Affiliation:
1. A.V. Vishnevsky National Medical Research Center for Surgery
2. National Medical Research Center Treatment and Rehabilitation Center
Abstract
Aim. To study the effect of mutations in the KRAS gene on the clinical course of intrahepatic cholangiocellular cancer (ICC) after surgical treatment in the Russian population.Materials and methods. A molecular genetic study of tumour tissue samples from 33 patients with intrahepatic cholangiocellular cancer obtained after surgical treatment was carried out using real-time polymerase chain reaction.Results. In the Russian population, the frequency of mutations in the KRAS gene in ICC was 27%, mainly in 12 (78%), 13 (33%), 61 (55%), 117 (44%) and 146 (44%) codons of 2, 3, 4 exons. In terms of KRAS gene mutations, intrahepatic cholangiocellular cancer is characterised by a pronounced heterogeneity. As a rule, the KRAS gene demonstrates multiple mutations at several loci and co-mutations in other genes, in particular, in IDH1/IDH2, PIK3CA, NRAS and BRAF genes. KRAS gene mutations in ICC were found to be significantly more common in women. The overall survival rate was significantly higher in patients with a KRAS mutation as compared to those with the wild type of the gene. Regarding the relapse-free survival rate in the groups of patients with the mutant and wild type of the KRAS gene, no significant differences were found.Conclusion. In the Russian population, no negative association between mutations in the KRAS gene and clinical outcomes was observed.
Publisher
Kuban State Medical University
Reference19 articles.
1. Pellino A., Loupakis F., Cadamuro M., Dadduzio V., Fassan M., Guido M., et al. Precision medicine in cholangiocarcinoma. Transl. Gastroenterol. Hepatol. 2018; 3: 40. DOI: 10.21037/tgh.2018.07.02
2. Mavros M.N., Economopoulos K.P., Alexiou V.G., Pawlik T.M. Treatment and prognosis for patients with intrahepatic cholangiocarcinoma: systematic review and meta-analysis. JAMA Surg. 2014; 149(6): 565–574. DOI: 10.1001/jamasurg.2013.5137
3. Rizvi S., Khan S.A., Hallemeier C.L., Kelley R.K., Gores G.J. Cholangiocarcinoma — evolving concepts and therapeutic strategies. Nat. Rev. Clin. Oncol. 2018; 15(2): 95–111. DOI: 10.1038/nrclinonc.2017.157
4. Churi C.R., Shroff R., Wang Y., Rashid A., Kang H.C., Weatherly J., et al. Mutation profiling in cholangiocarcinoma: Prognostic and therapeutic implications. PLoS One. 2014; 9(12): e115383. DOI: 10.1371/journal.pone.0115383
5. Vodolazhskii D.I., Antonets A.V., Dvadnenko K.V., Vladimirova L.Yu., Gevorkyan Yu.A., Kasatkin V.F., Maksimov A.Yu. Association of KRAS mutant type with clinico-pathological features of colorectal cancer in patients in the South of Russia. Mezhdunarodnyi Zhurnal Eksperimental’nogo Obrazovaniya. 2014; (1–1): 65–68 (In Russ., English abstract).