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Comparison of the Clinical Outcomes of Patients with Squamous Cell Carcinoma of the Tonsil Receiving Postoperative Ipsilateral Versus Bilateral Neck Radiotherapy: A Propensity Score Matching Analysis (KROG 11-07)

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dc.contributor.authorKim, Y-
dc.contributor.authorCho, KH-
dc.contributor.authorMoon, SH-
dc.contributor.authorLee, CG-
dc.contributor.authorKeum, KC-
dc.contributor.authorLee, SW-
dc.contributor.authorAhn, YC-
dc.contributor.authorOh, D-
dc.contributor.authorKim, YS-
dc.contributor.authorWon, YK-
dc.contributor.authorWu, HG-
dc.contributor.authorHah, JH-
dc.contributor.authorOh, YT-
dc.date.accessioned2018-08-24T01:50:16Z-
dc.date.available2018-08-24T01:50:16Z-
dc.date.issued2017-
dc.identifier.issn1598-2998-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/16152-
dc.description.abstractPURPOSE: The impact of postoperative ipsilateral neck radiotherapy (INRT) versus bilateral neck radiotherapy (BNRT) on the clinical outcomes of patients with tonsillar squamous cell carcinoma was analyzed retrospectively.
MATERIALS AND METHODS: Between October 2001 and June 2012, 241 patients with T1-2 and N0-N2b tonsillar carcinoma from 16 institutes underwent postoperative INRT (n=84) or BNRT (n=157) following a tonsillectomy. Seventy patients were identified from each group by propensity score matching and compared in terms of the overall survival (OS), disease-free survival (DFS), locoregional relapse-free survival (LRRFS), and distant metastasis-free survival (DMFS) rates calculated using the Kaplan-Meier method with a log-rank test.
RESULTS: The median follow-up was 55 months (range, 3 to 133 months). The survival outcomes in the INRT and BNRT groups were similar: 5-year OS (92.8% vs. 94.0%, p=0.985), DFS (80.5% vs. 94.2%. p=0.085), LRRFS (88.1% vs. 97.1%, p=0.083), and DMFS (92.7% vs. 97.0%, p=0.370). Subgroup analysis revealed no contralateral neck recurrence in 61 patients with T1-2N0-2a regardless of the treatment groups. For 79 patients with N2b, contralateral neck recurrence was more common in the INRT group than in the BNRT group (7.9% vs. 0.0%), but the difference was not significant (p=0.107). The overall grade >/= 2 toxicities were lower in the INRT group: acute (45.7% vs. 74.3%, p=0.001) and late (4.3% vs. 31.4%, p < 0.001), respectively.
CONCLUSION: INRT is an attractive strategy for patients with T1-2N0-2a tonsillar carcinoma compared to BNRT. For patients with N2b, there was a small risk of contralateral neck recurrence when treated with INRT, but its impact on the OS was limited with successful salvage treatment.
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dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHCarcinoma, Squamous Cell-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHFemale-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Grading-
dc.subject.MESHNeoplasm Recurrence, Local-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHPostoperative Care-
dc.subject.MESHPropensity Score-
dc.subject.MESHRadiotherapy, Adjuvant-
dc.subject.MESHSurvival Analysis-
dc.subject.MESHTonsillar Neoplasms-
dc.subject.MESHTonsillectomy-
dc.subject.MESHTreatment Failure-
dc.subject.MESHTreatment Outcome-
dc.titleComparison of the Clinical Outcomes of Patients with Squamous Cell Carcinoma of the Tonsil Receiving Postoperative Ipsilateral Versus Bilateral Neck Radiotherapy: A Propensity Score Matching Analysis (KROG 11-07)-
dc.typeArticle-
dc.identifier.pmid28183163-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654171/-
dc.contributor.affiliatedAuthor오, 영택-
dc.type.localJournal Papers-
dc.identifier.doi10.4143/crt.2016.425-
dc.citation.titleCancer research and treatment-
dc.citation.volume49-
dc.citation.number4-
dc.citation.date2017-
dc.citation.startPage1097-
dc.citation.endPage1105-
dc.identifier.bibliographicCitationCancer research and treatment, 49(4). : 1097-1105, 2017-
dc.identifier.eissn2005-9256-
dc.relation.journalidJ015982998-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Radiation Oncology
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