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Real-World Data on Subsequent Therapy for First-Line Osimertinib-Induced Pneumonitis: Safety of EGFR-TKI Rechallenge (Osi-risk Study TORG-TG2101).
Nishioka, Naoya; Imai, Hisao; Endo, Masahiro; Notsu, Akifumi; Doshita, Kosei; Igawa, Satoshi; Yokouchi, Hiroshi; Ninomiya, Takashi; Tokito, Takaaki; Soda, Sayo; Fujiwara, Takasato; Asao, Tetsuhiko; Nakamichi, Shinji; Kawamura, Takahisa; Inomata, Minehiko; Nakashima, Kazuhisa; Ito, Kentaro; Goto, Yasuhiro; Umeda, Yukihiro; Hirai, Soichi; Ushio, Ryota; Yokoo, Keiki; Takeda, Takayuki; Fukui, Tomoya; Ishihara, Masashi; Osaki, Takashi; Kubo, Sousuke; Fujiwara, Takumi; Yamamoto, Chie; Tsuda, Takeshi; Tamura, Nobumasa; Hosokawa, Shinobu; Chihara, Yusuke; Ikeda, Satoshi; Furuya, Naoki; Nakahara, Yoshiro; Miura, Satoru; Okamoto, Hiroaki.
Afiliación
  • Nishioka N; Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Imai H; Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Endo M; Department of Respiratory Medicine, Fukuchiyama City Hospital, Kyoto, Japan.
  • Notsu A; Department of Respiratory Medicine, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, Yamane 1397-1, Hidaka City, Saitama, Japan. m06701014@gunma-u.ac.jp.
  • Doshita K; Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Igawa S; Division of Diagnostic Radiology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Yokouchi H; Division of Clinical Research Center, Shizuoka Cancer Center, Shizuoka, Japan.
  • Ninomiya T; Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Tokito T; Department of Respiratory Medicine, Kitasato University School of Medicine, Kanagawa, Japan.
  • Soda S; Department of Respiratory Medicine, NHO Hokkaido Cancer Center, Hokkaido, Japan.
  • Fujiwara T; Department of Thoracic Oncology and Medicine, NHO Shikoku Cancer Center, Matsuyama, Ehime, Japan.
  • Asao T; Division of Respirology, Neurology, and Rheumatology, Department of Internal Medicine, Kurume University School of Medicine, Fukuoka, Japan.
  • Nakamichi S; Department of Pulmonary and Clinical Immunology, Dokkyo Medical University School of Medicine, Tohigi, Japan.
  • Kawamura T; Department of Respiratory Internal Medicine, Yokosuka Kyosai Hospital, Kanagawa, Japan.
  • Inomata M; Department of Respiratory Medicine, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
  • Nakashima K; Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
  • Ito K; Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.
  • Goto Y; 1st Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
  • Umeda Y; Division of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.
  • Hirai S; Respiratory Center, Matsusaka Municipal Hospital, Mie, Japan.
  • Ushio R; Department of Respiratory Medicine, Fujita Health University School of Medicine, Aichi, Japan.
  • Yokoo K; Third Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
  • Takeda T; Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Fukui T; Department of Thoracic Oncology, Kanagawa Cancer Center, Kanagawa, Japan.
  • Ishihara M; Department of Respiratory Medicine, Teine Keijinkai Hospital, Hokkaido, Japan.
  • Osaki T; Department of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan.
  • Kubo S; Department of Respiratory Medicine, Shonan Kamakura General Hospital, Kanagawa, Japan.
  • Fujiwara T; Division of Medical Oncology, Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
  • Yamamoto C; Department of Respiratory Medicine, Shibukawa Medical Center, Gunma, Japan.
  • Tsuda T; Department of Pulmonology, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Tamura N; Department of Genomic Medicine, Mie University Hospital, Mie, Japan.
  • Hosokawa S; Department of Respiratory Medicine, Fukuchiyama City Hospital, Kyoto, Japan.
  • Chihara Y; Division of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
  • Ikeda S; Division of Respiratory Diseases, Department of Internal Medicine, Atsugi City Hospital, Kanagawa, Japan.
  • Furuya N; Department of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama, Japan.
  • Nakahara Y; Department of Respiratory Medicine, Uji-Tokushukai Medical Center, Kyoto, Japan.
  • Miura S; Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Kanagawa, Japan.
  • Okamoto H; Division of Respiratory Medicine, Department of Internal Medicine, St Marianna University School of Medicine, Kanagawa, Japan.
Target Oncol ; 19(3): 423-433, 2024 May.
Article en En | MEDLINE | ID: mdl-38613731
ABSTRACT

BACKGROUND:

Although osimertinib is a promising therapeutic agent for advanced epidermal growth factor receptor (EGFR) mutation-positive lung cancer, the incidence of pneumonitis is particularly high among Japanese patients receiving the drug. Furthermore, the safety and efficacy of subsequent anticancer treatments, including EGFR-tyrosine kinase inhibitor (TKI) rechallenge, which are to be administered after pneumonitis recovery, remain unclear.

OBJECTIVE:

This study investigated the safety of EGFR-TKI rechallenge in patients who experienced first-line osimertinib-induced pneumonitis, with a primary focus on recurrent pneumonitis. PATIENTS AND

METHODS:

We retrospectively reviewed the data of patients with EGFR mutation-positive lung cancer who developed initial pneumonitis following first-line osimertinib treatment across 34 institutions in Japan between August 2018 and September 2020.

RESULTS:

Among the 124 patients included, 68 (54.8%) patients underwent EGFR-TKI rechallenge. The recurrence rate of pneumonitis following EGFR-TKI rechallenge was 27% (95% confidence interval [CI] 17-39) at 12 months. The cumulative incidence of recurrent pneumonitis was significantly higher in the osimertinib group than in the first- and second-generation EGFR-TKI (conventional EGFR-TKI) groups (hazard ratio [HR] 3.1; 95% CI 1.3-7.5; p = 0.013). Multivariate analysis revealed a significant association between EGFR-TKI type (osimertinib or conventional EGFR-TKI) and pneumonitis recurrence, regardless of severity or status of initial pneumonitis (HR 3.29; 95% CI 1.12-9.68; p = 0.03).

CONCLUSIONS:

Osimertinib rechallenge after initial pneumonitis was associated with significantly higher recurrence rates than conventional EGFR-TKI rechallenge.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neumonía / Acrilamidas / Inhibidores de Proteínas Quinasas / Receptores ErbB / Compuestos de Anilina / Neoplasias Pulmonares Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Target Oncol Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neumonía / Acrilamidas / Inhibidores de Proteínas Quinasas / Receptores ErbB / Compuestos de Anilina / Neoplasias Pulmonares Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Target Oncol Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: Japón
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