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Evaluation of Atezolizumab Plus Bevacizumab Versus Modified Lenvatinib Therapy in Child-Pugh A Unresectable Hepatocellular Carcinoma.
Kimura, Michio; Yamada, Shiori; Go, Makiko; Yasuda, Satoshi; Toyoda, Hidenori; Usami, Eiseki.
Afiliação
  • Kimura M; Department of Pharmacy, Ogaki Municipal Hospital, Gifu, Japan.
  • Yamada S; Department of Pharmacy, Ogaki Municipal Hospital, Gifu, Japan.
  • Go M; Department of Pharmacy, Ogaki Municipal Hospital, Gifu, Japan.
  • Yasuda S; Department of Gastroenterology and Hepatology, Ogaki Municipal Hospital, Gifu, Japan.
  • Toyoda H; Department of Gastroenterology and Hepatology, Ogaki Municipal Hospital, Gifu, Japan.
  • Usami E; Department of Pharmacy, Ogaki Municipal Hospital, Gifu, Japan.
Cancer Diagn Progn ; 4(2): 122-128, 2024.
Article em En | MEDLINE | ID: mdl-38434917
ABSTRACT
Background/

Aim:

Atezolizumab/bevacizumab (Atez/BV) and lenvatinib (LEN) are the recommended first-line treatments for patients with unresectable hepatocellular carcinoma (HCC). Previous reports have suggested that the tolerability and therapeutic efficacy of LEN could be enhanced by modifying its administration method. Therefore, this study compared the efficacy and safety of Atez/BV, the standard LEN therapy (standard LEN), and modified LEN therapy (modified LEN). Patients and

Methods:

The overall survival (OS) and the rate of discontinuation due to adverse events (AEs) were compared between groups treated with Atez/BV (n=36), standard LEN (n=30), and modified LEN (n=11).

Results:

Discontinuation due to AEs was required in 22.2%, 23.3%, and 9.1% of patients in the Atez/BV, standard LEN, and modified LEN groups (p=0.485). The median OS for the Atez/BV, standard LEN, and modified LEN groups was 523 [95% confidence interval (CI)=163-818], 382 (95%CI=330-547), and 604 (95% CI=257-656) days, respectively (log-rank test, p=0.949).

Conclusion:

Atez/BV and the standard and modified LEN regimens showed comparable efficacy and safety.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article