Methotrexate, Procarbazine, Lomustine, Dexamethasone, and Cytarabine in Treating Patients With Primary CNS Lymphoma
Information source: National Cancer Institute (NCI)
Information obtained from ClinicalTrials.gov on June 20, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Lymphoma
Intervention: cytarabine (Drug); dexamethasone (Drug); lomustine (Drug); methotrexate (Drug); procarbazine hydrochloride (Drug)
Phase: Phase 2
Status: Active, not recruiting
Sponsored by: Oregon Health and Science University Cancer Institute
Official(s) and/or principal investigator(s):
Edward A. Neuwelt, MD, Principal Investigator, Affiliation: Oregon Health and Science University Cancer Institute
RATIONALE: Drugs used in chemotherapy, such as methotrexate, procarbazine, lomustine,
dexamethasone, and cytarabine, use different ways to stop cancer cells from dividing so they
stop growing or die. Combining more than one drug may kill more cancer cells.
PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating
patients who have primary CNS lymphoma.
Official title: Combination Chemotherapy (Methotrexate, Procarbazine And CCNU), Intraventricular Cytarabine And Methotrexate, +/- Intra-Ocular Chemotherapy For Patients With Primary Central Nervous System Lymphoma
Study design: Treatment, Open Label
Primary outcome: Survival as measured by clinical and radiographic response at 5 years following completion of study treatment
Overall survival as measured by clinical and radiographic response
Progression-free survival as measured by clinical and radiographic response until tumor progression
Quality of Life (QOL) as measured by EORTC QOL before and after study treatment, every 6 months for 2 years, and then annually
- Determine the toxicity and efficacy of methotrexate, procarbazine, lomustine,
dexamethasone, and cytarabine in patients with primary CNS lymphoma.
- Determine the ability to recruit adequate numbers of patients for this study.
- Compare progression-free and dementia-free survival with standard measures of overall
survival, progression-free survival, disease-free survival, complete response rate,
cognitive function, and quality of life of patients treated with this regimen.
- Determine the feasibility of conducting a future phase III study of this treatment
regimen in these patients.
- Correlate neuropsychological outcomes with neuroimaging (MRI) outcomes in patients
treated with this regimen.
OUTLINE: This is a nonrandomized, multicenter study.
- Induction chemotherapy: Patients receive methotrexate IV over 3 hours on days 1, 10, and
20 and intraventricularly or intrathecally (IT) over 5 minutes on days 1, 5, 10, and 15;
oral procarbazine on days 1-7; oral lomustine on day 1; oral dexamethasone every 6 hours
on days 1-14 followed by a taper (as tolerated); and cytarabine intraventricularly or IT
over 5 minutes on days 1, 5, 10, and 15. Treatment repeats every 42 days for a total of
3 courses. Patients with intraocular lymphoma also receive methotrexate intravitreally
twice weekly until the vitreous is clear of cells by slit lamp exam. Patients with
stable or responding disease proceed to maintenance therapy.
- Maintenance chemotherapy: Patients receive methotrexate IV over 3 hours and IT over 5
minutes on day 1; oral procarbazine on days 1-7; oral lomustine on day 1; oral
dexamethasone every 6 hours on days 1-14 followed by a taper (as tolerated); and
cytarabine intraventricularly or IT over 5 minutes on day 1. Treatment repeats every 42
days for a total of 5 courses.
Patients with intraocular lymphoma also receive methotrexate intravitreally weekly for 1
month and then monthly for 1 year.
Quality of life is assessed at baseline, at 6 months, at the completion of treatment, every 6
months for 2 years, and then annually thereafter.
Patients are followed every 3 months for 1 year, every 6 months for 2 years, and then
PROJECTED ACCRUAL: A total of 180 patients will be accrued for this study within 3 years.
Minimum age: 16 Years.
Maximum age: 75 Years.
- Histologically or cytologically confirmed intermediate- or high-grade primary CNS
lymphoma documented by brain biopsy or cerebrospinal fluid or vitrectomy analysis
- Diagnosed within the past 90 days
- No systemic lymphoma NOTE: A new classification scheme for adult non-Hodgkin's
lymphoma has been adopted by PDQ. The terminology of "indolent" or "aggressive"
lymphoma will replace the former terminology of "low", "intermediate", or "high" grade
lymphoma. However, this protocol uses the former terminology.
- 16 to 75
- ECOG 0-3 OR
- Karnofsky 40-100%
- Not specified
- WBC at least 2,500/mm^3
- Hematocrit at least 25% (transfusion allowed)
- Absolute granulocyte count at least 1,200/mm^3
- Platelet count at least 100,000/mm^3 OR at least lower limit of normal (transfusion
- Bilirubin no greater than 2. 0 times upper limit of normal
- Creatinine clearance at least 30 mL/min
- Adequate cardiac function to tolerate general anesthesia
- Adequate pulmonary function to tolerate general anesthesia
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception for 2 months before and during study
- No other uncontrolled, clinically significant confounding medical condition within the
past 30 days
- No known allergy to study agents
- HIV negative
PRIOR CONCURRENT THERAPY:
- Not specified
- More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas)
- Single-agent methotrexate administered within the past 14 days allowed
- Not specified
- No prior cranial or spinal radiotherapy
- Prior surgery or biopsy allowed
Locations and Contacts
Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio 44195, United States
Oregon Health & Science University Cancer Institute, Portland, Oregon 97239-3098, United States
Clinical trial summary from the National Cancer Institute's PDQ® database
Starting date: March 2003
Last updated: May 23, 2008