The potential for malignancy from atopic disorders and allergic inflammation: A systematic review and meta‐analysis

医学 肺癌 哮喘 内科学 荟萃分析 恶性肿瘤 肿瘤科 癌症 皮肤癌 过敏 队列研究 入射(几何) 前瞻性队列研究 皮肤病科 免疫学 物理 光学
作者
Amanda B. Muir,Kelly A. Whelan,Michael Dougherty,Bailey Aaron,Brianna Navarre,Seema S. Aceves,Evan S. Dellon,Elizabeth T. Jensen
出处
期刊:Clinical & Experimental Allergy [Wiley]
卷期号:50 (2): 147-159 被引量:17
标识
DOI:10.1111/cea.13537
摘要

Abstract Objective While chronic inflammation is a well‐established risk factor for malignancy, studies evaluating the relationship between allergic inflammation and cancer have revealed conflicting results. Here, we aimed to assess the association between allergic inflammation in the lung (asthma), skin (eczema) or oesophagus (eosinophilic oesophagitis; EoE) and cancer at the organ site. Design We conducted a systematic review of the literature to identify observational studies (case‐control, cohort and cross‐sectional) evaluating the association between asthma and lung cancer, eczema and skin cancer, or EoE and oesophageal cancer. Random‐effects meta‐analysis was performed to define pooled estimates of effects. Data sources PubMed, EMBASE and Web of Science. Eligibility criteria for selection Included studies evaluated the incidence of cancer. Results Thirty‐two studies met the inclusion criteria, 27 in the lung, four in the skin and one in the oesophagus. Meta‐analysis of the three studies with prospective data collection of asthma diagnosis revealed a positive association with incident lung cancer (OR 1.27, 95% CI 1.09‐1.44); however, this result was not consistently supported by the larger dataset of retrospective studies (OR 1.37, 95% CI 0.90‐1.83). Overall, studies in the lung displayed significant heterogeneity ( I 2 98%, P < .0001), but no significant effect modification on the association between asthma and lung cancer was identified for the variables of sex, smoking or study design. Meta‐analysis could not be applied to the four papers reviewed in the skin, but three suggested an association between eczema and non‐melanoma skin cancer, while the remaining study failed to identify an association between melanoma and eczema. A single study meeting inclusion criteria showed no association between EoE and oesophageal malignancy. Conclusions The current data cannot exclude the possibility of an association between atopy and malignancy the lung, skin and oesophagus. The relationship between allergy and cancer should be explored further in prospective studies that any association identified between these conditions has the potential for significant public health implications.
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