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基于磁共振成像的瑞典胰腺癌风险人群筛查计划的短期结果。

Short-term Results of a Magnetic Resonance Imaging-Based Swedish Screening Program for Individuals at Risk for Pancreatic Cancer.

机构信息

Division of Surgery, Department of Clinical Science, Intervention, and Technology (CLINTEC), Karolinska Institute, Stockholm, Sweden.

Division of Pathology, Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.

出版信息

JAMA Surg. 2015 Jun;150(6):512-8. doi: 10.1001/jamasurg.2014.3852.

Abstract

IMPORTANCE

Pancreatic cancer is the fourth leading cause of cancer-related death in Western countries. In approximately 10% of all patients with pancreatic cancer, it is possible to define a positive family history for pancreatic cancer or for one of the other related genetic syndromes. A screening program for individuals at risk is recommended; however, surveillance modalities have not been defined yet.

OBJECTIVE

To analyze the short-term results of a prospective clinical surveillance program for individuals at risk for pancreatic cancer using a noninvasive magnetic resonance imaging (MRI)-based screening protocol.

DESIGN, SETTING AND PARTICIPANTS: A prospective observational study of all patients with a genetic risk for developing pancreatic cancer who were referred to Karolinska University Hospital between January 1, 2010, and January 31, 2013, using an MRI-based surveillance program. All patients were investigated for the most common genetic mutations associated with pancreatic cancer.

EXPOSURE

A noninvasive MRI-based screening protocol.

MAIN OUTCOMES AND MEASURES

The ability of MRI to identify potential precancerous or early cancers in individuals at risk for pancreatic cancer.

RESULTS

Forty patients (24 women and 16 men) were enrolled. The mean age was 49.9 years. The mean length of follow-up was 12.9 months. The numbers of relatives affected by pancreatic cancer were 5 in 2 patients (5%), 4 in 5 patients (12.5%), 3 in 17 patients (42.5%), 2 in 14 patients (35%), and 1 in 2 patients (5%). In 4 patients (10%), a p16 mutation was found; in 3, a BRCA2 mutation (7.5%); and in 1, a BRCA1 mutation (2.5%). In 16 patients (40%), MRI revealed a pancreatic lesion: intraductal papillary mucinous neoplasia (14 patients, 35%) and pancreatic ductal adenocarcinoma (2 patients, 5%). One patient had a synchronous intraductal papillary mucinous neoplasia and pancreatic ductal adenocarcinoma. Five patients (12.5%) required surgery (3 for pancreatic ductal adenocarcinoma and 2 for intraductal papillary mucinous neoplasia), while the remaining 35 are under continued surveillance.

CONCLUSIONS AND RELEVANCE

During a median follow-up of approximately 1 year, pancreatic lesions were detected in 40% of the patients, of whom 5 underwent surgery. Although the study time was relatively short, the surveillance program in individuals at risk seems to be effective.

摘要

重要性

在西方国家,胰腺癌是导致癌症相关死亡的第四大原因。在大约 10%的胰腺癌患者中,可以明确存在胰腺癌阳性家族史或其他相关遗传综合征。建议对高危个体进行筛查计划;然而,监测方式尚未确定。

目的

使用基于磁共振成像(MRI)的非侵入性筛查方案,分析针对胰腺癌高危个体的前瞻性临床监测计划的短期结果。

设计、地点和参与者:这是一项针对 2010 年 1 月 1 日至 2013 年 1 月 31 日期间在卡罗林斯卡大学医院就诊的具有遗传风险的胰腺癌患者的前瞻性观察性研究,采用基于 MRI 的监测方案。所有患者均接受了最常见的与胰腺癌相关的遗传突变检查。

暴露

基于 MRI 的非侵入性筛查方案。

主要结果和措施

MRI 识别具有胰腺癌遗传风险个体中潜在癌前或早期癌症的能力。

结果

共纳入 40 名患者(24 名女性和 16 名男性),平均年龄为 49.9 岁,平均随访时间为 12.9 个月。受胰腺癌影响的亲属数量如下:2 名患者(5%)5 名,5 名患者(12.5%)4 名,17 名患者(42.5%)3 名,14 名患者(35%)2 名,2 名患者(5%)1 名。4 名患者(10%)发现 p16 突变,3 名患者(7.5%)发现 BRCA2 突变,1 名患者(2.5%)发现 BRCA1 突变。16 名患者(40%)MRI 显示胰腺病变:导管内乳头状黏液性肿瘤(14 名患者,35%)和胰腺导管腺癌(2 名患者,5%)。1 名患者同时患有导管内乳头状黏液性肿瘤和胰腺导管腺癌。5 名患者(12.5%)需要手术(3 名用于胰腺导管腺癌,2 名用于导管内乳头状黏液性肿瘤),其余 35 名患者仍在继续监测。

结论和相关性

在大约 1 年的中位随访期间,40%的患者发现胰腺病变,其中 5 名患者接受了手术。尽管研究时间相对较短,但高危个体的监测计划似乎是有效的。

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