Please use this identifier to cite or link to this item:
10.3892/ol.2022.13613
Title: | Effects of BRAF V600E and NRAS mutational status on the progression-free survival and clinicopathological characteristics of patients with melanoma |
Authors: | Zablocka, Tatjana Kreismane, Madara Pjanova, Dace Isajevs, Sergejs |
Keywords: | BRAF V600;histopathology;melanoma;NRAS;progression-free survival;1.6 Biological sciences;3.1 Basic medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database;Oncology;Cancer Research;SDG 3 - Good Health and Well-being |
Issue Date: | Jan-2023 |
Citation: | Zablocka , T , Kreismane , M , Pjanova , D & Isajevs , S 2023 , ' Effects of BRAF V600E and NRAS mutational status on the progression-free survival and clinicopathological characteristics of patients with melanoma ' , Oncology Letters , vol. 25 , no. 1 , 27 , pp. 27 . https://doi.org/10.3892/ol.2022.13613 |
Abstract: | Hotspot mutations of the BRAF and NRAS genes are the most common genetic alterations in invasive cutaneous melanoma; however, the prognostic significance of BRAF and NRAS co-mutations remains controversial. The present study aimed to determine the association between NRAS and BRAF mutation status and the clinicopathological characteristics of patients with stage IA-IIC melanoma. A total of 118 patients who underwent surgical treatment for stage IA-IIC melanoma at the Riga East University Hospital between 2012 and 2018 were retrospectively enrolled in the present study. BRAF and NRAS mutation status was assessed by digital droplet PCR using the BRAFV600, NRAS Q61 and NRAS G12/G13 Screening Assays. The association between mutation status and clinicopathological features and progression-free survival (PFS) was then analyzed. The BRAF V600 mutation was detected in 67 out of 118 patients (56.8%). The PFS did not differ between patients with BRAF wild-type and BRAF-mutant melanoma. NRAS mutations were detected in 35 out of 118 patients (29.6%). The NRAS mutational status was associated with Breslow thickness (P=0.035), tumor type (P=0.020; χ2=0.20), mitotic rate (P=0.025) and lymphovascular invasion (P=0.02; χ2=0.20). Patients with NRAS-mutant melanoma had significantly worse PFS compared with NRAS wild-type melanoma (HR=12.30; 95% CI=5.78-26.21, P<0.0001). Furthermore, BRAF and NRAS co-mutant melanoma was associated with a significantly worse PFS compared with BRAF-mutant melanoma (HR=6.30; 95% CI=3.10-12.70, P<0.0001). In conclusion, NRAS-mutant and NRAS/BRAF co-mutant stage IA-IIC melanoma was associated with worse PFS compared with NRAS wild-type and BRAF-mutant melanoma. The assessment of NRAS mutation status in melanoma in routine clinical practice may be beneficial for the risk stratification of disease progression for primary non-metastatic malignant melanoma. |
Description: | Funding Information: The study was supported by the project ‘Strengthening of the capacity of doctoral studies at the University of Latvia within the framework of the new doctoral model’ (grant no. 8.2.2.0/20/I/006). Publisher Copyright: © 2023 Spandidos Publications. All rights reserved. |
DOI: | 10.3892/ol.2022.13613 |
ISSN: | 1792-1074 |
Appears in Collections: | Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure |
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