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Phase II study of durvalumab and tremelimumab with front-line neoadjuvant chemotherapy in patients with advanced-stage ovarian cancer: primary analysis in the original cohort of KGOG3046/TRU-D

DC Field Value Language
dc.contributor.author김성훈-
dc.contributor.author박준식-
dc.contributor.author이정윤-
dc.date.accessioned2024-01-03T00:58:48Z-
dc.date.available2024-01-03T00:58:48Z-
dc.date.issued2023-10-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/197419-
dc.description.abstractBackground: This study assessed the antitumor activity and safety of durvalumab plus tremelimumab combined with neoadjuvant chemotherapy (NAC) in patients newly diagnosed with advanced ovarian cancer. Here, we report the primary endpoint of the original cohort of the KGOG 3046/TRU-D study. Methods: In this investigator-initiated single-arm, phase II trial, patients with stage IIIC-IVB ovarian cancer were administered three cycles of durvalumab (1500 mg) and tremelimumab (75 mg) with NAC, followed by interval debulking surgery (IDS). After surgery, three cycles of durvalumab (1120 mg) and adjuvant chemotherapy followed by durvalumab maintenance (1120 mg [total 12 cycles]) were administered. The primary endpoint of the study was 12-month progression-free survival (PFS) rate. Results: Twenty-three patients were enrolled. The median patient age was 60 years (range 44-77 years), and most patients presented with high-grade serous carcinoma (87.0%) and stage IV disease (87.0%). At the time of data cut-off on January 17, 2023, the median follow-up duration was 29.2 months (range 12.0-42.2). The 12-month, 24-month, and 30 month PFS rates were 63.6%, 45.0%, and 40.0%, respectively. All patients underwent IDS, with an R0 resection rate of 73.9%, and 17.4% achieved pathological complete response. Skin rashes were the most common treatment-related adverse events (TRAEs, 69.6%). However, all TRAEs completely resolved after steroid use. Conclusion: This study showed promising activity with a durable clinical response, supporting the potential of NAC with dual immune checkpoint blockade in advanced-stage ovarian cancer.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfJOURNAL FOR IMMUNOTHERAPY OF CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols / adverse effects-
dc.subject.MESHCarcinoma, Ovarian Epithelial / drug therapy-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoadjuvant Therapy*-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHOvarian Neoplasms* / pathology-
dc.titlePhase II study of durvalumab and tremelimumab with front-line neoadjuvant chemotherapy in patients with advanced-stage ovarian cancer: primary analysis in the original cohort of KGOG3046/TRU-D-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics and Gynecology (산부인과학교실)-
dc.contributor.googleauthorJunsik Park-
dc.contributor.googleauthorJung Bok Lee-
dc.contributor.googleauthorMyong Cheol Lim-
dc.contributor.googleauthorByoung-Gie Kim-
dc.contributor.googleauthorJae-Weon Kim-
dc.contributor.googleauthorSunghoon Kim-
dc.contributor.googleauthorChel Hun Choi-
dc.contributor.googleauthorHee Seung Kim-
dc.contributor.googleauthorSang Yoon Park-
dc.contributor.googleauthorJung-Yun Lee-
dc.contributor.googleauthorKGOG investigators-
dc.identifier.doi10.1136/jitc-2023-007444-
dc.contributor.localIdA00595-
dc.contributor.localIdA05788-
dc.contributor.localIdA04638-
dc.relation.journalcodeJ03617-
dc.identifier.pmid37865397-
dc.subject.keywordclinical trials, phase II as topic-
dc.subject.keywordimmune checkpoint inhibitors-
dc.subject.keywordimmunotherapy-
dc.subject.keywordprogrammed cell death 1 receptor-
dc.contributor.alternativeNameKim, Sung Hoon-
dc.contributor.affiliatedAuthor김성훈-
dc.contributor.affiliatedAuthor박준식-
dc.contributor.affiliatedAuthor이정윤-
dc.citation.volume11-
dc.citation.number10-
dc.citation.startPagee007444-
dc.identifier.bibliographicCitationJOURNAL FOR IMMUNOTHERAPY OF CANCER, Vol.11(10) : e007444, 2023-10-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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