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
癌
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)
肺
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
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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