Pembrolizumab + Chemotherapy in Newly Diagnosed PCNSL

NCT ID: NCT06475235

Last Updated: 2025-12-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE1

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-18

Study Completion Date

2027-06-30

Brief Summary

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This research study is studying if the investigational drug, Pembrolizumab, in combination with chemotherapy helps primary central nervous system lymphoma with acceptable side effects.

This research study involves a combination of the below drugs:

* Pembrolizumab (a type of monoclonal antibody)
* Methotrexate (a type of anti-metabolite)
* Temozolomide (a type of alkylating agent)
* Rituximab (a type of antibody)

Detailed Description

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This is an open label, pilot trial of Pembrolizumab in combination with chemotherapy in participants with newly diagnosed Primary Central Nervous System Lymphoma (PCNSL).

The U.S. Food and Drug Administration (FDA) has not approved Pembrolizumab for Primary Central Nervous System Lymphoma (PCNSL) but it has been approved for other uses.

The FDA has approved Rituximab for PCNSL.

The FDA has not approved Temozolomide for PCNSL but it has been approved for other uses.

The FDA has not approved Methotrexate for PCNSL but it has been approved for other uses.

The research study procedures include screening for eligibility, blood and urine tests, Computerized Tomography (CT) scans, Magnetic Resonance Imaging (MRI) scans, Positron Emission Tomography (PET) scans, testicular ultrasounds, electrocardiograms (ECG), and eye exams.

It is expected that about 15 people will take part in this research study.

Merck \& Co. is supporting this research study by providing the study drug pembrolizumab.

Conditions

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Lymphoma Primary Central Nervous System Lymphoma

Keywords

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Lymphoma Primary Central Nervous System Lymphoma

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Induction Treatment:

Participants will be enrolled and will complete procedures as follows, starting at Dose Level 0 for Methotrexate and Temozolomide:

* Baseline visit with assessments and imaging.
* Imaging on cycles 3 and 6 only.

* Cycles 1 through 3:

---Days 3 and 10 of 14 day cycle: Predetermined dose of Rituximab 1x daily.
* Cycles 1, 3, 5, and 7:

---Days 7 through 11 of 14 day cycle: Predetermined dose of Temozolomide 1x daily.
* Cycles 1 through 8:

---Day 1 of 14 day cycle: Predetermined dose of Methotrexate 1x daily.
* Cycles 1, 4, 7
* Day 10 of 14 day cycle: Predetermined dose of Pembrolizumab 1x daily. Treatment will de-escalate per protocol if greater than or equal to 2 out of 6 participants experience a dose-limiting toxicity.

Group Type EXPERIMENTAL

Pembrolizumab

Intervention Type DRUG

Humanized immunoglobin G4 monoclonal antibody, 4 mL vials, via intravenous infusion (into the vein) per protocol.

Methotrexate

Intervention Type DRUG

Anti-metabolite, 50 mL vials, via intravenous infusion per protocol.

Temozolomide

Intervention Type DRUG

Alkylating agent, 5, 20, 100, 140, 180, or 250 mg capsules, taken orally per protocol.

Rituximab

Intervention Type DRUG

Anti-CD20 antibody, 10 or 50 mL single-use vials, via intravenous infusion per standard of care.

Consolidation Treatment:

4-8 weeks after the completion of Induction Cycle 8, the study doctor will determine if it is appropriate to move on to consolidation therapy and participants will complete:

* Imaging every other cycle.
* Cycles 1 through 15:

* Day 1 of 42 day cycle: Lumbar puncture
* Day 1 of 42 day cycle: Predetermined dose of Pembrolizumab 1x daily.
* End of treatment visit with lumbar puncture and imaging.
* Follow up

Group Type EXPERIMENTAL

Pembrolizumab

Intervention Type DRUG

Humanized immunoglobin G4 monoclonal antibody, 4 mL vials, via intravenous infusion (into the vein) per protocol.

Interventions

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Pembrolizumab

Humanized immunoglobin G4 monoclonal antibody, 4 mL vials, via intravenous infusion (into the vein) per protocol.

Intervention Type DRUG

Methotrexate

Anti-metabolite, 50 mL vials, via intravenous infusion per protocol.

