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A Phase II Open-Label Randomized Clinical Trial of Preoperative Durvalumab or Durvalumab plus Tremelimumab in Resectable Head and Neck Squamous Cell Carcinoma

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dc.contributor.author고윤우-
dc.contributor.author김경환-
dc.contributor.author김다희-
dc.contributor.author김종훈-
dc.contributor.author김창곤-
dc.contributor.author김혜련-
dc.contributor.author박진우-
dc.contributor.author윤선옥-
dc.contributor.author정인경-
dc.contributor.author홍민희-
dc.contributor.author김현욱-
dc.contributor.author이정은-
dc.contributor.author김세헌-
dc.contributor.author홍현준-
dc.contributor.author박영민-
dc.contributor.author심남석-
dc.contributor.author박희정-
dc.contributor.author이창걸-
dc.contributor.author박고은-
dc.date.accessioned2024-12-06T03:06:16Z-
dc.date.available2024-12-06T03:06:16Z-
dc.date.issued2024-05-
dc.identifier.issn1078-0432-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/200991-
dc.description.abstractPurpose: Clinical implications of neoadjuvant immunotherapy in patients with locally advanced but resectable head and neck squamous cell carcinoma (HNSCC) remain largely unexplored.Patients and Methods: Patients with resectable HNSCC were randomized to receive a single dose of preoperative durvalumab (D) with or without tremelimumab (T) before resection, followed by postoperative (chemo)radiotherapy based on multidisciplinary discretion and 1-year D treatment. Artificial intelligence (AI)-powered spatial distribution analysis of tumor-infiltrating lymphocytes and high-dimensional profiling of circulating immune cells tracked dynamic intratumoral and systemic immune responses.Results: Of the 48 patients enrolled (D, 24 patients; D+T, 24 patients), 45 underwent surgical resection per protocol (D, 21 patients; D+T, 24 patients). D +/- T had a favorable safety profile and did not delay surgery. Distant recurrence-free survival (DRFS) was significantly better in patients treated with D+T than in those treated with D monotherapy. AI-powered whole-slide image analysis demonstrated that D+T significantly reshaped the tumor microenvironment toward immune-inflamed phenotypes, in contrast with the D monotherapy or cytotoxic chemotherapy. High-dimensional profiling of circulating immune cells revealed a significant expansion of T-cell subsets characterized by proliferation and activation in response to D+T therapy, which was rare following D monotherapy. Importantly, expansion of specific clusters in CD8+ T cells and non-regulatory CD4+ T cells with activation and exhaustion programs was associated with prolonged DRFS in patients treated with D+T.Conclusions: Preoperative D +/- T is feasible and may benefit patients with resectable HNSCC. Distinct changes in the tumor microenvironment and circulating immune cells were induced by each treatment regimen, warranting further investigation.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherAmerican Association for Cancer Research-
dc.relation.isPartOfCLINICAL CANCER RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntibodies, Monoclonal* / administration & dosage-
dc.subject.MESHAntibodies, Monoclonal* / therapeutic use-
dc.subject.MESHAntibodies, Monoclonal, Humanized* / administration & dosage-
dc.subject.MESHAntibodies, Monoclonal, Humanized* / therapeutic use-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / adverse effects-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / therapeutic use-
dc.subject.MESHFemale-
dc.subject.MESHHead and Neck Neoplasms* / drug therapy-
dc.subject.MESHHead and Neck Neoplasms* / immunology-
dc.subject.MESHHead and Neck Neoplasms* / pathology-
