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이세민

Lee, Semin
Computational Biology Lab.
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dc.citation.endPage 2194 -
dc.citation.number 12 -
dc.citation.startPage 2182 -
dc.citation.title INTERNATIONAL JOURNAL OF CANCER -
dc.citation.volume 151 -
dc.contributor.author Yoon, Meesun -
dc.contributor.author Lee, Hyo Kyung -
dc.contributor.author Park, Eun Young -
dc.contributor.author Kim, Jin Hee -
dc.contributor.author Lee, Jong Hoon -
dc.contributor.author Kim, Young Seok -
dc.contributor.author Kim, Hak Jae -
dc.contributor.author Kim, Hunjung -
dc.contributor.author Yoo, Chong Woo -
dc.contributor.author Lee, Sun -
dc.contributor.author Hong, Eun Kyung -
dc.contributor.author Kim, Tae Hyun -
dc.contributor.author Kim, Tae-Sung -
dc.contributor.author Seo, Sang-soo -
dc.contributor.author Kang, Sokbom -
dc.contributor.author Chang, Suk-Joon -
dc.contributor.author Shin, Hye Jin -
dc.contributor.author Uong, Tung Nguyen Thanh -
dc.contributor.author Lee, Semin -
dc.contributor.author Kim, Joo-Young -
dc.date.accessioned 2023-12-21T13:16:47Z -
dc.date.available 2023-12-21T13:16:47Z -
dc.date.created 2022-07-28 -
dc.date.issued 2022-12 -
dc.description.abstract We conducted a prospective phase II study on whether extended-field irradiation (EFI) confers survival benefits depending on hypoxic markers in locally advanced uterine cervical cancer (LAUCC). RNA-seq was performed to identify immune and hypoxic gene signatures. A total of 288 patients were randomized to either EFI or pelvic radiotherapy (PRT). All patients completed chemoradiotherapy. Overall, significantly higher 5-year para-aortic recurrence free survival (PARFS) rate occurred in EFI (97.6%) than in PRT group (87.2%), with marginal tendency to improve disease-free survival (DFS; 78% vs 70%, P =.066). Subgroup analyses were performed based on carbonic anhydrase 9 (CA9)-only positive, CA9/hypoxia-inducible factor (HIF) double positive and CA9 negative. In the CA9-only positive, EFI successfully increased 5-year PARFS (100% vs 76.4%, P =.010), resulting in significantly improved long-term DFS (85.7% vs 54.7%, P =.023) compared to the PRT, while there was no such benefit of EFI in the CA9/HIFs double positive. RNA-seq analysis identified distinct immune(high) subgroup with negative correlation with hypoxia gene signatures (R = -.37, P <.01), which showed a higher 5-year DFS than the immune(low) (P =.032). Hypoxia-related genes were upregulated in the CA9/HIFs double positive compared to CA9 negative (P <.05). Only 17.4% of patients in CA9-negative group showed immune(low) signatures, while 40.0% of patients in the double-positive group exhibited immune(low) signatures. In conclusion, EFI improved PARFS significantly in all patients, but therapeutic efficacy of EFI in terms of improved DFS was solely observed in CA9-only positive LAUCC, and not in CA9/HIFs double-positive subgroup. RNA-seq analysis suggested that hypoxia-induced immunosuppression may be related to treatment resistance in LAUCC. -
dc.identifier.bibliographicCitation INTERNATIONAL JOURNAL OF CANCER, v.151, no.12, pp.2182 - 2194 -
dc.identifier.doi 10.1002/ijc.34190 -
dc.identifier.issn 0020-7136 -
dc.identifier.scopusid 2-s2.0-85133711144 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/59044 -
dc.identifier.url https://onlinelibrary.wiley.com/doi/10.1002/ijc.34190 -
dc.identifier.wosid 000822816800001 -
dc.language 영어 -
dc.publisher WILEY -
dc.title Randomized multicenter phase II trial of prophylactic irradiation of para-aortic lymph nodes in advanced cervical cancer according to tumor hypoxia: Korean Radiation Oncology Group (KROG 07-01) study -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Oncology -
dc.relation.journalResearchArea Oncology -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor CA9 -
dc.subject.keywordAuthor extended-field irradiation -
dc.subject.keywordAuthor HIF-1 alpha -
dc.subject.keywordAuthor HIF-2 alpha -
dc.subject.keywordAuthor locally advanced cervical cancer -
dc.subject.keywordPlus ENDOTHELIAL GROWTH-FACTOR -
dc.subject.keywordPlus EXPRESSION -
dc.subject.keywordPlus CARBONIC-ANHYDRASE-9 -
dc.subject.keywordPlus CARCINOMA -
dc.subject.keywordPlus MARKER -
dc.subject.keywordPlus CELLS -
dc.subject.keywordPlus METASTASES -
dc.subject.keywordPlus IX -

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