Multicenter phase II study of moderate low-dose radiotherapy in indolent non-Hodgkin lymphoma: CLCG-iNHL-01 protocol

Author:

Gao Lin-Rui1ORCID,Wang Xinyue1,Xia Changfa2,Song Yong-Wen1,Wang Liang3,Li Xin3,Yang Yong4,Cao Jian-Zhong5,Chen Ke6,Zhong Qiu-Zi7,Gao Yuyan8,Zhou Sheng-Yu9,Feng Xiao-Li10,Wang Xiaojun10,Li Ye-Xiong1ORCID,Qi Shu-Nan1

Affiliation:

1. Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, China

2. Office of Cancer Screening, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, China

3. Department of Hematology, Beijing TongRen Hospital, Capital Medical University, Beijing, 100730, China

4. Department of Radiation Oncology, Fujian Medical University Union Hospital, Fuzhou, Fujian, 350108, China

5. Shanxi Cancer Hospital & the Affiliated Cancer Hospital of Shanxi Medical University, Taiyuan, Shanxi, 030013, China

6. Department of Radiochemotherapy, The Affiliated People’s Hospital of Ningbo University, Ningbo, Zhejiang, 315100, China

7. Department of Radiation Oncology, Beijing Hospital, National Geriatric Medical Center, Beijing, 100005, China

8. The Department of Radiotherapy, Beijing Luhe Hospital, Capital Medical University, Beijing, 101199, China

9. Department of Medical Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC), Beijing, 100021, China

10. Department of Pathology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC), Beijing, 100021, China

Abstract

Background: Radiotherapy is an effective treatment for indolent non-Hodgkin lymphoma (iNHL); however, the optimal radiotherapy dose remains to be determined. We hypothesize that a suitable dose may exist between 4 and 24 Gy. Methods: This prospective multicenter phase II trial intends to recruit 73 sites of iNHL patients, who will receive involved-site radiotherapy of 12 Gy in four fractions. The primary objective is the 6-month clinical complete response rate. Tumor tissue, blood and conjunctival specimens will be collected to identify potential predictive biomarkers. Discussion: The CLCG-iNHL-01 trial will evaluate the efficacy and toxicity of 12 Gy in patients with iNHL and provide information on a novel hypofractionation regimen of low-dose radiotherapy. Clinical Trial Registration: NCT05543070 ( ClinicalTrials.gov )

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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