Calibrated Absolute Risk of Lymph-Node-Metastasis After Non-curative Endoscopic Resection of pT1 Colorectal Cancer.
2/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
1162 patients, LNM occurred for 148 patients (12.
I · Intervention 중재 / 시술
radical resection after endoscopic resection from 2004 to 2024 at a single tertiary center
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] A simple composite pathologic score integrating five adverse features provides a calibrated, clinically interpretable estimate of LNM risk after endoscopic resection of T1 CRC. By translating routine pathology into absolute risk and NNS, this model offers a practical framework to support individualized recommendations for completion radical surgery.
OpenAlex 토픽 ·
Gastric Cancer Management and Outcomes
Colorectal Cancer Surgical Treatments
Gastrointestinal Tumor Research and Treatment
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[BACKGROUND] After endoscopic resection of T1 colorectal cancer (CRC), the decision to recommend completion radical surgery is primarily driven by pathologic "high-risk" features.
APA
Jung Kyong Shin, Hee Cheol Kim, et al. (2026). Calibrated Absolute Risk of Lymph-Node-Metastasis After Non-curative Endoscopic Resection of pT1 Colorectal Cancer.. Annals of surgical oncology. https://doi.org/10.1245/s10434-026-19582-5
MLA
Jung Kyong Shin, et al.. "Calibrated Absolute Risk of Lymph-Node-Metastasis After Non-curative Endoscopic Resection of pT1 Colorectal Cancer.." Annals of surgical oncology, 2026.
PMID
41973291 ↗
Abstract 한글 요약
[BACKGROUND] After endoscopic resection of T1 colorectal cancer (CRC), the decision to recommend completion radical surgery is primarily driven by pathologic "high-risk" features. However, these binary criteria identify broad heterogeneous groups and do not provide individualized estimates of lymph-node-metastasis (LNM) risk.
[METHODS] This study analyzed patients with pathologic T1 CRC who underwent radical resection after endoscopic resection from 2004 to 2024 at a single tertiary center. Five histologic features (lymphatic/venous/perineural invasion, tumor budding, poor differentiation, submucosal invasion ≥2000 μm, and positive resection margin) were assigned one point each to construct a composite pathologic score (0-5).
[RESULTS] Among 1162 patients, LNM occurred for 148 patients (12.7 %). The composite score showed a stepwise gradient in LNM risk as follows: 6.6 % for score 0, 12.0 % for score 1, 29.2 % for score 2, and 66.7 % for scores 3 to 4. A threshold of ≥2 identified a high-risk group with substantially higher LNM prevalence than scores 0 to 1 (35.1 % vs 9.5 %; odds ratio [OR], 4.79), corresponding to an absolute risk difference of 24 % and number-needed-to-surgery (NNS) of 4.1. The score demonstrated acceptable discrimination (area under the curve, 0.673; 95 % confidence interval, 0.624-0.722) and good calibration, with close agreement between predicted and observed probabilities across all strata (29 % for score 2, 60 % for score 3, and 100 % for score 4).
[CONCLUSIONS] A simple composite pathologic score integrating five adverse features provides a calibrated, clinically interpretable estimate of LNM risk after endoscopic resection of T1 CRC. By translating routine pathology into absolute risk and NNS, this model offers a practical framework to support individualized recommendations for completion radical surgery.
[METHODS] This study analyzed patients with pathologic T1 CRC who underwent radical resection after endoscopic resection from 2004 to 2024 at a single tertiary center. Five histologic features (lymphatic/venous/perineural invasion, tumor budding, poor differentiation, submucosal invasion ≥2000 μm, and positive resection margin) were assigned one point each to construct a composite pathologic score (0-5).
[RESULTS] Among 1162 patients, LNM occurred for 148 patients (12.7 %). The composite score showed a stepwise gradient in LNM risk as follows: 6.6 % for score 0, 12.0 % for score 1, 29.2 % for score 2, and 66.7 % for scores 3 to 4. A threshold of ≥2 identified a high-risk group with substantially higher LNM prevalence than scores 0 to 1 (35.1 % vs 9.5 %; odds ratio [OR], 4.79), corresponding to an absolute risk difference of 24 % and number-needed-to-surgery (NNS) of 4.1. The score demonstrated acceptable discrimination (area under the curve, 0.673; 95 % confidence interval, 0.624-0.722) and good calibration, with close agreement between predicted and observed probabilities across all strata (29 % for score 2, 60 % for score 3, and 100 % for score 4).
[CONCLUSIONS] A simple composite pathologic score integrating five adverse features provides a calibrated, clinically interpretable estimate of LNM risk after endoscopic resection of T1 CRC. By translating routine pathology into absolute risk and NNS, this model offers a practical framework to support individualized recommendations for completion radical surgery.
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