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http://dx.doi.org/10.7314/APJCP.2015.16.17.7975

Predictive Value of IHC4 Score for Pathological Response to Neoadjuvant Chemotherapy in Hormone Receptor-Positive Breast Cancer  

Elsamany, Shereef (Oncology, King Abdullah Medical City)
Elmorsy, Soha (Pharmacology, Faculty of Medicine, Cairo University)
Alzahrani, Abdullah (Oncology, King Abdullah Medical City)
Rasmy, Ayman (Oncology, King Fahed Specialist Hospital)
Abozeed, Waleed N (Clinical Oncology, Mansoura University Hospital)
Mohammed, Amrallah A (Oncology, King Abdullah Medical City)
Sherisher, Mohamed A (Oncology, King Abdullah Medical City)
Abbas, Mohammed M (Pathology, King Fahed Specialist Hospital)
Mashhour, Miral (Pathology, King Fahed Specialist Hospital)
Publication Information
Asian Pacific Journal of Cancer Prevention / v.16, no.17, 2015 , pp. 7975-7979 More about this Journal
Abstract
Purpose: This study aimed to explore the value of IHC4 in predicting pathological response after neoadjuvant chemotherapy in patients with hormonal receptor (HR)-positive breast cancer (BC). Materials and Methods: In this retrospective exploratory study, data for 68 HR-positive BC patients who received neoadjuvant chemotherapy were recorded. IHC4 scores were calculated based on estrogen receptors/progesterone receptors, Ki-67 and HER2 status. Logistic and ordinal regression analyses in addition to likelihood ratio test were used to explore associations of IHC4 scores and other clinico-pathological parameters with pathological complete response (pCR) and pathological stage. Results: Taking the 25th percentile as the cut-off, a lower IHC4 score was associated with an increased probability of pCR (low; 52.9% vs. High; 21.6%, OR=4.1, 95% CI=1.28-13.16, p=0.018) and a lower pathological stage (OR=3.9, 95% CI=1.34-11.33, p=0.012). When the IHC4 score was treated as a continuous variable, a lower score was again associated with an increased probability of pCR (OR=1.010, 95% CI=1.001-1.018, p=0.025) and lower pathological stage (OR=1.009, 95% CI=1.002-1.017, P=0.008). Lower clinical stage was associated with a better pCR rate that was of borderline significance (P=0.056). When clinical stage and IHC4 score were incorporated together in a logistic model, the likelihood ratio test gave a P-value of 0.004 after removal of the IHC4 score and 0.011 after removal of the stage, indicating a more significant predictive value of the IHC4 score for pCR. Conclusions: This study suggests that the IHC4 score can predict pathological response to neoadjuvant chemotherapy in HR-positive BC patients. This finding now needs to be validated in a larger cohort of patients.
Keywords
IHC4 score; neoadjuvant chemotherapy; pathological response; hormonal receptors; breast cancer;
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