학술논문

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
Document Type
Author
Hollestelle, AntoinetteVan Der Baan, Frederieke H.Berchuck, AndrewJohnatty, Sharon E.Aben, Katja K.Agnarsson, Bjarni A.Aittomäki, KristiinaAlducci, ElisaAndrulis, Irene L.Anton-Culver, HodaAntonenkova, Natalia N.Antoniou, Antonis C.Apicella, CarmelArndt, VolkerArnold, NorbertArun, Banu K.Arver, BritaAshworth, AlanBaglietto, LauraBalleine, RosemaryBandera, Elisa V.Barrowdale, DanielBean, Yukie T.Beckmann, LarsBeckmann, Matthias W.Benitez, JavierBerger, AndreasBerger, RaananBeuselinck, BenoitBisogna, MariaBjorge, LineBlomqvist, CarlBogdanova, Natalia V.Bojesen, AndersBojesen, Stig E.Bolla, Manjeet K.Bonanni, BernardoBrand, Judith S.Brauch, HiltrudBrenner, HermannBrinton, LouiseBrooks-Wilson, AngelaBruinsma, FionaBrunet, JoanBrüning, ThomasBudzilowska, AgnieszkaBunker, Clareann H.Burwinkel, BarbaraButzow, RalfBuys, Saundra S.Caligo, Maria A.Campbell, IanCarter, JonathanChang-Claude, JennyChanock, Stephen J.Claes, Kathleen B MCollée, J. MargrietCook, Linda S.Couch, Fergus J.Cox, AngelaCramer, DanielCross, Simon S.Cunningham, Julie M.Cybulski, CezaryCzene, KamilaDamiola, FrancescaDansonka-Mieszkowska, AgnieszkaDarabi, HatefDe La Hoya, MiguelDefazio, AnnaDennis, JosephDevilee, PeterDicks, Ed M.Diez, OrlandDoherty, Jennifer A.Domchek, Susan M.Dorfling, Cecilia M.Dörk, ThiloSilva, Isabel Dos SantosDu Bois, AndreasDumont, MartineDunning, Alison M.Duran, MercedesEaston, Douglas F.Eccles, DianaEdwards, Robert P.Ehrencrona, HansEjlertsen, BentEkici, Arif B.Ellis, Steve D.Engel, ChristophEriksson, MikaelFasching, Peter A.Feliubadalo, LidiaFigueroa, JonineFlesch-Janys, DieterFletcher, OliviaFontaine, AnnetteFortuzzi, StefanoFostira, FlorentiaFridley, Brooke L.Friebel, TaraFriedman, EitanFriel, GraceFrost, DebraGarber, JudyGarcía-Closas, MontserratGayther, Simon A.Gentry-Maharaj, AleksandraGerdes, Anne MarieGiles, Graham G.Glasspool, RosalindGlendon, GordGodwin, Andrew K.Goodman, Marc T.Gore, MartinGreene, Mark H.Grip, MerviGronwald, JacekGschwantler Kaulich, DaphneGuénel, PascalGuzman, Starr R.Haeberle, LotharHaiman, Christopher A.Hall, PerHalverson, Sandra L.Hamann, UteHansen, Thomas V OHarter, PhilippHartikainen, Jaana M.Healey, SueHein, AlexanderHeitz, FlorianHenderson, Brian E.Herzog, JosefT Hildebrandt, Michelle A.Høgdall, Claus K.Høgdall, EstridHogervorst, Frans B LHopper, John L.Humphreys, KeithHuzarski, TomaszImyanitov, Evgeny N.Isaacs, ClaudineJakubowska, AnnaJanavicius, RamunasJaworska, KatarzynaJensen, AllanJensen, Uffe BirkJohnson, NicholaJukkola-Vuorinen, ArjaKabisch, MariaKarlan, Beth Y.Kataja, VesaKauff, NoahKelemen, Linda E.Kerin, Michael J.Kiemeney, Lambertus A.Kjaer, Susanne K.Knight, Julia A.Knol-Bout, Jacoba P.Konstantopoulou, IreneKosma, Veli MattiKrakstad, CamillaKristensen, VesselaKuchenbaecker, Karoline B.Kupryjanczyk, JolantaLaitman, YaelLambrechts, DietherLambrechts, SandrinaLarson, Melissa C.Lasa, AdrianaLaurent-Puig, PierreLazaro, ConxiLe, Nhu D.Le Marchand, LoicLeminen, ArtoLester, JennyLevine, Douglas A.Li, JingmeiLiang, DongLindblom, AnnikaLindor, NoralaneLissowska, JolantaLong, JirongLu, Karen H.Lubinski, JanLundvall, LeneLurie, GalinaMai, Phuong L.Mannermaa, ArtoMargolin, SaraMariette, FrederiqueMarme, FrederikMartens, John W MMassuger, Leon F A GMaugard, ChristineMazoyer, SylvieMcGuffog, LesleyMcGuire, ValerieMcLean, CatrionaMcNeish, IainMeindl, AlfonsMenegaux, FlorenceMenéndez, PrimitivaMenkiszak, JanuszMenon, UshaMensenkamp, Arjen R.Miller, NicolaMilne, Roger L.Modugno, FrancesmaryMontagna, MarcoMoysich, Kirsten B.Müller, HeikoMulligan, Anna MarieMuranen, Taru A.Narod, Steven A.Nathanson, Katherine L.Ness, Roberta B.Neuhausen, Susan L.Nevanlinna, HeliNeven, PatrickNielsen, Finn C.Nielsen, Sune F.Nordestgaard, Børge G.Nussbaum, Robert L.Odunsi, KunleOffit, KennethOlah, EdithOlopade, Olufunmilayo I.Olson, Janet E.Olson, Sara H.Oosterwijk, Jan C.Orlow, IreneOrr, NickOrsulic, SandraOsorio, AnaOttini, LauraPaul, JamesPearce, Celeste L.Pedersen, Inge SokildePeissel, BernardPejovic, TanjaPelttari, Liisa M.Perkins, JoPermuth-Wey, JennyPeterlongo, PaoloPeto, JulianPhelan, Catherine M.Phillips, Kelly