E. Wesselink , D.E. Kok , K.C. Smit , A.-S. van Lanen , J.W.G. Derksen , M. Koopman , M. Ligtenberg , I.D. Nagtegaal , P.D.M. Rombout , J.H.W. de Wilt , E. Kampman , A.M. May , F.J.B. van Duijnhoven
{"title":"基于共同分子肿瘤特征的患者亚组中饮食和生活方式炎症评分与结肠癌复发的关系","authors":"E. Wesselink , D.E. Kok , K.C. Smit , A.-S. van Lanen , J.W.G. Derksen , M. Koopman , M. Ligtenberg , I.D. Nagtegaal , P.D.M. Rombout , J.H.W. de Wilt , E. Kampman , A.M. May , F.J.B. van Duijnhoven","doi":"10.1016/j.esmogo.2025.100202","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>The aim of this study was to investigate associations between the inflammatory potential of diet and lifestyle in relation to colon cancer recurrence in subgroups of patients based on molecular tumour characteristics that also influence the inflammatory tumour microenvironment.</div></div><div><h3>Patients and methods</h3><div>A nested case-control study was implemented in two prospective cohort studies of colon cancer patients. Participants who developed a recurrence were included as cases (<em>n</em> = 167). Matched controls (<em>n</em> = 668) were selected based on incidence density sampling. Lifestyle factors were assessed at diagnosis using self-administered questionnaires and dietary intake was assessed using a food frequency questionnaire. The dietary inflammation score (DIS) and the lifestyle inflammation score (LIS) were constructed. High-throughput next-generation sequencing of tumour tissue was used for mutation and microsatellite instability (MSI) analysis. Associations between the DIS and LIS and recurrence were assessed with conditional logistic regression analyses in all patients, as well as in subgroups based on MSI. For patients with microsatellite stable (MSS) tumours, further stratification based on mutation status of <em>KRAS, BRAF, PIK3CA, TP53</em> and <em>APC</em> was performed.</div></div><div><h3>Results</h3><div>A more pro-inflammatory diet was not associated with risk of recurrence [incidence rate ratio (IRR) 1.04, 95% confidence interval (CI) 0.96-1.12]. Persons who have a more pro-inflammatory lifestyle may have an increased recurrence risk (IRR 1.21, 95% CI 0.97-1.52), which was most pronounced for persons with MSS and <em>KRAS</em> or <em>PIK3CA</em> wildtype tumours (IRR 1.31, 95% CI 0.90-1.90 and IRR 1.30, 95% CI 0.98-1.71, respectively).</div></div><div><h3>Conclusion</h3><div>Our results suggest that associations between the LIS and recurrence might differ based on molecular tumour characteristics.</div></div>","PeriodicalId":100490,"journal":{"name":"ESMO Gastrointestinal Oncology","volume":"9 ","pages":"Article 100202"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dietary and lifestyle inflammation scores in relation to colon cancer recurrence in subgroups of patients based on common molecular tumour characteristics\",\"authors\":\"E. Wesselink , D.E. Kok , K.C. Smit , A.-S. van Lanen , J.W.G. Derksen , M. Koopman , M. Ligtenberg , I.D. Nagtegaal , P.D.M. Rombout , J.H.W. de Wilt , E. Kampman , A.M. May , F.J.B. van Duijnhoven\",\"doi\":\"10.1016/j.esmogo.2025.100202\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>The aim of this study was to investigate associations between the inflammatory potential of diet and lifestyle in relation to colon cancer recurrence in subgroups of patients based on molecular tumour characteristics that also influence the inflammatory tumour microenvironment.</div></div><div><h3>Patients and methods</h3><div>A nested case-control study was implemented in two prospective cohort studies of colon cancer patients. Participants who developed a recurrence were included as cases (<em>n</em> = 167). Matched controls (<em>n</em> = 668) were selected based on incidence density sampling. Lifestyle factors were assessed at diagnosis using self-administered questionnaires and dietary intake was assessed using a food frequency questionnaire. The dietary inflammation score (DIS) and the lifestyle inflammation score (LIS) were constructed. High-throughput next-generation sequencing of tumour tissue was used for mutation and microsatellite instability (MSI) analysis. Associations between the DIS and LIS and recurrence were assessed with conditional logistic regression analyses in all patients, as well as in subgroups based on MSI. For patients with microsatellite stable (MSS) tumours, further stratification based on mutation status of <em>KRAS, BRAF, PIK3CA, TP53</em> and <em>APC</em> was performed.