LTA Pilot Study of Glucarpidase in Patients With Central Nervous System Lymphoma

Central Nervous System Lymphoma Clinical Trial

Official title:

LTA Pilot Study of Glucarpidase in Patients With Central Nervous System Lymphoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03684980
• Other study ID #: 18-410
• Status: Recruiting
• Phase: Early Phase 1
• Start date: November 14, 2018
• Est. completion date: November 2025

Study information

• Verified date: June 2024
• Source: Memorial Sloan Kettering Cancer Center
• Contact: Lauren Schaff, MD
• Phone: 212-610-0485
• Email: schaffl[@]mskcc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test the effects of a drug called Voraxaze when it's routinely given in combination with methotrexate and rituximab, the standard treatment for CNSL.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 64
• Est. completion date: November 2025
• Est. primary completion date: November 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Arm A:

• Histologically documented B-cell non-Hodgkin"s lymphoma involving the brain, spinal cord, and/or leptomeningeal space.

°Patients in whom the type of lymphoma could not be determined or is unknown (e.g., not enough tissue for further analysis) are assumed to have a B cell lymphoma and are eligible

• Patients with parenchymal lesions must have received no more than two cycles of treatment for treatment of CNS lymphoma or have unequivocal evidence of disease progression on imaging (MRI of the brain/spine or CT head) 28 days prior to study registration. For patients with leptomeningeal disease only, CSF cytology must document lymphoma cells and/or imaging findings must be consistent with CSF disease 28 days prior to study registration (at the discretion of the investigator).

• Patients who have already received two doses of treatment of CNS lymphoma are eligible for enrollment.

• (Arm A only) as long as they are planned for at least 6 additional doses of methotrexate. Patients must not have evidence of systemic non-Hodgkin lymphoma requiring active treatment.

• Men and woman must be at least 18 years of age on the day of consenting to the study.

• Patients must have a Karnofsky Performance Status (KPS) = 50 (See Appendix 2).

• Patients must be willing and able to comply with scheduled visits, treatment plan, and laboratory tests.

• Patients must have adequate bone marrow and organ function shown by:

• Absolute neutrophil count (ANC) = 1.0 x 10^9/L;

• Platelets = 100 x 10^9/L and no platelet transfusion within the past 28 days prior to study registration;

• Hemoglobin (Hgb) = 8 g/dL and no red blood cells (RBC) transfusion within the past 28 days prior to study registration;

• International Normalized Ratio (INR) = 1.5 and PTT (aPTT) = 1.5 times the upper limit of normal;

• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) = 3 times the upper limit of normal;

• Serum bilirubin = 1.5 times the upper limit of normal; or total bilirubin = 3 times the upper limit of normal with direct bilirubin within the normal range in patients with well documented Gilbert Syndrome;

• CrCl = 60 mL/min using the Cockcroft-Gault equation. Men: CrCl (min/mL) = (140-age) X (actual weight in kg) / 72 X serum creatinine (mg/dL) Women: CrCl (mL/min) = (140-age) X (actual weight in kg) X 0.85 / 72 X serum creatinine (mg/dL)

• Women of reproductive potential must agree to use highly effective methods of birth control during the period of therapy and for 30 days after the last dose of the study drug. Men who are sexually active must agree to use highly effective contraception during the period of therapy and for 3 months after the last dose.

• Female subjects of childbearing potential must have a negative plasma pregnancy test upon study entry.

• Patients must be able to tolerate MRI/CT scans.

• Patients must be able to tolerate lumbar puncture and/or Ommaya taps.

• Participants must have recovered to grade 1 toxicity from prior therapy. NOTE:

Patients who have initiated and received up to two cycles of treatment will NOT be excluded from study Arm A as long as all pretreatment assessments have been completed within 28 days of trial initiation.

Arms B and D:

• Histologically documented B-cell non-Hodgkin's lymphoma involving the brain, spinal cord, and/or leptomeningeal space

° Patients in whom the type of lymphoma could not be determined or is unknown (e.g., not enough tissue for further analysis) are assumed to have a B cell lymphoma and are eligible

• Patients must be treatment naïve or have unequivocal evidence of disease progression on imaging (MRI of the brain/spine or CT head) 28 days prior to initiation of MTX. For patients with leptomeningeal disease only, CSF cytology must document lymphoma cells and/or imaging findings must be consistent with CSF disease 28 days prior to initiation of MTX. (at the discretion of the investigator)

• Patients must not have evidence of systemic non-Hodgkin lymphoma requiring active treatment

• Men and woman must be at least 18 years of age on the day of consenting to the study

• Patients must have a Karnofsky Performance Status (KPS) >/= 70 or >/= 50 if KPS is due to a neurologic deficit attributed to active disease

• Patients must be willing and able to comply with scheduled visits, treatment plan, and laboratory tests

