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Adverse Event Profile of Atezolizumab, Bevacizumab, Carboplatin, and Paclitaxel Combination Therapy Based on JADER.
Endo, Kiri; Tanaka, Hiroyuki; Matsuo, Hajime; Onoda, Toshihisa; Iida, Ayaka; Ishii, Toshihiro.
Affiliation
  • Endo K; Department of Practical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Japan.
  • Tanaka H; Department of Practical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Japan; hiroyuki.tanaka@phar.toho-u.ac.jp.
  • Matsuo H; Department of Practical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Japan.
  • Onoda T; Clinical Development Department, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
  • Iida A; Department of Practical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Japan.
  • Ishii T; Department of Pharmacy, Toho University Ohashi Medical Center, Tokyo, Japan.
Anticancer Res ; 44(6): 2653-2660, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38821611
ABSTRACT
BACKGROUND/

AIM:

There have been advances in the development of immune checkpoint inhibitors for monotherapy and combination therapy with other anticancer agents in recent years. The combination of bevacizumab, carboplatin, and paclitaxel with atezolizumab, an anti-programmed death ligand 1 antibody (ABCP therapy), has been reported to be effective for treating non-small cell lung cancer. However, reports on its adverse events are limited. In this study, a survey and disproportionality analysis based on the Japanese Adverse Drug Event Report (JADER) database was conducted to elucidate the adverse event profile of ABCP therapy. MATERIALS AND

METHODS:

The reporting odds ratio (ROR) and information component were used as indicators for the disproportionality analysis. The ROR was also used to assess the changes in the reporting intensity with combination therapy, and the mutual exclusivity of the 95% confidence interval between the compared groups was considered.

RESULTS:

The reported adverse events of ABCP therapy mirrored those of the individual drugs that constituted it. ABCP therapy enhanced the reporting intensity of adverse events related to leukocytes and the skin, while decreased those related to interstitial lung disease and hepatic function abnormality as immune-related adverse events caused by atezolizumab, and gastrointestinal perforation caused by bevacizumab.

CONCLUSION:

Our analysis of data from the JADER database has revealed the adverse event profile of ABCP therapy. Our findings emphasize the importance of effectively managing febrile neutropenia and skin-related adverse events in ABCP therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Carboplatin / Paclitaxel / Antibodies, Monoclonal, Humanized / Bevacizumab Limits: Female / Humans / Male Language: En Journal: Anticancer Res Year: 2024 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Carboplatin / Paclitaxel / Antibodies, Monoclonal, Humanized / Bevacizumab Limits: Female / Humans / Male Language: En Journal: Anticancer Res Year: 2024 Document type: Article Affiliation country: Japan