Loncastuximab Tesirine and Rituximab Following Stereotactic Radiosurgery (SRS) in Patients With Primary and Secondary Central Nervous System Lymphomas (Lonca-R After SRS in CNSL)

Trial Title: Loncastuximab Tesirine and Rituximab Following Stereotactic Radiosurgery (SRS) in Patients With Primary and Secondary Central Nervous System Lymphomas (Lonca-R After SRS in CNSL)

NCT ID: NCT06607549

Condition: Central Nervous System Lymphoma

Conditions: Official terms:
Lymphoma
Rituximab
Loncastuximab tesirine

Study type: Interventional

Study phase: Phase 1

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Loncastuximab tesirine and rituximab (Lonca-R)
Description: Patients will receive stereotactic radiosurgery (SRS) followed by a brain MRI approx. 4 weeks after SRS. This will be followed by loncastuximab tesirine and rituximab administered intravenously for a total of 6 cycles (every 21 days).
Arm group label: Treatment: All Patients

Summary: The purpose of this clinical trial is to learn if drugs loncastuximab tesirine and rituximab (lonca-R) after stereotactic radiosurgery are safe and effective for treatment of central nervous system lymphomas.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Participant aged ≥ 18 years - ECOG Performance Status ≤ 3 - Histologically confirmed primary CNS lymphoma or secondary diffuse large B-cell lymphoma (DLBCL) with CNS involvement with either: - Relapsed or refractory disease with at least 1 prior therapy OR - Ineligible for high-dose methotrexate-based therapy as determined by the treating physician, including previously untreated patients. Examples of medical conditions for which a patient could be considered ineligible for high-dose methotrexate include but not limited to renal impairment, liver disease, heart failure. - Note: For patients with a history of histologically documented systemic DLBCL with CNS relapse, a biopsy of the CNS lesion is recommended but not required. - Must be a candidate for SRS. Lesion size must be < 6 cm and the number of lesions must be < 10. - Must have evaluable disease. This includes radiographic evidence of parenchymal disease or parenchymal disease and disease detected in the CSF. - Patients with vitreous or retinal involvement alone are not eligible. - Patients with leptomeningeal disease or spinal cord disease are not eligible. - Adequate organ function as defined as: - Hematologic: - Absolute neutrophil count ≥ 1000 cells/mm3 (1.00 x 109/L) independent of G-CSF support (i.e. no G-CSF within the past 3 days) unless there is documented bone marrow involvement. - Platelet count ≥ 75,000 cells/mm3 (75 x 109/L) independent of transfusion support (i.e. no transfusion within the past 3 days) unless there is documented bone marrow involvement. - Hemoglobin ≥ 8 g/dL (≥ 80 g/L) independent of transfusion support (i.e. no transfusion within the past 3 days) unless there is documented bone marrow involvement. - Hepatic: ---Total bilirubin ≤ 2.0 mg/dL (unless bilirubin rise is due to Gilbert's syndrome), if total bilirubin is > 2.0 mg/dL, the subject is eligible for the study if the direct bilirubin is normal; transaminases (AST/ALT) ≤2.5 x upper limit of normal (ULN) AST(SGOT)/ALT(SGPT) ≤ 3 × institutional ULN - Renal: - Estimated creatinine clearance ≥ 30 mL/min by Cockcroft-Gault formula: - Males: ((140-age)×weight[kg])/(serum creatinine [mg/dL]×72) - Females: (((140-age)×weight[kg])/(serum creatinine [mg/dL]×72))×0.85 - For subjects of childbearing potential: Negative pregnancy test or evidence of permanent surgical sterilization. The post-menopausal status will be defined as having been amenorrheic for 12 months without an alternative medical cause. The following age-specific requirements apply: - < 50 years of age: - Amenorrheic for ≥ 12 months following cessation of exogenous hormonal treatments; and - Luteinizing hormone and follicle-stimulating hormone levels in the post-menopausal range for the institution - ≥ 50 years of age: - Amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments; or - Had radiation-induced menopause with last menses >1 year ago; or - Had chemotherapy-induced menopause with last menses >1 year ago - Female participants of childbearing potential must agree to use a highly effective method of contraception as described in Section 