Hepatology Research

Antitumor effects and immune‐mediated adverse events of durvalumab plus tremelimumab treatment for unresectable hepatocellular carcinoma

Takanori Ito 1
Shigeo Shimose 2
Joji Tani 3
Tetsu Tomonari 4
Issei Saeki 5
Yasuto TAKEUCHI 6
Takeshi Hatanaka 7
Kyo Sasaki 8
Satoru Kakizaki 9
Yuki Kanayama 7
Naoki Yoshioka 10
Takehito Naito 11
Mamiko Takeuchi 12
Tetsuya Yasunaka 13
Masahiro Sakata 14
Hideki Iwamoto 2, 15
Satoshi ITANO 16
Tomotake Shirono 2
Norikazu Tanabe 17
Takafumi Yamamoto 1
Sohji Nishina 8
Motoyuki Otsuka 6
Taro Takami 5
Tetsuji Takayama 4
Takumi KAWAGUCHI 2
Hiroki Kawashima 1
Show full list: 27 authors
7
 
Department of Gastroenterology Gunma Saiseikai Maebashi Hospital Maebashi Japan
9
 
Department of Clinical Research NHO Takasaki General Medical Center Takasaki Japan
10
 
Department of Gastroenterology and Hepatology Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital Nagoya Japan
11
 
Department of Gastroenterology Toyohashi Municipal Hospital Toyohashi Japan
12
 
Department of Gastroenterology Anjo Kosei Hospital Anjo Japan
13
 
Department of Gastroenterology Fukuyama City Hospital Fukuyama Japan
14
 
Department of Gastroenterology National Hospital Organization Fukuyama Medical Center Fukuyama Japan
15
 
Department of Gastroenterology and Hepatology Iwamoto Internal Medical Clinic Kitakyusyu Japan
16
 
Department of Gastroenterology and Hepatology Kurume Central Hospital Kurume Japan
18
 
Department of Gastroenterology NHO Takasaki General Medical Center Takasaki Japan
Publication typeJournal Article
Publication date2024-12-15
scimago Q1
SJR1.241
CiteScore8.3
Impact factor3.9
ISSN13866346, 1872034X
Abstract
Aim

Durvalumab plus tremelimumab (Dur/Tre) is a first‐line systemic treatment option for unresectable hepatocellular carcinoma (uHCC). However, the management of severe immune‐mediated adverse events (imAEs) is challenging. Therefore, we investigated the relationship between severe imAEs and antitumor responses in patients with uHCC treated with Dur/Tre.

Methods

We included 157 patients with uHCC treated with Dur/Tre in this multicenter, retrospective study and analyzed the relationship between progression‐free survival (PFS)/antitumor response and severe imAEs requiring high‐dose corticosteroid treatment.

Results

Thirty‐two patients (20.4%) developed severe imAEs, including enterocolitis/diarrhea (n = 10), liver injury (n = 9), interstitial lung disease (n = 5), rashes (n = 4), cytokine‐release syndrome/fever (n = 2), pancreatitis (n = 2), and others (n = 4) (median follow‐up period, 6.8 months). Infliximab was administered in six patients with steroid‐refractory enterocolitis. Although the objective response rate (ORR) and disease control rate (DCR) were significantly higher with first‐line therapy than with later‐line therapy (p = 0.026), the frequency of severe imAEs was not significantly different (p = 0.221). The ORR and DCR in patients with and without severe imAEs were 15.6% and 17.6% and 65.6% and 47.2%, respectively, with no significant differences. Five patients with severe imAEs, including rashes and liver injury, showed objective responses (partial response + complete response). Among patients who achieved an objective response, the PFS at 10 months was good (100% and 70.3% with and without high‐dose corticosteroids, respectively).

Conclusions

Severe imAEs of Dur/Tre treatment requiring high‐dose corticosteroid treatment did not affect antitumor efficacy, which differed depending on the type of imAEs. Therefore, appropriately managing imAEs is essential to guide sequential treatment.

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