{"title":"儿科","authors":"J. Teruya","doi":"10.37573/9781585285525.008","DOIUrl":null,"url":null,"abstract":"Conclusions: BRAF mutation was more seen in a metastatic site rather than primary in melanoma (p=0.023). In colorectal adenocarcinoma, NRAS mutation was more likely persent in metastatic site than primary (p=0.048). We did not fi nd association with examined site in other analyzed mutations (KRAS, KIT, PIK3CA). These results suggest importance of consideration of disease site when analyzing mutational status. Probability of co-mutations in different pathways has signifi cance for decisions regarding therapy.","PeriodicalId":171073,"journal":{"name":"Demystifying Drug Dosing in Renal Dysfunction","volume":"49 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pediatrics\",\"authors\":\"J. Teruya\",\"doi\":\"10.37573/9781585285525.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Conclusions: BRAF mutation was more seen in a metastatic site rather than primary in melanoma (p=0.023). In colorectal adenocarcinoma, NRAS mutation was more likely persent in metastatic site than primary (p=0.048). We did not fi nd association with examined site in other analyzed mutations (KRAS, KIT, PIK3CA). These results suggest importance of consideration of disease site when analyzing mutational status. Probability of co-mutations in different pathways has signifi cance for decisions regarding therapy.\",\"PeriodicalId\":171073,\"journal\":{\"name\":\"Demystifying Drug Dosing in Renal Dysfunction\",\"volume\":\"49 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Demystifying Drug Dosing in Renal Dysfunction\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.37573/9781585285525.008\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Demystifying Drug Dosing in Renal Dysfunction","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37573/9781585285525.008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Conclusions: BRAF mutation was more seen in a metastatic site rather than primary in melanoma (p=0.023). In colorectal adenocarcinoma, NRAS mutation was more likely persent in metastatic site than primary (p=0.048). We did not fi nd association with examined site in other analyzed mutations (KRAS, KIT, PIK3CA). These results suggest importance of consideration of disease site when analyzing mutational status. Probability of co-mutations in different pathways has signifi cance for decisions regarding therapy.