A Multicenter Prospective Real-world Study of Zanubrutinib Combined With Rituximab (ZR) in the First-line Treatment for Patients With Marginal Zone Lymphoma (MZL)

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This is a prospective single arm, multi-center, real-world study to observe the efficacy and safety of ZR (Zanubrutinib combined with Rituximab) in the first-line treatment for patients with marginal zone lymphoma (MZL).

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Patients with CD20-positive marginal zone lymphoma diagnosed by histopathology

• First-line treatment with the combination regimen of zanubrutinib and rituximab

• No receiving systematic treatment before enrollment

• Having at least one measurable lesions. Measurable lesions were defined as: the longest diameter of lymph node lesions in CT cross-sectional images \> 1.5 cm, or the longest diameter of the extranodal lesion is greater than 1.0cm

• The patients voluntarily joined this study, signed the informed consent form, had good compliance and cooperated with the follow-up.

Locations
Other Locations
China
Henan Cancer Hospital/The affiliated Cancer Hospital of ZhengZhou university
RECRUITING
Zhengzhou
Contact Information
Primary
Zhihua Yao, M.D. Ph.D
zlyyyaozhihua1260@zzu.edu.cn
+8613592622292
Time Frame
Start Date: 2025-11-18
Estimated Completion Date: 2030-06
Participants
Target number of participants: 30
Treatments
Zanubrutinib Combined With Rituximab
Induction treatment:~Rituximab, 375mg/m2, Intravenous administration on day 1 (21 days/cycle); Zanubrutinib, 160mg twice daily continuous oral administration from 1 to 8 cycles (21 days/cycle)~Maintenance treatment:~Zanubrutinib, 160mg twice daily continuous oral administration for two years (28 days/cycle)
Related Therapeutic Areas
Sponsors
Leads: Henan Cancer Hospital

This content was sourced from clinicaltrials.gov

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