5.4.1 until 10 months after last dose of loncastuximab tesirine and 12 months after the last dose of rituximab. Male participants with female partners of childbearing potential must agree to use a highly effective method of contraception when sexually active until 7 months after the last dose of loncastuximab tesirine. - Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines. Exclusion Criteria: - Concurrent use of other approved or investigational antineoplastic agents (with the exception of corticosteroids). - History of intracranial hemorrhage or clinically significant stroke within 6 months prior to enrollment - History of prior radiation to the CNS. - Significant medical diseases or conditions, as assessed by the investigator, that would substantially increase the risk-to-benefit ratio of participating in the study. This includes, but is not limited to, acute myocardial infarction in the past 6 months, unstable angina, uncontrolled diabetes mellitus, significant active infections, severely immunocompromised state, and congestive heart failure, New York Heart Association Class III-IV. - Known bleeding diathesis (e.g., von Willebrand's disease), hemophilia, or active bleeding. - Known Human immunodeficiency virus (HIV) infection. - Prior allogeneic stem cell transplant (autologous stem cell transplant is NOT an exclusion). - Prior exposure to loncastuximab tesirine - Chemotherapy or targeted small molecule therapy (or other therapy for CNS lymphoma) within 3 weeks prior to the first day of study treatment (or 5 half-lives (whichever is shorter), or 2 weeks prior to the first day of study treatment for monoclonal antibodies. - The patient must have recovered to baseline or ≤ grade 1 from prior toxicities of therapy with the exception of alopecia and myelosuppression provided lab criteria met. Recovery to ≤ grade 2 neuropathy is permitted. - Cellular therapy within 8 weeks. - Presence of clinically significant pericardial or pleural effusions, or third space fluid accumulations (i.e., ascites requiring drainage or pleural effusion that is either requiring drainage or associated with shortness of breath). - Congenital long QT syndrome or a corrected QT measure (QTc) interval of >480 ms at screening (unless secondary to pacemaker or bundle branch block). - Known history of hypersensitivity to CD19 antibody, components of study medication. - All subjects must be screened for hepatitis B and C. Patients with evidence of active hepatitis B infection, based on positive surface antigen or Hepatitis B DNA PCR are excluded. Patients who are Hepatitis B core antibody positive must take prophylaxis with entecavir or equivalent and be willing to undergo monthly Hepatitis B DNA PCR testing. Subjects with active Hep C patients may be enrolled if other parameters precluding hepatic impairment are met and they are not undergoing active therapy for hepatitis C. - Active systemic bacterial, viral, fungal, or other infection requiring systemic treatment at time of screening. - Subjects with chronic liver disease with hepatic impairment Child-Pugh class C - Pregnant or lactating or intending to become pregnant during the study. - Patients diagnosed with another malignancy within three years or with any evidence of residual prior malignant disease (except nonmelanoma skin cancer, non-metastatic prostate cancer, in situ cervical cancer, or ductal or lobular carcinoma in situ). Patients meeting this exclusion criteria may be enrolled after approval from study PI. - Unable to tolerate corticosteroids - Medical, psychiatric, cognitive, or other conditions that may compromise the participant's ability to understand the participant information, give informed consent, comply with the study protocol or complete the study.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Huntsman Cancer Institute at University of Utah

Address:
City: Salt Lake City
Zip: 84112
Country: United States

Contact:
Last name: Catherine Cromar

Phone: 801-213-5652
Email: catherine.cromar@hci.utah.edu

Start date: November 2024

Completion date: November 2030

Lead sponsor:
Agency: University of Utah
Agency class: Other

Collaborator:
Agency: ADC Therapeutics S.A.
Agency class: Industry

Source: University of Utah

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06607549