Orelabrutinib,Rituximab and Methotrexate in Newly Diagnosed Primary Central Nervous System Lymphoma

Launched by SECOND AFFILIATED HOSPITAL, SCHOOL OF MEDICINE, ZHEJIANG UNIVERSITY · Oct 27, 2022

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment combination called OR-MTX, which includes Orelabrutinib, Rituximab, and Methotrexate, for patients with newly diagnosed primary central nervous system lymphoma, a type of cancer that affects the brain and spinal cord. The goal of the study is to see how effective and safe this treatment is compared to traditional therapies. The trial is currently recruiting participants aged 18 to 75 who have been diagnosed with this specific type of lymphoma and have not received any previous treatment (except for steroids).

To be eligible, participants need to have measurable cancer, good overall health, and the ability to understand and sign consent forms. They will undergo routine tests and evaluations, including MRIs, to monitor their progress. It's important to note that women who can become pregnant must use effective birth control during the study. Overall, participants can expect close monitoring and support from the research team throughout the trial.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Histologically confirmed Primary Central Nervous System (CNS) lymphoma Age range 18-75 years old.
• • 2. Eastern Cooperative Oncology Group performance status 0 to 3.
• • 3. Previously untreated. Patients treated with steroid alone are eligible.
• • 4. Measurable disease was defined as at least ≥1.0cm in short-diameter by MRI.
• • 5. Life expectancy of ≥ 3 months (in the opinion of the investigator).
• • 6. Participants must be able to understand and be willing to sign a written informed consent document.
• • 7. Women of reproductive potential must agree to use highly effective methods of birth control during the period of therapy and for 6 months 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 6 months after the last dose.
• • Women of childbearing potential must have a negative plasma pregnancy test upon study entry.
• • 8. Adequate renal function: Estimated glomerular filtration rate (GFR) or estimated creatinine clearance (CrCl) ≥ 50 mL/min;Serum creatinine ≤ 2 times the upper limit of normal.
• • 9. Adequate liver functions: Transaminase (AST/ALT) \< 3 X upper normal value \& Bilirubin \< 2 X upper normal value.
• • 10. Adequate hematological function: hemoglobin ≥ 9 g/dL absolute neutrophil count (ANC) ≥ 1,500/μL and platelet count ≥ 75,000/μL.
• • 11. Must be able to tolerate lumbar puncture and MRI/CT.
• • 12. Ability to swallow oral medications.
• Exclusion Criteria:
• • 1. Patient with systemic, non-CNS lymphoma metastatic to the CNS.
• • 2. Patient is concurrently using other approved or investigational antineoplastic agents.
• • 3. Presence of active hepatitis B virus(HBV) infection (HBsAg positive and HBV-DNA≥ 104), hepatitis C virus(HCV) infection, acquired and congenital immunodeficiency diseases include but not limited to HIV.
• • 4. Patient is allergic to components of the study drug.
• • 5. Patient has an active concurrent malignancy requiring active therapy.
• • 6. Patient has significant abnormalities on screening electrocardiogram (EKG) and active and significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, uncontrolled congestive heart failure, uncontrolled hypertension, valvular disease, pericarditis, or myocardial infarction within 6 months of screening.
• • 7. Patient is known to have an uncontrolled active systemic infection.
• • 8. 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.
• • 9. Women who are pregnant or nursing (lactating), where pregnancy is defined as a state of a female after conception until the termination of gestation, confirmed by a positive plasma human chorionic gonadotropin(hCG) laboratory test of \> 5 mIU/mL.
• • 10. The patient is unwell or unable to participate in all required study evaluations and procedures.
• • 11. Drug abuse, medical, psychological or social conditions which may interfering with subjects' participation in the study or evaluation of the results.
• • 12. History of intracranial hemorrhage or clinically significant stroke within 6 months prior to first day of study treatment
• • 13. History of significant gastrointestinal disease that would limit absorption of oral medications.
• • 14. Warfarin or any other Coumadin-derivative anticoagulant or vitamin K antagonists. Patients must be off warfarin-derivative anticoagulants for at least seven days prior to starting the study drug. Use of low molecular weight heparin and novel oral anticoagulants (eg. rivaroxaban, apixaban) is permitted if required.
• • 15. Concurrent use of a moderate or strong inhibitor or inducer of the P450 isoenzyme CYP3A. Participants must be off P450/CYP3A inhibitors and inducers prior to starting the study drug.
• • 16. Known bleeding diathesis (e.g. von Willebrand's disease), hemophilia, or active bleeding.
• • 17. History of invasive fungal infection, including invasive aspergillosis, or known active tuberculosis.
• • 18. Patients considered unsuitable to participate in the study by the researchers.