A Prospective, Single-arm, Multicenter Clinical Study of Polatuzumab, Rituximab and Orelabrutinib Combination Regimen (PRO) in the Treatment of Elderly Patients with Frail Treatment-naive Non-germinal Center Subtype Diffuse Large B-cell Lymphoma

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This prospective, single-arm, multicenter clinical study aims to enroll 30 frail elderly patients with Non-GCB DLBCL. This study is to evaluate the preliminary efficacy and safety of the combination of Polatuzumab, Rituximab, and orelabrutinib in this population. The primary endpoint is CR rate after induction therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Healthy Volunteers: f
View:

• Patients with histopathologically confirmed DLBCL;

⁃ The sGA evaluation result of octogenarians or 60-79 years old is unfit or f RA il;

‣ Non-germinal center (Non-GCB) type;

∙ ECOG performance status score of 0-3 points; ⑤ No previous treatment for Lymphoma (unless glucocorticoid); 6 Radiographic Investigation to measurable disease, defined as the longest diameter with at least one Lymph node disorder \> 1.5 cm, or at least one extranodal lesion \> 1.0 cm in the longest diameter; ⑦ Adequate organ function;

• Life expectancy ≥ 12 weeks; ⑨ Signed written informed consent.

Locations
Other Locations
China
Jiangsu Province Hospital
NOT_YET_RECRUITING
Nanjing
Affiliated hospital of Nantong University
RECRUITING
Nantong
Contact Information
Primary
Wenyu Shi
shiwenyu@hotmail.com
+86 13515203737
Time Frame
Start Date: 2024-08-01
Estimated Completion Date: 2026-08-01
Participants
Target number of participants: 30
Treatments
Experimental: PRO
The drugs involved in this trial include Polatuzumab, Rituximab, and orelabrutinib in 21-day cycles.~The dose and administration method of the study drug were as follows:~* Polatuzumab: 1.8 mg/kg, IV, D1;~* Rituximab: 375 mg/m2, IV, D1;~* Orelabrutinib: 150 mg/time, qd, po, D1-21;
Sponsors
Leads: Affiliated Hospital of Nantong University

This content was sourced from clinicaltrials.gov