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Long-Term Survival of Patients With Non-Small Cell Lung Cancer Treated With Immune Checkpoint Inhibitor Monotherapy in Real-World Settings.
Yoneda, Taro; Sone, Takashi; Koba, Hayato; Shibata, Kazuhiko; Suzuki, Junya; Tani, Mayuko; Nishitsuji, Masaru; Nishi, Koichi; Kobayashi, Takafumi; Shirasaki, Hiroki; Araya, Tomoyuki; Kita, Toshiyuki; Kase, Kazumasa; Yamamura, Kenta; Terada, Nanao; Nishikawa, Shingo; Tambo, Yuichi; Kimura, Hideharu; Kasahara, Kazuo.
Afiliación
  • Yoneda T; Department of Respiratory Medicine, Komatsu Municipal Hospital, Komatsu, Japan. Electronic address: taroyoneda@yahoo.co.jp.
  • Sone T; Department of Respiratory Medicine, Kanazawa University, Kanazawa, Japan.
  • Koba H; Department of Respiratory Medicine, Komatsu Municipal Hospital, Komatsu, Japan.
  • Shibata K; Department of Medical Oncology, Kouseiren Takaoka Hospital, Takaoka, Japan.
  • Suzuki J; Department of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
  • Tani M; Department of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
  • Nishitsuji M; Department of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
  • Nishi K; Department of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
  • Kobayashi T; Department of Respiratory Medicine, Fukui-ken Saiseikai Hospital, Fukui, Japan.
  • Shirasaki H; Department of Respiratory Medicine, Fukui-ken Saiseikai Hospital, Fukui, Japan.
  • Araya T; Department of Respiratory Medicine, National Hospital Organization Kanazawa Medical Center, Kanazawa, Japan.
  • Kita T; Department of Respiratory Medicine, National Hospital Organization Kanazawa Medical Center, Kanazawa, Japan.
  • Kase K; Department of Internal Medicine, Keiju Medical Center, Nanao, Japan.
  • Yamamura K; Department of Internal Medicine, Keiju Medical Center, Nanao, Japan.
  • Terada N; Department of Respiratory Medicine, Kanazawa University, Kanazawa, Japan.
  • Nishikawa S; Department of Respiratory Medicine, Kanazawa University, Kanazawa, Japan.
  • Tambo Y; Department of Respiratory Medicine, Kanazawa University, Kanazawa, Japan.
  • Kimura H; Department of Respiratory Medicine, Kanazawa University, Kanazawa, Japan.
  • Kasahara K; Department of Respiratory Medicine, Kanazawa University, Kanazawa, Japan.
Clin Lung Cancer ; 23(6): 467-476, 2022 09.
Article en En | MEDLINE | ID: mdl-35618628
ABSTRACT

BACKGROUND:

Immune checkpoint inhibitor (ICI) monotherapy is more effective than cytotoxic chemotherapy in improving overall survival (OS) among patients with advanced-stage non-small cell lung cancer (NSCLC). Recently, chemotherapy combined with ICI has been found to yield good outcomes. However, ICI monotherapy is still considered an important treatment option. Data on long-term progression-free survival (PFS) and OS in real-world settings are limited. PATIENTS AND

METHODS:

This was a multicenter retrospective observational study. A total of 435 consecutive patients histologically diagnosed with advanced, metastatic, or recurrent NSCLC treated with ICI monotherapy were enrolled in this study from December 2015 to December 2018. Clinical data were collected from electronic medical records and pharmacy databases.

RESULTS:

The PFS and OS of the patients were 3.4 and 13.0 months, respectively. The objective response and disease control rates were 22.8% and 54.9%, respectively, and the 4-year survival rate was 17.9%. Multivariate analyses revealed that elder patients (>70 years), good Eastern Cooperative Oncology Group Performance Status (ECOG PS) score, programmed death-ligand 1 tumor proportion score (PD-L1 TPS) of ≥ 50%, absence of bone metastasis, and presence of immune-related skin toxicity, which is an immune-related adverse event, were correlated with good PFS. Moreover, good ECOG PS score, PD-L1 TPS of ≥ 50%, absence of bone metastasis, and presence of skin toxicity were correlated with good OS.

CONCLUSIONS:

The 4-year survival rate was 17.9%. Good ECOG PS score, PD-L1 TPS of ≥ 50%, absence of bone metastasis, and presence of skin toxicity were correlated with good PFS and OS.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 / 6_ODS3_enfermedades_notrasmisibles Problema de salud: 1_sistemas_informacao_saude / 6_other_respiratory_diseases / 6_trachea_bronchus_lung_cancer Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans Idioma: En Revista: Clin Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 / 6_ODS3_enfermedades_notrasmisibles Problema de salud: 1_sistemas_informacao_saude / 6_other_respiratory_diseases / 6_trachea_bronchus_lung_cancer Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans Idioma: En Revista: Clin Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article
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