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Objectives: To determine the cost-effectiveness of combined durvalumab and tremelimumab in patients with metastatic colorectal cancer in the intention-to-treat (ITT) and biomarker-enriched populations using direct CCTG CO.26 phase-2 trial data.
Methods: A 4-state microsimulation model was used to evaluate the expected health outcomes in quality-adjusted life years (QALYs) and costs (2023 Canadian Dollars) over a lifetime horizon (5 years) from the Canadian public-payer perspective. Direct phase 2 CCTG CO.26 trial data informed model inputs, including overall survival Kaplan-Meier curves, progression-free survival Kaplan-Meier curves, and adverse event rates. Health-state utilities and costs of therapy, hospitalization, end-of-life care, sequencing panels, and physician care were obtained from published literature and Canadian costing databases. The incremental cost-utility ratios (ICURs) for the ITT and biomarker-enriched populations were determined.
Results: In the ITT population, expected QALYs for the treatment and best supportive care arms were 0.47 and 0.33 (incremental (Δ)0.14), respectively, and expected costs were $56 743 and $17 177 (Δ$39 566) for an ICUR of $277 661/QALY. In the plasma tumor mutation burden > 28 subgroup, expected QALYs were 0.43 and 0.21 (Δ0.21) and expected costs were $58 498 and $16 941 (Δ$41 557) for an ICUR of $193 945/QALY.
Conclusions: Combined durvalumab and tremelimumab is not cost-effective in refractory metastatic colorectal cancer per conventional cost-effectiveness thresholds. Cost-effectiveness is more favorable in the high-plasma tumor mutation burden subgroup, but costs of screening and cutoffs used must be considered.
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http://dx.doi.org/10.1016/j.jval.2025.04.2159 | DOI Listing |
Aims: This study aimed to evaluate the therapeutic efficacy of durvalumab and tremelimumab (Dur/Tre) in patients with hepatocellular carcinoma (HCC) who had a tumor thrombus in the main portal vein trunk (Vp4) or high tumor burden (HTB).
Methods: A total of 309 patients with BCLC stage B or C HCC who received Dur/Tre between March 2023 and October 2024 were included. HTB was defined as the presence of at least one of the following radiological findings: ≥ 50% liver involvement by HCC, bile duct invasion, or the presence of Vp4.
Intern Med
September 2025
Department of Gastroenterology, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Japan.
Objective This study aimed to evaluate the efficacy and safety of atezolizumab plus bevacizumab (Atez+Bev) as a second-line therapy after the administration of durvalumab plus tremelimumab (Dur+Tre) in patients with hepatocellular carcinoma (HCC). We focused on the treatment outcomes and adverse event profiles specific to this sequential regimen. Methods A retrospective analysis was conducted on 16 patients who received second-line Atez+Bev after Dur+Tre therapy between April 2023 and August 2024 in our hospital and associated institutions.
View Article and Find Full Text PDFCancer Diagn Progn
September 2025
Department of Gastroenterology, Saiseikai Niigata Hospital, Niigata, Japan.
Background/aim: Systemic therapy with immune checkpoint inhibitors for advanced hepatocellular carcinoma (HCC) treatment has demonstrated high response rates. Durvalumab plus tremelimumab (Dur/Tre) has been approved for HCC treatment and has become a first-line systemic therapy along with atezolizumab plus bevacizumab. However, there is early withdrawal owing to immune-related adverse effects, while others required sequential therapy owing to the lack of early therapeutic effects.
View Article and Find Full Text PDFCase Rep Oncol
February 2025
Department of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Introduction: SMARCB1 (INI1)-deficient intrathoracic neoplasms are rare and highly malignant. We report a case of a patient with this tumor who was initially diagnosed with non-small cell lung cancer and whose disease rapidly progressed to death despite chemotherapy.
Case Presentation: A man in his 60s was diagnosed with a mass exceeding 10 cm in the lower lobe of the right lung and a right pleural effusion on the first examination.
Hepatol Int
August 2025
Department of Gastroenterology and Hepatology, Graduate School of Medicine, Hokkaido University, North 15, West 7, Kita-Ku, Sapporo, Hokkaido, 060-8638, Japan.
Background: Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality. Although the atezolizumab/bevacizumab regimen demonstrated impressive efficacy in the IMbrave150 clinical trial, long-term outcomes, particularly 3-year overall survival (OS), remain unestablished because of limited follow-up. Long-term outcomes have been reported for the tremelimumab/durvalumab combination, highlighting the need for comparable data on atezolizumab/bevacizumab.
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