Aumolertinib with carboplatin–pemetrexed versus aumolertinib for nonsmall cell lung cancer with EGFR and concomitant tumor suppressor genes (ACROSS2): An open‐label, multicenter, randomized phase 3 study

医学 相伴的 内科学 肺癌 肿瘤科 危险系数 联合疗法 临床终点 不利影响 随机对照试验 癌症 靶向治疗 前瞻性队列研究 临床研究阶段 子群分析 无进展生存期 比例危险模型 置信区间 肿瘤进展 临床试验 原发性肿瘤 外科 性能状态 抑癌基因 存活率 生存分析 阶段(地层学)
作者
J. Duan,Jia Zhong,Bo‐Yang Sun,Wen‐Hua Zhao,Lin Wu,Kai‐Lun Fei,Qian Chu,Qi‐Sen Guo,Qi‐Bin Song,Yan Yu,Da‐Xing Zhu,Xin‐Yan Liu,Jun Zhao,Zhi‐Xiang Zhan,Shi Li,Lei Nie,J. Lin,Xiao‐Dong Peng,Dian‐Sheng Zhong,Jin Zhou
出处
期刊:CA: A Cancer Journal for Clinicians [Wiley]
卷期号:76 (2): e70071-e70071 被引量:3
标识
DOI:10.3322/caac.70071
摘要

Third-generation epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are standard first-line therapy for advanced, EGFR-mutated nonsmall cell lung cancer (NSCLC). However, their benefit is limited in patients who have co-existing tumor suppressor gene (TSG) mutations, highlighting a need for intensified strategies to improve outcomes. ACROSS2 (ClinicalTrials.gov identifier NCT04500717) is the first prospective, multicenter, randomized phase 3 study to compare the third-generation EGFR-TKI aumolertinib in combination with carboplatin-pemetrexed versus aumolertinib monotherapy in patients who had NSCLC with EGFR mutations and concomitant TSG mutations. In total, 126 patients were enrolled and randomly assigned to either combination therapy (n = 62) or monotherapy (n = 64). The primary end point was median progression-free survival (PFS). At a median follow-up of 25.3 months, combination therapy significantly prolonged median PFS compared with monotherapy (19.78 vs 16.53 months; hazard ratio, 0.58; 95% confidence interval, 0.34-0.97). Landmark PFS rates at 12, 18, and 24 months were 78.7% versus 65.3%, 67.2% versus 40.8%, and 41.0% versus 29.9%, respectively. Subgroup analyses demonstrated a clear PFS benefit in patients who had co-existing tumor protein p53 (TP53) mutations. Grade 3 or greater adverse events occurred in 25.9% of patients who received combination therapy versus 17.2% of those who received monotherapy; no drug-related deaths were observed. Overall survival data were immature (data maturity, 4%). The ACROSS2 trial provides the first prospective evidence supporting a genotype-directed, chemotherapy-targeted intensification approach favoring aumolertinib plus carboplatin-pemetrexed for this molecularly defined population.
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