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Clinical Trial Summary

This is a prospective multicenter single-arm phase II study, and the purpose of this study is to evaluate the efficiency of Orelabrutinib combined with PD-1 inhibitor regimen relapsed/refractory primary intraocular lymphoma. Overall response rate (ORR) after 4 cycles is the primary endpoint.


Clinical Trial Description

All the patients will be treated with Orelabrutinib combined with PD-1 inhibitor :Orelabrutinib 150mg qd,Tislelizumab Injection 200mg d1 or Sintilimab injection 200mg d1, every 21-day for 1 cycle). Patients will be evaluated every 2 cycles by MRI scan during the first 6 cycles,and then the interval of investigation will be prolonged to 12 weeks. The patients who achieved complete remission (CR) or partial remission (PR) or stable disease (SD) will receive further treatment. The patients progressed disease (PD) will withdraw from the trial and receive salvage regimens. The treatment will be continued for 2 years or until progression of the disease (PD), unacceptable toxicity, or patient/investigator discretion. During following-up, surveillance ophthalmologic examination and brain magnetic resonance imaging (MRI) scans can be performed every 3 months up for 2 years. ;


Study Design


Related Conditions & MeSH terms

  • Lymphoma
  • Primary Central Nervous System Lymphoma

NCT number NCT04899427
Study type Interventional
Source Peking Union Medical College Hospital
Contact
Status Recruiting
Phase Phase 2
Start date March 24, 2021
Completion date October 24, 2023

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