The Evaluation of Magee Equation 2 in Predicting Response and Outcome in Hormone Receptor-Positive and HER2-Negative Breast Cancer Patients Receiving Neoadjuvant Chemotherapy
Authors Saigosoom N, Sa-nguanraksa D, O-charoenrat E, Thumrongtaradol T, O-charoenrat P
Received 5 November 2019
Accepted for publication 27 March 2020
Published 8 April 2020 Volume 2020:12 Pages 2491—2499
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 5
Editor who approved publication: Dr Antonella D'Anneo
Napat Saigosoom,1,* Doonyapat Sa-nguanraksa,1,* Eng O-charoenrat,2 Thanawat Thumrongtaradol,1 Pornchai O-charoenrat1
1Division of Head, Neck and Breast Surgery, Department of Surgery, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand; 2Faculty of Medical Sciences, University College London, London WC1E 6BT, UK
*These authors contributed equally to this work
Correspondence: Pornchai O-charoenrat
Division of Head Neck and Breast Surgery, Department of Surgery, Faculty of Medicine, Siriraj Hospital, Mahidol University, 2 Wanglang Road, Bangkoknoi, Bangkok 10700, Thailand
Tel +66 2419 2837
Background and Purpose: Magee Equations have been developed as accurate tools for predicting response and clinical outcomes in breast cancer patients treated with adjuvant systemic therapy using basic clinicopathological parameters. This study aims to evaluate the alternative application of Magee Equation 2 score in predicting pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) in hormone receptor (HR)-positive, HER2-negative breast cancer.
Patients and Methods: Patients with HR-positive, HER2-negative breast cancer who received NAC from January 2010 to May 2018 at Siriraj Hospital, Mahidol University, Thailand, were recruited. Pre-treatment status of HR and HER2 was used to calculate the Magee Equation 2 scores. The pCR rates among different clinicopathological parameters were analyzed. Survival analysis was performed by Log-rank test. Kaplan–Meier survival curves were analyzed.
Results: A total of 215 patients were eligible. The pCR rates for low, intermediate, and high scores were 4.8%, 3.6%, and 23.8%, respectively. Patients with high scores had significantly higher size reduction and pCR rates compared to those with intermediate or low scores (p< 0.001). Those with high scores had higher rates of locoregional recurrence and death. The patients with high score had significantly lower overall survival (p=0.034).
Conclusion: Among patients with HR-positive and HER2-negative breast cancer treated with NAC, Magee Equation 2 might be used as a tool for predicting the pCR and clinical outcome.
Keywords: breast cancer, Magee Equation, neoadjuvant chemotherapy, pathologic complete response, survival
Breast cancer is the most common cancer in women worldwide and it is the leading cause of cancer-related death among females worldwide.1 Estrogen receptor (ER), progesterone receptor, and HER2 are considered as important biomarkers that can predict not only the response to treatment but also prognosis and disease recurrence.2–4 Ki-67 is known to be present in all proliferating cells and it has been used as a surrogate marker to assess proliferation index.5,6
Approximately 75% of invasive breast cancers are ER-positive and/or PR-positive tumors.7 Although approximately 85% of these women may be recurrence free at 10 years with adjuvant hormonal therapy alone, the addition of chemotherapy leads to relative reduction in the risk of recurrence of approximately 30% on average. This leads to an absolute benefit for an individual patient ranging from 1% to 5%.8,9 Many patients with ER-positive breast cancer would, therefore, be over treated with chemotherapy based on clinicopathologic features alone although most of them would have been adequately treated with hormonal therapy alone.10,11 On the other hand, neoadjuvant chemotherapy (NAC) before surgery is the standard therapy in the patients with locally advanced breast cancer12 and also increased the rate of breast conserving surgery in early breast cancer.13 The patients with pathological complete response (pCR) after NAC have improved survival.14
Gene expression profile assessed by the 21-gene assay (Oncotype Dx®; Genomic Health, Redwood City, CA) has been developed to precisely identify patients with ER-positive breast cancer who will benefit from chemotherapy using the result expressed as a recurrence score (RS).15 Furthermore, RS can discriminate pathological complete response (pCR) in the patients who received NAC.16 However, it has limitations, including a cost of over $4000 per test and a delay in treatment while waiting for the results. A recent study reported that biomarkers including ER, PR, and HER-2 can be incorporated into a multivariable model (known as Magee Equations; http://path.upmc.edu/onlineTools/MageeEquations.html) to predict the RS.17,18 The Magee Equations have been studied in both internal and external validation studies.19,20 Since the 21-gene assay has been shown to predict the benefit of adjuvant chemotherapy in women with hormone-receptor (HR)-positive, HER2-negative, axillary node-negative breast cancer, we hypothesized that Magee Equation 2 should also predict the response to NAC. This study aims to evaluate the alternative application of Magee Equation 2 score in predicting pCR after NAC in HR-positive, HER2-negative breast cancer.
