Real-world clinical efficacy of bevacizumab biosimilar in patients with advanced non-small-cell lung cancer.

IF 4.2 2区 医学 Q2 ONCOLOGY Therapeutic Advances in Medical Oncology Pub Date : 2024-10-17 eCollection Date: 2024-01-01 DOI:10.1177/17588359241290718
Wei-Fan Ou, Kuo-Hsuan Hsu, Jeng-Sen Tseng, Po-Hsin Lee, Kun-Chieh Chen, Yen-Hsiang Huang, Gee-Chen Chang, Tsung-Ying Yang
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Abstract

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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贝伐珠单抗生物仿制药在晚期非小细胞肺癌患者中的实际临床疗效。
背景:贝伐珠单抗被广泛用于治疗晚期非小细胞肺癌(NSCLC):贝伐珠单抗被广泛用于晚期非小细胞肺癌(NSCLC)的治疗。大量临床试验证明了贝伐珠单抗生物仿制药(BB)的临床疗效:我们的研究旨在比较贝伐珠单抗参考品(RP)和贝伐珠单抗生物仿制药在晚期NSCLC患者中的临床疗效:我们对接受贝伐珠单抗联合治疗的 IV 期转移性 NSCLC 患者进行了回顾性分析。患者被分为化疗(CT)组和表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKI)组。我们比较了两个治疗组中RP和BB患者的特征、疗效和不良事件:2020年1月至2022年7月,共筛选出171名接受贝伐珠单抗联合治疗的患者。其中79名患者符合研究的纳入标准,被纳入最终分析。我们采用卡普兰-梅耶法估算无进展生存期(PFS),并用对数秩检验比较不同组间的无进展生存期。我们使用 Cox 比例危险模型来确定无进展生存期的预测因素:在CT队列中,34名患者接受了RP联合铂类和培美曲塞治疗,25名患者接受了BB联合治疗。RP组的中位生存期为6.9个月,BB组为8.9个月(P = 0.255)。在EGFR-TKI队列中,20名EGFR突变NSCLC患者接受了EGFR-TKI加贝伐单抗的一线治疗。其中,9名患者接受了包括RP在内的联合方案治疗,11名患者接受了EGFR-TKI联合BB治疗。RP组的中位生存期为18.4个月,BB组为13.6个月(P = 0.363):结论:在晚期NSCLC患者中,我们发现接受RP或BB治疗的临床疗效没有差异。在联合治疗方案中,BB与RP以及CT或EGFR-TKIs的疗效相同。
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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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