Neoadjuvant immunochemotherapy for locally advanced resectable oral squamous cell carcinoma: a prospective single-arm trial (Illuminate Trial)

Author:

Huang Yingying1,Sun Jingjing2,Li Jun1,Zhu Dongwang1,Dong Minjun3,Dou Shengjin1,Tang Yong4,Shi Wentao5,Sun Qi3,Zhao Tongchao1,Zhou Zhihang1,Zhou Xinyu1,Liu Ying1,Li Jiang2,Zhu Guopei1,Zhang Ding6,Chen Yanan6,Zhu Qi14,Ju Wutong1ORCID,Zhong Laiping14789

Affiliation:

1. Department of Oral and Maxillofacial-Head and Neck Oncology

2. Department of Oral Pathology, Ninth People’s Hospital, College of Stomatology

3. Department of Radiology

4. Huangpu Branch

5. Department of Biostatistics in Clinical Research Unit, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine

6. The Medical Department, 3D Medicines Inc

7. National Center for Stomatology

8. National Clinical Research Center for Oral Diseases

9. Shanghai Key Laboratory of Stomatology, Shanghai, People’s Republic China

Abstract

Background: Locally advanced oral squamous cell carcinoma (LAOSCC) is associated with a high rate of recurrence and poor survival. Given the recent successes of neoadjuvant immunochemotherapy (NAICT) in solid tumors, it is promising to use this treatment modality to achieve a better pathological response and improve the survival of LAOSCC, and clinical evidence is needed to assess its safety and efficacy. Patients and Methods: A prospective trial of NAICT with toripalimab (PD-1 inhibitor) and albumin paclitaxel/cisplatin (TTP) was conducted in patients with clinical stage III and IVA OSCC. Intravenous albumin paclitaxel (260 mg/m2), cisplatin (75 mg/m2), and toripalimab (240 mg) were given in sequence on day 1 of each 21 day cycle for two cycles, followed by radical surgery and risk-adapted adjuvant (chemo)radiotherapy. The primary endpoints were safety and major pathological response (MPR). Targeted next generation sequencing and multiplex immunofluorescence were performed to assess clinical molecular characteristics and the tumor immune microenvironment in the pre-NAICT and post-NAICT tumor samples. Results: Twenty patients were enrolled. NAICT was well-tolerated with a low incidence of grades 3–4 adverse events in three patients. The completion rates of NAICT and subsequent R0 resection were 100%. The MPR rate was 60%, including a 30% pathological complete response. MPR was achieved in all four patients with a combined positive score of PD-L1>10. The density of tertiary lymphatic structure in post-NAICT tumor samples predicted the pathological response to NAICT. During the median 23-month follow-up, the disease-free survival was 90%, and the overall survival was 95%. Conclusions: NAICT with the TTP protocol in LAOSCC is feasible and well tolerated, with a promising MPR and no obstruction on subsequent surgery. This trial is supportive of further randomized trials using NAICT in LAOSCC.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Surgery

Reference37 articles.

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