Mi Rye Bae, Young Ha Lee, Jeong Heon Kim, Yoo-Sam Chung, Ji Heui Kim, Myeong Sang Yu
{"title":"鼻窦肉瘤的临床特征和预后:76例单院经验","authors":"Mi Rye Bae, Young Ha Lee, Jeong Heon Kim, Yoo-Sam Chung, Ji Heui Kim, Myeong Sang Yu","doi":"10.1002/lio2.70145","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objective</h3>\n \n <p>This study analyzed the clinical characteristics, treatment outcomes, and prognostic factors of sinonasal sarcomas through a single-institution experience involving 76 cases over 27 years.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A retrospective review was conducted on 76 patients diagnosed with sinonasal sarcoma at a tertiary medical center from 1995 to 2022. Data collected included demographic information, tumor characteristics, and treatment modalities. Survival outcomes were assessed using Kaplan–Meier analysis, and prognostic factors were identified through univariate and multivariate Cox proportional hazards models.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The cohort included 45 males and 31 females, with a mean age of 42.6 years. The most common presenting symptom was nasal obstruction (22%). Rhabdomyosarcoma was the most prevalent subtype, accounting for 27.6% of cases. The 5- and 10-year overall survival (OS) rates were 62% and 56%, while the disease-free survival (DFS) rates were 51% and 41%. Survival outcomes were significantly worse in patients aged ≥ 61 years (<i>p</i> = 0.030), with a smoking history (<i>p</i> = 0.005), or with neurovascular extension (<i>p</i> = 0.015). In the univariate analysis, smoking history increased the mortality risk by 2.95-fold (<i>p</i> = 0.008) and neurovascular involvement by 2.87-fold (<i>p</i> = 0.020). Multivariate Cox analysis confirmed smoking history as an independent predictor of mortality (HR = 2.38, 95% CI: 1.05–5.40, <i>p</i> = 0.038).</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>The results showed that advanced age, smoking history, and neurovascular involvement were key contributors to reduced survival, with identified as a significant independent predictors of higher mortality risk. These findings offer critical insight into the therapeutic management of this rare malignancy.</p>\n </section>\n \n <section>\n \n <h3> Level of Evidence</h3>\n \n <p>4</p>\n </section>\n </div>","PeriodicalId":48529,"journal":{"name":"Laryngoscope Investigative Otolaryngology","volume":"10 2","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.70145","citationCount":"0","resultStr":"{\"title\":\"Clinical Features and Prognostic Insights in Sinonasal Sarcomas: A 76-Case Single-Institution Experience\",\"authors\":\"Mi Rye Bae, Young Ha Lee, Jeong Heon Kim, Yoo-Sam Chung, Ji Heui Kim, Myeong Sang Yu\",\"doi\":\"10.1002/lio2.70145\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>This study analyzed the clinical characteristics, treatment outcomes, and prognostic factors of sinonasal sarcomas through a single-institution experience involving 76 cases over 27 years.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>A retrospective review was conducted on 76 patients diagnosed with sinonasal sarcoma at a tertiary medical center from 1995 to 2022. Data collected included demographic information, tumor characteristics, and treatment modalities. Survival outcomes were assessed using Kaplan–Meier analysis, and prognostic factors were identified through univariate and multivariate Cox proportional hazards models.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>The cohort included 45 males and 31 females, with a mean age of 42.6 years. The most common presenting symptom was nasal obstruction (22%). Rhabdomyosarcoma was the most prevalent subtype, accounting for 27.6% of cases. The 5- and 10-year overall survival (OS) rates were 62% and 56%, while the disease-free survival (DFS) rates were 51% and 41%. Survival outcomes were significantly worse in patients aged ≥ 61 years (<i>p</i> = 0.030), with a smoking history (<i>p</i> = 0.005), or with neurovascular extension (<i>p</i> = 0.015). In the univariate analysis, smoking history increased the mortality risk by 2.95-fold (<i>p</i> = 0.008) and neurovascular involvement by 2.87-fold (<i>p</i> = 0.020). Multivariate Cox analysis confirmed smoking history as an independent predictor of mortality (HR = 2.38, 95% CI: 1.05–5.40, <i>p</i> = 0.038).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>The results showed that advanced age, smoking history, and neurovascular involvement were key contributors to reduced survival, with identified as a significant independent predictors of higher mortality risk. These findings offer critical insight into the therapeutic management of this rare malignancy.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Level of Evidence</h3>\\n \\n <p>4</p>\\n </section>\\n </div>\",\"PeriodicalId\":48529,\"journal\":{\"name\":\"Laryngoscope Investigative Otolaryngology\",\"volume\":\"10 2\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-04-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.70145\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laryngoscope Investigative Otolaryngology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/lio2.70145\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OTORHINOLARYNGOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laryngoscope Investigative Otolaryngology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/lio2.70145","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
Clinical Features and Prognostic Insights in Sinonasal Sarcomas: A 76-Case Single-Institution Experience
Objective
This study analyzed the clinical characteristics, treatment outcomes, and prognostic factors of sinonasal sarcomas through a single-institution experience involving 76 cases over 27 years.
Methods
A retrospective review was conducted on 76 patients diagnosed with sinonasal sarcoma at a tertiary medical center from 1995 to 2022. Data collected included demographic information, tumor characteristics, and treatment modalities. Survival outcomes were assessed using Kaplan–Meier analysis, and prognostic factors were identified through univariate and multivariate Cox proportional hazards models.
Results
The cohort included 45 males and 31 females, with a mean age of 42.6 years. The most common presenting symptom was nasal obstruction (22%). Rhabdomyosarcoma was the most prevalent subtype, accounting for 27.6% of cases. The 5- and 10-year overall survival (OS) rates were 62% and 56%, while the disease-free survival (DFS) rates were 51% and 41%. Survival outcomes were significantly worse in patients aged ≥ 61 years (p = 0.030), with a smoking history (p = 0.005), or with neurovascular extension (p = 0.015). In the univariate analysis, smoking history increased the mortality risk by 2.95-fold (p = 0.008) and neurovascular involvement by 2.87-fold (p = 0.020). Multivariate Cox analysis confirmed smoking history as an independent predictor of mortality (HR = 2.38, 95% CI: 1.05–5.40, p = 0.038).
Conclusions
The results showed that advanced age, smoking history, and neurovascular involvement were key contributors to reduced survival, with identified as a significant independent predictors of higher mortality risk. These findings offer critical insight into the therapeutic management of this rare malignancy.