This is a prospective single-arm phase II study, with the purpose of evaluating the efficiency of ZR-MTX regimen (Rituximab, Zanubrutinib and methotrexate) combined with intravitreal methotrexate, then followed by minimal residual disease directed Zanubrutinib maintenance in newly-diagnosed primary intraocular lymphoma. The primary endpoint of this study is progression-free survival (PFS).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
2 years progression-free survival
Timeframe: from the date of treatment to the subject finished his 2 years follow-up phase or the disease relapsed or the death due to lymphoma