Functional hemodynamic imaging markers for the prediction of pathological outcomes in breast cancer patients treated with neoadjuvant chemotherapy
View abstract on PubMed
Summary
This summary is machine-generated.Early prediction of pathologic complete response (pCR) in breast cancer patients undergoing neoadjuvant chemotherapy (NACT) is possible using hemoglobin-based functional imaging biomarkers from diffuse optical tomography (DOT). These DOT markers show potential for personalized treatment adjustments.
Area Of Science
- Medical Imaging
- Oncology
- Biomedical Engineering
Background
- Pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) predicts survival in breast cancer.
- Early prediction of pCR is crucial for tailoring treatment strategies.
Purpose Of The Study
- To evaluate the association between diffuse optical tomography (DOT)-derived hemoglobin-based functional imaging biomarkers and pCR in breast cancer patients undergoing NACT.
- To assess the predictive performance of these biomarkers at different timepoints during NACT.
Main Methods
- Twenty-two breast cancer patients undergoing NACT were imaged using multimodal DOT and digital breast tomosynthesis (DBT).
- Logistic regression and receiver operating characteristic (ROC) curve analysis were used to correlate DOT markers with pCR status.
- Imaging was performed at different compression levels after the first and second chemotherapy cycles.
Main Results
- Normalized tumor total hemoglobin (HbT) under half compression was significantly lower in the pCR group after two cycles.
- The change in normalized tumor HbT with compression reduction after the first cycle also indicated pCR.
- Area under the curve (AUC) values for DOT markers reached up to 0.75, outperforming size-based changes from DBT and MRI.
Conclusions
- Breast DOT functional imaging biomarkers show potential for early response assessment during NACT.
- These findings suggest DOT can aid in personalizing breast cancer treatment regimens.
- DOT offers a critical tool for unmet clinical needs in monitoring NACT response.

