Riall Taylor S, Stager Victoria M, Nealon William H, Townsend Courtney M, Kuo Yong-fang, Goodwin James S, Freeman Jean L
Department of Surgery, The University of Texas Medical Branch, Galveston, TX 77555-0542, USA.
J Am Coll Surg. 2007 May;204(5):803-13; discussion 813-4. doi: 10.1016/j.jamcollsurg.2007.01.015. Epub 2007 Mar 23.
Recent small studies have reported an incidence of 23% to 39% for additional primary cancers in patients with intraductal papillary mucinous neoplasms (IPMN) of the pancreas. There have been no population-based studies evaluating this incidence rate.
Using the Surveillance, Epidemiology, and End Results (SEER) database (1983 to 1991), we identified all patients with primary pancreatic cancers (sporadic and adenocarcinomas arising in IPMNs). We determined the incidence of additional primary cancers that developed either before or after the diagnosis of invasive IPMN and compared it to the incidence of additional primary cancers in patients with sporadic pancreatic adenocarcinoma.
Nineteen thousand six hundred forty-seven patients were reported with pancreatic cancer. Ninety-five percent of cancers were sporadic and 5.0% were invasive IPMNs. Ten point three percent had one or more extra-pancreatic primary cancers in addition to their pancreatic primary (10.3% in patients with sporadic adenocarcinoma and 10.1% in patients with invasive IPMNs, p = NS). The most common sites of additional primary cancers were colorectal (20.1%), breast (19.9%), prostate (16.6%), urinary system (11.1%), and lung (9.8%). In the 2,017 patients with additional primary cancer, 86% occurred before the diagnosis of pancreatic cancer and 14% occurred after the diagnosis of pancreatic cancer.
Our population-based analysis shows that the incidence of additional primary malignancies in patients with invasive IPMNs is 10%. Although not as high as previously reported in smaller studies, the incidence is significant and comparable to the incidence seen in patients with adenocarcinoma. Surveillance for other common malignancies in patients with IPMNs and pancreatic adenocarcinomas should be performed.
近期的小型研究报告称,胰腺导管内乳头状黏液性肿瘤(IPMN)患者中额外原发性癌症的发生率为23%至39%。尚未有基于人群的研究评估这一发生率。
利用监测、流行病学和最终结果(SEER)数据库(1983年至1991年),我们确定了所有原发性胰腺癌患者(散发性以及IPMN中发生的腺癌)。我们确定了在侵袭性IPMN诊断之前或之后发生的额外原发性癌症的发生率,并将其与散发性胰腺腺癌患者中额外原发性癌症的发生率进行比较。
报告了19647例胰腺癌患者。95%的癌症为散发性,5.0%为侵袭性IPMN。10.3%的患者除胰腺原发性癌症外还患有一种或多种胰腺外原发性癌症(散发性腺癌患者中为10.3%,侵袭性IPMN患者中为10.1%,p = 无显著性差异)。额外原发性癌症最常见的部位是结肠(20.1%)、乳腺(19.9%)、前列腺(16.6%)、泌尿系统(11.1%)和肺(9.8%)。在2017例患有额外原发性癌症的患者中,86%发生在胰腺癌诊断之前,14%发生在胰腺癌诊断之后。
我们基于人群的分析表明,侵袭性IPMN患者中额外原发性恶性肿瘤的发生率为10%。虽然不像之前小型研究报告的那么高,但该发生率具有显著性,且与腺癌患者中的发生率相当。应对IPMN和胰腺腺癌患者进行其他常见恶性肿瘤的监测。