Small bowel cancers: A population-based analysis of epidemiology, treatment and outcomes in Ontario, Canada from 2005-2020

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Abstract

Introduction

Small bowel cancers are uncommon malignancies comprised of several histologies with variable treatments and prognoses. The current study describes the epidemiology, treatment, and outcomes of a large, population-based cohort of patients with small bowel cancers.

Methods

We performed a retrospective cohort study using linked administrative healthcare data from Ontario, Canada. Patients diagnosed with a small bowel cancer between 2005–2020 were included. Trends in incidence, treatments, and survival were explored by histology (adenocarcinoma, neuroendocrine tumors (NET), gastrointestinal stromal tumors (GIST), and lymphoma).

Results

A total of 5306 patients with small bowel cancers were identified. The most common histologies were NET (40.5 %) and adenocarcinoma (31.6 %). Over the study period the annual incidence of small bowel cancers increased from 1.54 to 2.78 per 100 000 and the likelihoods of receiving surgery and systemic therapy within one year of diagnosis both increased for all histologic subtypes except lymphoma. Median overall survival from diagnosis was 1.0 year for adenocarcinoma, 13.2 years for NET, 14.2 years for GIST, and 10.1 years for lymphoma. There was no trend towards improved median survival for adenocarcinoma by year of diagnosis; 0.94 years (2005–2010), 1.07 years (2011–2015), and 0.98 years (2016–2020).

Discussion

Small bowel cancers are increasing in incidence, with increasing use of surgery and systemic therapies. While survival is favourable for many small bowel cancers, it remains poor for adenocarcinoma. Better availability of cancer stage data and detailed histopathology within the database would facilitate future research.

Synopsis

This study of small bowel cancer in Ontario from 2005 to 2020 demonstrated increasing incidence, use of surgery, and systemic treatments. The most common histologies are neuroendocrine tumors and adenocarcinoma, with median survivals of 13.2 and 1.0 years respectively.

小肠癌:2005-2020 年加拿大安大略省基于人口的流行病学、治疗和结果分析
导言小肠癌是一种不常见的恶性肿瘤,由多种组织结构组成,治疗方法和预后各不相同。本研究描述了一个基于人群的大型小肠癌患者队列的流行病学、治疗和预后情况。方法我们利用加拿大安大略省的相关行政医疗数据进行了一项回顾性队列研究。研究纳入了 2005-2020 年间确诊的小肠癌患者。按组织学(腺癌、神经内分泌肿瘤(NET)、胃肠道间质瘤(GIST)和淋巴瘤)探讨了发病率、治疗和生存趋势。最常见的组织类型是NET(40.5%)和腺癌(31.6%)。在研究期间,小肠癌的年发病率从每十万人中 1.54 例增加到 2.78 例,除淋巴瘤外,所有组织学亚型的患者在确诊后一年内接受手术和系统治疗的几率都有所增加。腺癌确诊后的中位总生存期为 1.0 年,NET 为 13.2 年,GIST 为 14.2 年,淋巴瘤为 10.1 年。腺癌的中位生存期没有按诊断年份提高的趋势:0.94 年(2005-2010 年)、1.07 年(2011-2015 年)和 0.98 年(2016-2020 年)。虽然许多小肠癌的生存率较高,但腺癌的生存率仍然较低。这项关于 2005 年至 2020 年安大略省小肠癌的研究表明,小肠癌的发病率、手术和系统治疗的使用率都在上升。最常见的组织类型是神经内分泌肿瘤和腺癌,中位生存期分别为 13.2 年和 1.0 年。
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