彭布罗利珠单抗
医学
内科学
临床终点
肿瘤科
软组织肉瘤
队列
恶心
回顾性队列研究
代理终结点
置信区间
不利影响
环磷酰胺
无进展生存期
外科
临床试验
软组织
癌症
化疗
免疫疗法
作者
Antoîne Italiano,Alban Bessede,M. Pulido,Emmanuelle Bompas,Sophie Piperno‐Neumann,Christine Chevreau,Nicolas Penel,François Bertucci,Maud Toulmonde,Carine Bellera,Jean-Philippe Guégan,Christophe Rey,Catherine Sautès–Fridman,Antoine Bougouïn,Coralie Cantarel,Michèle Kind,Mariella Spalato Ceruso,Bérengère Dadone‐Montaudié,François Le Loarer,Jean‐Yves Blay,Wolf H. Fridman
出处
期刊:Nature Medicine
[Springer Nature]
日期:2022-05-26
卷期号:28 (6): 1199-1206
被引量:134
标识
DOI:10.1038/s41591-022-01821-3
摘要
Immune checkpoint inhibitors (ICIs) show limited clinical activity in patients with advanced soft-tissue sarcomas (STSs). Retrospective analysis suggests that intratumoral tertiary lymphoid structures (TLSs) are associated with improved outcome in these patients. PEMBROSARC is a multicohort phase 2 study of pembrolizumab combined with low-dose cyclophosphamide in patients with advanced STS (NCT02406781). The primary endpoint was the 6-month non-progression rate (NPR). Secondary endpoints included objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and safety. The 6-month NPR and ORRs for cohorts in this trial enrolling all comers were previously reported; here, we report the results of a cohort enrolling patients selected based on the presence of TLSs (n = 30). The 6-month NPR was 40% (95% confidence interval (CI), 22.7–59.4), so the primary endpoint was met. The ORR was 30% (95% CI, 14.7–49.4). In comparison, the 6-month NPR and ORR were 4.9% (95% CI, 0.6–16.5) and 2.4% (95% CI, 0.1–12.9), respectively, in the all-comer cohorts. The most frequent toxicities were grade 1 or 2 fatigue, nausea, dysthyroidism, diarrhea and anemia. Exploratory analyses revealed that the abundance of intratumoral plasma cells (PCs) was significantly associated with improved outcome. These results suggest that TLS presence in advanced STS is a potential predictive biomarker to improve patients’ selection for pembrolizumab treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI