Abstract

BackgroundBreast cancer patients who achieve pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) have favorable outcomes. Reliable predictors for pCR help to identify patients who will benefit most from NAC. The pretreatment serum albumin-to-alkaline phosphatase ratio (AAPR) has been shown to be a prognostic predictor in several malignancies, but its predictive value for pCR in breast cancer is still unknown. This study aims to investigate the predictive role of AAPR in breast cancer patients and develop an AAPR-based nomogram for pCR rate prediction.MethodsA total of 780 patients who received anthracycline and taxane-based NAC from January 2012 to March 2018 were retrospectively analyzed. Univariate and multivariate analyses were performed to assess the predictive value of AAPR and other clinicopathological factors. A nomogram was developed and calibrated based on multivariate logistic regression. A validation cohort of 234 patients was utilized to further validate the predictive performance of the model. The C-index, calibration plots and decision curve analysis (DCA) were used to evaluate the discrimination, calibration and clinical value of the model.ResultsPatients with a lower AAPR (<0.583) had a significantly reduced pCR rate (OR 2.228, 95% CI 1.246-3.986, p=0.007). Tumor size, clinical nodal status, histological grade, PR, Ki67 and AAPR were identified as independent predictors and included in the final model. The nomogram was used as a graphical representation of the model. The nomogram had satisfactory calibration and discrimination in both the training cohort and validation cohort (the C-index was 0.792 in the training cohort and 0.790 in the validation cohort). Furthermore, DCA indicated a clinical net benefit from the nomogram.ConclusionsPretreatment serum AAPR is a potentially valuable predictor for pCR in breast cancer patients who receive NAC. The AAPR-based nomogram is a noninvasive tool with favorable predictive accuracy for pCR, which helps to make individualized treatment strategy decisions.

Highlights

  • Breast cancer is the most common female malignancy and is one of the leading causes of female cancer morbidity and mortality [1]

  • We retrospectively reviewed the medical records of primary breast cancer patients at the First Affiliated Hospital of Chongqing Medical University from January 2012 to March 2018

  • According to the Miller-Payne grading system, 103 (13.2%) patients were evaluated as having pathological complete response (pCR) after Neoadjuvant chemotherapy (NAC)

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Summary

Introduction

Breast cancer is the most common female malignancy and is one of the leading causes of female cancer morbidity and mortality [1]. Neoadjuvant chemotherapy (NAC) is a standard treatment option for most breast cancer patients, especially those with locally advanced or inoperable breast cancer. It aims to reduce disease burden and make breast cancer operable in locally advanced patients [2]. NAC makes it possible to receive breast-conserving surgery. A recent meta-analysis of 52 clinical trials, including 27,895 patients, demonstrated that pathological complete response (pCR) after NAC was associated with better event-free survival and overall survival in all breast cancer molecular subtypes [4]. Breast cancer patients who achieve pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) have favorable outcomes. This study aims to investigate the predictive role of AAPR in breast cancer patients and develop an AAPR-based nomogram for pCR rate prediction

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