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Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Outcome for children and young people with Early T-cell precursor acute lymphoblastic leukaemia treated on a
Katharine Patrick1, Rachel Wade, Nick Goulden
1Sheffield Children's Hospital, Sheffield, UK.
Insights
Early T-precursor acute lymphoblastic leukaemia (ETP-ALL) shows intermediate outcomes in children and young people. This finding suggests ETP-ALL does not universally require experimental treatments or early allogeneic transplants.
Area of Science:
- Paediatric Oncology
- Hematology
- Leukemia Research
Background:
- Early T-precursor acute lymphoblastic leukaemia (ETP-ALL) is a distinct subtype of T-cell acute lymphoblastic leukaemia (T-ALL).
- ETP-ALL has been associated with a poorer prognosis in previous studies.
- Understanding the outcomes for ETP-ALL patients treated on contemporary protocols is crucial for refining treatment strategies.
Purpose of the Study:
- To evaluate the clinical outcomes of children and young people diagnosed with ETP-ALL.
- To compare the outcomes of ETP-ALL patients with those of typical T-ALL patients.
- To determine if ETP-ALL warrants universal experimental treatment or allogeneic stem cell transplantation in first remission.
Main Methods:
- Retrospective analysis of patients treated on the UKALL 2003 protocol.
- Comparison of event-free survival (EFS) and overall survival (OS) between ETP-ALL and typical T-ALL subgroups.
- Analysis of relapse rates in ETP-ALL patients.
Main Results:
- The ETP-ALL subgroup represented 16% of T-ALL patients in the study cohort.
- After a median follow-up of 4 years and 10 months, ETP-ALL patients showed non-significantly inferior 5-year EFS (76.7% vs. 84.6%, P=0.2) and OS (82.4% vs. 90.9%, P=0.1).
- ETP-ALL patients had a higher relapse rate (18.6% vs. 9.6%, P=0.1) compared to typical T-ALL.
Conclusions:
- ETP-ALL exhibits an intermediate risk outcome, rather than a universally poor prognosis.
- The current data do not support the universal application of experimental treatments for all ETP-ALL patients.
- Universal allogeneic transplantation in first remission is not indicated for the ETP-ALL group based on these findings.
Abstract:
We investigated the outcome for children and young people with Early T-precursor acute lymphoblastic leukaemia (ETP-ALL), a recently described poor prognosis sub-group of T-ALL, treated on a contemporary protocol, UKALL 2003. After a median follow-up of 4 years and 10 months, the ETP sub-group, representing 16% of T-ALL patients, had non-significantly inferior 5-year event-free survival (76·7% vs. 84·6%, P = 0·2) and overall survival (82·4% vs. 90·9%, P = 0·1), and a higher relapse rate (18·6% vs. 9·6%, P = 0·1) compared to typical T-ALL. ETP-ALL has an intermediate risk outcome, which does not warrant experimental treatment or first remission allogeneic transplant for the group universally.
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