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More than one-third of advanced non-small-cell lung cancer patients do not receive immunochemotherapy due to intolerance.
Ando, Chihiro; Ichihara, Eiki; Yokoyama, Toshihide; Inoue, Koji; Tamura, Tomoki; Fujiwara, Keiichi; Oda, Naohiro; Kano, Hirohisa; Kishino, Daizo; Watanabe, Kazuhiko; Inoue, Masaaki; Ochi, Nobuaki; Onishi, Fumie; Ichikawa, Hirohisa; Kobe, Hiroshi; Tachibana, Sayaka; Hotta, Katsuyuki; Maeda, Yoshinobu; Kiura, Katsuyuki.
Afiliación
  • Ando C; Department of Hematology and Oncology, Dentistry, and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama, Japan.
  • Ichihara E; Department of Allergy and Respiratory Medicine, Okayama University Hospital, 2-5-1 Shikata-Cho Kita-Ku Okayama City, Okayama, 700-8558, Japan. ichiha-e@md.okayama-u.ac.jp.
  • Yokoyama T; Department of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, Okayama, Japan.
  • Inoue K; Department of Respiratory Medicine, Ehime Prefectural Central Hospital, Matsuyama, Japan.
  • Tamura T; Department of Respiratory Medicine, NHO Iwakuni Clinical Center, Iwakuni, Japan.
  • Fujiwara K; Department of Respiratory Medicine, National Hospital Organization Okayama Medical Center, Okayama, Japan.
  • Oda N; Department of Internal Medicine, Fukuyama City Hospital, Fukuyama, Japan.
  • Kano H; Department of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama, Japan.
  • Kishino D; Department of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama, Japan.
  • Watanabe K; Department of Internal Medicine, Okayama Saiseikai General Hospital, Okayama, Japan.
  • Inoue M; Department of Chest Surgery, Shimonoseki City Hospital, Shimonoseki, Japan.
  • Ochi N; Department of General Internal Medicine 4, Kawasaki Medical School, Okayama, Japan.
  • Onishi F; Department of Respiratory Medicine, Okayama Rosai Hospital, Okayama, Japan.
  • Ichikawa H; Department of Respiratory Medicine, KKR Takamatsu Hospital, Takamatsu, Japan.
  • Kobe H; Department of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, Okayama, Japan.
  • Tachibana S; Department of Respiratory Medicine, Ehime Prefectural Central Hospital, Matsuyama, Japan.
  • Hotta K; Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
  • Maeda Y; Department of Hematology and Oncology, Dentistry, and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama, Japan.
  • Kiura K; Department of Allergy and Respiratory Medicine, Okayama University Hospital, 2-5-1 Shikata-Cho Kita-Ku Okayama City, Okayama, 700-8558, Japan.
J Cancer Res Clin Oncol ; 149(8): 4933-4938, 2023 Jul.
Article en En | MEDLINE | ID: mdl-36308525
BACKGROUND: Combination therapy with immune checkpoint inhibitors (ICIs) and chemotherapy (ICI + chemotherapy) has become the standard first line treatment for driver oncogene-negative advanced non-small-cell lung cancer (NSCLC). However, it may be more toxic compared to monotherapy, which limits its use. Moreover, the feasibility of the combination therapy in clinical practice remains unknown. METHODS: We conducted a cohort study to determine the implementation rate of ICI + chemotherapy in clinical practice. We retrospectively reviewed clinical data from advanced NSCLC patients who received systemic therapy at 13 institutions between December 2018 and December 2020. RESULTS: After excluding 154 patients with epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) gene alterations, a total of 919 NSCLC patients were included. Among them, 442 were treated with ICI + chemotherapy (48%), whereas 477 were treated with other therapies (52%). Among these 477 patients, 340 did not receive ICI + chemotherapy because of intolerance (71%); thus, more than one-third of the advanced NSCLC patients do not benefit from the combination therapy due to intolerance. Among the 659 NSCLC patients for whom PD-L1 was < 50% or unknown, only 342 received the ICI + chemotherapy combination (52%) even though it is considered preferable to either therapy alone; the remaining 318 patients were treated with other therapies (48%). Among the 318 patients who did not receive ICI + chemotherapy, 274 were intolerant to it (86%). CONCLUSION: Our results revealed that a substantial proportion of advanced NSCLC patients did not benefit from ICI + chemotherapy due to intolerance. As treatments for NSCLC are moving toward combinations for greater efficacy, their feasibility in clinical practice must be taken into consideration.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Cancer Res Clin Oncol Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Cancer Res Clin Oncol Año: 2023 Tipo del documento: Article País de afiliación: Japón