Marco Dal Molin, Aaron Brant, Amanda L Blackford, James F Griffin, Koji Shindo, Thomas Barkley, Neda Rezaee, Ralph H Hruban, Christopher L Wolfgang, Michael Goggins
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We hypothesized that pathological differences in pancreatic cancers from OSA cases compared to non-OSA cases would implicate OSA in pancreatic cancer progression.</p><p><strong>Methods: </strong>We reviewed the medical records of 1031 patients who underwent surgical resection without neoadjuvant therapy for pancreatic ductal adenocarcinoma (PDAC) at Johns Hopkins Hospital between 2003 and 2014 and compared the TNM classification of their cancer and their overall survival by patient OSA status.</p><p><strong>Results: </strong>OSA cases were significantly more likely than non-OSA cases to have lymph node-negative tumors (37.7% vs. 21.8%, p = 0.004). Differences in the prevalence of nodal involvement of OSA vs. non-OSA cases were not associated with differences in other pathological characteristics such as tumor size, tumor location, resection margin status, vascular or perineural invasion, or other comorbidities more common to OSA cases (BMI, smoking, diabetes). A logistic regression model found that a diagnosis of OSA was an independent predictor of lymph node status (hazard ratio, 0.051, p = 0.038). Patients with OSA had similar overall survival compared to those without OSA (HR, 0.89, (0.65-1.24), p = 0.41).</p><p><strong>Conclusion: </strong>The observed pathological differences between OSA-associated and non-OSA-associated pancreatic cancers supports the hypothesis that OSA can influence the pathologic features of pancreatic ductal adenocarcinoma.</p>","PeriodicalId":31105,"journal":{"name":"Boletim de Pesquisa NELIC","volume":"17 1","pages":"e0164195"},"PeriodicalIF":0.0000,"publicationDate":"2016-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1371/journal.pone.0164195","citationCount":"12","resultStr":"{\"title\":\"Obstructive Sleep Apnea and Pathological Characteristics of Resected Pancreatic Ductal Adenocarcinoma.\",\"authors\":\"Marco Dal Molin, Aaron Brant, Amanda L Blackford, James F Griffin, Koji Shindo, Thomas Barkley, Neda Rezaee, Ralph H Hruban, Christopher L Wolfgang, Michael Goggins\",\"doi\":\"10.1371/journal.pone.0164195\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Prospective studies have identified obstructive sleep apnea (OSA) as a risk factor for increased overall cancer incidence and mortality. 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引用次数: 12
摘要
背景:前瞻性研究已经确定阻塞性睡眠呼吸暂停(OSA)是增加总体癌症发病率和死亡率的危险因素。阻塞性睡眠呼吸暂停在特定癌症风险或进展中的潜在作用尚不清楚。我们假设,与非OSA患者相比,OSA患者胰腺癌的病理差异可能暗示OSA与胰腺癌进展有关。方法:回顾2003年至2014年在约翰霍普金斯医院接受胰腺导管腺癌(pancreatic ductal adenocarcinoma, PDAC)手术切除且未接受新辅助治疗的1031例患者的医疗记录,通过患者OSA状态比较其肿瘤的TNM分型和总生存期。结果:OSA患者发生淋巴结阴性肿瘤的可能性明显高于非OSA患者(37.7% vs. 21.8%, p = 0.004)。OSA与非OSA患者淋巴结受累患病率的差异与其他病理特征的差异无关,如肿瘤大小、肿瘤位置、切除边缘状态、血管或神经周围浸润,或其他OSA患者更常见的合并症(BMI、吸烟、糖尿病)。logistic回归模型发现,OSA诊断是淋巴结状态的独立预测因子(风险比,0.051,p = 0.038)。OSA患者与非OSA患者的总生存期相似(HR, 0.89, (0.65-1.24), p = 0.41)。结论:OSA相关性与非OSA相关性胰腺癌的病理差异支持OSA影响胰腺导管腺癌病理特征的假说。
Obstructive Sleep Apnea and Pathological Characteristics of Resected Pancreatic Ductal Adenocarcinoma.
Background: Prospective studies have identified obstructive sleep apnea (OSA) as a risk factor for increased overall cancer incidence and mortality. The potential role of OSA in the risk or progression of specific cancers is not well known. We hypothesized that pathological differences in pancreatic cancers from OSA cases compared to non-OSA cases would implicate OSA in pancreatic cancer progression.
Methods: We reviewed the medical records of 1031 patients who underwent surgical resection without neoadjuvant therapy for pancreatic ductal adenocarcinoma (PDAC) at Johns Hopkins Hospital between 2003 and 2014 and compared the TNM classification of their cancer and their overall survival by patient OSA status.
Results: OSA cases were significantly more likely than non-OSA cases to have lymph node-negative tumors (37.7% vs. 21.8%, p = 0.004). Differences in the prevalence of nodal involvement of OSA vs. non-OSA cases were not associated with differences in other pathological characteristics such as tumor size, tumor location, resection margin status, vascular or perineural invasion, or other comorbidities more common to OSA cases (BMI, smoking, diabetes). A logistic regression model found that a diagnosis of OSA was an independent predictor of lymph node status (hazard ratio, 0.051, p = 0.038). Patients with OSA had similar overall survival compared to those without OSA (HR, 0.89, (0.65-1.24), p = 0.41).
Conclusion: The observed pathological differences between OSA-associated and non-OSA-associated pancreatic cancers supports the hypothesis that OSA can influence the pathologic features of pancreatic ductal adenocarcinoma.