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Safety and tolerability of first-line durvalumab with tremelimumab and chemotherapy in esophageal squamous cell carcinoma

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dc.contributor.author김혜련-
dc.date.accessioned2024-05-30T06:57:26Z-
dc.date.available2024-05-30T06:57:26Z-
dc.date.issued2023-08-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/199473-
dc.description.abstractBackground: Advanced or metastatic esophageal squamous cell carcinoma (ESCC) is associated with poor prognosis; new first- line systemic treatment options are needed. Combining immuno-oncology therapies with standard chemo-therapy may represent a promising approach for the treatment of solid tumors. Results from a Phase Ib study evaluating durvalumab with tremelimumab and chemotherapy in patients with advanced or metastatic ESCC are reported.Methods: Adults with advanced or metastatic ESCC who were candidates for first- line platinum- based chemotherapy received durvalumab 1500 mg (Day 1), tremelimumab 75 mg (Day 1), cisplatin 80 mg/m(2) (Day 1) and 5-fluorouracil (5-FU) 800 mg/m(2) (Days 1- 5) in 28 -day cycles until disease progression or discontin-uation due to toxicity. The study consisted of safety run- in (Part A) and expansion (Part B) periods. The primary endpoint was safety. Antitumor activity was an exploratory endpoint.Results: Sixteen patients were enrolled, 6 in Part A and 10 in Part B, and re-ceived a median of 4.0 treatment cycles. All patients were Asian; median age was 65.0 years. All patients experienced adverse events (AEs) related to cisplatin and 5- FU, and 8 (50.0%) patients experienced AEs related to durvalumab and treme-limumab. Grade =3 treatment-related AEs occurred in 7 (43.8%) patients. There were no deaths associated with AEs. Six (37.5%) patients achieved an objective response. Median progression- free survival was 3.75 months, and median overall survival was 9.69 months.Conclusions: Durvalumab with tremelimumab and chemotherapy demonstrated manageable safety and antitumor activity in patients with advanced or metastatic ESCC, warranting further investigation in randomized trials. Registered with ClinicalTrials.gov: NCT02658214.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherJohn Wiley & Sons Ltd.-
dc.relation.isPartOfCANCER MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols / adverse effects-
dc.subject.MESHCisplatin / adverse effects-
dc.subject.MESHEsophageal Neoplasms* / drug therapy-
dc.subject.MESHEsophageal Neoplasms* / etiology-
dc.subject.MESHEsophageal Squamous Cell Carcinoma* / drug therapy-
dc.subject.MESHEsophageal Squamous Cell Carcinoma* / etiology-
dc.subject.MESHFluorouracil / adverse effects-
dc.subject.MESHHumans-
dc.titleSafety and tolerability of first-line durvalumab with tremelimumab and chemotherapy in esophageal squamous cell carcinoma-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorDae Ho Lee-
dc.contributor.googleauthorHye Ryun Kim-
dc.contributor.googleauthorBhumsuk Keam-
dc.contributor.googleauthorKen Kato-
dc.contributor.googleauthorYasutoshi Kuboki-
dc.contributor.googleauthorHaiyan Gao-
dc.contributor.googleauthorAlejandro Yovine-
dc.contributor.googleauthorScott H Robbins-
dc.contributor.googleauthorMyung-Ju Ahn-
dc.identifier.doi10.1002/cam4.6260-
dc.contributor.localIdA01166-
dc.relation.journalcodeJ00449-
dc.identifier.eissn2045-7634-
dc.identifier.pmid37489066-
dc.subject.keywordchemotherapy-
dc.subject.keywordclinical trials-
dc.subject.keywordesophageal squamous cell-
dc.subject.keywordimmunology-
dc.contributor.alternativeNameKim, Hye Ryun-
dc.contributor.affiliatedAuthor김혜련-
dc.citation.volume12-
dc.citation.number15-
dc.citation.startPage16066-
dc.citation.endPage16075-
dc.identifier.bibliographicCitationCANCER MEDICINE, Vol.12(15) : 16066-16075, 2023-08-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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