Knoblauch Mathilda, Kühn Florian, von Ehrlich-Treuenstätt Viktor, Werner Jens, Renz Bernhard Willibald
Department of General, Visceral, and Transplantation Surgery, LMU Klinikum, Munich, Germany.
Visc Med. 2023 Mar;39(1):10-16. doi: 10.1159/000526633. Epub 2022 Nov 30.
Early colorectal cancer (eCRC) is defined as cancer that does not cross the submucosal layer of the colon or rectum, including carcinoma in situ (pTis), pT1a, and pT1b. Early carcinomas differ in their prognosis depending on the risk profile. The differentiation between low and high risk is essential. The low-risk group includes R0-resected, well (G1) or moderately (G2) differentiated tumors without lymphatic vessel invasion (L0), without blood vessel invasion (V0) and a tumor size ≤3 cm. In this constellation, the estimated risk of lymph node metastasis is around 1% or below. The high-risk group includes tumors with incomplete resection (Rx), poor (G3) or undifferentiated (G4) carcinomas, and/or lymphatic and blood vessel invasion (L1) and size ≥3 cm. In a "high-risk" situation, there is a risk for lymph node metastasis of up to 23%.
The incidence of eCRC is rising with a rate of 10% in all endoscopically removed lesions during colonoscopy. For a correct histological evaluation, all suspected lesions should be completely resected. In case of a pT1 lesion in the rectum, pelvic magnetic resonance imaging should be performed to evaluate for suspicious lymph nodes. The therapeutic approach for eCRC is based on histological assessment and ranges from endoscopic resection to radical oncological surgery. The advantages, disadvantages, and associated risks of the individual treatment strategy need to be carefully discussed on a tumor board and with the patient.
Treatment options for early colorectal cancer depend on the histological assessment. Poorly differentiated carcinomas, a Kudo ≥ SM2 classified lesion, and a Haggitt level 4 always represent a "high-risk" situation. It should also be mentioned that in rectal cancer, local surgical tumor excision (full-wall excision) is also sufficient for pT1 carcinomas with a "low-risk" constellation (G1/G2; L0, size <3 cm) and an R0 resection.
早期结直肠癌(eCRC)定义为未侵犯结肠或直肠黏膜下层的癌症,包括原位癌(pTis)、pT1a和pT1b。早期癌的预后因其风险特征而异。区分低风险和高风险至关重要。低风险组包括R0切除、高分化(G1)或中分化(G2)、无淋巴管侵犯(L0)、无血管侵犯(V0)且肿瘤大小≤3 cm的肿瘤。在这种情况下,估计淋巴结转移风险约为1%或更低。高风险组包括切除不完全(Rx)、低分化(G3)或未分化(G4)癌,和/或有淋巴管和血管侵犯(L1)且大小≥3 cm的肿瘤。在“高风险”情况下,淋巴结转移风险高达23%。
在结肠镜检查中,所有经内镜切除的病变中,eCRC的发病率以10%的速度上升。为了进行正确的组织学评估,所有可疑病变都应完整切除。如果直肠出现pT1病变,应进行盆腔磁共振成像以评估可疑淋巴结。eCRC的治疗方法基于组织学评估,范围从内镜切除到根治性肿瘤手术。个体治疗策略的优缺点及相关风险需要在肿瘤专家委员会上与患者仔细讨论。
早期结直肠癌的治疗选择取决于组织学评估。低分化癌、Kudo≥SM2分级的病变以及Haggitt 4级总是代表“高风险”情况。还应提到,在直肠癌中,对于具有“低风险”特征(G1/G2;L0,大小<3 cm)且R0切除的pT1癌,局部手术肿瘤切除(全层切除)也足够。