Epcoritamab for the Treatment of Relapsed or Refractory Post Transplant Lymphoproliferative Disorders

Launched by TIMOTHY VOORHEES · Nov 1, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called epcoritamab for patients with a type of cancer known as post-transplant lymphoproliferative disorder (PTLD). This condition can occur when the immune system is weakened after an organ transplant, leading to abnormal growth of lymphocytes (a type of white blood cell). The trial is looking for people whose PTLD has either returned after treatment (relapsed) or did not respond to previous therapies (refractory). Epcoritamab works by helping the immune system target and attack the cancer cells.

To participate in this trial, patients must be at least 18 years old and have a confirmed diagnosis of B-cell PTLD. They should have already tried other treatments, such as reducing immunosuppression or using a drug called rituximab, without success. Participants will receive epcoritamab and will be monitored for its safety and effectiveness. It’s important for interested patients to discuss this trial with their doctor to see if they meet the specific eligibility criteria and to understand what participation would involve.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Written informed consent obtained to participate in the study and Health Insurance Portability and Accountability Act (HIPAA) authorization for release of personal health information to the sponsor, sites, and relevant study organizations.
• • Age ≥ 18 years at the time of consent.
• • Karnofsky scale ≥ 50% or Eastern Cooperative Oncology Group (ECOG) ≤ 2.
• • Histological evidence of B-cell PTLD (any histologic subtype) following solid organ transplantation; expresses CD20; with or without EBV association.
• • Treatment failure of immunosuppression reduction (ISR). NOTE: if ISR was deemed not feasible by treating physician, ISR treatment failure may be waived.
• • Treatment failure of rituximab or rituximab plus any concurrent or sequentially administered chemotherapy regimen.
• • Measurable disease of \> 1.5 cm in diameter and/or bone marrow involvement.
• • Subjects having undergone heart, lung, liver, kidney, pancreas, small intestine transplantation or a combination of the organ transplantations mentioned.
• • HIV infection is allowed if viral load is undetectable at time of enrollment, CD4+ count \> 200 cells/uL, and subject remains on anti-viral therapy.
• • Resolution of toxicities from prior therapy to a grade that does not contraindicate trial participation in the opinion of the investigator.
• • Expected survival greater than 60 days.
• • Absolute neutrophil count 1.0 ≥ x 10\^9/L.
• • Platelets 50 ≥ x 10\^9/L.
• • Creatinine clearance (mL/min) ≥ 30 mL/min - Cockcroft-Gault Equation.
• • Note: Hematology and other lab parameters that are ≤ grade 2 BUT still meet criteria for study entry are allowed. Furthermore, changes in laboratory parameters during the study should not be considered adverse events unless they meet criteria for dose modification(s) of study medication outlined by the protocol and/or worsen from baseline during therapy.
• • Bilirubin ≤ 3.0 x upper limit of normal (ULN). Subjects with Gilbert's syndrome may be enrolled despite a total bilirubin level \> 3.0 mg/dL if their conjugated bilirubin is ≤ 3.0 × ULN).
• • Note: Hematology and other lab parameters that are ≤ grade 2 BUT still meet criteria for study entry are allowed. Furthermore, changes in laboratory parameters during the study should not be considered adverse events unless they meet criteria for dose modification(s) of study medication outlined by the protocol and/or worsen from baseline during therapy.
• • Aspartate aminotransferase (AST) ≤ 3.0 x ULN.
• • Note: Hematology and other lab parameters that are ≤ grade 2 BUT still meet criteria for study entry are allowed. Furthermore, changes in laboratory parameters during the study should not be considered adverse events unless they meet criteria for dose modification(s) of study medication outlined by the protocol and/or worsen from baseline during therapy.
• • Alanine aminotransferase (ALT) ≤ 3.0 x ULN.
• • Note: Hematology and other lab parameters that are ≤ grade 2 BUT still meet criteria for study entry are allowed. Furthermore, changes in laboratory parameters during the study should not be considered adverse events unless they meet criteria for dose modification(s) of study medication outlined by the protocol and/or worsen from baseline during therapy.
• • Females of childbearing potential must have a negative serum pregnancy test within 3 days prior to registration. NOTE: Females are considered of childbearing potential unless they are surgically sterile (have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are naturally postmenopausal for at least 12 consecutive months. Documentation of postmenopausal status must be provided.
• • Females of childbearing potential must be willing to abstain from heterosexual activity or to use 2 forms of effective methods of contraception from the time of informed consent until 12 months after treatment the last dose of epcoritamab. The two contraception methods can be comprised of two barrier methods, or a barrier method plus a hormonal method or an intrauterine device.
• • Male subjects with female partners must have had a prior vasectomy or agree to use an adequate method of contraception (i.e., double barrier method: condom plus spermicidal agent) starting with the first dose of study therapy through 12 months after the last dose of epcoritamab.
• • Subjects with prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the experimental regimen are eligible for the trial.
• • Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee.
• Exclusion Criteria:
• • Uncontrolled active (symptomatic) infection. Patients requiring systemic therapy are eligible if the infection is deemed controlled by the investigator.
• • Post-transplant lymphoproliferative disorder following stem cell transplantation for hematologic malignancies or nonmalignant conditions.
• • Pregnant or breastfeeding (NOTE: breast milk cannot be stored for future use while the mother is being treated on study and lactating females must agree to not breastfeed while taking study drug).
• • Subjects with central nervous system (CNS) involvement by PTLD.
• • Seizure disorder requiring therapy (such as steroids or anti-epileptics).
• • Uncontrolled concomitant illness including, but not limited to, symptomatic congestive heart failure (New York Heart Association (NYHA) Class III or IV), unstable angina pectoris, myocardial infarction within 1 month prior to enrollment, uncontrolled cardiac arrhythmias, uncontrolled seizures, or severe non-compensated hypertension (systolic blood pressure \> 180mmHg or diastolic blood pressure \> 120mmHg).
• • History of progressive multifocal leukoencephalopathy.
• • Active Hepatitis B infection or Hepatitis C infection with positive viral polymerase chain reaction (PCR) from the blood. Subjects with active Hepatitis B infection and undetectable viral PCR from the blood will be allowed with concurrent use of entecavir suppression. Subjects with history of Hepatitis C infection (undetectable viral PCR) are allowed.
• • Electrocardiogram (ECG) abnormality at screening has to be documented by the investigator as not medically relevant.
• • Any condition, including the presence of laboratory values which is deemed by the clinician to place the subject at an unacceptable risk or confounds the ability to interpret the data from this study.
• • Live virus vaccines must not be administered within 28 days of the start of study treatment.
• • Any investigational treatments must have been completed at least 4 weeks or 5 half-lives, whichever is shorter, prior to the start of study treatment. Investigational antibody therapies are not included in this requirement.