The Efficacy and Safety of Zanubrutinib, Rituximab and Lenalidomide (ZR2) Versus Rituximab Combined With Low-dose CHOP (R-miniCHOP) in the Treatment of Unfit or Frail de Novo Diffuse Large B-cell Lymphoma Patients Aged Older Than or Equal to 70 Years: A Multicenter, Prospective, Randomized, Open-label, Controlled Trial

Who is this study for? Unfit or frail patients aged older than or equal to 70 years with de novo diffuse large B-cell lymphoma
What treatments are being studied? Zanubrutinib+Rituximab+Lenalidomide
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

A multicenter, prospective, randomized, open-label, controlled trial to evaluate the efficacy and safety of zanubrutinib, rituximab and lenalidomide (ZR2) versus rituximab combined with low-dose CHOP (R-miniCHOP) in the treatment of unfit or frail de novo diffuse large B-cell lymphoma patients aged older than or equal to 70 years

Eligibility
Participation Requirements
Sex: All
Minimum Age: 70
Healthy Volunteers: f
View:

⁃ Patients must satisfy all of the following criteria to be enrolled in the study:

• Histologically-confirmed diffuse large B-cell lymphoma (without central nervous system involvement)

• Eastern Cooperative Oncology Group performance status 0-3

• Aged ≥ 80 years old or aged 70-79 with comprehensive geriatric assessment stratified as unfit or frail

• International normalized ratio and activated partial thromboplastin time are both 1.5 times lower than the upper limits of normal (ULN).

• At least 1 measurable site of disease (defined as lymph nodes with the long diameters longer than 1.5cm, or extra-nodal sites with the long diameters longer than 1.0cm; meanwhile, any lesion site with at least 2 measurable vertical diameters)

• Life expectancy of at least 3 months determined by researchers

• The patient or his or her legal representative must provide written informed consent prior to any special examination or procedure for the research.

• Anti-lymphoma drugs have not been used before (except glucocorticoids).

Locations
Other Locations
China
Ruijin Hospital
RECRUITING
Shanghai
Contact Information
Primary
Weili ZHAO
zwl_trial@163.com
+862164370045
Backup
Pengpeng XU
pengpeng_xu@126.com
+862164370045
Time Frame
Start Date: 2022-03-02
Estimated Completion Date: 2025-12-25
Participants
Target number of participants: 280
Treatments
Experimental: ZR2
six courses of zanubrutinib, rituximab and lenalidomide
Active_comparator: R-miniCHOP
six courses of rituximab combined with low-dose CHOP
Sponsors
Collaborators: National Naval Medical Center, Huai'an First People's Hospital, Changzhou No.2 People's Hospital, The Second Affiliated Hospital of Dalian Medical University, Ningbo No. 1 Hospital, First Affiliated Hospital of Fujian Medical University, Sir Run Run Shaw Hospital, Qilu Hospital of Shandong University, Northern Jiangsu People's Hospital, Taizhou Hospital, HARBIN THE FIRST HOSPITAL, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, The First People's Hospital of Changde City, The First Hospital of Jilin University, Shandong Provincial Hospital, Hunan Cancer Hospital, The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, YANCHENG NO.1 PEOPLE'S HOSPITAL, Affiliated Hospital of Nantong University, The First Affiliated Hospital of Nanchang University, The Affiliated Hospital of Xuzhou Medical University, The First People's Hospital of Kunshan, THE FIRST AFFILIATED HOSPITAL, First Hospital of China Medical University, Shanghai Fengxian District Central Hospital, Henan Provincial People's Hospital, Huadong Hospital, SUZHOU HONGCI HEMATOLOGY HOSPITAL
Leads: Ruijin Hospital

This content was sourced from clinicaltrials.gov

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