A protocol for a randomized trial evaluating the role of carbon‐ion radiation therapy plus camrelizumab for patients with locoregionally recurrent nasopharyngeal carcinoma

Author:

Hu Jiyi1234,Huang Qingting1234ORCID,Hu Weixu1234,Gao Jing1234,Yang Jing1234,Zhang Haojiong1234,Lu Jiade Jay5,Kong Lin134

Affiliation:

1. Department of Radiation Oncology, Shanghai Proton and Heavy Ion Center Fudan University Cancer Hospital Shanghai China

2. Department of Radiation Oncology Shanghai Proton and Heavy Ion Center Shanghai China

3. Shanghai Key Laboratory of radiation oncology Shanghai China

4. Shanghai Engineering Research Center of Proton and Heavy Ion Radiation Therapy Shanghai China

5. Department of Radiation Oncology, Proton and Heavy Ion Center Heyou International Hospital Foshan China

Abstract

AbstractPurposeManagement of locoregionally recurrent nasopharyngeal carcinoma (LR NPC) is difficult. Although carbon‐ion radiation therapy (CIRT) could substantially improve the overall survival (OS) of those patients, around 40% of the patients may still develop local failure. Further improvement of the disease control is necessary. Immunotherapy, such as immune checkpoint inhibitors (ICIs) becomes a promising antitumor treatment. The role of ICIs was proved in head and neck cancers including recurrent/metastatic NPC. Preclinical studies indicated potential synergistic effects between radiation therapy and ICIs. Therefore, we conduct a randomized phase 2 trial to evaluate the efficacy and safety of camrelizumab, an anti‐PD‐1 monoclonal antibody, along with CIRT in patients with LR NPC.MethodsPatients will be randomly assigned at 1:1 to receive either standard CIRT with 63 Gy (relatively biological effectiveness, [RBE]) in 21 fractions, or standard CIRT plus concurrent camrelizumab. Camrelizumab will be administered intravenously with a dose of 200 mg, every 2 week, for a maximum of 1 year. We estimate addition of camrelizumab will improve the 2‐year progression‐free survival (PFS) from 45% to 60%. A total of 146 patients (with a 5% lost to follow‐up rate) is required to yield a type I error of 0.2, and a power of 0.8.Results and ConclusionThe results of the trial may shed insights on the combined therapy with ICIs and CIRT.

Publisher

Wiley

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