Efficacy, safety and single-cell analysis of neoadjuvant immunochemotherapy in locally advanced oral squamous cell carcinoma: a phase II trial
Zhongzheng Xiang,
Xiaoyuan Wei,
Zhuoyuan Zhang,
Yueyang Tang,
Linyan Chen,
Chenfeng Tan,
Yuanyuan Zeng,
Jun Wang,
Guile Zhao,
Zelei Dai,
Mingmin He,
Ningyue Xu,
Chunjie Li (),
Yi Li () and
Lei Liu ()
Additional contact information
Zhongzheng Xiang: Sichuan University
Xiaoyuan Wei: Sichuan University
Zhuoyuan Zhang: Sichuan University
Yueyang Tang: Sichuan University
Linyan Chen: Sichuan University
Chenfeng Tan: Sichuan University
Yuanyuan Zeng: Sichuan University
Jun Wang: Sichuan University
Guile Zhao: Sichuan University
Zelei Dai: Sichuan University
Mingmin He: Sichuan University
Ningyue Xu: Sichuan University
Chunjie Li: Sichuan University
Yi Li: Sichuan University
Lei Liu: Sichuan University
Nature Communications, 2025, vol. 16, issue 1, 1-17
Abstract:
Abstract The clinical activity of neoadjuvant immunochemotherapy (NAIC) for treating locally advanced oral squamous cell carcinoma (LA-OSCC) remains uncertain. This single-arm, phase II trial (ChiCTR2200066119) tested 2 cycles of NAIC with camrelizumab plus nab-paclitaxel and cisplatin in LA-OSCC patients. For primary endpoint, the major pathological response (MPR) rate was 69.0% (95% confidence interval (CI): 49.2%-84.7%). The treatment was well-tolerated, with only 2 patients (6.45%) having grade 3 or 4 treatment-related adverse events during neoadjuvant treatment. For secondary endpoints, the pathological complete response rate was 41.4% (95%CI: 23.5%-61.1%) and the objective response rate was 82.8% (24/29, 95%CI: 64.2%-94.2%). The 18-month overall survival and disease-free survival probabilities were 96.77% (95%CI: 79.23%-99.54%) and 85.71% (95%CI: 53.95%-96.22%), respectively. Exploratory analysis showed that patients with MPR exhibited higher density of baseline CD4_Tfh_CXCL13 cells, and increased density of tertiary lymphoid structures after NAIC. Baseline CD4_Tfh_CXCL13 cells might be potential predictive biomarker of efficacy. The interaction between CXCL13 on CD4_Tfh_CXCL13 cells and CXCR5 on B cells may play a role in treatment response. These findings suggest the potential of NAIC as a promising treatment for LA-OSCC and offer preliminary insights into responsive biomarkers.
Date: 2025
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DOI: 10.1038/s41467-025-59004-w
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