dc.subject.MESHHead and Neck Neoplasms* / therapy-
dc.subject.MESHHumans-
dc.subject.MESHLymphocytes, Tumor-Infiltrating / drug effects-
dc.subject.MESHLymphocytes, Tumor-Infiltrating / immunology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoadjuvant Therapy* / methods-
dc.subject.MESHSquamous Cell Carcinoma of Head and Neck* / drug therapy-
dc.subject.MESHSquamous Cell Carcinoma of Head and Neck* / pathology-
dc.subject.MESHSquamous Cell Carcinoma of Head and Neck* / therapy-
dc.subject.MESHTumor Microenvironment / drug effects-
dc.subject.MESHTumor Microenvironment / immunology-
dc.titleA Phase II Open-Label Randomized Clinical Trial of Preoperative Durvalumab or Durvalumab plus Tremelimumab in Resectable Head and Neck Squamous Cell Carcinoma-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Otorhinolaryngology (이비인후과학교실)-
dc.contributor.googleauthorChang Gon Kim-
dc.contributor.googleauthorMin Hee Hong-
dc.contributor.googleauthorDahee Kim-
dc.contributor.googleauthorBrian Hyohyoung Lee-
dc.contributor.googleauthorHyunwook Kim-
dc.contributor.googleauthorChan-Young Ock-
dc.contributor.googleauthorGeoffrey Kelly-
dc.contributor.googleauthorYoon Ji Bang-
dc.contributor.googleauthorGamin Kim-
dc.contributor.googleauthorJung Eun Lee-
dc.contributor.googleauthorChaeyeon Kim-
dc.contributor.googleauthorSe-Heon Kim-
dc.contributor.googleauthorHyun Jun Hong-
dc.contributor.googleauthorYoung Min Park-
dc.contributor.googleauthorNam Suk Sim-
dc.contributor.googleauthorHeejung Park-
dc.contributor.googleauthorJin Woo Park-
dc.contributor.googleauthorChang Geol Lee-
dc.contributor.googleauthorKyung Hwan Kim-
dc.contributor.googleauthorGoeun Park-
dc.contributor.googleauthorInkyung Jung-
dc.contributor.googleauthorDawoon Han-
dc.contributor.googleauthorJong Hoon Kim-
dc.contributor.googleauthorJunha Cha-
dc.contributor.googleauthorInsuk Lee-
dc.contributor.googleauthorMingu Kang-
dc.contributor.googleauthorHeon Song-
dc.contributor.googleauthorChiyoon Oum-
dc.contributor.googleauthorSeulki Kim-
dc.contributor.googleauthorSukjun Kim-
dc.contributor.googleauthorYoojoo Lim-
dc.contributor.googleauthorSeunghee Kim-Schulze-
dc.contributor.googleauthorMiriam Merad-
dc.contributor.googleauthorSun Och Yoon-
dc.contributor.googleauthorHyun Je Kim-
dc.contributor.googleauthorYoon Woo Koh-
dc.contributor.googleauthorHye Ryun Kim-
dc.identifier.doi10.1158/1078-0432.ccr-23-3249-
dc.contributor.localIdA00133-
dc.contributor.localIdA05226-
dc.contributor.localIdA04831-
dc.contributor.localIdA05233-
dc.contributor.localIdA05991-
dc.contributor.localIdA01166-
dc.contributor.localIdA06528-
dc.contributor.localIdA02566-
dc.contributor.localIdA03693-
dc.contributor.localIdA04393-
dc.relation.journalcodeJ00564-
dc.identifier.pmid38457288-
dc.identifier.urlhttps://aacrjournals.org/clincancerres/article/30/10/2097/745179/-
dc.contributor.alternativeNameKoh, Yoon Woo-
dc.contributor.affiliatedAuthor고윤우-
dc.contributor.affiliatedAuthor김경환-
dc.contributor.affiliatedAuthor김다희-
dc.contributor.affiliatedAuthor김종훈-
dc.contributor.affiliatedAuthor김창곤-
dc.contributor.affiliatedAuthor김혜련-
dc.contributor.affiliatedAuthor박진우-
dc.contributor.affiliatedAuthor윤선옥-
dc.contributor.affiliatedAuthor정인경-
dc.contributor.affiliatedAuthor홍민희-
dc.citation.volume30-
dc.citation.number10-
dc.citation.startPage2097-
dc.citation.endPage2110-
dc.identifier.bibliographicCitationCLINICAL CANCER RESEARCH, Vol.30(10) : 2097-2110, 2024-05-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biomedical Systems Informatics (의생명시스템정보학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

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