AnnePiedmonte, MarionPike, Malcolm C.Platte, RadkaPlisiecka-Halasa, JoannaPoole, Elizabeth M.Poppe, BrucePylkäs, KatriRadice, PaoloRamus, Susan J.Rebbeck, Timothy R.Reed, Malcolm W RRennert, GadRisch, Harvey A.Robson, MarkRodriguez, Gustavo C.Romero, AtochaRossing, Mary AnneRothstein, Joseph H.Rudolph, AnjaRunnebaum, IngoSalani, RituSalvesen, Helga B.Sawyer, Elinor J.Schildkraut, Joellen M.Schmidt, Marjanka K.Schmutzler, Rita K.Schneeweiss, AndreasSchoemaker, Minouk J.Schrauder, Michael G.Schumacher, FredrickSchwaab, IraScuvera, GiuliettaSellers, Thomas A.Severi, GianlucaSeynaeve, Caroline M.Shah, MitulShrubsole, MarthaSiddiqui, NadeemSieh, WeivaSimard, JacquesSinger, Christian F.Sinilnikova, Olga M.Smeets, DominiekSohn, ChristofSoller, MariaSong, HonglinSoucy, PennySouthey, Melissa C.Stegmaier, ChristaStoppa-Lyonnet, DominiqueSucheston, LaraSwerdlow, AnthonyTangen, Ingvild L.Tea, Muy KhengTeixeira, Manuel R.Terry, Kathryn L.Terry, Mary BethThomassen, MadsThompson, Pamela J.Tihomirova, LaimaTischkowitz, MarcToland, Amanda EwartTollenaar, Rob A E MTomlinson, IanTorres, DianaTruong, ThérèseTsimiklis, HelenTung, NadineTworoger, Shelley S.Tyrer, Jonathan P.Vachon, Celine M.Van 't Veer, Laura J.Van Altena, Anne M.Van Asperen, C. J.Van Den Berg, DavidVan Den Ouweland, Ans M WVan Doorn, Helena C.Van Nieuwenhuysen, ElsVan Rensburg, Elizabeth J.Vergote, IgnaceVerhoef, SennoVierkant, Robert A.Vijai, JosephVitonis, Allison F.Von Wachenfeldt, AnnaWalsh, ChristineWang, QinWang-Gohrke, ShanWappenschmidt, BarbaraWeischer, MarenWeitzel, Jeffrey N.Weltens, CarolineWentzensen, NicolasWhittemore, Alice S.Wilkens, Lynne R.Winqvist, RobertWu, Anna H.Wu, XifengYang, Hannah P.Zaffaroni, DanielaPilar Zamora, M.Zheng, WeiZiogas, ArgyriosChenevix-Trench, GeorgiaPharoah, Paul D PRookus, Matti A.Hooning, Maartje J.Goode, Ellen L.Breast Cancer Family Register, Cancer Family RegisterEMBRACEGENICA Network, NetworkHEBONSWE-BRCA
Source
Gynecologic Oncology BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation. 141(2):386-401
Subject
Breast cancer
Clinical outcome
Genetic association
KRAS variant
Ovarian cancer
Medicin och hälsovetenskap
Klinisk medicin
Cancer och onkologi
Medical and Health Sciences
Clinical Medicine
Cancer and Oncology
Medicinska och farmaceutiska grundvetenskaper
Medicinsk genetik
Basic Medicine
Medical Genetics
Language
English
ISSN
0090-8258
Abstract
Objective Clinical genetic testing is commercially available for rs61764370, an inherited variant residing in a KRAS 3′ UTR microRNA binding site, based on suggested associations with increased ovarian and breast cancer risk as well as with survival time. However, prior studies, emphasizing particular subgroups, were relatively small. Therefore, we comprehensively evaluated ovarian and breast cancer risks as well as clinical outcome associated with rs61764370. Methods Centralized genotyping and analysis were performed for 140,012 women enrolled in the Ovarian Cancer Association Consortium (15,357 ovarian cancer patients; 30,816 controls), the Breast Cancer Association Consortium (33,530 breast cancer patients; 37,640 controls), and the Consortium of Modifiers of BRCA1 and BRCA2 (14,765 BRCA1 and 7904 BRCA2 mutation carriers). Results We found no association with risk of ovarian cancer (OR = 0.99, 95% CI 0.94-1.04, p = 0.74) or breast cancer (OR = 0.98, 95% CI 0.94-1.01, p = 0.19) and results were consistent among mutation carriers (BRCA1, ovarian cancer HR = 1.09, 95% CI 0.97-1.23, p = 0.14, breast cancer HR = 1.04, 95% CI 0.97-1.12, p = 0.27; BRCA2, ovarian cancer HR = 0.89, 95% CI 0.71-1.13, p = 0.34, breast cancer HR = 1.06, 95% CI 0.94-1.19, p = 0.35). Null results were also obtained for associations with overall survival following ovarian cancer (HR = 0.94, 95% CI 0.83-1.07, p = 0.38), breast cancer (HR = 0.96, 95% CI 0.87-1.06, p = 0.38), and all other previously-reported associations. Conclusions rs61764370 is not associated with risk of ovarian or breast cancer nor with clinical outcome for patients with these cancers. Therefore, genotyping this variant has no clinical utility related to the prediction or management of these cancers.