Xiaotong He , Yi Xu , Yuqing Ren , Jiayi Wang , Youkang Ni , Yulong Zheng , Yanli Wang , Xiaofan Ding , Yining Li , Huiyong Zhu
{"title":"新辅助化疗联合抗pd -1单克隆抗体治疗局部晚期可切除口腔鳞状细胞癌的疗效评价及预测","authors":"Xiaotong He , Yi Xu , Yuqing Ren , Jiayi Wang , Youkang Ni , Yulong Zheng , Yanli Wang , Xiaofan Ding , Yining Li , Huiyong Zhu","doi":"10.1016/j.oraloncology.2025.107744","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Neoadjuvant chemotherapy (NAC) combined with anti-PD-1 antibody therapy is a potential treatment option for resectable oral squamous cell carcinoma (OSCC). Identifying biomarkers to predict therapeutic efficacy remains critical for optimizing this regimen.</div></div><div><h3>Methods</h3><div>Thirty patients with locally advanced, resectable OSCC (T3–T4, N0–N2, M0) who received two cycles of neoadjuvant chemoimmunotherapy (NACI) consisting of paclitaxel (175 mg/m<sup>2</sup>) and cisplatin (75 mg/m<sup>2</sup>) plus the anti-PD-1 monoclonal antibody sintilimab (200 mg) were enrolled in this single-arm phase II trial. Twenty-five patients underwent surgical resection and five received nonsurgical therapy. The primary and secondary end points were pathological response and clinical response, respectively. AI-powered nuclear segmentation and classification was applied to pre-treatment biopsy samples to spatially map inflammatory cell infiltration. Transcriptome RNA sequencing (RNA-seq) analysis and IHC were used to identify differentially expressed genes and immune cell subtypes between patients with and without major pathological response (MPR).</div></div><div><h3>Results</h3><div>The MPR rate was 44.0 % among the 25 patients who underwent surgical resection. The objective response rate (ORR) was 53.3 %. The primary tumor location significantly correlated with pathological response (<em>P</em> < 0.05). While AI analysis showed no significant difference in overall inflammatory cell infiltration between groups, immune infiltration analysis of the RNA-seq data revealed significant differences in the proportions of M1- and M2-type macrophages between the MPR and non-MPR groups. CD86 IHC validation across all 12 sequenced patients confirmed significantly elevated M1 infiltration in MPR tumors (13.75 % vs. 4.5 % CD86<sup>+</sup> cells, <em>P</em> < 0.001), directly linking M1 polarization to therapeutic sensitivity to PD-1 inhibition.</div></div><div><h3>Conclusions</h3><div>NAC combined with anti-PD-1 antibody therapy demonstrates clinically meaningful efficacy in OSCC, accompanied by a manageable toxicity profile. M1 macrophage infiltration, validated by both RNA-seq and IHC, emerges as a novel predictive biomarker for pathological response, providing mechanistic insight into PD-1 blockade efficacy within the tumor microenvironment.</div></div><div><h3>Trial registration</h3><div>Chinese clinical trial registry, ChiCTR2400091891.</div></div>","PeriodicalId":19716,"journal":{"name":"Oral oncology","volume":"170 ","pages":"Article 107744"},"PeriodicalIF":3.9000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neoadjuvant chemotherapy combined with anti-PD-1 monoclonal antibody in locally advanced resectable oral squamous cell carcinoma: efficacy evaluation and prediction\",\"authors\":\"Xiaotong He , Yi Xu , Yuqing Ren , Jiayi Wang , Youkang Ni , Yulong Zheng , Yanli Wang , Xiaofan Ding , Yining Li , Huiyong Zhu\",\"doi\":\"10.1016/j.oraloncology.2025.107744\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Neoadjuvant chemotherapy (NAC) combined with anti-PD-1 antibody therapy is a potential treatment option for resectable oral squamous cell carcinoma (OSCC). Identifying biomarkers to predict therapeutic efficacy remains critical for optimizing this regimen.</div></div><div><h3>Methods</h3><div>Thirty patients with locally advanced, resectable OSCC (T3–T4, N0–N2, M0) who received two cycles of neoadjuvant chemoimmunotherapy (NACI) consisting of paclitaxel (175 mg/m<sup>2</sup>) and cisplatin (75 mg/m<sup>2</sup>) plus the anti-PD-1 monoclonal antibody sintilimab (200 mg) were enrolled in this single-arm phase II trial. Twenty-five patients underwent surgical resection and five received nonsurgical therapy. The primary and secondary end points were pathological response and clinical response, respectively. AI-powered nuclear segmentation and classification was applied to pre-treatment biopsy samples to spatially map inflammatory cell infiltration. Transcriptome RNA sequencing (RNA-seq) analysis and IHC were used to identify differentially expressed genes and immune cell subtypes between patients with and without major pathological response (MPR).