Intervention Type DRUG

Temozolomide

Alkylating agent, 5, 20, 100, 140, 180, or 250 mg capsules, taken orally per protocol.

Intervention Type DRUG

Rituximab

Anti-CD20 antibody, 10 or 50 mL single-use vials, via intravenous infusion per standard of care.

Intervention Type DRUG

Other Intervention Names

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Keytruda MK-3475 Humanized X PD-1 mAb (H409A11) IgG4 MTX Temodar Temodal Riabni Rituxan Ruxience Truxima

Eligibility Criteria

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Inclusion Criteria

* Subjects with pathologically confirmed newly diagnosed primary CNS diffuse large B-cell lymphoma (DLBCL) confirmed by one of the following:

* Brain biopsy or resection
* Cerebrospinal fluid
* Vitreous fluid
* Participants must not have any evidence or history of DLBCL outside of the CNS. Participants with prior history of isolated intraocular lymphoma (primary vitreoretinal lymphoma/PVRL) who have received only local therapy are allowed.
* Participants must not have received any systemic chemotherapy or whole brain radiation therapy directed to PCNSL.
* Age ≥18 years.
* ECOG performance status ≤2 (Karnofsky ≥70% will be considered if related to PCNSL, see Appendix A).
* Participants must have adequate organ function as defined below.
* Hematology

* Absolute neutrophil count (ANC) ≥1000/µL
* Platelets ≥100 000/µL
* Hemoglobin ≥9.0 g/dL or ≥5.6 mmol/L (Criteria must be met without erythropoietin dependency and without packed red blood cell (pRBC) transfusion within last 2 weeks)
* Renal

\-- Creatinine ≤1.5 x ULN OR Measured or calculated creatinine clearance ≥40 mL/min for participant with creatinine levels \>1.5 × institutional ULN (Creatinine clearance (CrCl) should be calculated per institutional standard.)
* Hepatic

* Total bilirubin ≤1.5 x ULN OR direct bilirubin ≤ULN for participants with total bilirubin levels \>1.5 x ULN
* AST (SGOT) and ALT (SGPT) ≤2.5 × ULN (≤5 × ULN for participants with liver metastases)
* Coagulation

--International normalized ratio (INR) OR prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤1.5 × ULN unless participant is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants
* Participants must have negative HIV serology.
* Participants must have no history of organ transplantation or ongoing immunosuppressant therapy.
* Women of child-bearing potential (WOCBP), defined as all women physiologically capable of becoming pregnant, must have a negative serum pregnancy within 72 hours prior to registration.
* Women in the following categories are not considered WOCBP:

* Premenarchal
* Premenopausal female with 1 of the following:

* Documented hysterectomy
* Documented bilateral salpingectomy
* Documented bilateral oophorectomy
* Note: Documentation can come from the site personnel's review of the participant's medical records, medical examination, or medical history interview.
* Post-menopausal female is defined as no menses for 12 months without an alternative medical cause.

* A high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a postmenopausal state in women not using hormonal contraception or hormonal replacement therapy (HRT). However, in the absence of 12 months of amenorrhea, confirmation with two FSH measurements in the postmenopausal range is required.
* Females on HRT and whose menopausal status is in doubt will be required to use one of the non-hormonal highly effective contraception methods if they wish to continue their HRT during the study. Otherwise, they must discontinue HRT to allow confirmation of postmenopausal status before study enrollment.
* Women of child-bearing potential (WOCBP; see definition above), must agree to use a highly effective method of contraception consistently and correctly as described below during study treatment and for 120 days after study discontinuation.

* 1\. Highly Effective Contraceptive Methods That Are User Dependent (Failure rate of \< 1% per year when used consistently and correctly.)

* a. Combined (estrogen- and progestogen- containing) hormonal contraception

* i. Oral
* ii. Intravaginal
* iii. Transdermal
* iv. Injectable
* b. Progestogen-only hormonal contraception b, c

* i. Oral
* ii. Injectable
* 2\. Highly Effective Methods That Have Low User Dependency (Failure rate of \<1% per year when used consistently and correctly)

* a. Progestogen- only contraceptive implant b, c
* b. Intrauterine hormone-releasing system (IUS) b
* c. Intrauterine device (IUD)
* d. Bilateral tubal occlusion
* e. Vasectomized partner: A vasectomized partner is a highly effective contraception method provided that the partner is the sole male sexual partner of the WOCBP and the absence of sperm has been confirmed. If not, an additional highly effective method of contraception should be used.
* f. Sexual abstinence: Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatment. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the study and the preferred and usual lifestyle of the participant.
* NOTES: Use should be consistent with local regulations regarding the use of contraceptive methods for participants of clinical studies.