Patients and Methods
This study was approved by Siriraj Institutional Review Board. The patient consent to review their medical records was not required due to this study involved the collection of existing data recorded by the investigator in such a manner that subjects cannot be identified, directly or through identifiers linked to the subject. This study was conducted in accordance with the Declaration of Helsinki. Patients with HR-positive, HER2-negative breast cancer who received NAC from January 2010 to May 2018 at Siriraj Hospital, Mahidol University, Thailand were retrospectively reviewed. pCR was defined as the absence of invasive tumor in the surgical specimen (pCR in both breast and axillary nodes). Residual carcinoma in situ without invasive carcinoma was allowed for pCR.21 Estimated tumor size reduction in the breast was calculated using the following equation: Estimated percent tumor size reduction= ((pre-therapy clinical size-pathology size)/pre-therapy clinical size) x100.
The pathology size is the largest dimension of the gross tumor bed by the invasive tumor cellularity. Pre-treatment status of ER, PR, HER2, and Ki-67 was available from core biopsy pathology reports and were used to calculate Magee Equation 2 scores using the equation:
The H-score was calculated by summation of the results of multiplication of the percentage of cells (0–100%) with staining intensity (0 for negative, 1 for weak, 2 for moderate, and 3 for strong intensity). The results can be ranged from 0 to 300.22 Magee Equation 2 scores were divided into 3 categories according to the RS obtained from Oncotype Dx: 0-<18=low; 18-<31=intermediate; and ≥31=high.
Statistical analysis was performed using SPSS version 25.0® (SPSS Inc., Chicago, USA). Continuous parameters were compared by independent t-test or Wilcoxon rank sum test. Categorical parameters were analyzed by chi-square statistics and the p-values were obtained from a two-sided Fisher exact test. Patients with missing or unknown information were excluded from the test. Confidence intervals were obtained using Wald normal approximation. Multivariable analysis for prediction of pCR was performed after including variables that were significant on univariable analysis. Survival analyses were performed using the Log-rank (univariate analysis) and Cox regression (multivariate analysis) methods. Two-sided tests were used in all analyses. The significance level was set at P<0.05.
Breast cancer cohort was searched for the term NAC and resulted in 757 patients. Of the 757 patients, 215 patients with ER-positive, HER2-negative or equivocal were eligible for participation (excluding 75 patients without NAC; 293 patients with HR-negative or HER2-positive; 127 patients with de novo metastatic breast cancer; and 47 patients with incomplete data or incomplete treatment). The demographic and tumor characteristics data with respect to pCR for the 215 ER-positive, HER2-negative/equivocal patients are shown in Table 1.
Table 1 Patient and Tumor Characteristics
NAC regimens were chosen at the discretion of the medical oncologists and resulting in different NAC regimens. However, the majority (96.3%) received an anthracycline (AC) and a sequential anthracycline and taxane (AC-T) regimens. Five patients (2.3%) had received neoadjuvant endocrine therapy for 6 months before surgery. After neoadjuvant treatment, 49 patients underwent breast conserving surgery, while 166 patients underwent total mastectomy. Axillary lymph node dissection was performed in 181 patients and sentinel lymph node biopsy was performed in 34 patients. All pathological reports of both breast conserving surgery and mastectomy specimens showed free surgical margin.
Overall, 17 patients (7.9%) had pCR. The patients with pCR had significantly lower ER H-score and PR H-score (p=0.003 and p=0.027, respectively). Of the 215 patients, the distribution of Magee Equation 2 scores was low in 62 (28.8%), intermediate in 111 (51.6%), and high in 42 (19.5%) patients. The pCR rates for low, intermediate, and high Magee Equation 2 scores were 4.8%, 3.6%, and 23.8%, respectively (Table 2). Patients with high Magee Equation 2 scores were more likely to have pCR compare to those with intermediate or low scores (OR= 7.41, 95% CI 2.63–20.91, p<0.001). Subgroup analysis of those who received AC-based regimen showed that the patients with high scores were more likely to have pCR (OR=14.17, 95% CI 2.58–77.87, p=0.002). The rate of pCR was significantly higher in those who received AC-T chemotherapy than those who received AC-based chemotherapy (13.3% vs 4.8%, p=0.031, respectively). The estimated tumor size reduction was also significantly higher in the patients with high Magee Equation 2 score when compare to those with low and intermediate scores. Multivariate analysis by binary logistic regression showed that Magee Equation 2 score was the only independent predictor for pCR (Table 3). The factors that were utilized to calculate Magee 2 score (tumor size, Nottingham score, ER H-score, PR H-score, and HER2 status) were not included in this multivariate analysis.
