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Real-World Pharmacokinetics, Effectiveness, and Safety of Atezolizumab in Patients With Unresectable Advanced or Recurrent NSCLC: An Exploratory Study of J-TAIL.
Yagishita, Shigehiro; Goto, Yasushi; Nishio, Makoto; Akamatsu, Hiroaki; Hayashi, Hidetoshi; Miura, Satoru; Tamada, Koji; Kagamu, Hiroshi; Hamada, Akinobu; Ohuchi, Mayu; Gemma, Akihiko; Yoshino, Ichiro; Misumi, Toshihiro; Hata, Akito; Hara, Satoshi; Kijima, Takashi; Masaki, Fujita; Iwasawa, Shunichiro; Nakagawa, Shintaro; Tatsuno, Masahiro; Mitsudomi, Tetsuya.
Afiliación
  • Yagishita S; Division of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan.
  • Goto Y; Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Nishio M; Department of Thoracic Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Akamatsu H; Internal Medicine III, Wakayama Medical University, Wakayama, Japan.
  • Hayashi H; Department of Medical Oncology, Faculty of Medicine, Kindai University, Osaka, Japan.
  • Miura S; Department of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.
  • Tamada K; Department of Immunology, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
  • Kagamu H; Department of Respiratory Medicine, International Medical Center, Saitama Medical University, Saitama, Japan.
  • Hamada A; Division of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan.
  • Ohuchi M; Department of Pharmacology and Therapeutics, Fundamental Innovative Oncology Core, National Cancer Center Research Institute, Tokyo, Japan.
  • Gemma A; Department of Pulmonary Medicine and Oncology, Nippon Medical School, Graduate School of Medicine, Tokyo, Japan.
  • Yoshino I; Department of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Misumi T; Department of Thoracic Surgery, International University of Health and Welfare Narita Hospital, Narita, Japan.
  • Hata A; Department of Biostatistics, Yokohama City University School of Medicine, Kanagawa, Japan.
  • Hara S; Department of Data Science, National Cancer Center Hospital East, Chiba, Japan.
  • Kijima T; Department of Thoracic Oncology, Kobe Minimally Invasive Cancer Center, Hyogo, Japan.
  • Masaki F; Department of Respiratory Medicine, Itami City Hospital, Hyogo, Japan.
  • Iwasawa S; Department of Respiratory Medicine and Hematology, Hyogo Medical University, Nishinomiya, Hyogo, Japan.
  • Nakagawa S; Department of Respiratory Medicine, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
  • Tatsuno M; Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.
  • Mitsudomi T; Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.
JTO Clin Res Rep ; 5(7): 100683, 2024 Jul.
Article en En | MEDLINE | ID: mdl-39091595
ABSTRACT

Introduction:

This study validated real-world pharmacokinetic (PK) data using an established population PK (PopPK) model for atezolizumab in Japanese patients with NSCLC and explored the relationship between PK parameters, effectiveness, and adverse events (AEs) for the 1200 mg once every three weeks regimen.

Methods:

A subgroup of 262 of 1039 patients from J-TAIL consented to this exploratory research for PK evaluation of atezolizumab monotherapy for unresectable advanced/recurrent NSCLC (August 2018 to October 2019; 197 institutions). We evaluated plasma concentrations before the start of the third cycle of atezolizumab infusion classified into quartiles 1 to 4, their association with effectiveness, and the association between atezolizumab maximum plasma concentrations (Cmax) calculated using the existing PopPK model and AEs of special interest (AESIs).

Results:

Overall, 175 of 262 patients were included; baseline characteristics were similar to those of patients enrolled in J-TAIL (Eastern Cooperative Oncology Group performance status ≥ 2, 12.0%; age ≥ 75 y, 28.9%; atezolizumab as more than or equal to third-line treatment, 57.5%). Atezolizumab plasma concentrations were similar to previously reported data among Japanese/non-Japanese patients. The overall survival was significantly shorter in patients with lower atezolizumab plasma concentrations in Q1 versus Q2 to Q4, although progression-free survival remained the same. The PK data adequately fit the PopPK model, with the frequency of AESIs increasing as the calculated Cmax at cycle 1 increased.

Conclusions:

In real-world Japanese patients with unresectable advanced/recurrent NSCLC, PKs were similar to previous reports. Certain patient populations had shorter overall survival, and atezolizumab plasma concentrations in cycle 3 were lower in this population. Elevated Cmax at cycle 1 may be associated with an increased frequency of AESIs.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: JTO Clin Res Rep Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: JTO Clin Res Rep Año: 2024 Tipo del documento: Article País de afiliación: Japón