* a. Typical use failure rates are lower than perfect-use failure rates (i.e. when used consistently and correctly).
* b. If hormonal contraception efficacy is potentially decreased due to interaction with study treatment, condoms must be used in addition to the hormonal contraception during the treatment period and for at least during study treatment and for 120 days after study discontinuation after the last dose of study treatment.
* c. If locally required, in accordance with Clinical Trial Facilitation Group (CTFG) guidelines, acceptable contraceptive implants are limited to those which inhibit ovulation.
* Male participants must to use at least one of the following methods of contraception starting with the first dose of study therapy through 120 days after the last dose of therapy:

* Be abstinent from penile-vaginal intercourse as their usual and preferred lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent
* Use a male condom plus partner use of a contraceptive method with a failure rate of \<1% per year as described in Eligibility criterion 3.1.11 when having penile-vaginal intercourse with a woman of childbearing potential who is not currently pregnant.
* Note: Men with a pregnant or breastfeeding partner must agree to remain abstinent from penile- vaginal intercourse or use a male condom during each episode of penile penetration.

Exclusion Criteria

* Participants who cannot undergo MRI
* Intraocular PCNSL without evidence of brain or spinal cord disease.
* Participants who are receiving any other investigational agents.
* History of allergic reactions or severe hypersensitivity reactions (≥grade 3) attributed to compounds of similar chemical or biologic composition to study agent and/or any of its excipients.
* Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4, OX-40, CD137)
* Has active autoimmune disease requiring immunosuppressives or steroids
* Has received a live vaccine within 30 days prior to the first dose of study drug. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (eg, FluMist®) are live attenuated vaccines and are not allowed. COVID19 vaccines are allowed.
* Has a known additional malignancy that is progressing or has required active treatment within the past 3 years. Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, transitional cell carcinoma of urothelial cancer, or carcinoma in situ (e.g. breast carcinoma, cervical cancer in situ) that have undergone potentially curative therapy are not excluded.
* Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis.
* Patient has poorly controlled diabetes mellitus with a glycosylated hemoglobin \>8% or poorly controlled steroid-induced diabetes mellitus with a glycosylated hemoglobin of \>8%.
* Unable to swallow capsules or disease significantly affecting gastrointestinal function, such as malabsorption syndrome, resection of the stomach or small bowel, or complete bowel obstruction.
* Enzyme-inducing antiepileptic drugs (EIAED) need to be discontinued and switched to a non-EIAED 2 weeks prior to starting on trial drugs
* Has a known history of Hepatitis B (defined as Hepatitis B surface antigen \[HBsAg\] reactive) or known active Hepatitis C virus (defined as HCV RNA \[qualitative\] is detected) infection.
* Has a known history of active TB (Bacillus Tuberculosis)
* Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent)
* Patients who have undergone prior allogeneic stem cell transplant
* Patients who have large pleural effusions, ascites or full body edema
* Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
* Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the study, starting with the screening visit through 120 days after the last dose of trial treatment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role collaborator

Dana-Farber Cancer Institute

OTHER

Sponsor Role lead

Responsible Party

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Lakshmi Nayak, MD

Sponsor Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Lakshmi Nayak, MD

Role: PRINCIPAL_INVESTIGATOR

Dana-Farber Cancer Institute

Locations

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Brigham and Women's Hospital

Boston, Massachusetts, United States

Site Status RECRUITING

Dana Farber Cancer Institute

Boston, Massachusetts, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Lakshmi Nayak, MD

Role: CONTACT

Phone: 617-632-2166

Email: [email protected]

DFCI Clinical Trials Hotline

Role: CONTACT

Phone: 877-338-7425

Facility Contacts

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Lakshmi Nayak, MD

Role: primary

Lakshmi Nayak, MD

Role: primary

Other Identifiers

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24-246

Identifier Type: -

Identifier Source: org_study_id