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Risk and survival of patients with non-small cell lung cancer and pre-existing autoimmune disorders receiving immune checkpoint blockade therapy: Survival analysis with inverse probability weighting from a nationwide, multi-institutional, retrospective study (NEJ047).
Asao, Tetsuhiko; Shukuya, Takehito; Uemura, Kohei; Kitadai, Rui; Yamamoto, Gaku; Mouri, Atsuto; Tamaoka, Meiyo; Imai, Ryosuke; Tsukita, Yoko; Isobe, Kazutoshi; Watanabe, Satoshi; Kamimura, Mitsuhiro; Morita, Ryo; Kudo, Keita; Inomata, Minehiko; Tateishi, Kazunari; Kakinuma, Kazutaka; Yoshioka, Hiroshige; Namba, Yukiko; Sumiyoshi, Issei; Nakagawa, Taku; Watanabe, Kana; Kobayashi, Kunihiko; Takahashi, Kazuhisa.
Afiliação
  • Asao T; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Shukuya T; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan. Electronic address: tshukuya@juntendo.ac.jp.
  • Uemura K; Interfaculty Initiative in Information Studies, The University of Tokyo, Tokyo, Japan.
  • Kitadai R; Department of Thoracic Oncology and Respiratory Medicine, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan; Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Yamamoto G; Department of Respiratory Medicine, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
  • Mouri A; Department of Respiratory Medicine, Saitama Medical University International Medical Center, Saitama, Japan.
  • Tamaoka M; Department of Respiratory Medicine, Toranomon Hospital, Tokyo, Japan.
  • Imai R; Department of Pulmonary Medicine, St. Luke's International Hospital, Tokyo, Japan.
  • Tsukita Y; Department of Respiratory Medicine, Tohoku University Graduate School of Medicine, Miyagi, Japan.
  • Isobe K; Division of Respiratory Medicine, Toho University School of Medicine, Tokyo, Japan.
  • Watanabe S; Department of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Kamimura M; Department of Pulmonology, National Hospital Organization Disaster Medical Center, Tokyo, Japan.
  • Morita R; Department of Respiratory Medicine, Akita Kousei Medical Center, Akita, Japan.
  • Kudo K; Department of Medical Oncology, National Hospital Organization Osaka Minami Medical Center, Osaka, Japan.
  • Inomata M; First Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
  • Tateishi K; First Department of Internal Medicine, Shinshu University School of Medicine, Nagano, Japan.
  • Kakinuma K; Division of Respiratory Medicine, Department of Internal Medicine, St. Marianna University School of Medicine, Kanagawa, Japan.
  • Yoshioka H; Department of Thoracic Oncology, Kansai Medical University Hospital, Osaka, Japan.
  • Namba Y; Department of Respiratory Medicine, Juntendo University Urayasu Hospital, Chiba, Japan.
  • Sumiyoshi I; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan; Department of Respiratory Medicine, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
  • Nakagawa T; Department of Thoracic Surgery, Omagari Kosei Medical Center, Akita, Japan.
  • Watanabe K; Department of Respiratory Medicine, Miyagi Cancer Center, Miyagi, Japan.
  • Kobayashi K; Department of Respiratory Medicine, Saitama Medical University International Medical Center, Saitama, Japan.
  • Takahashi K; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Lung Cancer ; 194: 107894, 2024 Jul 14.
Article em En | MEDLINE | ID: mdl-39029359
ABSTRACT

BACKGROUND:

The risk and survival of patients with non-small cell lung cancer (NSCLC) with pre-existing autoimmune disorders (AIDs) receiving immune checkpoint blockade (ICB) therapy have not been clearly established. PATIENTS AND

METHODS:

This multi-institutional, retrospective cohort study was conducted in collaboration with 20 centers in Japan.

RESULTS:

In total, 229 patients with advanced or recurrent NSCLC and pre-existing AID, with or without ICB treatment from January 2010-February 2020, were included and analyzed. Among 69 patients who received ICB, 2 received two lines of ICBs with a total of 71 ICB treatments; 57 (80.3 %) and 14 (19.7 %) patients received ICB monotherapy and combination therapy, respectively. AID flares were observed in 18 patients (25.4 %, 95 % confidence interval [CI], 15.8-37.1 %) receiving ICB. AID exacerbations were more likely when NSCLC was diagnosed less than 1 year after the AID diagnosis (odds ratio 5.26 [95 % CI, 1.40-21.61]; P = 0.016). Immune-related adverse events were observed in 32 patients (45.1 %, 95 % CI, 33.2-57.3 %); 17 had grade 3 or higher. The safety profile of combination immunotherapy was not significantly different from that of the monotherapy. After inverse probability weighting, the use of ICB prolonged survival (hazard ratio 0.43 [95 % CI, 0.26-0.70]; P = 0.0006).

CONCLUSIONS:

These findings revealed a novel risk factor for AID flares following ICB treatment, that is the diagnosis of NSCLC within 1 year of AID diagnosis, and showed that ICBs may improve survival in this population. These results support the utilization of ICB in patients with NSCLC and pre-existing AID.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão