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Is Ki-67 Really Useful as a Predictor for Response to Neoadjuvant Chemotherapy in Locally Advanced Breast Cancer?
Sukruti Dave1, Arpan Choudhury2, Shirish S Alurkar1
1Department of Medical Oncology, Apollo Hospitals International Limited: Apollo Hospitals Ahmedabad, Ahmedabad, Gujarat India.
This study investigated Ki-67's ability to predict pathological complete response (pCR) in locally advanced breast cancer (LABC) patients receiving neoadjuvant chemotherapy (NACT). Results showed no significant association between Ki-67 and pCR, suggesting other factors like hormone receptor status are more predictive.
Area of Science:
- Oncology
- Biomarkers
- Clinical Research
Background:
- Neoadjuvant chemotherapy (NACT) is standard for locally advanced breast cancer (LABC), aiming for breast conservation or operability.
- Pathological complete response (pCR) after NACT is a key surrogate for improved survival, especially in high-grade tumors.
- Identifying predictors of pCR is crucial for tailoring treatment strategies.
Purpose of the Study:
- To evaluate the predictive value of the Ki-67 protein index for achieving pCR in LABC patients undergoing NACT.
- To explore other clinicopathological factors associated with pCR in this patient cohort.
Main Methods:
- Retrospective analysis of 105 LABC patients who completed NACT and surgery.
- Ki-67 scores assessed on pre-treatment core biopsies.
- Clinical and histopathological evaluation for response assessment (pCR and clinical complete response - cCR).
- Statistical analysis including univariate analysis and ROC curve analysis for Ki-67.
Main Results:
- 33 out of 105 patients (31.4%) achieved pCR.
- Mean Ki-67 index was 46.44% ± 22.92% in the overall population.
- No significant association was found between Ki-67 levels and pCR (pCR group mean Ki-67: 51.60% vs. no pCR group: 44.06%).
- Estrogen receptor negativity, progesterone receptor negativity, and HER2 positivity were predictive of pCR.
- Triple-negative breast cancer (TNBC) and HER2-positive subgroups showed higher rates of cCR and pCR.
Conclusions:
- Ki-67 index did not demonstrate significant predictive value for pCR in this LABC cohort treated with NACT.
- Hormone receptor status and HER2 status appear to be stronger predictors of pCR.
- The COVID-19 pandemic may have confounded results; further validation in larger prospective studies is warranted.
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