Olamide O. Omidele, Christopher Connors, Nikhil Wainganker, Ketan Badani, John Sfakianos, Reza Mehrazin, Isuru Jayaratna
{"title":"预后因素和治疗对肾脏神经内分泌肿瘤患者总生存期的影响","authors":"Olamide O. Omidele, Christopher Connors, Nikhil Wainganker, Ketan Badani, John Sfakianos, Reza Mehrazin, Isuru Jayaratna","doi":"10.1002/bco2.341","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Renal neuroendocrine neoplasms (R-NEN) are exceptionally rare tumours characterized by high mortality rates.</p>\n </section>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>The objective of this study is to analyse prognostic factors and treatment impact on overall survival in patients with R-NEN.</p>\n </section>\n \n <section>\n \n <h3> Design, setting and participants</h3>\n \n <p>We identified all patients with R-NEN in the National Cancer Database (NCDB) from 2004 to 2019 and identified prognostic factors for improved survival.</p>\n </section>\n \n <section>\n \n <h3> Results and limitations</h3>\n \n <p>Of 542 R-NEN cases, 166 (31%) were neuroendocrine tumour grade 1 (NET-G1), 14 (3%) were neuroendocrine tumour grade 2 (NET-G2), 169 (31%) were neuroendocrine carcinoma (NEC-NOS), 18 (3%) were large cell neuroendocrine carcinoma (LC-NEC) and 175 (32%) were small cell neuroendocrine carcinoma (SC-NEC). Median overall survival for all patients in the study was 44.88 months (SE, 4.265; 95% CI, 27.57–62.19). Median overall survival was 7.89 months (SE 0.67; 95% CI, 6.58–9.20) for patients without surgical intervention and 136.61 months (SE 16.44; 95% CI, 104.38–168.84, <i>p</i> < 0.001) for patients who underwent surgery. Increased age (HR, 1.05; 95% CI, 1.03–1.06; <i>p</i> < 0.001), T4 stage disease (HR, 3.17; 95% CI, 1.96–5.1; <i>p</i> < 0.001), NEC-NOS histology (HR, 2.82; 95% CI, 1.64–4.86; <i>p</i> < 0.001), LC-NEC histology (HR, 2.73; 95% CI, 1.04–7.17; <i>p</i> = 0.041) and SC-NEC histology (HR, 5.17; 95% CI, 2.95–9.05; <i>p</i> < 0.001) were all positive predictors of worsening overall survival. The main limitation of the study is its retrospective design.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>R-NEN is an aggressive tumour characterized by high mortality rates. Surgery continues to be the mainstay of treatment and has shown to provide a survival benefit for most patients.</p>\n </section>\n \n <section>\n \n <h3> Patient Summary</h3>\n \n <p>R-NEN is composed of several tumour histologies that differ based on their aggressiveness with NEC-NOS and SC-NEC being the most lethal. Surgery, predominantly through minimally invasive approaches, is the mainstay of treatment and has a clear survival benefit.</p>\n </section>\n </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"5 6","pages":"576-584"},"PeriodicalIF":1.6000,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bco2.341","citationCount":"0","resultStr":"{\"title\":\"Prognostic factors and treatment impact on overall survival in patients with renal neuroendocrine tumour\",\"authors\":\"Olamide O. Omidele, Christopher Connors, Nikhil Wainganker, Ketan Badani, John Sfakianos, Reza Mehrazin, Isuru Jayaratna\",\"doi\":\"10.1002/bco2.341\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Renal neuroendocrine neoplasms (R-NEN) are exceptionally rare tumours characterized by high mortality rates.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>The objective of this study is to analyse prognostic factors and treatment impact on overall survival in patients with R-NEN.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Design, setting and participants</h3>\\n \\n <p>We identified all patients with R-NEN in the National Cancer Database (NCDB) from 2004 to 2019 and identified prognostic factors for improved survival.