R-MPV Followed by Nivolumab in Older (≥65) Pts With Previously Untreated Primary CNS Lymphoma

Clinical Trial ID: NCT04022980


The primary objective of Stage 1 is to evaluate the safety of nivolumab consolidation after R-MPV induction chemotherapy in older subjects with previously untreated PCNSL in terms of a tolerated dose (based on dose-limiting toxicities) for the expansion phase of the study (Stage 2). The primary objective of Stage 2 is to evaluate the efficacy of nivolumab consolidation after R-MPV induction chemotherapy in terms of the 2-year progression-free survival rate.

This is a 2-stage phase 1B study of R-MPV (rituximab, methotrexate, procarbazine, vincristine) induction chemotherapy followed by nivolumab consolidation in older (≥ 65 years old) patients with previously untreated primary CNS lymphoma. Stage 1 is designed to evaluate the safety of nivolumab consolidation after R-MPV induction chemotherapy. We plan to use 3+3 design and start at the FDA approved single agent dose of nivolumab 480 mg intravenously every 4 weeks. Stage 2 is designed to evaluate the safety as well as efficacy of nivolumab consolidation after R-MPV induction chemotherapy in an expansion cohort.


Subjects must meet all of the following criteria to participate in this study: 1. Written informed consent and HIPAA authorization for release of personal health information of subject or subject's legally authorized representative. 2. Age ≥ 65 years at the time of consent 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 3 within 14 days prior to day 1 of treatment 4. Previously untreated histological or cytological confirmation of PCNSL, CD20 positive by immunohistochemistry 5. Measurable disease including lesions that can be accurately measured in 2 dimensions by CT or MRI of brain and with a greatest transverse diameter of ≥ 1 cm. 6. Deemed poor candidate for whole brain irradiation (WBI) or autologous stem cell transplant (ASCT) due to advanced age, ECOG performance status of 2, or in the opinion of the treating physician, subject would not tolerate the administration of WBI or ASCT for other reasons 7. Life expectancy of at least 3 months 8. Demonstrate adequate organ function as defined below (all screening labs to be obtained within 14 days prior to day 1 of treatment): 1. Absolute Neutrophil Count (ANC) ≥ 1000K/mm3 2. Platelet Count ≥ 75 K/mm3 3. Hemoglobin (Hgb) ≥ 8 g/dL 4. Serum creatinine ≥ 1.5 mg/dL OR creatinine clearance ≥ 50 cc/minute as measured by a 24-hour urine collection or estimated by the Cockcroft and Gault formula 5. Bilirubin ≤ 1.5 x upper limit of normal (ULN) (except subjects with Gilbert Syndrome who must have a total bilirubin level of < 3.0 x ULN) 6. Aspartate aminotransferase (AST) ≤ 3 x ULN 7. Alanine aminotransferase (ALT) ≤ 3 x ULN 9. Females of childbearing potential (FCBP) must have a negative serum pregnancy test within 3 days prior to day 1 of treatment. NOTE: Females are considered of child bearing potential unless they are surgically sterile (have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or are postmenopausal (at least 12 consecutive months with no menses without an alternative medical cause). 10. FCBP must be willing to use a highly effective contraceptive method (i.e., achieves a failure rate of <1% per year when used consistently and correctly) from the time of informed consent until 5 months after treatment discontinuation. Contraceptive methods with low user dependency are preferable but not required. (http://www.hma.eu/fileadmin/dateien/Human_Medicines/01-About_HMA/Working_Groups/CTFG/ 2014_09_HMA_CTFG_Contraception.pdf) 11. Male subjects must be willing to use condoms from the time of treatment initiation until 7 months after treatment discontinuation. For a non-pregnant FCBP partner, contraception recommendations should also be considered. 12. As determined by the enrolling physician, ability of the subject to understand and comply with study procedures for the entire length of the study. Subjects must not meet any of the following criteria: 1. Any concurrent systemic involvement by lymphoma outside CNS or intraocular lymphoma without evidence of brain disease 2. Any previous chemotherapy or radiation therapy for PCNSL. Subjects treated with corticosteroids for PCNSL are allowed. 3. Pregnant or breastfeeding (NOTE: breast milk cannot be stored for future use while the mother is being treated on study) 4. Has a known additional malignancy within the past 5 years that is active and/or progressive requiring treatment; exceptions include basal cell or squamous cell skin cancer, in situ cervical or bladder cancer. 5. Treatment with any investigational drug (including drugs not FDA-approved for the indication for which they are given) within 28 days prior to day 1 of treatment 6. Subjects with active, uncontrolled infections (subjects must be afebrile for >48 hours off systemic antibiotics). 7. Uncontrolled intercurrent illness including, but not limited to, ongoing or active symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements as determined by the investigator. 8. Major surgery and/or radiotherapy within 14 days prior to initiation of study treatment 9. Known history of positive test for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS). NOTE: Testing for HIV must be performed at sites where mandated locally. 10. Active infectious hepatitis, type B or C. Subjects with a past or resolved HBV infection (defined as the presence of hepatitis B core antibody anti-HBc and absence of HBsAg) may be included if HBV DNA is undetectable. If enrolled, subjects must be willing to undergo monthly HBV DNA testing. 11. Subjects with active interstitial pneumonitis. 12. Subjects with active, known or suspected autoimmune disease. Subjects with vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger are permitted to enroll.

  • Start Date


  • Last Updated


  • Sponsor

    Bristol-Myers Squibb

  • Condition Name

    Eye and Orbit

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