T-cell (T-lineage) acute lymphoblastic leukemia (T-ALL) is a distinct immunophenotypic subtype of ALL. T-ALL comprises approximately 25% of adult ALL cases, and its treatment follows a similar overall framework to that used for B-lineage ALL, with specific risk-stratified considerations.
This protocol applies to patients with confirmed T-cell (T-lineage) ALL. Certain high-risk features within T-ALL — including early T-cell precursor (ETP) ALL and unfavourable oncogenetics — significantly affect treatment planning and transplant decision-making. Measurable residual disease (MRD) response is a central factor in determining escalation of care.
For patients with T-ALL who demonstrate a poor MRD response, have ETP ALL, or carry unfavourable oncogenetic features, allogeneic transplantation is among the approaches considered in the structured protocol. For older patients with high-risk disease and an appropriate donor, a modified conditioning approach may be relevant.
DOI: 10.1182/blood.2023023568
T-ALL comprises 25% of adult ALL and treatment is similar to that for B-LIN ALL.
ETP ALL appears to have a poor prognosis with chemotherapy and unfavourable oncogenetics should also lead to consideration of SCT indication.
Older patients with high-risk T-ALL may benefit from a RIC if they have a well-matched donor.
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