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results and limitations</h3>\\n \\n <p>Of 542 R-NEN cases, 166 (31%) were neuroendocrine tumour grade 1 (NET-G1), 14 (3%) were neuroendocrine tumour grade 2 (NET-G2), 169 (31%) were neuroendocrine carcinoma (NEC-NOS), 18 (3%) were large cell neuroendocrine carcinoma (LC-NEC) and 175 (32%) were small cell neuroendocrine carcinoma (SC-NEC). Median overall survival for all patients in the study was 44.88 months (SE, 4.265; 95% CI, 27.57–62.19). Median overall survival was 7.89 months (SE 0.67; 95% CI, 6.58–9.20) for patients without surgical intervention and 136.61 months (SE 16.44; 95% CI, 104.38–168.84, <i>p</i> < 0.001) for patients who underwent surgery. Increased age (HR, 1.05; 95% CI, 1.03–1.06; <i>p</i> < 0.001), T4 stage disease (HR, 3.17; 95% CI, 1.96–5.1; <i>p</i> < 0.001), NEC-NOS histology (HR, 2.82; 95% CI, 1.64–4.86; <i>p</i> < 0.001), LC-NEC histology (HR, 2.73; 95% CI, 1.04–7.17; <i>p</i> = 0.041) and SC-NEC histology (HR, 5.17; 95% CI, 2.95–9.05; <i>p</i> < 0.001) were all positive predictors of worsening overall survival. The main limitation of the study is its retrospective design.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>R-NEN is an aggressive tumour characterized by high mortality rates. Surgery continues to be the mainstay of treatment and has shown to provide a survival benefit for most patients.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Patient Summary</h3>\\n \\n <p>R-NEN is composed of several tumour histologies that differ based on their aggressiveness with NEC-NOS and SC-NEC being the most lethal. Surgery, predominantly through minimally invasive approaches, is the mainstay of treatment and has a clear survival benefit.</p>\\n </section>\\n </div>\",\"PeriodicalId\":72420,\"journal\":{\"name\":\"BJUI compass\",\"volume\":\"5 6\",\"pages\":\"576-584\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2024-03-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bco2.341\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BJUI compass\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/bco2.341\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BJUI compass","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bco2.341","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Prognostic factors and treatment impact on overall survival in patients with renal neuroendocrine tumour
Background
Renal neuroendocrine neoplasms (R-NEN) are exceptionally rare tumours characterized by high mortality rates.
Objective
The objective of this study is to analyse prognostic factors and treatment impact on overall survival in patients with R-NEN.
Design, setting and participants
We identified all patients with R-NEN in the National Cancer Database (NCDB) from 2004 to 2019 and identified prognostic factors for improved survival.
Results and limitations
Of 542 R-NEN cases, 166 (31%) were neuroendocrine tumour grade 1 (NET-G1), 14 (3%) were neuroendocrine tumour grade 2 (NET-G2), 169 (31%) were neuroendocrine carcinoma (NEC-NOS), 18 (3%) were large cell neuroendocrine carcinoma (LC-NEC) and 175 (32%) were small cell neuroendocrine carcinoma (SC-NEC). Median overall survival for all patients in the study was 44.88 months (SE, 4.265; 95% CI, 27.57–62.19). Median overall survival was 7.89 months (SE 0.67; 95% CI, 6.58–9.20) for patients without surgical intervention and 136.61 months (SE 16.44; 95% CI, 104.38–168.84, p < 0.001) for patients who underwent surgery. Increased age (HR, 1.05; 95% CI, 1.03–1.06; p < 0.001), T4 stage disease (HR, 3.17; 95% CI, 1.96–5.1; p < 0.001), NEC-NOS histology (HR, 2.82; 95% CI, 1.64–4.86; p < 0.001), LC-NEC histology (HR, 2.73; 95% CI, 1.04–7.17; p = 0.041) and SC-NEC histology (HR, 5.17; 95% CI, 2.95–9.05; p < 0.001) were all positive predictors of worsening overall survival. The main limitation of the study is its retrospective design.
Conclusion
R-NEN is an aggressive tumour characterized by high mortality rates. Surgery continues to be the mainstay of treatment and has shown to provide a survival benefit for most patients.
Patient Summary
R-NEN is composed of several tumour histologies that differ based on their aggressiveness with NEC-NOS and SC-NEC being the most lethal. Surgery, predominantly through minimally invasive approaches, is the mainstay of treatment and has a clear survival benefit.