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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

Authors
 Kim, Chang Gon  ;  Hong, Min Hee  ;  Kim, Dahee  ;  Lee, Brian Hyohyoung  ;  Kim, Hyunwook  ;  Ock, Chan-Young  ;  Kelly, Geoffrey  ;  Bang, Yoon Ji  ;  Kim, Gamin  ;  Lee, Jung Eun  ;  Kim, Chaeyeon  ;  Kim, Se-Heon  ;  Hong, Hyun Jun  ;  Park, Young Min  ;  Sim, Nam Suk  ;  Park, Heejung  ;  Park, Jin Woo  ;  Lee, Chang Geol  ;  Kim, Kyung Hwan  ;  Park, Goeun  ;  Jung, Inkyung  ;  Han, Dawoon  ;  Kim, Jong Hoon  ;  Cha, Junha  ;  Lee, Insuk  ;  Kang, Mingu  ;  Song, Heon  ;  Oum, Chiyoon  ;  Kim, Seulki  ;  Kim, Sukjun  ;  Lim, Yoojoo  ;  Kim-Schulze, Seunghee  ;  Merad, Miriam  ;  Yoon, Sun Och  ;  Kim, Hyun Je  ;  Koh, Yoon Woo  ;  Kim, Hye Ryun 
Citation
 CLINICAL CANCER RESEARCH, Vol.30(10) : 2097-2110, 2024-05 
Journal Title
CLINICAL CANCER RESEARCH
ISSN
 1078-0432 
Issue Date
2024-05
Abstract
Purpose: 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.
DOI
10.1158/1078-0432.CCR-23-3249
Appears in Collections:
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
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
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
Yonsei Authors
Koh, Yoon Woo(고윤우)
Kim, Kyung Hwan(김경환)
Kim, Da Hee(김다희) ORCID logo https://orcid.org/0000-0001-7286-1334
Kim, Se Heon(김세헌)
Kim, Jong Hoon(김종훈) ORCID logo https://orcid.org/0000-0002-3385-8180
Kim, Chang Gon(김창곤)
Kim, Hyunwook(김현욱) ORCID logo https://orcid.org/0000-0002-9560-4768
Kim, Hye Ryun(김혜련) ORCID logo https://orcid.org/0000-0002-1842-9070
Park, Goeun(박고은)
Park, Young Min(박영민) ORCID logo https://orcid.org/0000-0002-7593-8461
Park, Jin Woo(박진우)
Park, Heejung(박희정)
Sim, Nam Suk(심남석)
Yoon, Sun Ock(윤선옥) ORCID logo https://orcid.org/0000-0002-5115-1402
Lee, Jung Eun(이정은) ORCID logo https://orcid.org/0000-0003-0917-2872
Lee, Chang Geol(이창걸) ORCID logo https://orcid.org/0000-0002-8702-881X
Jung, Inkyung(정인경) ORCID logo https://orcid.org/0000-0003-3780-3213
Hong, Min Hee(홍민희) ORCID logo https://orcid.org/0000-0003-3490-2195
Hong, Hyun Jun(홍현준) ORCID logo https://orcid.org/0000-0002-7808-7877
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200991
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