Early-onset colorectal cancer: A review of current knowledge

被引:64
作者
Saraiva, Margarida R. [1 ]
Rosa, Isadora [1 ,2 ]
Claro, Isabel [1 ]
机构
[1] Inst Portugues Oncol Francisco Gentil, Dept Gastroenterol, P-1099023 Lisbon, Portugal
[2] Inst Portugues Oncol Francisco Gentil, Dept Gastroenterol, Rua Prof Lima Bastos, P-1099023 Lisbon, Portugal
关键词
Colorectal cancer; Early-onset; Adenocarcinoma; Hereditary; Birth-cohort effect; Risk factors; CLINICAL-PRACTICE GUIDELINES; SUSCEPTIBILITY GENE-MUTATIONS; COLON-CANCER; YOUNG-ONSET; AMERICAN-SOCIETY; AVERAGE-RISK; CLINICOPATHOLOGICAL FEATURES; MICROSATELLITE INSTABILITY; MOLECULAR-FEATURES; AGE;
D O I
10.3748/wjg.v29.i8.1289
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colorectal cancer (CRC) is one of the most prevalent malignancies worldwide. Although most prevalent among older people, its incidence above 50 years old has been decreasing globally in the last decades, probably as a result of better screening. Paradoxically, its incidence in patients below 50 years old [early-onset CRC (EO-CRC)] has been increasing, for reasons not yet fully understood. EO-CRC's increasing incidence is genre independent but shows racial disparities and has been described to occur worldwide. It follows a birth-cohort effect which probably reflects a change in exposure to CRC risk factors. Its incidence is predicted to double until 2030, which makes EO-CRC a serious public health issue. Both modifiable and non-modifiable risk factors have been identified - some are potential targets for preventive measures. EO-CRC is often diagnosed at advanced stages and histological features associated with poor prognosis have been described. EO-CRC presents some distinctive features: Microsatellite in-stability is common, but another subtype of tumours, both microsatellite and chromosome stable also seems relevant. There are no age-specific treatment protocols and studies on EO-CRC survival rates have shown conflicting data. Due to the higher germline pathological mutations found in EO-CRC patients, an accurate genetic risk evaluation should be performed. In this review, we summarize the current evidence on epidemiological, clinical, histopathological and molecular features of EO-CRC and discuss the contribution of genetics and lifestyle risk factors. We further comment on screening strategies and specific dimensions to consider when dealing with a younger cancer patient.
引用
收藏
页码:1289 / 1303
页数:15
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