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Identify high-risk patients of T1-2N1M0 breast cancer who benefit from postmastectomy radiotherapy: a dual-center retrospective propensity score-matched study.

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European radiology 📖 저널 OA 35.1% 2022: 1/4 OA 2023: 0/7 OA 2024: 2/11 OA 2025: 18/71 OA 2026: 72/165 OA 2022~2026 2026 Vol.36(4) p. 3002-3014 cited 2 Breast Cancer Treatment Studies
TL;DR This multimodal nomogram served as a clinical decision-support tool for clinicians to assess the risk-benefit balance of PMRT and had potential clinical application to guide further personalized adjuvant therapy for women with pT1-2N1M0 breast cancer.
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PubMed DOI OpenAlex Semantic 마지막 보강 2026-05-01
연도별 인용 (2025–2026) · 합계 2
OpenAlex 토픽 · Breast Cancer Treatment Studies Breast Implant and Reconstruction Breast Lesions and Carcinomas

Xu Z, Zhang Y, Zou Y, He Y, Zhang L, Huo J

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This multimodal nomogram served as a clinical decision-support tool for clinicians to assess the risk-benefit balance of PMRT and had potential clinical application to guide further personalized adjuv

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p < 0.05
  • 95% CI 0.774-0.859
  • HR 0.392

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APA Ziting Xu, Yanyan Zhang, et al. (2026). Identify high-risk patients of T1-2N1M0 breast cancer who benefit from postmastectomy radiotherapy: a dual-center retrospective propensity score-matched study.. European radiology, 36(4), 3002-3014. https://doi.org/10.1007/s00330-025-12091-1
MLA Ziting Xu, et al.. "Identify high-risk patients of T1-2N1M0 breast cancer who benefit from postmastectomy radiotherapy: a dual-center retrospective propensity score-matched study.." European radiology, vol. 36, no. 4, 2026, pp. 3002-3014.
PMID 41139173 ↗

Abstract

[OBJECTIVE] To develop a personalized risk stratification nomogram, integrating clinicopathological, sonographic, and mammographic features, to identify high-risk patients who may benefit from postmastectomy radiotherapy (PMRT).

[MATERIALS AND METHODS] A retrospective analysis was conducted on 408 patients from Medical Center 1 (January 2011 to June 2019) and 190 patients from Medical Center 2 (January 2017 to June 2019) with pathologically staged pT1-2N1M0 breast cancer following mastectomy, with preoperative mammography (MG) and ultrasound (US) imaging. After propensity score matching (PSM), the multimodal nomogram was developed using univariate and multivariate Cox regression analyses.

[RESULTS] With multivariate analysis, independent risk factors were identified, including age, pathologic T stage, positive axillary lymph nodes, lymphovascular invasion, microcalcifications, and vascularity on US, architectural distortion, and suspicious calcifications on MG (all p < 0.05). The C-index for the multimodal nomogram was 0.816 (95% CI: 0.774-0.859) in the training and 0.846 (95% CI: 0.772-0.920) in the external validation cohort, demonstrating superior prognostic accuracy, discriminative ability, and clinical applicability than clinicopathological and imaging-only models. Risk stratification using this nomogram showed that PMRT significantly improved RFS in the high-risk group (training cohort: HR = 0.392; external validation cohort: HR = 0.358, both p < 0.05), while patients in the low-risk group did not derive benefit from PMRT (training cohort: HR = 0.173; external validation cohort: HR = 0, both p > 0.05).

[CONCLUSION] This multimodal nomogram served as a clinical decision-support tool for clinicians to assess the risk-benefit balance of PMRT and had potential clinical application to guide further personalized adjuvant therapy for women with pT1-2N1M0 breast cancer.

[KEY POINTS] Question Can the multimodal nomogram integrating clinicopathological, ultrasonic, and mammographic parameters identify high-risk pT1-2N1M0 patients who may benefit from postmastectomy radiation therapy? Findings By effectively risk-stratifying, the nomogram identified high-risk patients who derived significant benefit from PMRT while distinguishing low-risk patients who could potentially avoid unnecessary treatment. Clinical relevance The multimodal nomogram served as a clinical decision-support tool for clinicians to optimize personalized adjuvant therapeutic approaches and improve survival outcomes for patients with pT1-2N1M0 breast cancer.

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