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R2 in the Treatment of Follicular Lymphoma

Phase 2
Conditions
Follicular Lymphoma
Interventions
Registration Number
NCT03715309
Lead Sponsor
Ruijin Hospital
Brief Summary

Lenalidomide Based Immunotherapy in the Treatment of FL

Detailed Description

Lenalidomide Based Immunotherapy efficacy related molecular biomarker in follicular lymphoma

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
115
Inclusion Criteria

Patients diagnose as de novo or relapse refractory FL grade 1-3A .

No history of stem cell transplantation.

Written informed consent.

Exclusion Criteria

Chemotherapy or large field radiotherapy within 3 weeks prior to entering the study.

Clinically significant active infection.

Impaired liver, renal or other organ function not caused by lymphoma, which will interfere with the treatment schedule.

Any significant medical or psychiatric condition that might prevent the patient from complying with all study procedures.

Subject has ≥grade 2 peripheral neuropathy or grade 1 with pain within 14 days before enrollment.

Patients who are pregnant or breast-feeding.

HIV infection.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
RevlimdRevlimid-
Primary Outcome Measures
NameTimeMethod
CR12 weeks

Complete response rate

Secondary Outcome Measures
NameTimeMethod
PFS1 year

Progression free survival rate

OS1 year

Overall survival rate

ORR12 weeks

Overall response rate

Trial Locations

Locations (1)

Ruijin Hospital

🇨🇳

Shanghai, Shanghai, China

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