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Study of the TBFC/V regimen (thiotepa combined with busulfan, fludarabine and cyclophosphamide (TBFC) or thiotepa combined with busulfan, fludarabine and venetoclax (TBFV) in a pretreatment regimen for allogeneic haematopoietic stem cell transplantation

Study of the TBFC/V regimen (thiotepa combined with busulfan, fludarabine and cyclophosphamide (TBFC) or thiotepa combined with busulfan, fludarabine and venetoclaxe (TBFV) in a pretreatment regimen for allogeneic haematopoietic stem cell transplantation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074726
Enrollment
Unknown
Registered
2023-08-14
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Malignant hematology disease

Interventions

Group myeloid malignant disease ( Thiotepa combined with busulfan, fludarabine and venetoclaxe (TBFV) ):NA
Group Lymphoid malignant disease (Thiotepa combined with busulfan, fludarabine and cyclophosphamide (TBFC) ):NA

Sponsors

The First Affiliated Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. age 14-70 years (including 14 & 70 years); 2. an ECOG score of <3; 3. Liver function ALT or AST less than 2 times the upper limit of normal, renal function Cr less than 2 times the upper limit of normal and can tolerate high-dose chemotherapy; 4. Agreed to participate in the study protocol.

Exclusion criteria

Exclusion criteria: 1. Under 14 years of age or above 70 years of age; 2. Liver glutamic aminotransferase (ALT) or glutamic oxalacetic aminotransferase (AST) more than 2 times the upper limit of normal; 3. Cr value more than 2 times the upper limit of normal or intolerance of high-dose chemotherapy 4. During pregnant or breastfeeding period; 5. who are unable to cooperate with treatment in the transplantation compartment.

Design outcomes

Secondary

MeasureTime frame
graft-versus-host disease;CMV effective rate;

Primary

MeasureTime frame
2 year OS;2 year DFS;relapse rate;

Countries

China

Contacts

Public ContactPing Zhang

The First Affiliated Hospital of Ningbo University

lingdujianke@163.com+86 19811995

Outcome results

None listed

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