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Association Between Early Immune-related Adverse Events and Clinical Outcomes in Patients With Non-Small Cell Lung Cancer Treated With Immune Checkpoint Inhibitors.
Hosoya, Kazutaka; Fujimoto, Daichi; Morimoto, Takeshi; Kumagai, Toru; Tamiya, Akihiro; Taniguchi, Yoshihiko; Yokoyama, Toshihide; Ishida, Tadashi; Hirano, Katsuya; Matsumoto, Hirotaka; Kominami, Ryota; Tomii, Keisuke; Suzuki, Hidekazu; Hirashima, Tomonori; Uchida, Junji; Morita, Mitsunori; Kanazu, Masaki; Sawa, Nobuhiko; Makio, Takeshi; Hara, Satoshi; Tamiya, Motohiro.
Afiliação
  • Hosoya K; Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
  • Fujimoto D; Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan. Electronic address: daichi@kcho.jp.
  • Morimoto T; Clinical Research Center, Kobe City Medical Center General Hospital, Kobe, Japan; Department of Clinical Epidemiology, Hyogo College of Medicine, Nishinomiya, Japan.
  • Kumagai T; Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.
  • Tamiya A; Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
  • Taniguchi Y; Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
  • Yokoyama T; Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.
  • Ishida T; Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.
  • Hirano K; Department of Respiratory Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
  • Matsumoto H; Department of Respiratory Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
  • Kominami R; Department of Respiratory Medicine, Himeji Medical Center, Himeji, Japan.
  • Tomii K; Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
  • Suzuki H; Department of Thoracic Oncology, Osaka Habikino Medical Center, Habikino, Osaka, Japan.
  • Hirashima T; Department of Thoracic Oncology, Osaka Habikino Medical Center, Habikino, Osaka, Japan.
  • Uchida J; Department of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.
  • Morita M; Department of Respiratory Medicine, Kobe City Medical Center West Hospital, Kobe, Japan.
  • Kanazu M; Department of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Toyonaka, Japan.
  • Sawa N; Department of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Toyonaka, Japan.
  • Makio T; Department of Respiratory Medicine, Itami City Hospital, Itami, Japan.
  • Hara S; Department of Respiratory Medicine, Itami City Hospital, Itami, Japan.
  • Tamiya M; Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Clin Lung Cancer ; 21(4): e315-e328, 2020 07.
Article em En | MEDLINE | ID: mdl-32113737
ABSTRACT

INTRODUCTION:

Previous studies have described an association between immune-related adverse events (irAEs) and better outcomes in patients administered nivolumab for advanced non-small-cell lung cancer. However, the patients in previous studies were not stratified by potential predictive factors, such as programmed cell death ligand 1 status and treatment lines. Additionally, little is known of whether the timing and type of irAEs can inform the prediction of outcomes. PATIENTS AND

METHODS:

We prospectively investigated the association between irAEs and outcomes in the single-center cohort that included patients administered nivolumab in the second or later line of therapy. Subsequently, we confirmed these findings in a retrospective multicenter cohort that included patients with programmed cell death ligand 1 tumor proportion score of ≥ 50% who had received first-line pembrolizumab. The primary outcome was progression-free survival (PFS).

RESULTS:

In the prospective cohort (n = 76), the median PFS was significantly longer for the patients experiencing irAEs within 2 weeks of beginning nivolumab compared with the PFS for those who did not (median, 5.0 months [95% confidence interval (CI), 2.1-8.6 months] vs. median, 2.0 months [95% CI, 1.9-2.5 months]; P = .046). The association was stronger with earlier (within 2 weeks) than with later (within 6 weeks) irAEs. In the retrospective cohort (n = 148), the median PFS was significantly longer for the patients with early irAEs (within 3 weeks) than for those without (median, not reached [95% CI, 5.9 months to not reached] vs. median, 6.9 months [95% CI, 4.2-9.7 months]; P = .04). Rash was common and a better predictor of outcomes in both cohorts.

CONCLUSION:

Our results have provided firmer evidence of the association between the occurrence of irAEs and outcomes and suggest that early irAEs (especially rash) might better predict outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Carcinoma Pulmonar de Células não Pequenas / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Inibidores de Checkpoint Imunológico / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Carcinoma Pulmonar de Células não Pequenas / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Inibidores de Checkpoint Imunológico / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão