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Therapeutic Effect and Safety Study of IH-2014A regimen in Adult Lymphoblastic Leukemia/ Lymphoma Patients

Prognosis stratification and individual treatment regimen of leukemia and lymphoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15006328
Enrollment
Unknown
Registered
2015-01-27
Start date
2015-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Adult Lymphoblastic Leukemia/ Lymphoma

Interventions

Case series:Nil

Sponsors

Hospital of Blood Diseases, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. De novo and primary Ph/BCR-ABL1 negative adult lymphoblastic leukemia/ lymphoma patients diagnosed by the bone marrow cytomorphology, immunophenotyping, cytogenetics and molecular biology according to WHO classification; 2. Male or female, Age (years) >=15; 3. ECOG Performance status of 0,1, or 2; 4.Predicted survival time >=3 months; 5.Contraception should be agreed and performed for reproductive age men and women; 6.Patients must have the following laboratory values 1) Total bilirubin 45%; 7. Patient must sign the informed consent prior to study.

Exclusion criteria

Exclusion criteria: 1. Diagnosed as MPAL, Burkitt lymphoma/leukemia according to WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues(2008); 2. Other serious or life threatening diseases:Patients with another primary malignancy (requiring active intervention at the same starting study time);hepatitis, serious pancreatic or kidney disease; 3. Female who are pregnant, breast feeding or childbearing potential; 4. HIV positive patients; 5. Mental disorders which may interfere the patients to sign the informed consent or to complete the treatment; 6. The investigator believe that patient who are not suitable for involvement.

Design outcomes

Primary

MeasureTime frame
Overall survival(OS);

Secondary

MeasureTime frame
DFS;CR rate;EFS;IRM;TRM;

Contacts

Public ContactJianxiang Wang
wangjx@medmail.com.cn+86 22 23909120

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026