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Decrease of peripheral blood lymphocyte count predicts response to neoadjuvant chemotherapy in breast cancer
1Department of Surgery, Kyung Hee University College of Medicine, Seoul, Korea.
Korean Journal of Clinical Oncology
|March 22, 2023
Summary
A decrease in peripheral blood lymphocyte (PBL) count after neoadjuvant chemotherapy (NAC) is linked to pathologic complete response (pCR) in breast cancer. Monitoring PBL changes can help predict treatment effectiveness.
Area of Science:
- Oncology
- Immunology
- Medical Diagnostics
Background:
- Pathologic complete response (pCR) is a key indicator of neoadjuvant chemotherapy (NAC) efficacy in breast cancer.
- Peripheral blood lymphocyte (PBL) counts have emerged as potential biomarkers for predicting NAC response.
Purpose of the Study:
- To investigate the association between changes in PBL count and pCR in breast cancer patients undergoing NAC.
- To determine if PBL count dynamics can serve as a prognostic factor for NAC response.
Main Methods:
- Retrospective analysis of 61 breast cancer patients treated with NAC and mastectomy.
- Correlational analyses and logistic regression to evaluate the relationship between PBL count changes and pCR.
- Receiver operating characteristic (ROC) curve analysis to identify optimal PBL decrease cutoff values.
Main Results:
- 14 patients (22.9%) achieved pCR, with most showing a decrease in PBL count post-NAC.
- A smaller decrease in PBL count was significantly associated with achieving pCR (P=0.028).
- A PBL decrease cutoff of 755×10^6/L differentiated groups with significantly different pCR rates (38.46% vs 11.43%).
Conclusions:
- Decreased PBL count after NAC is significantly associated with pCR in breast cancer patients.
- Monitoring PBL count reduction post-NAC may offer a valuable tool for predicting treatment response.
- These findings support the utility of PBL dynamics as a predictive biomarker for NAC in breast cancer.
Keywords:
Breast neoplasmsNeoadjuvant chemotherapyPathological complete remissionPeripheral blood lymphocytes
