Hatanaka Takeshi, Yata Yutaka, Hiraoka Atsushi, Tada Toshifumi, Hirooka Masashi, Kariyama Kazuya, Tani Joji, Atsukawa Masanori, Takaguchi Koichi, Itobayashi Ei, Kakizaki Satoru, Fukunishi Shinya, Tsuji Kunihiko, Ishikawa Toru, Tajiri Kazuto, Toyoda Hidenori, Koshiyama Yuichi, Ogawa Chikara, Nishikawa Hiroki, Nishimura Takashi, Kawata Kazuhito, Kosaka Hisashi, Matsui Kosuke, Naganuma Atsushi, Tanaka Hironori, Ohama Hideko, Kuroda Hidekatsu, Matono Tomomitsu, Aoki Tomoko, Ochi Hironori, Imai Michitaka, Nakamura Shinichiro, Kanayama Yuki, Tanaka Kazunari, Tada Fujimasa, Yoshida Osamu, Nouso Kazuhiro, Morishita Asahiro, Tsutsui Akemi, Nagano Takuya, Itokawa Norio, Okubo Tomomi, Arai Taeang, Enomoto Hirayuki, Kaibori Masaki, Hiasa Yoichi, Kudo Masatoshi, Kumada Takashi
Department of Gastroenterology, Gunma Saiseikai Maebashi Hospital, Maebashi, Japan.
Department of Gastroenterology, Hanwa Memorial Hospital, Osaka, Japan.
Liver Int. 2025 Jul;45(7):e70192. doi: 10.1111/liv.70192.
This study aimed to evaluate the therapeutic efficacy and prognostic significance of C-reactive protein (CRP) in patients with advanced hepatocellular carcinoma (HCC) receiving durvalumab and tremelimumab (Dur/Tre).
A total of 167 patients treated with Dur/Tre between March 2023 and March 2024 in Japanese hospitals were included in this retrospective multicentre study. Patients were divided into two groups based on pre-treatment serum CRP levels: the low-CRP group (< 1 mg/dL, n = 106) and the high-CRP group (≥ 1 mg/dL, n = 61).
The median age of the cohort was 74.0 years (interquartile range, 67.5-79.5), and 139 patients (83.2%) were male. The median progression-free survival (PFS) was 3.6 months (95% CI: 2.6-5.4) in the low-CRP group and 2.4 months (95% CI: 1.9-4.1) in the high-CRP group, with statistical significance (p = 0.02). The median overall survival (OS) was not reached in the low-CRP group, with a 1-year survival rate of 64.7% (95% CI: 49.0-76.7), while it was 7.9 months (95% CI: 5.8-11.8) in the high-CRP group. The low-CRP group demonstrated significantly better survival outcomes compared to the high-CRP group (p < 0.001). Multivariate analysis identified serum CRP level as an independent predictive factor for both PFS and OS (p = 0.04 and < 0.001, respectively). No significant differences in immune-related adverse events were observed between the two groups.
Serum CRP may serve as a prognostic biomarker in HCC patients receiving Dur/Tre, with a potential association with treatment efficacy.