Immune checkpoint inhibitors in the treatment of pleural mesothelioma: insights from real-world data

被引:0
|
作者
Kanayama, Masatoshi [1 ]
Manabe, Takehiko [1 ]
Yoshimatsu, Katsuma [1 ]
Oyama, Rintaro [1 ]
Matsumiya, Hiroki [1 ]
Mori, Masataka [1 ]
Takenaka, Masaru [1 ]
Kuroda, Koji [1 ]
Tanaka, Fumihiro [1 ]
机构
[1] Univ Occupat & Environm Hlth, Dept Surg 2, 1-1 Iseigaoka,Yahatanishi Ku, Kitakyushu 8078555, Japan
关键词
Immune checkpoint inhibitor; Ipilimumab; Nivolumab; Pleural mesothelioma; NIVOLUMAB PLUS IPILIMUMAB; EXPRESSION; TOXICITY; CRITERIA;
D O I
10.1007/s10147-025-02706-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Immune checkpoint inhibitors (ICIs) have recently emerged as a promising strategy for the treatment of pleural mesothelioma (PM). Methods This retrospective study evaluated treatment efficacy and safety in Japanese patients with PM treated with nivolumab and ipilimumab (N + I group: 41 patients) as first-line therapy and nivolumab monotherapy (N group: 33 patients) as second- or later-line treatment. Results The median overall survival (OS) and progression-free survival (PFS) were not reached and 10.4 months in the N + I group, and 8.6 months and 3.5 months in the N group, respectively. Treatment-related adverse events (TRAEs) of any grade occurred in 68.3% of the N + I group and 72.7% of the N group, with grade 3-4 TRAEs in 19.5% and 12.1% of patients, respectively. Patients with an ECOG PS 0-1 had significantly better OS and PFS in both treatment groups (p < 0.001). In the N + I group, OS was significantly better in patients with TRAEs (p = 0.020) and in those with the epithelioid subtype (p = 0.047), although PFS was not significantly different (p = 0.138 and p = 0.154, respectively). In the N group, both OS (p = 0.007) and PFS (p = 0.048) were significantly longer in patients with TRAEs. Conclusion This study provides valuable real-world clinical evidence of the efficacy and safety of nivolumab plus ipilimumab and nivolumab monotherapy in Japanese patients with PM. These results support the use of ICIs as a viable treatment option for advanced or relapsed disease.
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页码:705 / 717
页数:13
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