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Updated: Jun 25, 2025

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
[Prognostic analysis of childhood T-lymphoblastic lymphoma treated with leukemia regimen]
Shu-Min Hou1, Jing-Bo Shao1, Hong Li1
1Department of Hematology/Oncology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200040, China.
Insights
Childhood T-lymphoblastic lymphoma (T-LBL) shows good prognosis with acute lymphoblastic leukemia (ALL) regimens, achieving 84% overall survival. However, B systemic symptoms, high platelet counts, and mediastinal/lymph node involvement indicate a poorer outcome for T-LBL patients.
Area of Science:
- Pediatric Oncology
- Hematology
- Lymphoma Research
Background:
- Childhood T-lymphoblastic lymphoma (T-LBL) is an aggressive subtype of non-Hodgkin lymphoma.
- Treatment often involves regimens designed for acute lymphoblastic leukemia (ALL).
- Understanding prognostic factors is crucial for optimizing T-LBL management.
Purpose of the Study:
- To evaluate the prognosis of childhood T-lymphoblastic lymphoma (T-LBL) treated with acute lymphoblastic leukemia (ALL) chemotherapy regimens.
- To identify factors influencing survival outcomes in pediatric T-LBL patients.
Main Methods:
- Retrospective analysis of 29 pediatric T-LBL patients treated with ALL-2009 or CCCG-ALL-2015 regimens between May 2010 and May 2022.
- Evaluation of prognostic characteristics, including clinical symptoms, laboratory findings, and treatment regimens.
Main Results:
- The 5-year overall survival (OS) and event-free survival (EFS) rates were 84%±7% and 81%±8%, respectively.
- Factors associated with poorer prognosis included B systemic symptoms, platelet count >400×10^9/L, and involvement of both mediastinum and lymph nodes.
- The CCCG-ALL-2015 regimen reduced high-dose methotrexate frequency and severe infections compared to the ALL-2009 regimen without affecting survival rates.
Conclusions:
- Acute lymphoblastic leukemia (ALL) regimens are effective and safe for treating childhood T-lymphoblastic lymphoma (T-LBL).
- Identifying patients with B systemic symptoms, elevated platelet counts, or mediastinal and lymph node involvement is key for predicting poor prognosis.
- Modifying chemotherapy protocols, such as reducing high-dose methotrexate, can decrease infection rates without compromising patient outcomes.
Objectives:
To investigate the prognosis of childhood T-lymphoblastic lymphoma (T-LBL) treated with acute lymphoblastic leukemia (ALL) regimen and related influencing factors.
Methods:
A retrospective analysis was performed for the prognostic characteristics of 29 children with T-LBL who were treated with ALL regimen (ALL-2009 or CCCG-ALL-2015 regimen) from May 2010 to May 2022.
Results:
The 29 children with T-LBL had a 5-year overall survival (OS) rate of 84%±7% and an event-free survival (EFS) rate of 81%±8%. The children with B systemic symptoms (unexplained fever >38°C for more than 3 days; night sweats; weight loss >10% within 6 months) at initial diagnosis had a lower 5-year EFS rate compared to the children without B symptoms (P<0.05). The children with platelet count >400×109/L and involvement of both mediastinum and lymph nodes at initial diagnosis had lower 5-year OS rates (P<0.05). There were no significant differences in 5-year OS and EFS rates between the children treated with CCCG-ALL-2015 regimen and those treated with ALL-2009 regimen (P>0.05). Compared with the ALL-2009 regimen, the CCCG-ALL-2015 regimen reduced the frequency of high-dose methotrexate chemotherapy and the incidence rate of severe infections (P<0.05).
Conclusions:
The ALL regimen is safe and effective in children with T-LBL. Children with B systemic symptoms, platelet count >400×109/L, and involvement of both mediastinum and lymph nodes at initial diagnosis tend to have a poor prognosis. Reduction in the frequency of high-dose methotrexate chemotherapy can reduce the incidence rate of severe infections, but it does not affect prognosis.
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