{"title":"Palbociclib and Exemestane are Active in Pretreated Low-Grade Serous Ovarian Cancer","authors":"B. Thürlimann, Gesa Isensee","doi":"10.31487/j.crogr.2020.03.04","DOIUrl":null,"url":null,"abstract":"We describe a case of a 55-year-old woman with a rare metastatic micropapillary low-grade serous ovarian\ncancer who had been heavily pretreated. A KRAS-mutation and c-MYC-amplification were detected, and\nwe initiated a therapy with the CDK4/6- inhibitor Palbociclib in combination with the steroidal aromatase\ninhibitor exemestane. We postulated that the combination therapy leads to a blocking of the c-MYCamplification-activated cell cycle, proliferation, and inhibition of apoptosis, further enhanced by other\noncogenes like mutated RAS. This therapy showed a good and lasting response representing a new\nopportunity for therapy in heavily pretreated metastatic micropapillary low-grade serous ovarian cancer.","PeriodicalId":416165,"journal":{"name":"Case Reports in Obstetrics Gynecology and Reproductive","volume":"33 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Obstetrics Gynecology and Reproductive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.crogr.2020.03.04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We describe a case of a 55-year-old woman with a rare metastatic micropapillary low-grade serous ovarian
cancer who had been heavily pretreated. A KRAS-mutation and c-MYC-amplification were detected, and
we initiated a therapy with the CDK4/6- inhibitor Palbociclib in combination with the steroidal aromatase
inhibitor exemestane. We postulated that the combination therapy leads to a blocking of the c-MYCamplification-activated cell cycle, proliferation, and inhibition of apoptosis, further enhanced by other
oncogenes like mutated RAS. This therapy showed a good and lasting response representing a new
opportunity for therapy in heavily pretreated metastatic micropapillary low-grade serous ovarian cancer.