Initial treatment efficacy and safety of durvalumab plus tremelimumab combination therapy in unresectable hepatocellular carcinoma in clinical practice

被引:0
|
作者
Tomonari, Tetsu [1 ]
Tani, Joji [3 ]
Sato, Yasushi [2 ]
Tanaka, Hironori [1 ]
Morishita, Akihiro [3 ]
Okamoto, Koichi [1 ]
Kawano, Yutaka [1 ]
Sogabe, Masahiro [1 ]
Miyamoto, Hiroshi [1 ]
Takayama, Tetsuji [1 ]
机构
[1] Tokushima Univ, Grad Sch Med, Inst Biomed Sci, Dept Gastroenterol & Oncol, Tokushima, Japan
[2] Tokushima Univ, Dept Community Med Gastroenterol & Oncol, Grad Sch Med, Inst Biomed Sci, 2-50-1 Kuramoto Cho, Tokushima, Tokushima 770042, Japan
[3] Kagawa Univ, Grad Sch Med, Dept Gastroenterol & Neurol, Takamatsu, Kagawa, Japan
来源
JGH OPEN | 2024年 / 8卷 / 10期
关键词
durvalumab; hepatocellular carcinoma; tremelimumab; ATEZOLIZUMAB; BEVACIZUMAB;
D O I
10.1002/jgh3.70033
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimsWe aimed to evaluate the efficacy and safety of durvalumab plus tremelimumab (Dur + Tre) combination therapy in patients with unresectable hepatocellular carcinoma (uHCC) in clinical practice.MethodsWe retrospectively evaluated 37 patients with uHCC from our institutions between April 2023 and January 2024. Patients were divided into first- and later-line groups for analysis of antitumor efficacy, adverse events (AEs), and transition rate to second-line treatment according to the Response Evaluation Criteria in Solid Tumors (RECIST).ResultsThe disease control rate (DCR) for the first-line group was 80.9%, which was significantly higher than that for the later-line group (50%). The incidence of immune-related AEs (irAEs) was 24.3%, with grade 3 or higher irAEs including increased transaminase (8.1%), diarrhea (8.1%), and adrenal insufficiency (2.7%). The rates of drug withdrawal and discontinuation owing to AEs were 23.8% and 19%, respectively, in the first-line treatment and 31.2% and 12.5%, respectively, in the later-line treatment, with no significant difference. Analysis of changes in liver reserve using the albumin-bilirubin (ALBI) score showed no obvious loss of liver reserve for up to 12 weeks. The transition rate from first- to second-line therapy after progressive disease (PD) was as high as 94.7%.ConclusionThe efficacy and safety of Dur + Tre in clinical practice were comparable to those reported in a recent phase III trial. The first-line Dur + Tre therapy had a higher DCR than that of the later lines, and the transition rate to second-line therapy was considerably high, suggesting that Dur + Tre therapy would be more beneficial in first-line treatment. In this study, we analyzed the changes in tumor markers, both AFP and DCP, which were linked to the tumor evaluation decision in RECIST, especially at the time of PD evaluation, with a significant increase in AFP and DCP after one month, suggesting that they may be useful in determining early efficacy.image
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页数:8
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