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Efficacy and safety of a modified dual-epitope multi-target regimen for the treatment of first diagnosis of high-risk acute T-lymphoblastic leukemia

Efficacy and safety of a modified dual-epitope multi-target regimen for the treatment of first diagnosis of high-risk acute T-lymphoblastic leukemia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083581
Enrollment
Unknown
Registered
2024-04-29
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

T-ALL

Interventions

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 90 Years

Inclusion criteria

Inclusion criteria: (i) Age =14 years; (ii) Diagnosis meets the criteria for T-ALL in the Blood Diagnostic and Therapeutic Criteria (Fourth Edition); (iii) All were treated with a modified dual-epi multi-targeting regimen, with the following specific dosages: cedarbenazine 30mg biw; azacitidine 75mg/m2 d1-d7; ;Venetoclax 100mg d1, 200mg d2, 300mg d3, 400mg qd d4-d14; dexamethasone 10mg d1-d7/d1-d10. The specific application dose is appropriately increased or decreased according to the patient's physical condition.

Exclusion criteria

Exclusion criteria: (i) women who are preparing for pregnancy, pregnant or breastfeeding; (ii) patients with serious underlying diseases of important organs, progressive tumors and other diseases that affect the prognosis of the treatment; (iii) poor adherence, inability to cooperate with the treatment, and any conditions that, after evaluation by the investigator, may increase the risk to the subject or interfere with the results of the trial.

Design outcomes

Primary

MeasureTime frame
Complete remission rate, CR;

Secondary

MeasureTime frame
Progression free survival, PFS;Overall survival, OS;

Countries

China

Contacts

Public ContactLi Hui

Sichuan Provincial People's Hospital

lihui606606@163.com+86 189 8183 8256

Outcome results

None listed

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