False-positive MRI Findings in Breast Cancer After Neoadjuvant Chemotherapy and Correlation Between Tumor Response Patterns and HER2 Status
ACTA ONCOLOGICA TURCICA, cilt.56, ss.97-105, 2023 (TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 56
- Basım Tarihi: 2023
- Doi Numarası: 10.5505/aot.2023.60973
- Dergi Adı: ACTA ONCOLOGICA TURCICA
- Derginin Tarandığı İndeksler: TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.97-105
- Gazi Üniversitesi Adresli: Evet
Özet
Objective: To demonstrate false-positive MRI findings after neoadjuvant chemotherapy (NAC) in
patients with pathologic complete response (pCR) and investigate the correlation between post-NAC
MRI findings and tumor response patterns based on human epidermal growth factor receptor 2 (HER2)
status.
Methods: This retrospective multicenter study enrolled 118 patients with breast cancer who received
NAC and achieved pCR. Tumors were evaluated with MRI pre- and post-NAC. MRI evaluation
included lesion characteristics, kinetic curve analysis, background parenchymal enhancement (BPE),
and post-NAC changes of MRI features. Tumor response patterns were also assessed and categorized
based on MRI findings. Tumor response patterns and post-NAC MRI findings were correlated with
HER2 status.
Results: The residual MRI findings following NAC differed significantly between HER2+ and HER2−
groups (p=0.02). The most frequent false-positive MRI finding was focus and foci in HER2+ tumors,
whereas non-mass enhancement (NME) in HER2− group. The presence of ductal carcinoma in situ
(DCIS) and fibrosis in surgical pathology is significantly associated with NME on post-NAC MRI
(p<0.001). Axillary pCR was achieved significantly higher in the HER2+ group (p=0.04).
Conclusion: Although MRI is considered the most reliable method for evaluating tumor response after
NAC, over and underestimation is still possible. This study revealed that tumor response patterns and
post-NAC MRI findings differ according to HER2 status. The diagnostic accuracy of post-NAC MRI is
evolving by understanding the underlying mechanisms and tumor biology.