BMJ Open (Nov 2024)

Safety and efficacy of intralesional rituximab injection versus involved site radiation therapy in primary ocular adnexal MALT lymphoma: study protocol for a multicentre randomised controlled trial

  • Lu Chen,
  • Wei Liu,
  • Ling Jin,
  • Xiaohui Wang,
  • Qing Zhou,
  • Fei Han,
  • Honglei Liu,
  • Yi Wang,
  • Yang Gao,
  • Cheng Li,
  • Lili Wang,
  • Hong Chen,
  • Yu Zhu,
  • Jia Tan,
  • Rong Lu,
  • Weifeng Huang,
  • Yaoming Liu,
  • Yujie Wu,
  • Jichao Zhou,
  • Yuying Dong,
  • Yajing Zheng,
  • Jinmiao Li,
  • Shicai Su,
  • Junjie Tang,
  • Yinghao Wang,
  • Ningyu An,
  • Huiyu Guo

DOI
https://doi.org/10.1136/bmjopen-2024-084904
Journal volume & issue
Vol. 14, no. 11

Abstract

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Introduction Involved site radiation therapy (ISRT) is a widely used treatment for primary ocular adnexal mucosa-associated lymphoid tissue (MALT) lymphoma with control rates over 85%; however, its complications could reach 30%–50%. Intralesional rituximab injection has shown promising results with remission rates between 65% and 100% and minimal complications. This study aimed to conduct a multicentre randomised controlled clinical trial to compare the safety and efficacy of intralesional rituximab injection versus ISRT on primary ocular adnexal MALT lymphoma.Methods and analysis This is a multicentre randomised controlled trial and will be conducted at eight ophthalmic departments and institutes in China. 108 patients with primary ocular adnexal MALT lymphoma will be enrolled and randomised to undergo intralesional rituximab injection or ISRT. Comprehensive examinations will be performed before and after the treatment. The primary outcome is the cumulative occurrence rate of complications of grade ≥2 within 5 years after treatment commencement. The main secondary outcome is overall response rate, and progression-free survival, time to next treatment and overall survival will also be compared between the groups.Ethics and dissemination Ethical approval has been obtained from the Ethics Committee of the Zhongshan Ophthalmic Center (ID: 2023KYPJ125-3; V.20240818) and the ‘5010 Plan’ evaluation committee at Sun Yat-sen University, Guangzhou, China, and all subcentres. All the participants will be required to provide written informed consent. The results will be disseminated through scientific meetings and published in peer-reviewed journals.Trial registration number NCT06190301.