Department of Radiation Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, Sichuan, 610041, China.
Department of Thoracic Surgery, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, Sichuan, 610041, China.
Nat Commun. 2024 Aug 20;15(1):7116. doi: 10.1038/s41467-024-51105-2.
This single-arm phase 2 trial (ChiCTR2100046715) examined previously untreated patients with advanced esophageal squamous cell carcinoma (ESCC) who received four cycles of paclitaxel with carboplatin every 3 weeks. Toripalimab was infused intravenously every 3 weeks for 12 months, or until disease progression or intolerable toxicity. Radiotherapy that encompassed the primary lesions and metastases commenced in the third cycle. The median progression-free survival time was 9.8 months (95% confidence interval [CI]: 6.8-not estimable) in the intent-to-treat population, failing to meet the pre-specified primary endpoints. Secondary endpoints included an objective response rate of 45.5%, a disease control rate of 57.6%, and a median duration of response of 11.5 months (interquartile range, 6.4-15.0). The 1-year progression-free survival and overall survival rates were 41.9% (95% CI: 27.7-63.5) and 69.7% (95% CI: 55.7-87.3), respectively. Lymphopenia was the most frequent grade ≥3 adverse event (82%), and an esophageal fistula developed in three patients (9.1%). No treatment-related deaths occurred. In prespecified exploratory biomarker analysis, higher densities of CD8 + T cells, CD11c+ dendritic cells, and CD68+ macrophages correlated with improved tumor response and prognosis. Radiotherapy supplementation to first-line chemo-immunotherapy for treatment-naive advanced ESCC demonstrated some antitumor activity and manageable safety profiles, warranting further randomized controlled trials.
这项单臂 2 期临床试验(ChiCTR2100046715)纳入了未经治疗的晚期食管鳞癌(ESCC)患者,这些患者每 3 周接受 4 个周期紫杉醇联合卡铂治疗。替雷利珠单抗每 3 周静脉输注 12 个月,或直至疾病进展或不可耐受的毒性。在第 3 个周期开始进行涵盖原发病灶和转移灶的放疗。在意向治疗人群中,中位无进展生存期为 9.8 个月(95%置信区间[CI]:6.8-不可估计),未达到预设的主要终点。次要终点包括客观缓解率 45.5%、疾病控制率 57.6%和中位缓解持续时间 11.5 个月(四分位距[IQR]:6.4-15.0)。1 年无进展生存率和总生存率分别为 41.9%(95%CI:27.7-63.5)和 69.7%(95%CI:55.7-87.3)。最常见的 3 级及以上不良事件是淋巴细胞减少症(82%),3 例(9.1%)发生食管瘘。无治疗相关死亡。在预设的探索性生物标志物分析中,较高密度的 CD8+T 细胞、CD11c+树突状细胞和 CD68+巨噬细胞与肿瘤缓解和预后改善相关。一线化疗免疫治疗联合放疗治疗未经治疗的晚期 ESCC 显示出一定的抗肿瘤活性和可管理的安全性特征,值得进一步开展随机对照试验。