Skip to content

Venetoclax combined with HAG regimen in the treatment of adult refractory/relapsed ETP-ALL

A prospective, multi-center clinical study on the efficacy of Venetoclax combined with HAG (low-dose homoharringtonine and cytarabine, G-CSF) regimen in the treatment of adults with refractory/relapsed early T-cell acute lymphoblastic leukemia (ETP-ALL)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048966
Enrollment
Unknown
Registered
2021-07-19
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early precursor T-cell acute lymphoblastic leukemia

Interventions

Case series:Venetoclax+HAG solution

Sponsors

The First Affiliated Hospital, Zhejiang University College of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged > 18 years; 2. The cell morphology and immunophenotype at the initial diagnosis are consistent with the diagnosis of ETP-ALL; 3. Refractory ETP-ALL (initially diagnosed ETP-ALL, failed to achieve remission after 2 standard treatment regimens) or relapsed ETP-ALL (after remission, the bone marrow blast cells were again greater than 20%, and the leukemia cell morphology and immunophenotype were consistent with ETP- ALL); 4. The ECOG score during screening is 0-2 points; 5. Expected survival period >= 2 months; 6. During the screening period, there is no abnormal organ function that restricts the use of the program; 7. Understand the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Refractory/relapsed ETP-ALL patients who cannot be treated with Venetoclax due to economic constraints; 2. History of other malignant tumors in the past 5 years; 3. Serum total bilirubin > 1.5 ULN (upper limit of normal); ALT or AST or ALP > 5 ULN; serum creatinine > 1.5 ULN; 4. Known HIV infection, or chronic infection with hepatitis B virus (HbsAg positive) or hepatitis C virus (anti-HCV positive); 5. The general condition is not suitable for chemotherapy; 6. Failure to comply with the research protocol.

Design outcomes

Primary

MeasureTime frame
Complete remission rate;Partial remission rate;

Secondary

MeasureTime frame
Mutational analysis;Gene fusion analysis;Karyotype analysis;

Countries

China

Contacts

Public ContactJin Jie

The First Affiliated Hospital, Zhejiang University College of Medicine

jiej0503@163.com+86 13505716779

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026