Abstract
Background and Objective
Durvalumab plus tremelimumab (Durva/Treme) has recently been approved as a first-line or later-line treatment for patients with unresectable hepatocellular carcinoma (u-HCC) in Japan. We assessed the real-world outcomes of Durva/Treme for u-HCC, with a focus on treatment efficacy and safety.
Methods
We retrospectively evaluated 22 patients with u-HCC treated with Durva/Treme at Iwate Medical University during the period from 2023 to 2024, with a comparison of the clinical outcomes between patients who received Durva/Treme as first-line and later-line treatments. We further evaluated changes in the modified albumin-bilirubin (mALBI) grade during treatment.
Results
There were 10 patients in the first-line group and 12 patients in the later-line treatment group. During the follow-up with a median duration of 7.6 months, the median progression-free survival (first-line versus later-line: 4.7 months versus 2.9 months, p = 0.85), the objective response rate (0.0% versus 16.7%, p = 0.48), the disease control rate (60.0% versus 58.4%, p = 1.00), and the incidence of any adverse event (50.0% versus 75.0%, p = 0.38) were not statistically different between the two groups. The changes in the mALBI scores were not statistically significant (p = 0.75).
Conclusions
Durva/Treme may be effective and safe for patients with u-HCC, even in patients who receive Durva/Treme as a later-line treatment.
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Details
; Kuroda, Hidekatsu 1 ; Abe, Tamami 1 ; Kakisaka, Keisuke 1 ; Nakaya, Ippeki 1 ; Ito, Asami 1 ; Watanabe, Takuya 1 ; Yusa, Kenji 1 ; Nagasawa, Tomoaki 1 ; Sato, Hiroki 1 ; Suzuki, Akiko 1 ; Endo, Kei 1 ; Yoshida, Yuichi 1 ; Oikawa, Takayoshi 1 ; Sawara, Kei 1 ; Miyasaka, Akio 1 ; Matsumoto, Takayuki 1 1 Iwate Medical University, Division of Gastroenterology and Hepatology, Department of Internal Medicine, Iwate, Japan (GRID:grid.411790.a) (ISNI:0000 0000 9613 6383)





