Study of Venetoclax Combined With Azacitidine Regimen in Newly Diagnosed T-ALL Patients

Prior treatment

• Surgery on the main organs within the past six weeks.
• Drug abuse or long-term alcohol abuse that would affect the evaluation results.
• Patients who have received chemotherapy treatments related to the disease.

Other illness

• Patients who are allergic to the study drug or drugs with similar chemical structures.
• Patients with uncontrolled active infection
• Patients with active bleeding.
• Patients with new thrombosis, embolism, cerebral hemorrhage, or other diseases or a medical history within one year before enrollment.
• Patients with mental disorders or other conditions whereby informed consent cannot be obtained and where the requirements of the study treatment and procedures cannot be met.

Lab values

• Liver dysfunction (total bilirubin \> 1.5 times the upper limit of the normal range, ALT/AST \> 2.5 times the upper limit of the normal range or patients with liver involvement whose ALT/AST \> 1.5 times the upper limit of the normal range), or renal anomalies (serum creatinine \> 1.5 times the upper limit of the normal value).
• Patients with a history of clinically significant QTc interval prolongation (male \> 450 ms; female \> 470 ms), ventricular heart tachycardia and atrial fibrillation, II-degree heart block, myocardial infarction attack within one year before enrollment, and congestive heart failure, and patients with coronary heart disease who have clinical symptoms and requiring drug treatment.

Age

• Pregnant or lactating women, and women of childbearing age who do not want to practice effective methods of contraception.

• Patients aged ≥ 15.
• Patients diagnosed with T-ALL according to 2016 WHO criteria for precursor lymphoid neoplasms.
• ECOG performance status score less than 3.
• Patients without serious heart, lung, liver, or kidney dysfunction.
• Ability to understand and voluntarily provide informed consent.