A Trial to Assess Cobicistat Boosted Venetoclax in Combination With Azacitidine in Adult Patients With Newly Diagnosed AML

Prior treatment

• Patients previously treated for AML or MDS (any anti-leukemic therapy including investigational agents; excluding: 1) erythropoiesis stimulating agents (ESAs); 2) hydroxyurea ((previous treatment with hydroxyurea is allowed for the control of peripheral leukemic blasts in patients with leukocytosis).
• Diagnosis of any previous or concomitant malignancy is an exclusion criterion:
  • except when the patient successfully completed treatment (chemotherapy and/or surgery and/or radiotherapy) with curative intent for this malignancy at least 24 months prior to registration;
  • except for basal and squamous cell carcinoma of the skin or in situ carcinoma of the cervix.
• Concurrent severe and/or uncontrolled medical condition (e.g. uncontrolled diabetes, infection, hypertension, pulmonary disease etc.).
• History of stroke or intracranial haemorrhage within 6 months prior to registration.
• Current concomitant chemotherapy, radiation therapy, or immunotherapy; other than hydroxyurea.

Other illness

• Myelodysplastic syndrome (MDS).
• History of non-compliance to medical regimens or considered unreliable with respect to compliance.
• Senile dementia, mental impairment or any other psychiatric disorder that prohibits the patient from understanding and giving informed consent.
• Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.
• Unreplaceable use of strong inhibitors or inducers of CYP3A or CYP3A/p-GP substrates with a narrow therapeutic window (e.g. cobicistat or ritonavir for HIV treatment). Please check with Appendix I.
• Intolerability, contra-indication or allergy to one of the study drugs.

Lab values

• Cardiac dysfunction as defined by:
  • Myocardial infarction within the last 3 months of study entry, or
  • Reduced left ventricular function with an ejection fraction \< 40% as measured by MUGA scan or echocardiogram, or
  • Unstable angina or New York Heart Association (NYHA) grade IV congestive heart failure (see Appendix G), or
  • Unstable cardiac arrhythmias.

Other

• A patient who meets any of the following criteria cannot be included in this study:
• Acute promyelocytic leukemia.
• Blast crisis of chronic myeloid leukemia.
• Symptomatic central nervous system (CNS) leukemia (NO routinely lumbar puncture required to investigate CNS involvement).

• In order to be eligible to participate in this study, a patient must meet all of the following criteria:
• Patients with: a diagnosis of AML and related precursor neoplasms according to ICC-2022 classification (excluding acute promyelocytic leukaemia) (appendix A). Patients may have had previous treatment with erythropoiesis stimulating agents (ESA) for an antecedent phase of MDS. ESAs must be stopped at least two weeks before registration.
• Patients 18 years and older who are considered not fit for intensive chemotherapy or who decline the option of intensive chemotherapy.
• WHO performance status 0, 1 or 2 (appendix E).
• Leukocytes \< 30 x109/L
• Adequate renal and hepatic functions unless clearly disease related as indicated by the following laboratory values:
  • Adequate renal function as demonstrated by a creatinine clearance ≥ 30 mL/min; calculated by the Cockcroft Gault formula or measured by 24 hours urine collection.
  • Serum bilirubin ≤ 3 x upper limit of normal (ULN), unless considered AML-related or due to Gilbert's syndrome.
  • Alanine transaminase (ALT) ≤ 3 x ULN, unless considered AML-related.
• Male subjects who are sexually active, must agree, from Study Day 1 until at least 90 days after the last dose of study drug, to practice the protocol specified contraception. Male subjects must agree to refrain from sperm donation from initial study drug administration through at least 90 days after the last dose of study drug.
• Female subjects must be either postmenopausal defined as: Age \>55 years with no menses for ≥12 months, without an alternative medical cause. OR willing and able to use adequate contraception during and until 180 days after the last protocol treatment.
• Written informed consent.
• Patient is capable of giving informed consent.
• Patient agrees not to participate in another interventional study while on treatment without approval of the (co-) Principal Investigator.