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Influence of age on the efficacy of immune checkpoint inhibitors in advanced cancers: a systematic review and meta-analysis.
Ninomiya, Kiichiro; Oze, Isao; Kato, Yuka; Kubo, Toshio; Ichihara, Eiki; Rai, Kammei; Ohashi, Kadoaki; Kozuki, Toshiyuki; Tabata, Masahiro; Maeda, Yoshinobu; Kiura, Katsuyuki; Hotta, Katsuyuki.
Afiliação
  • Ninomiya K; Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Oze I; Division of Cancer Epidemiology and Prevention, Aichi Cancer Center, Nagoya, Japan.
  • Kato Y; Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
  • Kubo T; Center for Clinical Oncology, Okayama University Hospital, Okayama, Japan.
  • Ichihara E; Department of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
  • Rai K; Department of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
  • Ohashi K; Department of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
  • Kozuki T; Department of Thoracic Oncology and Medicine, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.
  • Tabata M; Center for Clinical Oncology, Okayama University Hospital, Okayama, Japan.
  • Maeda Y; Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Kiura K; Department of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
  • Hotta K; Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
Acta Oncol ; 59(3): 249-256, 2020 Mar.
Article em En | MEDLINE | ID: mdl-31782328
Background: Immune checkpoint inhibitors (ICIs) represent a paradigm shift in the development of cancer treatment. However, it remains to be clarified whether the benefits that they confer differ according to patient age. We conducted a systematic review and meta-analysis to assess age differences in the benefits of ICI treatment.Methods: We systematically searched the PubMed database for randomised controlled trials of ICIs, including PD-1, PD-L1 and CTLA-4 inhibitors across multiple cancer types, such as melanoma, lung cancer and gastric cancer. We extracted trials including hazard ratios (HRs) for death stratified by patient age (cut-off age, 65 years). The primary objective of this study was to assess the difference in ICI efficacy between younger and older patients. We calculated pooled HRs and 95% confidence intervals (CIs) for younger and older cancer patients, and assessed data heterogeneity.Results: We identified 3999 studies in our search. Of these, 24 eligible randomised trials, including a total of 8157 (57%) younger and 6104 (43%) older cancer patients, fulfilled the criteria for our study and were thus further analysed. The pooled HRs of the younger and older patients were 0.76 (95% CI: 0.69-0.84) and 0.80 (95% CI: 0.71-0.86), respectively; the difference in ICI efficacy between younger and older cancer patients was not significant (p = .82). Regarding the PD-1 and PD-L1 inhibitors, the survival benefit was similar in both age groups (HR: 0.74; p = .96), whereas for the CTLA-4 inhibitors, there tended to be less survival benefit for older versus younger patients (HR: 0.90 and 0.77, respectively; p = .26).Conclusions: The survival benefit conferred by ICI was not age-dependent, amongst patients aged 65 years or younger. However, age-dependent benefits may vary amongst different types of ICIs.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígeno B7-H1 / Antígeno CTLA-4 / Receptor de Morte Celular Programada 1 / Neoplasias Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Aged / Humans / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígeno B7-H1 / Antígeno CTLA-4 / Receptor de Morte Celular Programada 1 / Neoplasias Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Aged / Humans / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article