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A clinical-molecular nomogram for predicting early recurrence following resection of initially unresectable colorectal liver metastases.

1/5 보강
Therapeutic advances in medical oncology 2026 Vol.18() p. 17588359251411660
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
411 patients with initially unresectable CRLM undergoing curative resection after conversion therapy were analyzed.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Calibration curves showed good agreement ( > 0.05), and DCA indicated clinical benefit at recurrence risk thresholds above 30%. [CONCLUSION] We identified 4 months as the optimal RFS threshold for PER and proposed a novel nomogram integrating molecular and clinical factors for perioperative decision-making in patients with initially unresectable CRLM.

Lu YT, Huang XX, Chen WC, Xiao QY, Duan JL, Li ZJ, Pat Fong W, Wang FH, Li YH, Wang DS

📝 환자 설명용 한 줄

[BACKGROUND] Postoperative early recurrence (PER) remains a major challenge to long-term survival after successful conversion therapy and curative resection for initially unresectable colorectal liver

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 95% CI 0.670-0.723
  • OR 1.061
  • 연구 설계 cohort study

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BibTeX ↓ RIS ↓
APA Lu YT, Huang XX, et al. (2026). A clinical-molecular nomogram for predicting early recurrence following resection of initially unresectable colorectal liver metastases.. Therapeutic advances in medical oncology, 18, 17588359251411660. https://doi.org/10.1177/17588359251411660
MLA Lu YT, et al.. "A clinical-molecular nomogram for predicting early recurrence following resection of initially unresectable colorectal liver metastases.." Therapeutic advances in medical oncology, vol. 18, 2026, pp. 17588359251411660.
PMID 41567811

Abstract

[BACKGROUND] Postoperative early recurrence (PER) remains a major challenge to long-term survival after successful conversion therapy and curative resection for initially unresectable colorectal liver metastases (CRLM). Existing prediction models rely heavily on clinicopathological parameters and lack molecular biomarkers, limiting their predictive accuracy.

[OBJECTIVES] To define the optimal recurrence-free survival (RFS) cutoff for PER and develop a comprehensive predictive nomogram incorporating molecular and clinical variables to predict PER in patients with initially unresectable CRLM who undergo curative resection following conversion therapy.

[DESIGN] Retrospective cohort study.

[METHODS] Clinicopathological and molecular data from 411 patients with initially unresectable CRLM undergoing curative resection after conversion therapy were analyzed. The minimum value approach determined the optimal RFS cutoff for PER. Least absolute shrinkage and selection operator regression identified significant predictors, followed by multivariate logistic regression to build a nomogram. Model performance was assessed using the area under the curve (AUC), calibration curves, and decision curve analysis (DCA).

[RESULTS] PER was defined as recurrence within 4 months postoperatively. Independent predictors included dual preoperative positivity for CEA and CA19-9 (odds ratio (OR) = 2.437, < 0.001), number of liver metastases (OR = 1.061, < 0.001), tumor progression during the chemotherapy-to-surgery interval (OR = 2.837, = 0.003), exon 2 mutations (OR = 1.927, = 0.006), and mutations (OR = 2.410, = 0.002). An AUC of 0.703 (95% confidence intervals (CI): 0.650-0.756) was achieved, with an internal validation AUC of 0.697 (95% CI: 0.670-0.723). Calibration curves showed good agreement ( > 0.05), and DCA indicated clinical benefit at recurrence risk thresholds above 30%.

[CONCLUSION] We identified 4 months as the optimal RFS threshold for PER and proposed a novel nomogram integrating molecular and clinical factors for perioperative decision-making in patients with initially unresectable CRLM.

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