Integrating Clinical–Pathological–MRI features to construct a prediction model for pathological complete remission of axillary lymph nodes after neoadjuvant therapy: a retrospective study

医学 乳腺癌 腋窝淋巴结 新辅助治疗 病态的 放射科 磁共振成像 淋巴结 肿瘤科 内科学 癌症
作者
Jiabei Shang,Jianzhe Chen,Xudong Gao,Zhipeng Wan,Ruirong Yang,Zhenli Lei,Siqi Chen,Meining Chen,Yi Quan,Jiao Bai
出处
期刊:International Journal of Surgery [Wolters Kluwer]
卷期号:111 (11): 7633-7646 被引量:1
标识
DOI:10.1097/js9.0000000000003070
摘要

BACKGROUND: Accurate assessment of axillary lymph node (ALN) metastasis is essential for developing an effective treatment strategy for breast cancer (BC). Despite advancements in imaging and surgical techniques, a critical need remains for reliable, non-invasive methods to predict axillary response to neoadjuvant therapy (NAT). This study aimed to identify key factors influencing ALN pathological complete response (pCR) following NAT and develop a predictive model for axillary pCR (apCR) to support clinical decision-making regarding the necessity of axillary lymph node dissection (ALND). MATERIALS AND METHODS: Clinical data from female patients diagnosed with BC between January 2019 and December 2024 were retrospectively collected. All patients had biopsy-confirmed metastasis to ipsilateral ALNs at initial presentation, received standardized NAT, and subsequently underwent ALND. Patients were randomly divided into a training set (n = 354) and a test set (n = 151) in a ratio of 7:3. Based on ALND results, patients were classified into the apCR and non-apCR groups, and their clinicopathological and magnetic resonance imaging (MRI) features were compared. Independent predictors of apCR were identified using multivariate logistic regression analysis, and feature selection was performed using the Least Absolute Shrinkage and Selection Operator method. Two predictive models were developed, a Clinical-Pathological-MRI model and a Clinical-Pathological-Delta-MRI model. The predictive performance of both models was evaluated and compared. RESULTS: A total of 505 patients were enrolled, including 237 patients in the apCR group and 268 in the non-apCR group. The AUC values for the Clinical-Pathological-MRI model were 0.817 in the training set and 0.680 in the test set. For the Clinical-Pathological-Delta-MRI model, the AUC values were 0.844 in the training set and 0.793 in the test set, indicating superior predictive performance. Decision curve analysis further demonstrated that the Clinical-Pathological-Delta-MRI model provided greater net clinical benefit compared to the Clinical-Pathological-MRI model in both the training and test sets. CONCLUSION: This model may provide valuable support for individualized surgical decision-making and help guide the selective omission of ALN dissection in appropriate candidates.
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