Abstract

Materials and methods. The study included 18 samples of patients with ACC stages I–III who received treatment from 2003 to 2021. Samples from 6 (33 %) patients with stage I, 5 (28 %) patients with stage II, and 7 (39 %) patients with stage III ACC were analyzed. The average age of patients is 61.6 (12–216) months. Four subgroups of patients were identified: with an isolated mutation in the TP-53 gene, with an isolated mutation in the IGF-2 gene, with simultaneous mutations in the TP-53 and IGF-2 genes and no mutations in the studied genes.Results. In 12 out of 18 (67 %) of the studied samples, mutations in the TP-53 and IGF-2 genes and their combination were detected. A mutation in the TP-53 gene was present in 8 patients, in the IGF-2 gene in 8 patients, and a combination of TP-53 + IGF-2 in 4 patients. The five-year OS and DFS in the groups of patients with mutations in TP-53 and/or IGF-2 were 45.5 % and 41.6 % versus 83.3 % and 83.3 % in the group without mutations (p = 0.15 and p = 0.18, respectively). The five-year overall (OS) and disease-free (DFS) survival in the TP-53 group compared with the group without the mutation was 50 % and 50 % versus 62.2 % and 66.7 % (p = 0.6 and p = 0.5, respectively). The five-year OS and DFS in the IGF-2 group compared with the group without mutation was 14.3 % and 0 % versus 90 % and 90 % (p = 0.001 and p = 0.0009, respectively). The five-year OS and DFS in the group in which the combination of mutations in the TP-53 + IGF-2 genes was present compared with patients without the combination of these mutations was 0 % vs. 75.2 % and 76.9 % (p = 0.002 and p = 0.003, respectively).Conclusion. The presence of a mutated IGF-2 gene is combined with a high Ki-67 index and is a factor in poor prognosis in children with localized forms of ACC. The simultaneous presence of mutations in the TP-53 and IGF-2 genes in the tumor also significantly negatively affects survival rates. Further prospective studies are needed to confirm the data and develop tactics for this group of patients.

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