and safety. Survival outcomes were analyzed using the Kaplan–Meier method and Cox proportional hazards regression models. Results: A total of 78 patients were analyzed; 53.8% were male, and the median age was 62 years. Primary tumor sites were intrahepatic (55.1%), extrahepatic (30.8%), and gallbladder (14.1%). After a median follow-up of 12.58 months, median OS was 11.59 months and median PFS was 6.80 months. The ORR was 50.6%, including complete and partial responses in 2.7% and 47.9% of patients, respectively. Treatment-related adverse events occurred in 97.4% of patients, with grade 3–4 events in 37.2%. Immune-related adverse events were observed in 19.2%, including one case of grade 3 pneumonitis. No patient permanently discontinued durvalumab due to toxicity, and no durvalumab-related mortality occurred. In multivariable analysis, ECOG performance status 2 (HR 3.43; 95% CI 1.33–8.80) and ALBI grade 2–3 (HR 2.54; 95% CI 1.24–5.19) independently predicted worse OS, while ECOG performance status 2 also predicted shorter PFS (HR 5.91; 95% CI 2.30–15.17). Conclusions: In this multicenter real-world Turkish cohort, first-line durvalumab plus chemotherapy showed effectiveness and tolerability comparable to clinical trial data. Baseline ECOG performance status and ALBI grade were independent prognostic factors, supporting their use for risk stratification in advanced biliary tract cancer. © 2025 by the authors. en_US
dc.identifier.doi 10.3390/cancers18010101
dc.identifier.issn 2072-6694
dc.identifier.scopus 2-s2.0-105027628940
dc.identifier.uri https://doi.org/10.3390/cancers18010101
dc.language.iso en en_US
dc.publisher Multidisciplinary Digital Publishing Institute (MDPI) en_US
dc.relation.ispartof Cancers en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Albumin–Bilirubin Grade (Albi) en_US
dc.subject Biliary Tract Cancer en_US
dc.subject Durvalumab en_US
dc.subject Gemcitabine–Cisplatin en_US
dc.subject Prognostic Factors en_US
dc.subject Real-World Data en_US
dc.title Durvalumab-Based First-Line Chemoimmunotherapy in Advanced Biliary Tract Cancer: Real-World Outcomes and Prognostic Factors—A Turkish Oncology Group Study en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Alan, Ozkan/0000-0002-6635-2012
gdc.author.id Akbaş, Sinem/0000-0002-7197-211X
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gdc.description.department İzmir Ekonomi Üniversitesi en_US
gdc.description.departmenttemp [Efil] Safa Can, Department of Medical Oncology, Ankara Bilkent City Hospital, Ankara, Ankara, Turkey; [Kus] Fatih, Department of Medical Oncology, Hacettepe Üniversitesi, Ankara, Turkey; [Köylü] Bahadır, Department of Medical Oncology, Koç University, Istanbul, Turkey; [Durukan] Bekir Mert, Department of Medical Oncology, Hacettepe Üniversitesi, Ankara, Turkey; [Bayram] Selami, Department of Medical Oncology, Antalya Training and Research Hospital, Antalya, Antalya, Turkey; [Guzel] Halil Göksel, Department of Medical Oncology, University of Health Sciences, Istanbul, Turkey; [Öztürk] Banu, Department of Medical Oncology, University of Health Sciences, Istanbul, Turkey; [Muglu] Harun, Department of Medical Oncology, İstanbul Medipol Üniversitesi, Istanbul, Turkey; [Bilici] Ahmet Erkan, Department of Medical Oncology, İstanbul Medipol Üniversitesi, Istanbul, Turkey; [Köse] Fatih, Department of Medical Oncology, Başkent Üniversitesi, Ankara, Turkey; [Alan] Ozkan, Department of Medical Oncology, Istanbul University-Cerrahpasa, Istanbul, Turkey; [Karapelit Agitoglu] Eda, Department of Medical Oncology, Necmettin Erbakan Üniversitesi, Meram, Konya, Turkey; [Güner] Gürkan, Department of Medical Oncology, Izmir Ekonomi Üniversitesi, Izmir, Turkey; [Beşen] Ali Ayberk, Department of Medical Oncology, İstanbul Aydın Üniversitesi, Istanbul, Turkey; [Helvaci] Kaan, Department of Medical Oncology, Ankara Numune Hospital, Ankara, Turkey; [Araz] Murat, Department of Medical Oncology, Necmettin Erbakan Üniversitesi, Meram, Konya, Turkey; [Kaçan] Turgut, Department of Medical Oncology, Doruk Health Group Nilüfer Hospital, Bursa, Turkey; [Arslan] Çaǧatay, Department of Medical Oncology, Izmir Ekonomi Üniversitesi, Izmir, Turkey; [Unal] Ahmet, Department of Medical Oncology, Dokuz Eylül Üniversitesi, Izmir, Turkey; [Eniseler] Emine Bihter, Department of Medical Oncology, Manisa Celâl Bayar Üniversitesi, Manisa, Manisa, Turkey; [Biter] Sedat, Department of Medical Oncology, Çukurova Üniversitesi, Adana, Adana, Turkey; [Ekinci] Ferhat, Department of Medical Oncology, Manisa Celâl Bayar Üniversitesi, Manisa, Manisa, Turkey; [Aslan] Ferit Ferhat, Department of Medical Oncology, Medical Park Batıkent Private Hospital, Ankara, Turkey; [Ünek] Ilkay Tuǧba, Department of Medical Oncology, Dokuz Eylül Üniversitesi, Izmir, Turkey; [Tas] Semra, Department of Medical Oncology, Pamukkale Üniversitesi, Denizli, Denizli, Turkey; [Acar] Ömer, Department of Medical Oncology, Mardin Training and Research Hospital, Mardin, Mardin, Turkey; [Ateş] Öztürk, Department of Medical Oncology, Ankara Oncology Education and Research Hospital, Ankara, Turkey; [Şakalar] Teoman, Department of Medical Oncology, Kahramanmaras Sütçü Imam Üniversitesi, Kahramanmaras, Kahramanmaras, Turkey; [Akbas] Sinem, Department of Medical Oncology, Koç University, Istanbul, Turkey; [Karakaş] Hilal, Department of Medical Oncology, Ankara Bilkent City Hospital, Ankara, Ankara, Turkey; [Akinci] Muhammed Bölent, Department of Medical Oncology, Ankara Bilkent City Hospital, Ankara, Ankara, Turkey; [Yalçin] Bülent, Department of Medical Oncology, Ankara Bilkent City Hospital, Ankara, Ankara, Turkey; [Yalçın] Şuayip, Department of Medical Oncology, Hacettepe Üniversitesi, Ankara, Turkey; [Şendur] Mehmet Ali Nahit, Department of Medical Oncology, Ankara Bilkent City Hospital, Ankara, Ankara, Turkey en_US
gdc.description.issue 1 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality N/A
gdc.description.volume 18 en_US
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