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Pediatric-Inspired versus Adult Chemotherapy Regimens on Survival of Adult Philadelphia-Negative Acute Lymphoblastic Leukemia Underwent Allogeneic Hematopoietic Stem Cell Transplantation, A PASS-ALL Cohort Study

Pediatric-Inspired versus Adult Chemotherapy Regimens on Survival of Adult Philadelphia-negative Acute Lymphoblastic Leukemia received HSCT:A Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053227
Enrollment
Unknown
Registered
2021-11-16
Start date
2016-06-01
Completion date
Unknown
Last updated
2022-09-20

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

Conditions

Adult Philadelphia-negative Acute Lymphoblastic Leukemia

Interventions

pediatric-regimen group:Nil
adult-regimen group:Nil

Sponsors

Nanfang Hospital of Nanfang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 60 Years

Inclusion criteria

Inclusion criteria: The subjects must meet the following criteria to be eligible for study entry: 1.Aged 14-60 years; 2.Newly diagnosed Ph-negative B-ALL; 3.Eligible for allo-HSCT; 4.The functions of vital organs meet the following requirements: LVEF >= 50%; TBIL <= 1.5ULN; AST/ALT <= 2.5ULN; Serum creatinine <= 1.5ULN. 5.Researchers assess expected lifetime is more than 3 months; 6.Informed consent was obtained.

Exclusion criteria

Exclusion criteria: 1.Burkitt lymphoma/leukemia; 2.T-cell precursor acute lymphoblastic lymphoma/leukemia; 3.Acute undifferentiated leukemia; 4.Being pregnant; 5.Severe active infection; 6.History of gastrointestinal bleeding during the past 6 months; 7.History of artery/vein thrombosis during the past 6 months; 8.Other active malignancy.

Design outcomes

Primary

MeasureTime frame
leukemia free survival;

Secondary

MeasureTime frame
overall survival;

Countries

China

Contacts

Public ContactLiu Qifa

Nanfang Hospital affiliated to Southern Medical University

liuqifa628@163.com+86 13602791429

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026