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阿特珠单抗、贝伐单抗与化疗用于EGFR突变型非小细胞肺癌获得性耐药的随机非对照II期研究——ETOP 15-19 ABC-肺癌试验

A randomised non-comparative phase II study of atezolizumab, bevacizumab and chemotherapy in EGFR-mutant NSCLC with acquired resistance - The ETOP 15-19 ABC-lung trial.

作者信息

Soo R A, Vervita K, Früh M, Cho B C, Majem M, Rodriguez Abreu D, Ribi K, Callejo A, Moran T, Domine Gomez M, Provencio M, Addeo A, Han J Y, Ortega Granados A L, Reck M, Blasco A, Garcia Campelo R, Sala González M A, Britschgi C, Roschitzki-Voser H, Ruepp B, Gasca-Ruchti A, Haberecker M, Dafni U, Peters S, Stahel R A

机构信息

Department of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.

ETOP Statistical Office, FSF-H - Frontier Science Foundation Hellas, Athens, Greece.

出版信息

Lung Cancer. 2025 Apr;202:108454. doi: 10.1016/j.lungcan.2025.108454. Epub 2025 Feb 20.

Abstract

BACKGROUND

ABC-lung explores the potential effect of combining atezolizumab and bevacizumab with either carboplatin/paclitaxel (ABCPac) or pemetrexed (ABPem) in patients with EGFR-mutant NSCLC, resistant to tyrosine kinase inhibitors (TKIs).

METHODS

ABC-lung is a 1:1 randomised, non-comparative, phase II trial, stratified by prior treatment with a third-generation EGFR TKI, evaluating atezolizumab (1200 mg, Q3W) and bevacizumab (15mg/kg, Q3W) with either 4-6 cycles of carboplatin (AUC5, Q3W) and paclitaxel (175-200mg/m2, Q3W) or pemetrexed (500 mg/m2, Q3W) until progression (PD). The study aimed to improve the 1-year progression-free survival (PFS) rate from 18% to 37%, assessed per RECISTv1.1, separately in each arm. To reject the null hypothesis, at least 14 of 45 evaluable patients in each arm needed to be progression-free at 1-year (power 83%, 1-sided a=0.023). Secondary endpoints included overall survival (OS), objective response rate (ORR), PFS, quality of life (QoL) and adverse events (AEs).

RESULTS

Between 09/2020 and 09/2022, 95 patients were randomized (ABCPac:45; ABPem:50) with median follow-up time of 19 months. From the evaluable patients, 9 in ABCPac and 11 in ABPem arms reached 1-year without progression, lower than the success criterion of 14patients. Median PFS was 6.4 months in ABCPac and 7.6 months in the ABPem arms, while median OS was 15.4 months and 15.6 months, respectively. Grade ≥3 treatment-related AEs were experienced by 50% and 42% of patients in ABCPac and ABPem arms, respectively, while no grade 5 AEs were recorded.

CONCLUSIONS

The observed 1-year PFS rate with atezolizumab, bevacizumab in combination with either carboplatin-paclitaxel or pemetrexed was below the aspired rate of 37% in both arms. The safety is consistent with the known toxicity profiles. Clinical trial identification: NCT04245085.

摘要

背景

ABC-肺癌研究探索了阿替利珠单抗和贝伐单抗联合卡铂/紫杉醇(ABCPac)或培美曲塞(ABPem),用于对酪氨酸激酶抑制剂(TKIs)耐药的表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者的潜在疗效。

方法

ABC-肺癌研究是一项1:1随机、非对照的II期试验,根据既往使用第三代EGFR TKI的治疗情况进行分层,评估阿替利珠单抗(1200mg,每3周一次)和贝伐单抗(15mg/kg,每3周一次)联合4-6周期的卡铂(AUC5,每3周一次)和紫杉醇(175-200mg/m²,每3周一次)或培美曲塞(500mg/m²,每3周一次),直至疾病进展(PD)。该研究旨在将1年无进展生存期(PFS)率从18%提高到37%,根据RECISTv1.1标准在每个治疗组中分别评估。为了拒绝原假设,每个治疗组中45例可评估患者中至少14例需要在1年时无疾病进展(检验效能83%,单侧α=0.023)。次要终点包括总生存期(OS)、客观缓解率(ORR)、PFS、生活质量(QoL)和不良事件(AE)。

结果

在2020年9月至2022年9月期间,95例患者被随机分组(ABCPac组45例;ABPem组50例),中位随访时间为19个月。在可评估患者中,ABCPac组9例和ABPem组11例在1年时无疾病进展,低于成功标准的14例。ABCPac组的中位PFS为6.4个月,ABPem组为7.6个月,而中位OS分别为15.4个月和15.6个月。ABCPac组和ABPem组分别有50%和42%的患者发生≥3级治疗相关AE,未记录到5级AE。

结论

观察到阿替利珠单抗、贝伐单抗联合卡铂-紫杉醇或培美曲塞的1年PFS率在两个治疗组中均低于预期的37%。安全性与已知的毒性特征一致。临床试验注册号:NCT04245085。

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