Abstract PS3-11-15: Comprehensive Analysis and Prediction of HER2-targeted Therapy Insensitivity among HER2-Positive Breast Cancer Patients Undergoing Neoadjuvant treatment

Abstract Background: HER2-targeted therapy has been incorporated into the standard neoadjuvant treatment regimen for HER2-positive early-stage breast cancer, yet a subset of patients show limited pathological response. Early identification of these treatment-insensitive individuals may improve therapeutic decision-making. Methods: This retrospective study included 13,004 HER2-positive breast cancer patients from the National Cancer Database (2010-2022) who received neoadjuvant chemotherapy plus HER2-targeted therapy. Neoadjuvant treatment (NAT) insensitivity was defined as the absence of pathologic T-stage downstaging after treatment. Pathological complete response (pCR) was defined as no residual invasive carcinoma in the breast and axillary lymph nodes (ypT0/is, ypN0). Baseline characteristics and overall survival (OS) were compared between NAT-sensitive and NAT-insensitive groups. A multivariable logistic regression model was developed using significant clinicopathological variables. Categorical variables and interaction terms were also tested by the likelihood ratio test. Model performance was assessed using the area under the receiver operating characteristic curve (AUC), Hosmer-Lemeshow test, and calibration curves. Results: Among all patients, 22.5% (n = 2926) were classified as NAT-insensitive, 49.4% (n = 6418) were partial responders, and 28.1% (n = 3660) achieved pCR. NAT-insensitive patients were older and more likely to have HR-positive, low-grade, and non-ductal tumors. They experienced significantly worse OS compared to NAT-sensitive patients (log-rank p < 0.0001). Patients who achieved pCR were more likely to be younger, have poorly differentiated tumors, HR-negative status, and invasive ductal carcinoma, indicating a more responsive biological subtype. The predictive model showed good discrimination (AUC = 0.760 in training, 0.753 in validation) and calibration. Conclusion: Younger age, HR negativity, high tumor grade, and ductal histology were associated with higher pCR rates, whereas the opposite traits characterized treatment-insensitive patients. The predictive model developed in this study demonstrated good performance and may assist in early identification of individuals unlikely to benefit from neoadjuvant HER2-targeted therapy. Citation Format: Q. Shang, L. Zian, L. Sheng, W. Xin. Comprehensive Analysis and Prediction of HER2-targeted Therapy Insensitivity among HER2-Positive Breast Cancer Patients Undergoing Neoadjuvant treatment [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS3-11-15.

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Journal
Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps3-11-15
Primary Topic
Advanced Breast Cancer Therapies
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article
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article

Abstract PS3-11-15: Comprehensive Analysis and Prediction of HER2-targeted Therapy Insensitivity among HER2-Positive Breast Cancer Patients Undergoing Neoadjuvant treatment

Qingyao Shang, W. Xin, L. Zian, L. Sheng
Clinical Cancer Research
Advanced Breast Cancer Therapies
article

Abstract PS3-11-15: Comprehensive Analysis and Prediction of HER2-targeted Therapy Insensitivity among HER2-Positive Breast Cancer Patients Undergoing Neoadjuvant treatment

Qingyao Shang, W. Xin, L. Zian, L. Sheng
article en

Abstract

Abstract Background: HER2-targeted therapy has been incorporated into the standard neoadjuvant treatment regimen for HER2-positive early-stage breast cancer, yet a subset of patients show limited pathological response. Early identification of these treatment-insensitive individuals may improve therapeutic decision-making. Methods: This retrospective study included 13,004 HER2-positive breast cancer patients from the National Cancer Database (2010-2022) who received neoadjuvant chemotherapy plus HER2-targeted therapy. Neoadjuvant treatment (NAT) insensitivity was defined as the absence of pathologic T-stage downstaging after treatment. Pathological complete response (pCR) was defined as no residual invasive carcinoma in the breast and axillary lymph nodes (ypT0/is, ypN0). Baseline characteristics and overall survival (OS) were compared between NAT-sensitive and NAT-insensitive groups. A multivariable logistic regression model was developed using significant clinicopathological variables. Categorical variables and interaction terms were also tested by the likelihood ratio test. Model performance was assessed using the area under the receiver operating characteristic curve (AUC), Hosmer-Lemeshow test, and calibration curves. Results: Among all patients, 22.5% (n = 2926) were classified as NAT-insensitive, 49.4% (n = 6418) were partial responders, and 28.1% (n = 3660) achieved pCR. NAT-insensitive patients were older and more likely to have HR-positive, low-grade, and non-ductal tumors. They experienced significantly worse OS compared to NAT-sensitive patients (log-rank p < 0.0001). Patients who achieved pCR were more likely to be younger, have poorly differentiated tumors, HR-negative status, and invasive ductal carcinoma, indicating a more responsive biological subtype. The predictive model showed good discrimination (AUC = 0.760 in training, 0.753 in validation) and calibration. Conclusion: Younger age, HR negativity, high tumor grade, and ductal histology were associated with higher pCR rates, whereas the opposite traits characterized treatment-insensitive patients. The predictive model developed in this study demonstrated good performance and may assist in early identification of individuals unlikely to benefit from neoadjuvant HER2-targeted therapy. Citation Format: Q. Shang, L. Zian, L. Sheng, W. Xin. Comprehensive Analysis and Prediction of HER2-targeted Therapy Insensitivity among HER2-Positive Breast Cancer Patients Undergoing Neoadjuvant treatment [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS3-11-15.

Clinical Cancer ResearchVol. 32(4_Supplement)
Duke University (US), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), University of Michigan (US)
Peace, Justice and strong institutions
Openalex Percentile: Top 52%
Advanced Breast Cancer Therapies
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