Rituximab Plus Methotrexate With or Without Lenalidomide in Treating Patients With Newly Diagnosed Primary Central Nervous System Lymphoma

PCNSL Clinical Trial

Official title:

Efficacy and Safety Study of Lenalidomide Plus Rituximab and Methotrexate Chemotherapy（R2-MTX） Versus Rituximab and Methotrexate Chemotherapy（R-MTX） in Newly Diagnosed Primary Central Nervous System Lymphoma: a Multicenter, Open-Label, Randomised Phase 2 Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04481815
• Other study ID #: IR2020001238
• Status: Recruiting
• Phase: Phase 2
• Start date: October 1, 2020
• Est. completion date: December 30, 2025

Study information

• Verified date: October 2022
• Source: Second Affiliated Hospital, School of Medicine, Zhejiang University
• Contact: Xianggui Yuan, MD,PhD
• Phone: +8613989883884
• Email: yuanxg[@]zju.edu.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

It is a multicenter, open-Label, randomised phase 2 study to compare the efficacy and safety study of R2-MTX chemotherapy（Lenalidomide, Rituximab and Methotrexate）with R-MTX chemotherapy（Rituximab and Methotrexate ）as first-line regimens in the treatment of newly diagnosed primary central nervous system lymphoma.2-year Progression free survival (PFS) is the primary endpoint.

Description:

This is a multicenter, open-Label, randomised phase 2 study designed to evaluate the efficacy and safety of rituximab plus methotrexate with or without lenalidomide as first-line regimens in the treatment of primary central nervous system lymphoma. A total of 240 patients plan to participate in this study to receive a total 6 cycles of induction chemotherapy followed by 4 cycles of maintenance chemotherapy. Follow-ups should be taken up to the first 3 years.The primary endpoints were 2-year PFS rate and and secondary endpoints including objective response rate (ORR), PFS, overall survival (OS), and adverse events.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 240
• Est. completion date: December 30, 2025
• Est. primary completion date: December 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Histologically confirmed Primary Central Nervous System (CNS) lymphoma

2. Age range 18-75 years old.

3. Eastern Cooperative Oncology Group performance status 0 to 3.

4. Previously untreated. Patients treated with steroid alone are eligible.

5. Patient's who are not planned to undergo consolidation with autologous hematopoietic stem cell transplantation(HSCT).

6. Measurable disease was defined as at least =1.0cm in short-diameter by MRI.

7. Life expectancy of = 3 months (in the opinion of the investigator).

8. Participants must be able to understand and be willing to sign a written informed consent document.

9. Women of reproductive potential must agree to use highly effective methods of birth control during the period of therapy and for 6 months after the last dose of the study drug. Men who are sexually active must agree to use highly effective contraception during the period of therapy and for 6 months after the last dose.

10. Women of childbearing potential must have a negative plasma pregnancy test upon study entry.

11. Adequate renal function: Estimated glomerular filtration rate (GFR) or estimated creatinine clearance (CrCl) = 50 mL/min;Serum creatinine = 2 times the upper limit of normal.

12. Adequate liver functions: Transaminase (AST/ALT) < 3 X upper normal value & Bilirubin < 2 X upper normal value.

13. Adequate hematological function: hemoglobin = 9 g/dL absolute neutrophil count (ANC) = 1,500/µL and platelet count = 75,000/µL.

Exclusion Criteria:

1. Patient with systemic, non-CNS lymphoma metastatic to the CNS.

2. Patient is concurrently using other approved or investigational antineoplastic agents.

3. Presence of active hepatitis B virus(HBV) infection (HBsAg positive and HBV-DNA= 104), hepatitis C virus(HCV) infection, acquired and congenital immunodeficiency diseases include but not limited to HIV.

4. Patient is allergic to components of the study drug.

5. Patient has an active concurrent malignancy requiring active therapy.

6. Patient has significant abnormalities on screening electrocardiogram (EKG) and active and significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, uncontrolled congestive heart failure, uncontrolled hypertension, valvular disease, pericarditis, or myocardial infarction within 6 months of screening.

7. Patient is known to have an uncontrolled active systemic infection.

8. Patient has a life-threatening illness, medical condition, or organ system dysfunction that, in the opinion of the investigator, could compromise the subject's safety or put the study outcomes at undue risk.

9. Women who are pregnant or nursing (lactating), where pregnancy is defined as a state of a female after conception until the termination of gestation, confirmed by a positive plasma human chorionic gonadotropin(hCG) laboratory test of > 5 mIU/mL.

10. The patient is unwell or unable to participate in all required study evaluations and procedures.

11. Drug abuse, medical, psychological or social conditions which may interfering with subjects' participation in the study or evaluation of the results.

12. Patients considered unsuitable to participate in the study by the researchers.

Related Conditions & MeSH terms

• PCNSL

Intervention

Drug:
• Rituximab
375mg/m2 intravenous infusion d1, every 3 weeks for 1 cycle, 6 cycles will be prescribed for induction therapy. 375mg/m2 intravenous infusion d1, every 8 weeks for 1 cycle, 4 cycles will be prescribed for maintenance therapy.
• Lenalidomide
25mg orally d1-10 every 3 weeks for 1 cycle, 6 cycles will be prescribed for induction therapy. 25mg orally d1-14,d29-42 every 8 weeks for 1 cycle, 4 cycles will be prescribed for maintenance therapy.
• Methotrexate
3.5g/m2 intravenous infusion for 4 hours in d1, every 21 days for 1 cycle, 6 cycles will be prescribed.

Locations

Country	Name	City	State
China	2nd Affiliated Hospital, School of Medicine, Zhejiang University	Hangzhou	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Serum ctDNA biomarkers and tissue biomarkers	Next generation sequencing of serum and tissue samples to identify circulating tumor DNA(ctDNA)and tissue biomarkers before and after treatment	Up to 3 years
Primary	2-year progression free survival	From date of patients sign informed consent until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 years	2 years
Secondary	Objective response rate	At the end of Cycle 6 (each cycle is 21 days) the ratio of numbers of patients with complete response and partial response to all the participants receiving treatment	At the end of Cycle 6 chemotheray
Secondary	Overall survival	From date of patients sign informed consent until the date of death or the date of last follow-up time, whichever came first, assessed up to 3 years	3 years
Secondary	Progression free survival	From date of patients sign informed consent until the date of progression or death or the date of last follow-up time, whichever came first, assessed up to 3 years	3 years
Secondary	Treatment-related adverse events	Number of participants with treatment-related adverse events as assessed by CTCAE v4.0	1 year