Jayakrishnan Thejus, Ng Kimmie
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
JAMA. 2025 Jul 17. doi: 10.1001/jama.2025.10218.
Early-onset gastrointestinal (GI) cancer is typically defined as GI cancer diagnosed in individuals younger than 50 years. The incidence of early-onset GI cancer is rising globally, and early-onset GI cancers represent the most rapidly increasing early-onset cancer in the US.
Worldwide, among early-onset GI cancers reported in 2022, colorectal cancer (CRC) was the most common (54.3%; 184 709 cases), followed by gastric cancer (23.8%; 80 885 cases), esophageal cancer (13.2%; 45 056 cases), and pancreatic cancer (8.6%; 29 402 cases). In the US, among early-onset GI cancers reported in 2022, 20 805 individuals were diagnosed with early-onset CRC, 2689 with early-onset gastric, 2657 with early-onset pancreatic, and 875 with early-onset esophageal cancer. Most early-onset GI cancers are associated with modifiable risk factors including obesity, poor-quality diet (eg, sugar-sweetened beverages, ultraprocessed foods), sedentary lifestyle, cigarette smoking, and alcohol consumption. Nonmodifiable risk factors include family history, hereditary syndromes (eg, Lynch syndrome), and inflammatory bowel disease for patients with early-onset CRC. Approximately 15% to 30% of early-onset GI cancers have pathogenic germline variants in genes such as DNA mismatch repair genes and BRCA1/2. All patients with early-onset GI cancers should undergo germline and somatic genetic testing to guide treatment, screen for other cancers (eg, endometrial cancer in Lynch syndrome), and assess familial risk. Treatment for early-onset GI cancers are similar to later-onset GI cancers and may include chemotherapy, surgery, radiation, and therapies such as poly-adenosine diphosphate ribose polymerase inhibitors for BRCA-associated pancreatic cancer. Compared with GI cancers diagnosed after age 50 years, patients with early-onset GI cancers typically receive more treatments but often have similar or shorter survival. Specialized centers and multidisciplinary teams can support patients with challenges around fertility preservation, parenting with cancer, financial difficulty, and psychosocial distress. Currently, screening is not recommended for most early-onset GI cancers, although in the US, screening for CRC is recommended for average-risk individuals starting at age 45 years. High-risk individuals (eg, those with Lynch syndrome, a first-degree relative with CRC, or advanced colorectal adenoma) should begin CRC screening earlier, at an age determined by the specific risk factor.
Early-onset GI cancers, typically defined as cancer diagnosed in individuals younger than 50 years, are among the largest subset of early-onset cancers globally. Treatment is similar to later-onset GI cancers and typically involves a combination of chemotherapy, surgery, and radiation, depending on the cancer type and stage. The prognosis for patients with early-onset GI cancers is similar to or worse than that for patients with later-onset GI cancers, highlighting the need for improved methods of prevention and early detection.
早发性胃肠道(GI)癌通常定义为在50岁以下个体中诊断出的胃肠道癌。早发性胃肠道癌的发病率在全球范围内呈上升趋势,在美国,早发性胃肠道癌是增长最为迅速的早发性癌症。
在全球范围内,2022年报告的早发性胃肠道癌中,结直肠癌(CRC)最为常见(54.3%;184709例),其次是胃癌(23.8%;80885例)、食管癌(13.2%;45056例)和胰腺癌(8.6%;29402例)。在美国,2022年报告的早发性胃肠道癌中,20805人被诊断为早发性结直肠癌,2689人被诊断为早发性胃癌,2657人被诊断为早发性胰腺癌,875人被诊断为早发性食管癌。大多数早发性胃肠道癌与可改变的风险因素有关,包括肥胖、低质量饮食(如含糖饮料、超加工食品)、久坐的生活方式、吸烟和饮酒。不可改变的风险因素包括家族史、遗传性综合征(如林奇综合征)以及早发性结直肠癌患者的炎症性肠病。大约15%至30%的早发性胃肠道癌在DNA错配修复基因和BRCA1/BRCA2等基因中存在致病性种系变异。所有早发性胃肠道癌患者都应接受种系和体细胞基因检测,以指导治疗、筛查其他癌症(如林奇综合征中的子宫内膜癌)并评估家族风险。早发性胃肠道癌的治疗与晚发性胃肠道癌相似,可能包括化疗、手术、放疗以及针对BRCA相关胰腺癌的聚腺苷二磷酸核糖聚合酶抑制剂等治疗方法。与50岁以后诊断出的胃肠道癌相比,早发性胃肠道癌患者通常接受更多治疗,但生存期往往相似或更短。专业中心和多学科团队可以为患者在生育保留、患癌育儿、经济困难和心理社会困扰等方面提供支持。目前,不建议对大多数早发性胃肠道癌进行筛查,不过在美国,建议平均风险个体从45岁开始进行结直肠癌筛查。高危个体(如患有林奇综合征、有结直肠癌一级亲属或晚期结直肠腺瘤的个体)应根据具体风险因素在更早的年龄开始进行结直肠癌筛查。
早发性胃肠道癌通常定义为在50岁以下个体中诊断出的癌症,是全球早发性癌症中最大的子集之一。治疗与晚发性胃肠道癌相似,通常根据癌症类型和阶段采用化疗、手术和放疗相结合的方法。早发性胃肠道癌患者的预后与晚发性胃肠道癌患者相似或更差,这突出了改进预防和早期检测方法的必要性。