</div></div><div><h3>Results</h3><div>A more pro-inflammatory diet was not associated with risk of recurrence [incidence rate ratio (IRR) 1.04, 95% confidence interval (CI) 0.96-1.12]. Persons who have a more pro-inflammatory lifestyle may have an increased recurrence risk (IRR 1.21, 95% CI 0.97-1.52), which was most pronounced for persons with MSS and <em>KRAS</em> or <em>PIK3CA</em> wildtype tumours (IRR 1.31, 95% CI 0.90-1.90 and IRR 1.30, 95% CI 0.98-1.71, respectively).</div></div><div><h3>Conclusion</h3><div>Our results suggest that associations between the LIS and recurrence might differ based on molecular tumour characteristics.</div></div>\",\"PeriodicalId\":100490,\"journal\":{\"name\":\"ESMO Gastrointestinal Oncology\",\"volume\":\"9 \",\"pages\":\"Article 100202\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ESMO Gastrointestinal Oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949819825000718\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ESMO Gastrointestinal Oncology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949819825000718","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本研究的目的是基于影响炎症性肿瘤微环境的分子肿瘤特征,调查饮食和生活方式与结肠癌复发相关亚组患者炎症潜力之间的关系。患者和方法在两项结肠癌患者前瞻性队列研究中实施巢式病例对照研究。复发的参与者被纳入病例(n = 167)。根据发病率密度抽样选择匹配对照(n = 668)。生活方式因素在诊断时使用自我管理问卷进行评估,饮食摄入使用食物频率问卷进行评估。构建饮食炎症评分(DIS)和生活方式炎症评分(LIS)。肿瘤组织的高通量下一代测序用于突变和微卫星不稳定性(MSI)分析。在所有患者以及基于MSI的亚组中,通过条件logistic回归分析评估DIS和LIS与复发之间的关系。对于微卫星稳定型(MSS)肿瘤患者,根据KRAS、BRAF、PIK3CA、TP53和APC的突变状态进行进一步分层。结果促炎饮食与复发风险无相关性[发病率比(IRR) 1.04, 95%可信区间(CI) 0.96 ~ 1.12]。具有更促炎生活方式的人可能有更高的复发风险(IRR 1.21, 95% CI 0.97-1.52),这在MSS和KRAS或PIK3CA野生型肿瘤患者中最为明显(IRR 1.31, 95% CI 0.90-1.90和IRR 1.30, 95% CI 0.98-1.71)。结论:LIS与复发的关系可能因肿瘤分子特征而异。
Dietary and lifestyle inflammation scores in relation to colon cancer recurrence in subgroups of patients based on common molecular tumour characteristics
Background
The aim of this study was to investigate associations between the inflammatory potential of diet and lifestyle in relation to colon cancer recurrence in subgroups of patients based on molecular tumour characteristics that also influence the inflammatory tumour microenvironment.
Patients and methods
A nested case-control study was implemented in two prospective cohort studies of colon cancer patients. Participants who developed a recurrence were included as cases (n = 167). Matched controls (n = 668) were selected based on incidence density sampling. Lifestyle factors were assessed at diagnosis using self-administered questionnaires and dietary intake was assessed using a food frequency questionnaire. The dietary inflammation score (DIS) and the lifestyle inflammation score (LIS) were constructed. High-throughput next-generation sequencing of tumour tissue was used for mutation and microsatellite instability (MSI) analysis. Associations between the DIS and LIS and recurrence were assessed with conditional logistic regression analyses in all patients, as well as in subgroups based on MSI. For patients with microsatellite stable (MSS) tumours, further stratification based on mutation status of KRAS, BRAF, PIK3CA, TP53 and APC was performed.
Results
A more pro-inflammatory diet was not associated with risk of recurrence [incidence rate ratio (IRR) 1.04, 95% confidence interval (CI) 0.96-1.12]. Persons who have a more pro-inflammatory lifestyle may have an increased recurrence risk (IRR 1.21, 95% CI 0.97-1.52), which was most pronounced for persons with MSS and KRAS or PIK3CA wildtype tumours (IRR 1.31, 95% CI 0.90-1.90 and IRR 1.30, 95% CI 0.98-1.71, respectively).
Conclusion
Our results suggest that associations between the LIS and recurrence might differ based on molecular tumour characteristics.