The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing.

Journal Article (Journal Article)

PURPOSE: An assay for the single-nucleotide polymorphism (SNP), rs61764370, has recently been commercially marketed as a clinical test to aid ovarian cancer risk evaluation in women with family histories of the disease. rs67164370 is in a 3'-UTR miRNA binding site of the KRAS oncogene and is a candidate for epithelial ovarian cancer (EOC) susceptibility. However, only one published article, analyzing fewer than 1,000 subjects in total, has examined this association. EXPERIMENTAL DESIGN: Risk association was evaluated in 8,669 cases of invasive EOC and 10,012 controls from 19 studies participating in the Ovarian Cancer Association Consortium, and in 683 cases and 2,044 controls carrying BRCA1 mutations from studies in the Consortium of Investigators of Modifiers of BRCA1/2. Prognosis association was also examined in a subset of five studies with progression-free survival (PFS) data and 18 studies with all-cause mortality data. RESULTS: No evidence of association was observed between genotype and risk of unselected EOC (OR = 1.02, 95% CI: 0.95-1.10), serous EOC (OR = 1.08, 95% CI: 0.98-1.18), familial EOC (OR = 1.09, 95% CI: 0.78-1.54), or among women carrying deleterious mutations in BRCA1 (OR = 1.09, 95% CI: 0.88-1.36). There was little evidence for association with survival time among unselected cases (HR = 1.10, 95% CI: 0.99-1.22), among serous cases (HR = 1.12, 95% CI = 0.99-1.28), or with PFS in 540 cases treated with carboplatin and paclitaxel (HR = 1.18, 95% CI: 0.93-1.52). CONCLUSIONS: These data exclude the possibility of an association between rs61764370 and a clinically significant risk of ovarian cancer or of familial ovarian cancer. Use of this SNP for ovarian cancer clinical risk prediction, therefore, seems unwarranted.

Full Text

Duke Authors

Cited Authors

  • Pharoah, PDP; Palmieri, RT; Ramus, SJ; Gayther, SA; Andrulis, IL; Anton-Culver, H; Antonenkova, N; Antoniou, AC; Goldgar, D; BCFR Investigators, ; Beattie, MS; Beckmann, MW; Birrer, MJ; Bogdanova, N; Bolton, KL; Brewster, W; Brooks-Wilson, A; Brown, R; Butzow, R; Caldes, T; Caligo, MA; Campbell, I; Chang-Claude, J; Chen, YA; Cook, LS; Couch, FJ; Cramer, DW; Cunningham, JM; Despierre, E; Doherty, JA; Dörk, T; Dürst, M; Eccles, DM; Ekici, AB; Easton, D; EMBRACE Investigators, ; Fasching, PA; de Fazio, A; Fenstermacher, DA; Flanagan, JM; Fridley, BL; Friedman, E; Gao, B; Sinilnikova, O; GEMO Study Collaborators, ; Gentry-Maharaj, A; Godwin, AK; Goode, EL; Goodman, MT; Gross, J; Hansen, TVO; Harnett, P; Rookus, M; HEBON Investigators, ; Heikkinen, T; Hein, R; Høgdall, C; Høgdall, E; Iversen, ES; Jakubowska, A; Johnatty, SE; Karlan, BY; Kauff, ND; Kaye, SB; Chenevix-Trench, G; kConFab Investigators and the Consortium of Investigators of Modifiers of BRCA1/2, ; Kelemen, LE; Kiemeney, LA; Kjaer, SK; Lambrechts, D; Lapolla, JP; Lázaro, C; Le, ND; Leminen, A; Leunen, K; Levine, DA; Lu, Y; Lundvall, L; Macgregor, S; Marees, T; Massuger, LF; McLaughlin, JR; Menon, U; Montagna, M; Moysich, KB; Narod, SA; Nathanson, KL; Nedergaard, L; Ness, RB; Nevanlinna, H; Nickels, S; Osorio, A; Paul, J; Pearce, CL; Phelan, CM; Pike, MC; Radice, P; Rossing, MA; Schildkraut, JM; Sellers, TA; Singer, CF; Song, H; Stram, DO; Sutphen, R; Lindblom, A; SWE-BRCA Investigators, ; Terry, KL; Tsai, Y-Y; van Altena, AM; Vergote, I; Vierkant, RA; Vitonis, AF; Walsh, C; Wang-Gohrke, S; Wappenschmidt, B; Wu, AH; Ziogas, A; Berchuck, A; Risch, HA; Ovarian Cancer Association Consortium,

Published Date

  • June 1, 2011

Published In

Volume / Issue

  • 17 / 11

Start / End Page

  • 3742 - 3750

PubMed ID

  • 21385923

Pubmed Central ID

  • PMC3107901

Electronic International Standard Serial Number (EISSN)

  • 1557-3265

Digital Object Identifier (DOI)

  • 10.1158/1078-0432.CCR-10-3405


  • eng

Conference Location

  • United States