Diffuse Large B-Cell Lymphoma (DLBCL) Clinical Trials

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Pomalidomide, Anti-PD-1 Antibody Combined With Selinexor (PPS) in Relapsed/Refractory Primary Central Nervous System Diffuse Large B-Cell Lymphoma: A Prospective, Multicenter, Single-Arm, Phase II Clinical Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Primary central nervous system diffuse large B-cell lymphoma (PCNSL-DLBCL) is a highly aggressive malignancy accounting for over 80% of primary CNS lymphomas, with an annual incidence of 0.4-0.6 per 100,000 people globally and a rising trend in immunocompetent patients. First-line high-dose methotrexate-based chemotherapy causes severe toxicities and nearly 50% of patients relapse within 1-2 years, developing relapsed/refractory (R/R) disease. Treatment options for R/R PCNSL are scarce, with low response rates, median survival of only 3-6 months, and 5-year survival below 5%. The blood-brain barrier and tumor heterogeneity further worsen outcomes. This prospective, multicenter, single-arm phase II study evaluates the efficacy and safety of pomalidomide, PD-1 inhibitor, and selinexor (PPS) in R/R PCNSL, aiming to provide a new effective treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Histologically confirmed primary central nervous system diffuse large B-cell lymphoma (PCNSL-DLBCL).

• Disease progression or relapse after prior treatment with high-dose methotrexate and/or BTK inhibitors.

• Age between 18 and 75 years.

• ECOG performance status score 0-4.

• Expected overall survival \> 3 months.

• No known hypersensitivity to any study drug.

• White blood cell count ≥ 3×10⁹/L; absolute neutrophil count ≥ 1.0×10⁹/L; platelet count ≥ 50×10⁹/L.

• Serum creatinine ≤ 1.5 mg/dL; creatinine clearance ≥ 50 mL/min.

• ALT and AST ≤ 3× upper limit of normal (ULN); total bilirubin ≤ 2× ULN.

• Signed written informed consent.

Locations
Other Locations
China
Beijing Tongren Hospital, Capital Medical University
RECRUITING
Beijing
Contact Information
Primary
Liang Wang, M.D.
wangliangtrhos@126.com
+861058266633
Backup
Jia Cong, M.D.
congjia21@163.com
+861058268442
Time Frame
Start Date: 2026-04-01
Estimated Completion Date: 2028-08-31
Participants
Target number of participants: 43
Treatments
Experimental: PPS group
All enrolled patients may initiate induction therapy after completing baseline imaging and relevant laboratory examinations:~Pomalidomide: 4 mg on days 1-14, every 3 weeks (q3w), for a total of 6 cycles; Selinexor: 60 mg on days 1, 8, and 15, q3w, for a total of 6 cycles; PD-1 monoclonal antibody: tislelizumab 200 mg on day 1, q3w, for a total of 6 cycles.~During induction therapy, patients who achieve complete response (CR) may discontinue from the study to receive consolidation therapy with autologous hematopoietic stem cell transplantation (AHSCT) or dose-optimized whole-brain radiotherapy (WBRT), at the investigator's discretion or the patient's choice.~For patients not discontinuing for consolidation therapy, maintenance therapy may be administered after 6 cycles of induction therapy: pomalidomide 4 mg every other day (qod) plus selinexor 40-60 mg once weekly (qw), until disease progression or unacceptable toxicity.
Sponsors
Leads: Beijing Tongren Hospital

This content was sourced from clinicaltrials.gov

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