Impact of metformin on clinical outcomes in advanced hepatocellular carcinoma treated with immune checkpoint inhibitors

• Published in: Liver cancer international Vol. 4; no. 2; pp. 77 - 88
• Main Authors: Kang, Sandra, Khalil, Lana, McCook‐Veal, Ashley, Liu, Yuan, Galvin, John, Draper, Amber, Kokabi, Nima, Diab, Maria, Shaib, Walid, Alese, Olatunji, Gbolahan, Olumide, El‐Rayes, Bassel, Akce, Mehmet
• Format: Journal Article
• Language: English
• Published: Hoboken John Wiley & Sons, Inc 01.06.2023
• Subjects: Alcohol; Antidiabetics; Body mass index; Cancer therapies; Clinical outcomes; Diabetes; Etiology; Hepatitis; hepatocellular carcinoma; immune checkpoint inhibitors; Immunotherapy; Kinases; Liver cancer; Liver cirrhosis; Liver diseases; Lung cancer; Medical prognosis; Melanoma; non‐alcoholic steatohepatitis; Ovaries; Patients; Response rates; White people
• ISSN: 2642-3561; 2642-3561
• DOI: 10.1002/lci2.71

Background and Aims Non‐alcoholic steatohepatitis (NASH) is a common cause of hepatocellular carcinoma (HCC) worldwide. Emerging data suggests NASH‐induced HCC could be associated with less response to immune checkpoint inhibitor (ICI)‐based therapy. Metformin has been associated with improved outcomes in cancers like melanoma treated with ICIs, but its impact on HCC is not well defined. The purpose of this study was to examine the effect of metformin on clinical outcomes in patients with advanced HCC treated with ICIs. Methods We retrospectively analysed patients with advanced HCC treated with ICIs in first and later‐line settings between 2015 and 2021. The primary endpoints were overall survival (OS), progression‐free survival (PFS), and objective response rate (ORR) as assessed according to Response Evaluation Criteria in Solid Tumours (RECIST) version 1.1. Patients were stratified based on their usage of metformin. Results Our study included 18 patients in the metformin group and 93 patients in the non‐metformin group. The most common causes of HCC were viral hepatitis (52%), NASH (29%), and alcohol (8%). ORR was 5.6% in the metformin group vs 22.6% in the non‐metformin group (P = .0987). Median OS was 10.8 months versus 45.9 months (HR = 1.99, 95% CI = 0.95–4.21, P = .065) and median PFS was 2.5 months versus 6.6 months (P = .077) in the metformin and non‐metformin groups, respectively. Regardless of metformin usage, OS was significantly worse in patients with poor ECOG performance status, HCC aetiology of NASH, MELD score 10–23, AFP >= 400, and use of ICIs in later lines of therapy. Conclusions Metformin use was associated with a trend, although not statistically significant, toward a worse ORR, OS and PFS in advanced HCC patients treated with ICIs.