• Patients must have adequate bone marrow and organ function shown by:

• Absolute neutrophil count (ANC) >/= 1.0 x 10^9/L

• Platelets >/= 100 x 10^9/L and no platelet transfusion within the past 28 days prior to study registration

• Hemoglobin (Hgb) >/= 8g/dL and no red blood cells (RBC) transfusion within the past 28 days prior to study registration

• International Normalized Ratio (INR) </= 1.5 and PTT (aPTT) </= 1.5 times the upper limit of normal

• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) </= 3 times the upper limit of normal

• Serum bilirubin </= 1.5 times the upper limit of normal; or total bilirubin </= 3 times the upper limit of normal with direct bilirubin within the normal range in patients with well documented Gilbert Syndrome

• CrCl >/= 60 mL/min using the Cockcroft-Gault equation Men: CrCl (min/mL) = (140-age) X (actual weight in kg) / 72 X serum creatinine (mg/dL) Women: CrCl (mL/min) = (140-age) X (actual weight in kg) X 0.85 / 72 X serum creatinine (mg/dL)

• Women of reproductive potential must agree to use highly effective methods of birth control during the period of therapy and for 30 days after the last dose of the study drug. Men who are sexually active must agree to use highly effective contraception during the period of therapy and for 3 months after the last dose.

• Female subjects of childbearing potential must have a negative plasma pregnancy test upon study entry

• Patients must be able to tolerate MRI/CT scans

• Patients must be able to tolerate lumbar puncture and/or Ommaya taps

• Participants must have recovered to grade 1 toxicity from prior therapy

• Patients with ocular manifestation of systemic lymphoma are allowed if repeat ophthalmologic exam is planned for the end of therapy. If ocular disease remains present, ocular-directed therapy may be administered after treatment with methotrexate.

• Patients must be able to tolerate po hydration (Arm D only)

NOTE: Prior autologous stem cell transplant as well as prior radiation to the CNS does NOT prevent patients from enrollment into the trial.

Arm Outpatient MTX Therapy in times of COVID-19:

• Patients eligible for inclusion in this arm must be eligible for inpatient MTX administration for treatment of CNS lymphoma. Patients should have received prior MTX therapy without major adverse events.

• Female subjects of childbearing potential must have a negative plasma pregnancy test upon study entry.

Arm E:

• Documented history of CNS lymphoma, appropriate for standard of care inpatient MTX administration as determined by their treating physician

• Men and woman must be at least 18 years of age on the day of consenting to the study.

• Patients must be willing and able to comply with scheduled visits, treatment plan, and laboratory tests.

• Patients must meet at least ONE of the following additional criteria

• MTX >100 nmol/L = 72 hours after initiation of MTX

• History of prolonged MTX clearance (= 72 hours) after prior MTX administration of equal or higher dose (g/m2)

• CrCl < 60 ml/min calculated by Cockroft-Gault equation oHistory of MTX-related toxicity, CTCAE v5 grade 2 or higher (must have recovered to a grade 1 toxicity)

Exclusion Criteria:

Arms A, B and D:

• Patient with SCNSL requiring treatment for extra-CNS disease are excluded.

• Patient concurrently using other approved or investigational antineoplastic agents.

• Patient has received chemotherapy, monoclonal antibodies or targeted anticancer therapy = 4 weeks or 5 half-lives, whichever is shorter, or 6 weeks for nitrosoureas or mitomycin-C prior to starting the study drug, or the patient has not recovered from the side effects of such therapy. Exceptions are allowed for rituximab and methotrexate for patients enrolling Arm A as long as patients have recovered from side effects.

• Patient has received external beam radiation therapy to the CNS within 28 days of the first dose of the study drug.

• Patient has an active concurrent malignancy requiring active therapy.

• The patient has been treated with radio- or toxin-immunoconjugates within 70 days of the first dose of the study drug.

• Patient weighs <40kg

• Patient is allergic to components of the study drug.

• Patient is known to have human immunodeficiency virus (HIV) infection.

• Patient is known to have a history of active or chronic infection with hepatitis C virus (HCV) or hepatitis B virus (HBV) as determined by serologic tests.

• Severe, active medical co-morbidity such as unstable angina and/or congestive heart failure, coronary artery disease, significant abnormalities on electrocardiogram (EKG), uncontrolled or symptomatic arrhythmias or valvular disease; active infection, severe chronic obstructive pulmonary disease or other respiratory illness, hepatic insufficiency, known pre-existing immunodeficiency as seen in organ transplant recipients, renal failure with CrCl <60 mL/min.

• Patient has a life-threatening illness, medical condition, or organ system dysfunction that, in the opinion of the investigator, could compromise the subject"s safety or put the study outcomes at undue risk.

• Patient has large pleural or ascetic fluid collection.

• Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; this exclusion is necessary because the treatment involved in this study may be significantly teratogenic.

• Prior severe allergic reaction to any of the study drugs that cannot be resolved with medication.

• Patient has undergone prior allogenic stem cell transplant (autologous stem cell transplant is NOT an exclusion).

Arm Outpatient MTX Therapy in times of COVID-19:

Patients eligible for this arm must not meet any of the following criteria:

• Patients with SCNSL requiring treatment for extra-CNS disease are excluded.

• Patients weighing <40kg

• Inadequate bone marrow and organ function shown by:

• Absolute neutrophil count (ANC) </= 0.5 x 10^9/L

• Platelets </= 75 x 10^9/L

• Hemoglobin (Hgb) </= 8 g/dL

• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) >/= 3 times the upper limit of normal

• Serum bilirubin >/= 1.5 times the upper limit of normal; or total bilirubin >/= 3 times the upper limit of normal with direct bilirubin outside of the normal range in patients with well documented Gilbert Syndrome

• Creatinine >/= 1.3 mg/dL

• Patients allergic to components of the study drug.

• Patients with severe, active medical co-morbidity such as unstable angina and/or congestive heart failure, coronary artery disease, significant abnormalities on electrocardiogram (EKG), uncontrolled or symptomatic arrhythmias or valvular disease; active infection, severe chronic obstructive pulmonary disease or other respiratory illness, hepatic insufficiency, known pre-existing immunodeficiency as seen in organ transplant recipients, renal failure with creatinine >/= 1.3 mg/dL.

• Patients with a life-threatening illness, medical condition, or organ system dysfunction that, in the opinion of the investigator, could compromise the subject's safety or put the study outcomes at undue risk

• Patients with large pleural or ascetic fluid collection

• Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; this exclusion is necessary because the treatment involved in this study may be significantly teratogenic. Women of reproductive potential must agree to use highly effective methods of birth control during the period of therapy and for 30 days after the last dose of the study drug. Men who are sexually active must agree to use highly effective contraception during the period of therapy and for 3 months after the last dose

Arm E:

Patients eligible for this arm must not meet any of the following criteria:

• Weight <40kg

• Prior severe allergic reaction to methotrexate or glucarpidase that cannot be resolved withmedication.

• Severe, active medical co-morbidity such as unstable angina and/or congestive heart failure, coronary artery disease, significant abnormalities on electrocardiogram (EKG), uncontrolled or symptomatic arrhythmias or valvular disease; active uncontrolled infection, severe chronic obstructive pulmonary disease or other respiratory illness, hepatic insufficiency

• Patient has a life-threatening illness, medical condition, or organ system dysfunctionthat, in the opinion of the investigator, could compromise the subject's safety or put the study outcomes at undue risk.

• Presence of large pleural or ascetic fluid collection.

• Treatment with MTX dose greater than 8 g/m2

Related Conditions & MeSH terms

• Central Nervous System Lymphoma
• Lymphoma

Intervention

Drug:
• Methotrexate
(Cohort A) will receive MTX 3 g/m2 or (Cohort B) will receive MTX 8 g/m^2 (Cohort E) will receive MTX = 3.5 g/ m2
• Rituximab
Patients will be treated with rituximab 500 mg/m^2.
• leucovorin
Patients will also receive standard of care leucovorin rescue starting at least 24 hours after MTX and 2 hours after Voraxaze. Cycles will be 14 days long.
• Glucarpidase
Glucarpidase 2000 units. Arm E 1000 units.

Locations

Country	Name	City	State
United States	Memorial Sloan Kettering Basking Ridge	Basking Ridge	New Jersey
United States	University of Alabama at Birmingham	Birmingham	Alabama
United States	Dana Farber Cancer Institute (Data Collection and Specimen Analysis)	Boston	Massachusetts
United States	Cleveland Clinic (Data Collection and Specimen Collection)	Cleveland	Ohio
United States	Memorial Sloan Kettering Commack	Commack	New York
United States	Memorial Sloan Kettering Westchester	Harrison	New York
United States	Memorial Sloan Kettering Monmouth	Middletown	New Jersey
United States	Memorial Sloan Kettering Bergen	Montvale	New Jersey
United States	Memorial Sloan Kettering Cancer Center	New York	New York
United States	Memorial Sloan Kettering Nassau	Uniondale	New York

Sponsors (2)

Lead Sponsor	Collaborator
Memorial Sloan Kettering Cancer Center	University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	number of patients that have significant reduction of serum methotrexate levels	All serum samples will be tested via MTX immunoassay (measures MTX levels in addition to byproducts) as well as HPLC or mass spectroscopy which will reveal plasma concentrations of MTX and DAMPA separately.	1 year

External Links

•   Memorial Sloan Kettering Cancer Center