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Toripalimab plus nab-paclitaxel in metastatic or recurrent triple-negative breast cancer: a randomized phase 3 trial

  • Zefei Jiang,
  • Quchang Ouyang,
  • Tao Sun,
  • Qingyuan Zhang,
  • Yuee Teng,
  • Jiuwei Cui,
  • Haibo Wang,
  • Yongmei Yin,
  • Xiaojia Wang,
  • Xin Zhou,
  • Yongsheng Wang,
  • Gang Sun,
  • Jingfen Wang,
  • Lili Zhang,
  • Jin Yang,
  • Jun Qian,
  • Min Yan,
  • Xinlan Liu,
  • Tienan Yi,
  • Ying Cheng,
  • Man Li,
  • Aimin Zang,
  • Shusen Wang,
  • Chuan Wang,
  • Xinhong Wu,
  • Jing Cheng,
  • Hui Li,
  • Ying Lin,
  • Cuizhi Geng,
  • Kangsheng Gu,
  • Chunwei Xie,
  • Huihua Xiong,
  • Xiaohong Wu,
  • Junlan Yang,
  • Qingshan Li,
  • Yiding Chen,
  • Fanfan Li,
  • Anqin Zhang,
  • Yongqiang Zhang,
  • Yudong Wu,
  • Jianyun Nie,
  • Qiang Liu,
  • Kun Wang,
  • Xueli Mo,
  • Lilin Chen,
  • Yueyin Pan,
  • Peifen Fu,
  • Helong Zhang,
  • Danmei Pang,
  • Yuan Sheng,
  • Yunwei Han,
  • Hongxia Wang,
  • Shundong Cang,
  • Xianming Luo,
  • Wenbo Yu,
  • Rong Deng,
  • Chaoqiang Yang,
  • Patricia Keegan

摘要

The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) (n = 353; experimental arm) versus placebo and nab-P (n = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470–0.906, P = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414–0.914, P = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579.