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Safety and tolerability of first-line durvalumab with tremelimumab and chemotherapy in esophageal squamous cell carcinoma
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Dae Ho | - |
| dc.contributor.author | Kim, Hye Ryun | - |
| dc.contributor.author | Keam, Bhumsuk | - |
| dc.contributor.author | Kato, Ken | - |
| dc.contributor.author | Kuboki, Yasutoshi | - |
| dc.contributor.author | Gao, Haiyan | - |
| dc.contributor.author | Yovine, Alejandro | - |
| dc.contributor.author | Robbins, Scott H. H. | - |
| dc.contributor.author | Ahn, Myung-Ju | - |
| dc.date.accessioned | 2024-05-30T06:57:26Z | - |
| dc.date.available | 2024-05-30T06:57:26Z | - |
| dc.date.created | 2024-04-17 | - |
| dc.date.issued | 2023-08 | - |
| dc.identifier.issn | 2045-7634 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/199473 | - |
| dc.description.abstract | Background: 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.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | John Wiley & Sons Ltd. | - |
| dc.relation.isPartOf | CANCER MEDICINE | - |
| dc.relation.isPartOf | CANCER MEDICINE | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.title | Safety and tolerability of first-line durvalumab with tremelimumab and chemotherapy in esophageal squamous cell carcinoma | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Lee, Dae Ho | - |
| dc.contributor.googleauthor | Kim, Hye Ryun | - |
| dc.contributor.googleauthor | Keam, Bhumsuk | - |
| dc.contributor.googleauthor | Kato, Ken | - |
| dc.contributor.googleauthor | Kuboki, Yasutoshi | - |
| dc.contributor.googleauthor | Gao, Haiyan | - |
| dc.contributor.googleauthor | Yovine, Alejandro | - |
| dc.contributor.googleauthor | Robbins, Scott H. H. | - |
| dc.contributor.googleauthor | Ahn, Myung-Ju | - |
| dc.identifier.doi | 10.1002/cam4.6260 | - |
| dc.relation.journalcode | J00449 | - |
| dc.identifier.eissn | 2045-7634 | - |
| dc.identifier.pmid | 37489066 | - |
| dc.subject.keyword | chemotherapy | - |
| dc.subject.keyword | clinical trials | - |
| dc.subject.keyword | esophageal squamous cell | - |
| dc.subject.keyword | immunology | - |
| dc.contributor.alternativeName | Kim, Hye Ryun | - |
| dc.contributor.affiliatedAuthor | Kim, Hye Ryun | - |
| dc.identifier.scopusid | 2-s2.0-85165553017 | - |
| dc.identifier.wosid | 001035647600001 | - |
| dc.citation.volume | 12 | - |
| dc.citation.number | 15 | - |
| dc.citation.startPage | 16066 | - |
| dc.citation.endPage | 16075 | - |
| dc.identifier.bibliographicCitation | CANCER MEDICINE, Vol.12(15) : 16066-16075, 2023-08 | - |
| dc.identifier.rimsid | 83178 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | chemotherapy | - |
| dc.subject.keywordAuthor | clinical trials | - |
| dc.subject.keywordAuthor | esophageal squamous cell | - |
| dc.subject.keywordAuthor | immunology | - |
| dc.subject.keywordPlus | PHASE-II EVALUATION | - |
| dc.subject.keywordPlus | ANTITUMOR-ACTIVITY | - |
| dc.subject.keywordPlus | EFFICACY | - |
| dc.subject.keywordPlus | CANCER | - |
| dc.subject.keywordPlus | 5-FLUOROURACIL | - |
| dc.subject.keywordPlus | CISPLATIN | - |
| dc.subject.keywordPlus | DEATH | - |
| dc.subject.keywordPlus | COMBINATION | - |
| dc.subject.keywordPlus | NIVOLUMAB | - |
| dc.subject.keywordPlus | MEDI4736 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Oncology | - |
| dc.relation.journalResearchArea | Oncology | - |
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