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Clinical Trial Summary

This is a prospective, single-arm, multi-center, phase Ib/II clinical trial to evaluate the safety, tolerability, and efficacy of selinexor in combination with R-CHOP (rituximab, cyclophosphamide, vincristine, doxorubicin, and prednisone) followed by selinexor maintenance for untreated EBV-positive diffuse large B-cell lymphoma (DLBCL) patients.


Clinical Trial Description

This is a prospective, single-arm, multi-center, phase Ib/II clinical trial to explore the maximum tolerated dose (MTD) of selinexor when combined with R-CHOP regimen for untreated EBV-positive DLBCL patients. Phase Ib study: Selinexor will be given orally at two different doses (40mg qw, and 60mg qw ) and combined with the R-CHOP regimen from the second cycle based on the "3+3" principle. In the induction therapy period, 6 cycles of R-CHOP regimen and 2 cycles of rituximab in combination with selinexor are planned. The dose limited toxicity (DLT) will be evaluated after the first cycle of selinexor in combination with R-CHOP. Phase II study: The phase II study of selinexor at recommended phase II dose (RP2D) dose level combined with R-CHOP regimen was conducted to explore the efficacy and safety of the combined regimen. After 8 cycles of induction therapy, if the response is assessed as complete remission (CR), maintenance therapy with selinexor will be conducted. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05577364
Study type Interventional
Source Sun Yat-sen University
Contact Qingqing Cai, MD. PhD.
Phone 0086-20-87342823
Email caiqq@sysucc.org.cn
Status Recruiting
Phase Phase 1/Phase 2
Start date November 1, 2022
Completion date February 28, 2026