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

被引:1
|
作者
Hu, Jiyi [1 ,2 ,3 ,4 ]
Huang, Qingting [1 ,2 ,3 ,4 ]
Hu, Weixu [1 ,2 ,3 ,4 ]
Gao, Jing [1 ,2 ,3 ,4 ]
Yang, Jing [1 ,2 ,3 ,4 ]
Zhang, Haojiong [1 ,2 ,3 ,4 ]
Lu, Jiade Jay [5 ,6 ]
Kong, Lin [1 ,3 ,4 ,6 ]
机构
[1] Fudan Univ, Shanghai Proton & Heavy Ion Ctr, Dept Radiat Oncol, Canc Hosp, Shanghai, Peoples R China
[2] Shanghai Proton & Heavy Ion Ctr, Dept Radiat Oncol, Shanghai, Peoples R China
[3] Shanghai Key Lab Radiat Oncol, Shanghai, Peoples R China
[4] Shanghai Engn Res Ctr Proton & Heavy Ion Radiat Th, Shanghai, Peoples R China
[5] Heyou Int Hosp, Proton & Heavy Ion Ctr, Dept Radiat Oncol, Foshan, Peoples R China
[6] Shanghai Proton & Heavy Ion Ctr, 4365 Kangxin Rd, Shanghai 201321, Peoples R China
来源
CANCER MEDICINE | 2024年 / 13卷 / 03期
关键词
camrelizumab; carbon ion; radiotherapy (RT); randomized trial; recurrent nasopharyngeal carcinoma; SQUAMOUS-CELL CARCINOMA; INTENSITY-MODULATED RADIOTHERAPY; OPEN-LABEL; HEAD; PEMBROLIZUMAB; MULTICENTER; IMMUNOTHERAPY; CETUXIMAB;
D O I
10.1002/cam4.6742
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Management 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.Methods: Patients 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 Conclusion: The results of the trial may shed insights on the combined therapy with ICIs and CIRT.
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页数:7
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