Efficacy of Lenalidomide Maintenance in Primary Central Nervous System Lymphoma and Primary Vitreoretinal Lymphoma: a Phase II, Open-label, Single-arm Study

NCT05901324 | Not Yet Recruiting Phase 2

• 1 other identifier: 202303123MIPA
• Study Type: interventional
• Target: 20
• Locations: 0 countries
• Sites: N/A

Brief Summary

Therefore, we intend to conduct a phase II study to evaluate the efficacy of maintenance therapy with lenalidomide as the maintenance therapy for patients with PCNSL or PVRL who have achieved CR or partial response after HD-MTX-based induction therapy followed by reduced-dose WBRT.Twentypatients with PCNSL or PVRL will be recruited. The primary outcome is 2-year progression-free survival from the first date of reduced-dose WBRT. Besides, the safety and the incidence of cute and late neurotoxicity related to reduced-dose WBRT, the single nucleotide polymorphism assay,and the clinical applications of plasma and CSF circulating tumor DNA and CSF lactate level will be investigated.

Conditions

Primary Central Nervous System Lymphoma and Primary Vitreoretinal Lymphoma

Keywords

primary central nervous system lymphoma and primary vitreoretinal lymphoma; primary vitreoretinal lymphoma

Outcome Measures

Primary Outcomes (1)

• The incidence of tumor progression or death from all causes from the starting date of reduced-dose WBRT to the end of maintenance therapy

  2-year

Secondary Outcomes (2)

• The time from the starting date of reduced-dose WBRTto death from any cause.

  24months

• The proportion of patients who achieve CR and PR.

  24months

Study Arms (1)

Maintenance therapy with lenalidomide as the maintenance therapy for patients with PCNSL or PVRL

EXPERIMENTAL

Radiation: intensity-modulated radiotherapy (IMRT)

Interventions

intensity-modulated radiotherapy (IMRT) RADIATION

1.8 Gy of 4-6 MV X-ray to a total dose of 23.4 Gy (13 fractions) will be delivered.

Maintenance therapy with lenalidomide as the maintenance therapy for patients with PCNSL or PVRL

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Those who have been diagnosed with histopathological- or CSF/vitreous fluid flow cytometry- confirmedPCNSL/PVRL, DLBCL subtype and who are above 18 years of age.
• Those who have completed standard HD-MTX-based remission induction chemotherapy followed by reduced-dose WBRT and reached a CR or PR
• Patients must be able to tolerate MRI scans and lumbar punctures and/or Ommaya taps.
• With sufficient organ and bone marrow function, and no severe hematopoietic, heart, lung, liver, kidney, thyroid dysfunction, and immune deficiency
• ECOG PS 0-2
• Those who can take oral medication
• Written informed consent under institutional guidelines.
• Female patients of child-bearing potential (FCBP) must have two negative pregnancy tests (sensitivity of at least 25 mIU/mL) prior to starting lenalidomide. The first pregnancy test must be performed within 10 to 14 days prior to the start of lenalidomide, and the second pregnancy test must be performed within 24 hours prior to the start of lenalidomide
• Effective method of contraception should be used during and for 28 days following the last dose of the drug
• Male patients must use an effective barrier method of contraception during study and 28 days following the last dose if sexually active with a FCBP

You may not qualify if:

• Patients who are planned to undergo auto-SCT after induction chemotherapy
• Disease involving extra-CNSat the time of initial diagnosis
• Previous treatment with lenalidomide or WBRT
• Active congestive heart failure (New York Heart Association \[NYHA\] Class III to IV), symptomatic ischemia, or conduction abnormalities uncontrolled by conventional intervention. Myocardial infarction within six months prior to 1st day of 1st cycle
• Acute active infection requiring systemic antibiotics, antiviral (except antiviral therapy directed at hepatitis B) or antifungal agents
• Known human immunodeficiency (HIV) seropositive
• Those who are unable to take oral medication or unable to take antiplatelet therapy for the purpose of thromboembolism prevention.
• Patients with a history of malignant tumors other than the target diseases except for the following cases oIf the tumor has not been treated for at least 5 years or is disease-free oPatients at least 1 year after complete resection of basal cell carcinoma / squamous cell carcinoma or successful treatment of cervical epithelial cancer
• Adverse reactions within 30 days prior to screening Severe gastrointestinal bleeding exceeding Grade 2 according to the Common Terms Criteria 4.03 version criteria
• Occurrence of blood clots or embolism within 6 months before starting screening
• Patients with hypersensitivity to THIS DRUG and other ingredients of THIS DRUG (e.g., angioedema, Stevens-Jones syndrome, toxic epidermal necrosis, etc.)
• Female patients who are pregnant or lactating
• The Patient is unwell or unable to participate in all required study evaluations and procedures.

Sponsors & Collaborators

• National Taiwan University Hospital: lead

MeSH Terms

Interventions

Radiotherapy, Intensity-Modulated

Intervention Hierarchy (Ancestors)

Radiotherapy, Conformal; Radiotherapy, Computer-Assisted; Radiotherapy; Therapeutics

Central Study Contacts

Chieh Lung Cheng, doctoral degree

CONTACT

+886972651893; Jerome010471@gmail.com

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Attending Physician

Study Record Dates

• First Submitted: June 4, 2023
• First Posted: June 13, 2023
• Study Start: July 1, 2023
• Primary Completion (Estimated): May 31, 2031
• Study Completion (Estimated): May 31, 2031
• Last Updated: June 13, 2023

Record last verified: 2023-06

Data Sharing

• IPD Sharing: Will share
• Shared Documents: ICF