Abstract PS3-11-19: Guiding the Axilla: Combining SUVmax and Monocytes to Predict Response to Neoadjuvant Therapy in HER2 positive Breast Cancer

Abstract Introduction: The prognostic significance of achieving axillary pathologic complete response (AxpCR) following neoadjuvant chemotherapy (NAT) in clinically node-positive (cN+) breast cancer (BC) is well established. However, consensus regarding the optimal strategy for axillary management—particularly in patients with HER2-positive BC—remains lacking. This study aims to evaluate the predictive value of the maximum standardized uptake value of axillary lymph nodes (N-SUVmax) obtained from baseline 18F-FDG PET/CT scans, in combination with the absolute monocyte count (AMC), for AxpCR following NAT in patients with cN+ HER2-positive BC. Methods: A retrospective analysis was conducted on HER2-positive cN+ BC patients treated with NAT. All patients received the same chemotherapy regimen, including dual HER2 blockade. ROC curves were used to determine cut-off values for N-SUVmax and AMC. Associations with AxpCR were analyzed using logistic regression models. Results: Among 285 patients diagnosed with HER2-positive BC, 215 presented with cN+ disease at baseline. Of these, 155 patients (72.1%) achieved AxpCR following NAT. All patients underwent axillary lymph node dissection (ALND) according to current guidelines, regardless of imaging or biomarker results. Notably, a large proportion showed no residual nodal disease at pathology, confirming AxpCR despite initial cN+ status.Patients with an N-SUVmax ≥ 3.5 had a 4.9-fold higher likelihood of achieving AxpCR (p = 0.039; odds ratio [OR] = 4.938 [95% CI: 1.081-1.904]). In contrast, patients with an AMC > 340/mm3 had a 90.4% lower probability of achieving AxpCR (p < 0.001; OR = 0.096 [95% CI: 0.028-0.324]). Notably, the interaction between N-SUVmax and AMC was significant: higher AMC levels diminished the predictive value of N-SUVmax for AxpCR (p = 0.002; OR = 0.999 [95% CI: 0.997-1.000]). Based on N-SUVmax and AMC values, patients were stratified into three groups. Group 1: High N-SUVmax - Low AMC; Group 2: High N-SUVmax - High AMC or Low N-SUVmax - Low AMC; Group 3: Low N-SUVmax - High AMC. Compared to Group 1, both Group 2 (p < 0.001; OR = 0.047 [95% CI: 0.009-0.237]) and Group 3 (p < 0.001; OR = 0.017 [95% CI: 0.002-0.137]) showed significantly reduced probabilities of achieving AxpCR. Conclusions: Assessing axillary response to NAT in HER2-positive BC provides a critical opportunity to tailor surgical management. The combination of baseline N-SUVmax and AMC improves prediction of AxpCR and may support more individualized axillary treatment strategies, ultimately contributing to better patient outcomes. Citation Format: L. Raimondi, M. Cuzzocrea, C. Oliva, N. Peradze, Y. Harder, D. Schmauss, R. Graffeo Galbiati, L. Rossi. Guiding the Axilla: Combining SUVmax and Monocytes to Predict Response to Neoadjuvant Therapy in HER2 positive Breast Cancer [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 PS3-11-19.

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Journal
Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps3-11-19
Primary Topic
Breast Cancer Treatment Studies
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article

Abstract PS3-11-19: Guiding the Axilla: Combining SUVmax and Monocytes to Predict Response to Neoadjuvant Therapy in HER2 positive Breast Cancer

Marco Cuzzocrea, Daniel Schmauß, R. Graffeo Galbiati, C. Oliva et al.
Clinical Cancer Research
Breast Cancer Treatment Studies
article

Abstract PS3-11-19: Guiding the Axilla: Combining SUVmax and Monocytes to Predict Response to Neoadjuvant Therapy in HER2 positive Breast Cancer

Marco Cuzzocrea, Daniel Schmauß, R. Graffeo Galbiati, C. Oliva, L. Rossi, L. Raimondi, N. Peradze, Y. Harder
article en

Abstract

Abstract Introduction: The prognostic significance of achieving axillary pathologic complete response (AxpCR) following neoadjuvant chemotherapy (NAT) in clinically node-positive (cN+) breast cancer (BC) is well established. However, consensus regarding the optimal strategy for axillary management—particularly in patients with HER2-positive BC—remains lacking. This study aims to evaluate the predictive value of the maximum standardized uptake value of axillary lymph nodes (N-SUVmax) obtained from baseline 18F-FDG PET/CT scans, in combination with the absolute monocyte count (AMC), for AxpCR following NAT in patients with cN+ HER2-positive BC. Methods: A retrospective analysis was conducted on HER2-positive cN+ BC patients treated with NAT. All patients received the same chemotherapy regimen, including dual HER2 blockade. ROC curves were used to determine cut-off values for N-SUVmax and AMC. Associations with AxpCR were analyzed using logistic regression models. Results: Among 285 patients diagnosed with HER2-positive BC, 215 presented with cN+ disease at baseline. Of these, 155 patients (72.1%) achieved AxpCR following NAT. All patients underwent axillary lymph node dissection (ALND) according to current guidelines, regardless of imaging or biomarker results. Notably, a large proportion showed no residual nodal disease at pathology, confirming AxpCR despite initial cN+ status.Patients with an N-SUVmax ≥ 3.5 had a 4.9-fold higher likelihood of achieving AxpCR (p = 0.039; odds ratio [OR] = 4.938 [95% CI: 1.081-1.904]). In contrast, patients with an AMC > 340/mm3 had a 90.4% lower probability of achieving AxpCR (p < 0.001; OR = 0.096 [95% CI: 0.028-0.324]). Notably, the interaction between N-SUVmax and AMC was significant: higher AMC levels diminished the predictive value of N-SUVmax for AxpCR (p = 0.002; OR = 0.999 [95% CI: 0.997-1.000]). Based on N-SUVmax and AMC values, patients were stratified into three groups. Group 1: High N-SUVmax - Low AMC; Group 2: High N-SUVmax - High AMC or Low N-SUVmax - Low AMC; Group 3: Low N-SUVmax - High AMC. Compared to Group 1, both Group 2 (p < 0.001; OR = 0.047 [95% CI: 0.009-0.237]) and Group 3 (p < 0.001; OR = 0.017 [95% CI: 0.002-0.137]) showed significantly reduced probabilities of achieving AxpCR. Conclusions: Assessing axillary response to NAT in HER2-positive BC provides a critical opportunity to tailor surgical management. The combination of baseline N-SUVmax and AMC improves prediction of AxpCR and may support more individualized axillary treatment strategies, ultimately contributing to better patient outcomes. Citation Format: L. Raimondi, M. Cuzzocrea, C. Oliva, N. Peradze, Y. Harder, D. Schmauss, R. Graffeo Galbiati, L. Rossi. Guiding the Axilla: Combining SUVmax and Monocytes to Predict Response to Neoadjuvant Therapy in HER2 positive Breast Cancer [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 PS3-11-19.

Clinical Cancer ResearchVol. 32(4_Supplement)
Humanitas University (IT), Ente Ospedaliero Cantonale (CH), Ospedale Humanitas Gradenigo (IT), European Institute of Oncology (IT)
Good health and well-being
Openalex Percentile: Top 55%
Breast Cancer Treatment Studies
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