Risk of metachronous neoplasia in early-onset colorectal cancer: meta-analysis

被引:0
作者
Pellino, Gianluca [1 ]
Fuschillo, Giacomo [2 ]
Gonzalez-Sarmiento, Rogelio [3 ]
Marti-Gallostra, Marc [1 ]
Selvaggi, Francesco [2 ]
Espin-Basany, Eloy [1 ]
Perea, Jose [3 ,4 ]
机构
[1] Univ Autonoma Barcelona UAB, Vall dHebron Univ Hosp, Colorectal Surg, Passeig Vall Hebron 119-129, Barcelona 08035, Spain
[2] Univ Studi Campania Luigi Vanvitelli, Dept Adv Med & Surg Sci, Colorectal Surg, Naples, Italy
[3] Biomed Res Inst Salamanca IBSAL, Mol Med, Salamanca, Spain
[4] Vithas Arturo Soria Univ Hosp, Dept Surg, Madrid 28043, Spain
关键词
MICROSATELLITE INSTABILITY; COLONOSCOPY SURVEILLANCE; YOUNG-PATIENTS; COLON-CANCER; RESECTION; SURGERY; CARCINOMAS; PREDICTS; OUTCOMES; AGE;
D O I
10.1093/bjsopen/zrae092
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Metachronous colorectal cancer refers to patients developing a second colorectal neoplasia diagnosed at least 6 months after the initial cancer diagnosis, excluding recurrence. The aim of this systematic review is to assess the incidence of metachronous colorectal cancer in early-onset colorectal cancer (defined as age at diagnosis of less than 50 years) and to identify risk factors.Methods This is a systematic review and meta-analysis performed following the PRISMA statement and registered on PROSPERO. The literature search was conducted in PubMed and Embase. Only studies involving patients with early-onset colorectal cancer (less than 50 years old) providing data on metachronous colorectal cancer were included in the analysis. The primary endpoint was the risk of metachronous colorectal cancer in patients with early-onset colorectal cancer. Secondary endpoints were association with Lynch syndrome, family history and microsatellite instability.Results Sixteen studies met the inclusion criteria. The incidence of metachronous colorectal cancer was 2.6% (95% c.i. 2.287-3.007). The risk of developing metachronous colorectal cancer in early-onset colorectal cancer versus non-early-onset colorectal cancer patients demonstrated an OR of 0.93 (95% c.i. 0.760-1.141). The incidence of metachronous colorectal cancer in patients with Lynch syndrome was 18.43% (95% c.i. 15.396-21.780), and in patients with family history 10.52% (95% c.i. 5.555-17.659). The proportion of metachronous colorectal cancer tumours in the microsatellite instability population was 19.7% (95% c.i. 13.583-27.2422).Conclusion The risk of metachronous colorectal cancer in patients with early-onset colorectal cancer is comparable to those with advanced age, but it is higher in patients with Lynch syndrome, family history and microsatellite instability. This meta-analysis demonstrates the need to personalize the management of patients with early-onset colorectal cancer according to their risk factors. The risk of metachronous colorectal cancers in patients with early-onset colorectal cancer is comparable to those with advanced age, but they can occur later and be associated with family history and Lynch syndrome, advocating the need to identify the ideal follow-up pathways in this patient population.
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