Authors
Sinuo Gao, Zhaoqi Zhang, Chao Shi, Cheng Cheng, Xindi Ma, Xinming Zhao, Yunjiang Liu
Published in
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. Aug 06, 2026. Epub Aug 06, 2026.
Abstract
This study aimed to evaluate the predictive performance of 68Ga-HER2 PET/CT in assessing pathologic response to neoadjuvant therapy (NAT) in human epidermal growth factor receptor 2 (HER2)-positive breast cancer. Methods: In total, 45 patients with newly diagnosed HER2-positive breast cancer eligible for NAT were enrolled. All participants received at least 4 cycles of trastuzumab combined with pertuzumab or pyrotinib-based therapy, followed by surgery. 68Ga-HER2 PET/CT was performed at baseline (PET1), at the end of the second therapy cycle (PET2), and before surgery (PET3). The SUVmax of primary breast tumors and metastatic lymph nodes were recorded. Results: Pathologic complete response (pCR) was achieved in 31 patients (70%), whereas 13 (30%) showed non-pCR. The SUVmax at PET1 did not differ significantly between pCR and non-pCR groups (3.76 ± 1.97 vs. 3.79 ± 2.71, P = 0.349). However, the SUVmax at PET2 and PET3 were significantly lower in the pCR group compared with the non-pCR group (PET 2: 0.45 ± 0.71 vs. 2.01 ± 2.36, P = 0.008; PET3: 0.12 ± 0.39 vs. 1.67 ± 2.94, P = 0.014). The optimal cutoff values for predicting pCR included an SUVmax of no more than 1.15 (area under the curve [AUC] = 0.738) at PET2 and no more than 0.50 (AUC = 0.735) at PET3 and a ΔSUVmax of at least 61% (AUC = 0.742) at PET2 and at least 72% (AUC = 0.743) at PET3. Application of the PET2 cutoff thresholds for SUVmax and ΔSUVmax identified a therapy-sensitive subgroup, which had a positive predictive value for pCR of 85%-representing a 15% higher absolute likelihood of pCR compared with the nonsensitive subgroup-while the method provided a negative predictive value of approximately 60%. Conclusion: Dynamic changes in 68Ga-HER2 PET/CT uptake during NAT provide an effective early indicator of therapeutic sensitivity in HER2-positive breast cancer, supporting its value for predicting pathologic response at both early treatment and preoperative stages.
PMID:
42562610
Bibliographic data and abstract were imported from PubMed on 07 Aug 2026.
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