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Alkylating agents
Rituximab, Methotrexate, Vincristine, Procarbazine, PBPCs collection, Busulfan, Thiotepa, and Cyclophosphamide for Central Nervous System Lymphoma (PCNSL Trial)
Phase 2
Waitlist Available
Led By Christian Grommes, MD
Research Sponsored by Memorial Sloan Kettering Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
PCNSL Trial Summary
This trial is testing a new cancer treatment to see if it is safe and effective. The current standard treatment for this cancer only cures less than half of patients, and often has serious side effects.
Eligible Conditions
- Central Nervous System Lymphoma
- Brain Cancer
- Non-Hodgkin's Lymphoma
PCNSL Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants Evaluated for Toxicity
Secondary outcome measures
Overall Response Rates
Side effects data
From 2023 Phase 2 trial • 33 Patients • NCT0059615433%
Fatigue
21%
Death not related to disease
21%
Neuropathy: sensory
15%
Constipation
12%
Neuropathy: motor
9%
ALT, SGPT
9%
Nausea
9%
Infection, other
9%
Thrombosis/thrombus/embolism
9%
AST, SGOT
6%
Dysgeusia
6%
Rash: erythema multiforme
6%
Rash/desquamation
6%
Lymphopenia
6%
Pain - Head/headache
6%
Vomiting
6%
Diarrhea
3%
Ophthalmoplegia/diplopia (double vision)
3%
Obstruction, GI- Small bowel NOS
3%
Confusion
3%
Pain - Chest/thorax NOS
3%
Seizure
3%
Liver dysfunction/failure
3%
Fever (in the absence of neutropenia)
3%
Creatinine
3%
Osteonecrosis (avascular necrosis)
100%
80%
60%
40%
20%
0%
Study treatment Arm
Newly Diagnosed Primary CBS Lymphoma/PCNSL
PCNSL Trial Design
1Treatment groups
Experimental Treatment
Group I: 1Experimental Treatment1 Intervention
Rituximab, methotrexate (MTX), procarbazine and vincristine (R-MPV). The peripheral blood stem cell (PBSC) harvest procedure will be performed at the discretion of the hematology attending (usually after the 1st or 2nd cycle of R-MPV)and high dose chemotherapy Busulfan, Thiotepa, and Cyclophosphamide. Patients will be off study at the time of death. All patients will be followed for survival every 6 months throughout their lifetime. Survival status may be obtained by phone call, clinical visit or medical records (e.g. physician notes/laboratory results of clinic or hospital visit.
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Who is running the clinical trial?
Memorial Sloan Kettering Cancer CenterLead Sponsor
1,935 Previous Clinical Trials
588,822 Total Patients Enrolled
3 Trials studying Central Nervous System Lymphoma
128 Patients Enrolled for Central Nervous System Lymphoma
Christian Grommes, MDPrincipal InvestigatorMemorial SloanKettering Cancer Center
6 Previous Clinical Trials
209 Total Patients Enrolled
Frequently Asked Questions
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