Cited 0 times in Scipus Cited Count

Treatment strategy and outcomes in locally advanced head and neck squamous cell carcinoma: a nationwide retrospective cohort study (KCSG HN13-01)

DC Field Value Language
dc.contributor.authorLee, YG-
dc.contributor.authorKang, EJ-
dc.contributor.authorKeam, B-
dc.contributor.authorChoi, JH-
dc.contributor.authorKim, JS-
dc.contributor.authorPark, KU-
dc.contributor.authorLee, KE-
dc.contributor.authorKwon, JH-
dc.contributor.authorLee, KW-
dc.contributor.authorKim, MK-
dc.contributor.authorAhn, HK-
dc.contributor.authorShin, SH-
dc.contributor.authorKim, HR-
dc.contributor.authorKim, SB-
dc.contributor.authorYun, HJ-
dc.date.accessioned2022-11-29T01:43:35Z-
dc.date.available2022-11-29T01:43:35Z-
dc.date.issued2020-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/23028-
dc.description.abstractBACKGROUND: By investigating treatment patterns and outcomes in locally advanced head and neck squamous cell carcinoma (LA-HNSCC), we aimed at providing valuable insights into the optimal therapeutic strategy for physicians in real-world practice. METHODS: This is a multi-institutional study enrolled the patients with stage III to IVB LA-HNSCC, except for nasopharyngeal carcinoma, from 2004 to 2015 in thirteen referral hospitals capable of multidisciplinary care. RESULTS: A total of 445 LA-HNSCC patients were analyzed. The median age was 61 years (range, 24-89). The primary tumor location was the oropharynx in 191 (43%), oral cavity in 106 (24%), hypopharynx in 64 (14%), larynx in 57 (13%) and other sites in 27 (6%). The most common stage was T2 in 172 (39%), and N2 in 245 (55%). Based on treatment intents, 229 (52%) of the patients received definitive concurrent chemoradiotherapy (CCRT) and 187 (42%) underwent surgery. Approximately 158 (36%) of the study population received induction chemotherapy (IC). Taken together, 385 (87%) of the patients underwent combined therapeutic modalities. The regimen for definitive CCRT was weekly cisplatin in 58%, 3-weekly cisplatin in 28% and cetuximab in 3%. The preferred regimen for IC was docetaxel with cisplatin in 49%, and docetaxel, cisplatin plus fluorouracil in 27%. With a median follow-up of 39 months, one-year and two-year survival rates were 89 and 80%, respectively. Overall survival was not significantly different between CCRT and surgery group (p = 0.620). CONCLUSIONS: In patients with LA-HNSCC, the majority of patients received combined therapeutic modalities. Definitive CCRT, IC then definitive CCRT, and surgery followed by adjuvant CCRT or radiotherapy are the preferred multidisciplinary strategies in real-world practice.-
dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAntimetabolites, Antineoplastic-
dc.subject.MESHAntineoplastic Agents, Immunological-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols-
dc.subject.MESHCetuximab-
dc.subject.MESHChemoradiotherapy-
dc.subject.MESHCisplatin-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHDocetaxel-
dc.subject.MESHFemale-
dc.subject.MESHFluorouracil-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHHead and Neck Neoplasms-
dc.subject.MESHHumans-
dc.subject.MESHInduction Chemotherapy-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHProgression-Free Survival-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHSquamous Cell Carcinoma of Head and Neck-
dc.subject.MESHSurvival Rate-
dc.subject.MESHYoung Adult-
dc.titleTreatment strategy and outcomes in locally advanced head and neck squamous cell carcinoma: a nationwide retrospective cohort study (KCSG HN13-01)-
dc.typeArticle-
dc.identifier.pmid32854649-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450571-
dc.subject.keywordLocally advanced head and neck cancer-
dc.subject.keywordSquamous cell carcinoma-
dc.subject.keywordMultidisciplinary treatment-
dc.subject.keywordStrategy-
dc.contributor.affiliatedAuthorChoi, JH-
dc.type.localJournal Papers-
dc.identifier.doi10.1186/s12885-020-07297-z-
dc.citation.titleBMC cancer-
dc.citation.volume20-
dc.citation.number1-
dc.citation.date2020-
dc.citation.startPage813-
dc.citation.endPage813-
dc.identifier.bibliographicCitationBMC cancer, 20(1). : 813-813, 2020-
dc.identifier.eissn1471-2407-
dc.relation.journalidJ014712407-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
Files in This Item:
32854649.pdfDownload

qrcode

해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse