The Profile of Immunophenotype and Genotype Aberrations in Subsets of Pediatric T-Cell Acute Lymphoblastic Leukemia

Elda Pereira Noronha; Luísa Vieira Codeço Marques; Francianne Gomes Andrade; Luiz Claudio Santos Thuler; Eugênia Terra-Granado; Maria S Pombo-de-Oliveira; Brazilian Collaborative Study Group of Acute Leukemia

doi:10.3389/fonc.2019.00316

The Profile of Immunophenotype and Genotype Aberrations in Subsets of Pediatric T-Cell Acute Lymphoblastic Leukemia

Front Oncol. 2019 Apr 30:9:316. doi: 10.3389/fonc.2019.00316. eCollection 2019.

Authors

Elda Pereira Noronha¹, Luísa Vieira Codeço Marques¹, Francianne Gomes Andrade¹, Luiz Claudio Santos Thuler², Eugênia Terra-Granado¹, Maria S Pombo-de-Oliveira¹; Brazilian Collaborative Study Group of Acute Leukemia

Collaborators

Affiliations

¹ Pediatric Hematology-Oncology Program, Research Center, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
² Clinical Research Division, Research Center, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Abstract

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^mut (17%). ETP-ALL had frequent FLT3^mut (22.2%) and SUZ12^del (16.7%) (p < 0.001), while CDKN2A/B^del were rarely found in this subtype (p < 0.001). The early cortical T-ALL subtype had high frequencies of NOTCH1^mut and IL7R^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/NF1^del/IL7R^mut, were characterized with statistical significance (p < 0.05) but only STIL-TAL1 (pOS 47.5%) and NOTCH1^WT/FBXW7^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.

Keywords: T-cell acute lymphoblastic leukemia; childhood; early T-cell precursor acute lymphoblastic leukemia; immunophenotypic subtypes; molecular alterations; overall survival.