drugset / Trial / NCT04541277

Combined Inhibition of PD-1 and DNA Hypomethylating Agent +/- Chemotherapy in High-risk AML or Elderly Patients With AML Who Are Unfit for Intensive Chemotherapy

NCT04541277

Phase 2 Unknown 55 enrolled Chinese PLA General Hospital
NaSingle-groupOpen-labelTreatment

Summary

This phase II trial studies how well tislelizumab combined with DNA hypomethylation agent +/- CAG regimen (cytarabine, idarubicin / Aclarithromycin, rhG-CSF/ PEG-rhG-CSF) work in treating patients with high-risk acute myeloid leukemia (AML) or AML patients older than 60 years of age who are unfit for standard-dose chemotherapy. The expressions of PD-1 and PD-L1 are increased in AML cells. However, blocking the immune checkpoint alone has limited efficacy as a single agent in highly proliferative leukemia cells. During the recovery period after cytotoxic chemotherapy, the activation of PD-1/PD-L1 pathway may be increased and DNA hypomethylation agents can also up-regulate PD-1, PD-L1 and PD-L2 in AML patients. The up-regulation and activation of above immune checkpoint molecules are related to chemotherapy resistance. Therefore, adding chemotherapy and epigenetic regulation agents to Immune checkpoint blockade therapy may work better through overcoming drug resistance in AML treatment.

Timeline

Start
2020-09-01
Primary completion
2021-08-30
Completion
2022-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Aclamycin Unknown 20 mg Intravenous
Subject Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Subject Cytarabine Small molecule 10 mg Intravenous
Subject Cytarabine Small molecule 100 mg Intravenous
Subject Decitabine Small molecule 20 mg/m2 Intravenous
Subject Idarubicin Small molecule 10 mg Intravenous
Subject Tislelizumab Monoclonal antibody 200 mg
Background Pegylated Recombinant Human Granulocyte Stimulating Factor Protein / enzyme biologic 100 ug/kg Subcutaneous
Background filgrastim Protein / enzyme biologic 5 ug/kg Subcutaneous