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An umbrella study of biomarker-driven targeted therapy in patients with platinum-resistant recurrent ovarian cancer: a Korean Gynecologic Oncology Group study (KGOG 3045), AMBITION

DC Field Value Language
dc.contributor.authorLee, Jung-Yun-
dc.contributor.authorYi, Ju Yeon-
dc.contributor.authorKim, Hyun-Soo-
dc.contributor.authorLim, June-
dc.contributor.authorKim, Sunghoon-
dc.contributor.authorNam, Byoung Ho-
dc.contributor.authorKim, Hee Seung-
dc.contributor.authorKim, Jae Weon-
dc.contributor.authorChoi, Chel Hun-
dc.contributor.authorKim, Byoung-Gie-
dc.creator김희승-
dc.date.accessioned2020-01-23T07:41:29Z-
dc.date.available2020-04-05T07:41:29Z-
dc.date.created2019-12-04-
dc.date.created2019-12-04-
dc.date.created2019-12-04-
dc.date.issued2019-08-
dc.identifier.citationJapanese Journal of Clinical Oncology, Vol.49 No.8, pp.789-792-
dc.identifier.issn0368-2811-
dc.identifier.urihttps://hdl.handle.net/10371/163921-
dc.description.abstractA pilot study of biomarker-driven targeted therapy in patients with platinum-resistant recurrent ovarian cancer has been started in Korea. Archival tumor samples were tested for HRD and PD-L1 status. Treatment arms will be allocated according to the test results. For HRD+ patients, we tested the synergistic effects of olaparib and other agents; treatment arms will randomly be allocated. (Arm 1: olaparib and cediranib; Arm 2: olaparib and durvalumab). For HRD- patients, we tested the role of biomarker-driven immunotherapy according to PD-L1 expression (Arm 3: durvalumab and chemotherapy in patients with high PD-L1 expression; Arm 4: durvalumab, tremelimumab, and chemotherapy in patients with low PD-L1 expression). Sixty-eight patients will be included from three Korean institutions within 1 year. The primary endpoint is the response rate according to RECIST 1.1 (6 months after treatment initiation).-
dc.language영어-
dc.language.isoENGen
dc.publisherOxford University Press-
dc.titleAn umbrella study of biomarker-driven targeted therapy in patients with platinum-resistant recurrent ovarian cancer: a Korean Gynecologic Oncology Group study (KGOG 3045), AMBITION-
dc.typeArticle-
dc.identifier.doi10.1093/jjco/hyz085-
dc.citation.journaltitleJapanese Journal of Clinical Oncology-
dc.identifier.wosid000493068900016-
dc.identifier.scopusid2-s2.0-85074351167-
dc.description.srndOAIID:RECH_ACHV_DSTSH_NO:T201916095-
dc.description.srndRECH_ACHV_FG:RR00200001-
dc.description.srndADJUST_YN:-
dc.description.srndEMP_ID:A080402-
dc.description.srndCITE_RATE:2.183-
dc.description.srndDEPT_NM:의학과-
dc.description.srndEMAIL:bboddi0311@snu.ac.kr-
dc.description.srndSCOPUS_YN:Y-
dc.citation.endpage792-
dc.citation.number8-
dc.citation.startpage789-
dc.citation.volume49-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Hee Seung-
dc.identifier.srndT201916095-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordAuthorplatinum-resistant-
dc.subject.keywordAuthorovarian cancer-
dc.subject.keywordAuthorbiomarker-
dc.subject.keywordAuthorumbrella study-
dc.subject.keywordAuthortargeted therapy-
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