The Profile of Immunophenotype and Genotype Aberrations in Subsets of Pediatric T-Cell Acute Lymphoblastic Leukemia (vol 9, 316, 2019)

T-cell acute lymphoblastic leukemia (T-ALL) is a biologically heterogeneous malignancy, which reflects distinctive stages of T-cell differentiation arrest. We have revisited a cohort of pediatric T-ALL, in order to test if immunophenotypes associated with molecular alterations would predict the patient's outcome. Genetic mutations, translocations and copy number alterations were identified through Sanger sequencing, RT-PCR, FISH and multiplex ligation-dependent probe amplification (MLPA). We defined 8 immunophenotypic T-ALL subtypes through multiparametric flow cytometry: early T-cell precursor (ETP, n = 27), immature (n = 38), early cortical (n = 15), cortical (n = 50), late cortical (n = 53), CD4/CD8 double negative mature (n = 31), double positive mature (n = 35) and simple positive mature (n = 31) T-ALL. Deletions (del) or amplifications (amp) in at least one gene were observed in 87% of cases. The most frequent gene alterations were CDKN2A/B-del (71.4%), NOTCH1(mut) (47.6%) and FBXW7(mu)(t )(17%). ETP-ALL had frequent FLT3(mut) (22.2%) and SUZ12(de)(l) (16.7%) (p < 0.001), while CDKN2A/B(del )were rarely found in this subtype (f) < 0.001). The early cortical T-ALL subtype had high frequencies of NOTCH1(mut) and /L7R(mut) (71%, 28.6%, respectively), whereas, mature T-ALL with double positive CD4/CD8 had the highest frequencies of STIL-TAL1 (36.7%), LEF1(del)(27.3%) and CASP8AP2(del) (22.7%). The co-existence of two groups of T-ALL with NOTCH1(mut)/IL7R(mut), and with TLX3/SUZ12(del)/NFl(del)/IL7R(mut), were characterized with statistical significance (p < 0.05) but only STIL-TAL1 (pOS 47.5%) and NOTCH1(WT)/FBXVV7(WT) (pOS 55.3%) are predictors of poor T-ALL outcomes. In conclusion, we have observed that 8 T-ALL subgroups are characterized by distinct molecular profiles. The mutations in NOTCH1/FBXW7 and STIL-TAL1 rearrangement had a prognostic impact, independent of immunophenotype.