
| ID | 69982 |
| フルテキストURL | |
| 著者 |
Sagara, Yasuaki
Department of Breast and Thyroid Surgical Oncology, Hakuaikai Sagara Hospital
Yoshida, Atsushi
Department of Breast Surgical Oncology, St Luke's International Hospital
Kimura, Yuri
Department of Breast Surgical Oncology, The Cancer Institute Hospital of JFCR
Ishitobi, Makoto
Department of Breast Surgery, Osaka Habikino Medical Center
Ono, Yuka
Department of Radiation Oncology and Image-Applied Therapy, Kyoto University
Takahashi, Yuko
Department of Breast and Endocrine Surgery, Okayama University Hospital
Tsukioki, Takahiro
Department of Breast and Endocrine Surgery, Okayama University Hospital
Takada, Koji
Department of Breast Surgical Oncology, Osaka Metropolitan University Graduate School of Medicine
Ito, Yuri
Department of Medical Statistics, Osaka Medical and Pharmaceutical University
Osako, Tomo
Division of Pathology, The Cancer Institute of Japanese Foundation for Cancer Research
Sakai, Takehiko
Department of Breast Surgical Oncology, The Cancer Institute Hospital of JFCR
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| 抄録 | Purpose Ipsilateral breast tumor recurrence (IBTR) remains a critical concern for patients undergoing breast-conserving surgery (BCS). Reliable risk estimation tools for IBTR risk can support personalized surgical and adjuvant treatment decisions, especially in the era of evolving systemic therapies. We aimed to develop and validate models to estimate IBTR risk.
Patients and Methods This multicenter retrospective cohort study included 8,938 women who underwent partial mastectomy for invasive breast cancer between 2008 and 2017. Prediction models were developed using Cox proportional hazards regression and validated via bootstrap resampling. Model performance was assessed using Harrell's C-index, Brier scores, calibration plots, and goodness-of-fit tests. Results During a median follow-up of 9.0 years (IQR, 6.6-10.9), IBTR occurred in 320 patients (3.6%). The initial model, based on variables from Sanghani et al, achieved a Harrell's C-index of 0.74. Incorporating hormonal receptor status, human epidermal growth factor receptor 2 status, radiotherapy, and targeted therapy as predictors reduced the C-index to 0.65, despite their clinical relevance. Importantly, the inclusion of these factors improved calibration, demonstrating better alignment between predicted and observed IBTR probabilities. Although the hazard ratios (HRs) for radiotherapy aligned with the Early Breast Cancer Trialists’ Collaborative Group meta-analyses (MA), those for chemotherapy and endocrine therapy showed slight differences. Therefore, HRs from the MA were used to represent treatment effects in our model. Conclusion We have developed and internally validated a new risk estimation model for IBTR using Cox regression and bootstrap methods. A Web-based risk estimation tool is now available to facilitate individualized risk assessment and treatment planning. |
| 発行日 | 2025-09
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| 出版物タイトル |
JCO Clinical Cancer Informatics
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| 巻 | 9巻
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| 出版者 | American Society of Clinical Oncology (ASCO)
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| 開始ページ | e2500182
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| ISSN | 2473-4276
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| OAI-PMH Set |
岡山大学
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| 著作権者 | © 2025 by American Society of Clinical Oncology.
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| 論文のバージョン | publisher
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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| 関連URL | isVersionOf https://doi.org/10.1200/cci-25-00182
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| ライセンス | http://creativecommons.org/licenses/by-nc-nd/4.0/
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| Citation | Yasuaki Sagara et al. Development and Validation of an Ipsilateral Breast Tumor Recurrence Risk Estimation Tool Incorporating Real-World Data and Evidence From Meta-Analyses: A Retrospective Multicenter Cohort Study. JCO Clin Cancer Inform 9, e2500182(2025). DOI:10.1200/CCI-25-00182
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