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Real-world clinical efficacy of bevacizumab biosimilar in patients with advanced non-small-cell lung cancer
被引:0
|作者:
Ou, Wei-Fan
[1
]
Hsu, Kuo-Hsuan
[1
,2
]
Tseng, Jeng-Sen
[1
,2
,3
,4
,5
]
Lee, Po-Hsin
[1
,3
,6
,7
]
Chen, Kun-Chieh
[8
,9
,10
]
Huang, Yen-Hsiang
[1
,2
,3
]
Chang, Gee-Chen
[3
,5
,8
,9
,10
]
Yang, Tsung-Ying
[1
,2
,6
]
机构:
[1] Taichung Vet Gen Hosp, Dept Chest Med, 1650,Sect 4,Taiwan Blvd, Taichung 407, Taiwan
[2] Taichung Vet Gen Hosp, Lung Canc Comprehens Care & Res Ctr, 1650,Sect 4,Taiwan Blvd, Taichung 407, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Coll Med, Sch Med, 155,Sec 2,Linong St, Taipei 112, Taiwan
[4] Natl Chung Hsing Univ, Coll Med, Dept Postbaccalaureate Med, Taichung, Taiwan
[5] Natl Chung Hsing Univ, Inst Biomed Sci, Taichung, Taiwan
[6] Natl Chung Hsing Univ, Doctoral Program Translat Med, Taichung, Taiwan
[7] Natl Chung Hsing Univ, Rong Hsing Translat Med Res Ctr, Taichung, Taiwan
[8] Chung Shan Med Univ Hosp, Dept Internal Med, Div Pulm Med, Taichung, Taiwan
[9] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[10] Chung Shan Med Univ, Sch Med, Taichung, Taiwan
关键词:
anti-angiogenesis therapy;
bevacizumab;
biosimilar;
chemotherapy;
non-small-cell lung cancer;
PHASE-III;
GEMCITABINE;
CARBOPLATIN;
CISPLATIN;
HALLMARKS;
D O I:
10.1177/17588359241290718
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Bevacizumab is extensively used in the treatment of advanced non-small-cell lung cancer (NSCLC). Numerous clinical trials have proven the clinical efficacies of bevacizumab biosimilars (BB).Objective: Our study aimed to compare the clinical outcomes between bevacizumab reference product (RP) and BB among advanced NSCLC patients in a real-world setting.Design: We retrospectively analyzed stage IV metastatic NSCLC patients who were treated with bevacizumab as part of a combination therapy. Patients were categorized into chemotherapy (CT) and epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) groups. We compared the patients' characteristics, treatment efficacy, and adverse events between RP and BB in the two treatment groups.Methods: From January 2020 to July 2022, a total of 171 patients who underwent combination therapy with bevacizumab were screened. Seventy-nine of these patients met the study's inclusion criteria and were enrolled in the final analysis. We utilized the Kaplan-Meier method to estimate progression-free survival (PFS) and the log-rank test to compare PFS between groups. The Cox proportional hazards model was used to identify predictors of PFS.Results: Within the CT cohort, 34 patients were treated with RP in combination with platinum and pemetrexed, and 25 patients received a combination regimen with BB. The median PFS was 6.9 months in the RP group and 8.9 months in the BB group (p = 0.255). Within the EGFR-TKI cohort, 20 patients with EGFR-mutant NSCLC received first-line treatment with EGFR-TKI plus bevacizumab. Of these patients, 9 were treated with a combination regimen that included RP, and 11 patients received EGFR-TKI in combination with BB. The median PFS was 18.4 months for the RP group and 13.6 months for the BB group (p = 0.363).Conclusion: In our advanced NSCLC patients, we found no difference in clinical outcomes when receiving treatment with RP or BB. Given a combination regimen, BB was as effective as RP together with either CT or EGFR-TKIs.
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