Safety and Efficacy of Durvalumab After Chemoradiotherapy in Antinuclear Antibody-positive Patients With Non-small Cell Lung Cancer

被引:0
作者
Tsukaguchi, Akihiro [1 ]
Tamiya, Akihiro [1 ]
Fukuda, Shoichi [2 ]
Iwahashi, Yuki [1 ]
Kanaoka, Kensuke [3 ]
Tanaka, Yuya [1 ]
Inagaki, Yuji [1 ]
Taniguchi, Yoshihiko [1 ]
Nakao, Keiko [1 ]
Kagawa, Tomoko [1 ]
Matsuda, Yoshinobu [1 ]
Okishio, Kyoichi [4 ]
机构
[1] NHO Kinki Chuo Chest Med Ctr, Dept Internal Med, Kitaku Nagasone Cho 1180, Sakai, Osaka 5918555, Japan
[2] NHO Kinki Chuo Chest Med Ctr, Dept Radiol, Osaka, Japan
[3] Osaka Univ, Grad Sch Med, Dept Resp Med & Clin Immunol, Osaka, Japan
[4] NHO Kinki Chuo Chest Med Ctr, Dept Clin Res Ctr, Osaka, Japan
关键词
Antinuclear antibodies; chemoradiotherapy; durvalumab; non-small-cell lung cancer; pneumonitis; ADVERSE EVENTS; INHIBITORS; NIVOLUMAB;
D O I
10.21873/anticanres.17280
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/aim: Pneumonitis during durvalumab consolidation therapy after chemoradiotherapy (CRT) is a major cause of treatment discontinuation. Although previous studies have revealed an association between antinuclear antibody (ANA) positivity and the safety and efficacy of immune checkpoint inhibitors in advanced non-small cell lung cancer (NSCLC), there are no reports on durvalumab consolidation therapy. This study investigated the safety and efficacy of durvalumab after CRT in ANA-positive patients. Patients and methods: We retrospectively reviewed patients with unresectable NSCLC treated with durvalumab after CRT between August 2018 and July 2022 at our institution. We evaluated the association among ANA positivity, treatment-related adverse events (AEs), and survival outcomes. Results: Overall, 80 patients were enrolled, 39 of whom were ANA-positive. Although there were no significant differences in the incidence of each AE of any grade, ANA-positive patients tended to have a higher frequency of pneumonitis of grade 3 to 5 than ANA-negative patients (12.8% vs. 2.4%, p=0.104). ANA-positive patients had a significantly shorter median progression-free survival (PFS) and overall survival (OS) than ANA-negative patients [14.9 months vs. not reached (NR), p=0.005; NR vs. NR, p=0.013]. Multivariate analysis revealed that ANA positivity was an independent predictor of shorter PFS (HR=2.23; 95% CI=1.16-4.29; p=0.016) and OS (HR=2.28; 95% CI=1.01-5.12; p=0.046). Conclusion: ANA-positive patients receiving durvalumab after CRT tended to have a higher frequency of severe pneumonitis and significantly worse PFS and OS compared with ANA-negative patients.
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收藏
页码:4517 / 4524
页数:8
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