</div></div><div><h3>Results</h3><div>The MPR rate was 44.0 % among the 25 patients who underwent surgical resection. The objective response rate (ORR) was 53.3 %. The primary tumor location significantly correlated with pathological response (<em>P</em> < 0.05). While AI analysis showed no significant difference in overall inflammatory cell infiltration between groups, immune infiltration analysis of the RNA-seq data revealed significant differences in the proportions of M1- and M2-type macrophages between the MPR and non-MPR groups. CD86 IHC validation across all 12 sequenced patients confirmed significantly elevated M1 infiltration in MPR tumors (13.75 % vs. 4.5 % CD86<sup>+</sup> cells, <em>P</em> < 0.001), directly linking M1 polarization to therapeutic sensitivity to PD-1 inhibition.</div></div><div><h3>Conclusions</h3><div>NAC combined with anti-PD-1 antibody therapy demonstrates clinically meaningful efficacy in OSCC, accompanied by a manageable toxicity profile. M1 macrophage infiltration, validated by both RNA-seq and IHC, emerges as a novel predictive biomarker for pathological response, providing mechanistic insight into PD-1 blockade efficacy within the tumor microenvironment.</div></div><div><h3>Trial registration</h3><div>Chinese clinical trial registry, ChiCTR2400091891.</div></div>\",\"PeriodicalId\":19716,\"journal\":{\"name\":\"Oral oncology\",\"volume\":\"170 \",\"pages\":\"Article 107744\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oral oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1368837525005731\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral oncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1368837525005731","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
Neoadjuvant chemotherapy combined with anti-PD-1 monoclonal antibody in locally advanced resectable oral squamous cell carcinoma: efficacy evaluation and prediction
Background
Neoadjuvant chemotherapy (NAC) combined with anti-PD-1 antibody therapy is a potential treatment option for resectable oral squamous cell carcinoma (OSCC). Identifying biomarkers to predict therapeutic efficacy remains critical for optimizing this regimen.
Methods
Thirty patients with locally advanced, resectable OSCC (T3–T4, N0–N2, M0) who received two cycles of neoadjuvant chemoimmunotherapy (NACI) consisting of paclitaxel (175 mg/m2) and cisplatin (75 mg/m2) plus the anti-PD-1 monoclonal antibody sintilimab (200 mg) were enrolled in this single-arm phase II trial. Twenty-five patients underwent surgical resection and five received nonsurgical therapy. The primary and secondary end points were pathological response and clinical response, respectively. AI-powered nuclear segmentation and classification was applied to pre-treatment biopsy samples to spatially map inflammatory cell infiltration. Transcriptome RNA sequencing (RNA-seq) analysis and IHC were used to identify differentially expressed genes and immune cell subtypes between patients with and without major pathological response (MPR).
Results
The MPR rate was 44.0 % among the 25 patients who underwent surgical resection. The objective response rate (ORR) was 53.3 %. The primary tumor location significantly correlated with pathological response (P < 0.05). While AI analysis showed no significant difference in overall inflammatory cell infiltration between groups, immune infiltration analysis of the RNA-seq data revealed significant differences in the proportions of M1- and M2-type macrophages between the MPR and non-MPR groups. CD86 IHC validation across all 12 sequenced patients confirmed significantly elevated M1 infiltration in MPR tumors (13.75 % vs. 4.5 % CD86+ cells, P < 0.001), directly linking M1 polarization to therapeutic sensitivity to PD-1 inhibition.
Conclusions
NAC combined with anti-PD-1 antibody therapy demonstrates clinically meaningful efficacy in OSCC, accompanied by a manageable toxicity profile. M1 macrophage infiltration, validated by both RNA-seq and IHC, emerges as a novel predictive biomarker for pathological response, providing mechanistic insight into PD-1 blockade efficacy within the tumor microenvironment.
Trial registration
Chinese clinical trial registry, ChiCTR2400091891.
期刊介绍:
Oral Oncology is an international interdisciplinary journal which publishes high quality original research, clinical trials and review articles, editorials, and commentaries relating to the etiopathogenesis, epidemiology, prevention, clinical features, diagnosis, treatment and management of patients with neoplasms in the head and neck.
Oral Oncology is of interest to head and neck surgeons, radiation and medical oncologists, maxillo-facial surgeons, oto-rhino-laryngologists, plastic surgeons, pathologists, scientists, oral medical specialists, special care dentists, dental care professionals, general dental practitioners, public health physicians, palliative care physicians, nurses, radiologists, radiographers, dieticians, occupational therapists, speech and language therapists, nutritionists, clinical and health psychologists and counselors, professionals in end of life care, as well as others interested in these fields.