Table 2 Magee Equation 2 Score Categories and Outcomes
Table 3 Multivariate Analysis of Predictive Factors for pCR
Median follow-up time was 33 months (1–106 months). There were 30 locoregional recurrences, 59 distant metastasis, and 36 deaths occurred. Those with high Magee Equation 2 scores had higher rates of locoregional recurrence and death when compared to those with low/intermediate score (OR=2.47, 95% CI 1.05–5.78, p=0.033, and OR=2.57, 95% CI 1.16–5.71, p=0.018, respectively) (Table 2). Five-year disease-free survival (DFS) rates for low, intermediate, and high Magee Equation 2 scores were 69.7%, 50.8%, and 54.9%, respectively. The survival analysis by Log-rank test showed worse DFS for high Magee Equation 2 category but the level of statistically significant was not reached (p=0.101). Five-year overall survival (OS) rates for low, intermediate, and high Magee Equation 2 scores were 80.2%, 81.0%, and 61.8%, respectively. Univariate analysis by Log-rank test showed that the patients with high Magee Equation 2 scores had significantly lower OS (p=0.034). The survival curves estimated by Kaplan–Meier method are shown in Figures 1 and 2. Multivariate analysis by Cox regression revealed that N stage and Magee Equation 2 score were the independent predictors for both DFS and OS. The factors that were utilized to calculate Magee 2 score (tumor size, Nottingham score, ER H-score, PR H-score, and HER2 status) were not included in this multivariate analysis (Tables 4 and 5).
Table 4 Multivariate Analysis of Independent Prognostic Factors for DFS
Table 5 Multivariate Analysis of Independent Prognostic Factors for OS
Figure 1 DFS by Magee Equation 2 score category. ME: Magee Equation 2 score. Abbreviation: ME, Magee Equation 2 score.
Figure 2 OS by Magee Equation 2 score category. Abbreviation: ME, Magee Equation 2 score.
Achievement of pCR following NAC was associated with better DFS and OS, especially in the patients with triple-negative or HER2-positive breast cancer.23 Several clinicopathological parameters were reported to be the predictors for response to NAC.24,25 Luminal breast cancer subtype had lower response to NAC when compare to other subtypes.26,27
Although there were higher proportion of T4 breast cancer recruited in this current study, the rate of pCR in the current study was similar to the recent report of clinically node-positive breast cancer receiving NAC.25 However, approximately 70% of the patients received neoadjuvant AC regimen which resulted in lower response when compare to the addition of taxane-based regimen.28
Gene expression profiles assessed by Oncotype DX in the patients with locally advanced breast cancer who received neoadjuvant paclitaxel and doxorubicin revealed that high RS were strongly associated with pCR.16 In a study by Yardley et al, 108 patients with HER2-negative breast cancer who received neoadjuvant ixabepilone and cyclophosphamide were assessed for pCR rate. The patients with a high-risk score had a pCR rate of 26% compared to 0% in patients with low or intermediate risk scores.29 These patients were most likely to receive the greatest clinical benefit from NAC. However, the Oncotype DX carries a high cost and may not be widely available in Thailand. Utilization of conventional clinicopathological parameters derived from pretreatment core biopsy might be suitable in this situation. Magee Equation score can accurately estimate the RS and might be used as an alternative predictor for response to chemotherapy.18 Magee Equation 3 score was previously reported to be accurately predict the response to NAC in HR-positive, HER2-negative breast cancer.30 Due to Ki67 was not available in a significant proportion of the patients in our cohort, Magee Equation 2 that does not require Ki67 results was utilized in the current study. High Magee Equation 2 score was the independent predictor for pCR in HR-positive, HER2-negative breast cancer. In contrast, high Magee Equation 2 score was also the independent predictor of lower DFS and OS. The patients with high score had unfavorable clinicopathological parameters and aggressive tumor biology. However, the rate of pCR is also higher in the tumor that had more aggressive biology when compared to the tumor that had favorable biology (eg Luminal breast cancer). Subgroup analysis of the patients with high score showed that among 37 patients with high score, approximately one-fourth of the patients (24.3%) had pCR. Lower percentage of death was occurred in the patients with pCR when compared with the patients without pCR (11.8% vs 17.2%, respectively). pCR was not a significant predictor for DFS and OS. This finding might be due to a small number of patients with pCR. Furthermore, pooled analysis of more than 11,000 patients among 12 studies suggested that achievement of pCR was associated with better OS in non-luminal (HER2-positive or triple-negative), and grade 3 luminal, HER2-negative breast cancer. In contrast, pCR failed to demonstrate this association in grade 1/2 HR-positive, HER2-negative breast cancer14 which accounted for the major proportion of the patients in this current study.
High Magee Equation 2 score was associated with tumor size reduction after NAC. This finding might suggest the application of Magee Equation for prediction of NAC in HR-positive, HER2-negative breast cancer patients who will receive NAC with the aim of downsizing for conversion from total mastectomy to breast conserving surgery. However, this was not the objective of this study and further study is required to address this issue.
Our study had some limitations as follows. Due to a retrospective study, selection bias might be occurred. Majority of the patients had locally advanced breast cancer and might result in lower pCR rate. The follow up time was relatively short as the HR-positive breast cancers tend to recur later.
Our findings demonstrate an association between high Magee Equation 2 scores and pCR after NAC. The Magee Equation 2 might be used for predicting pCR and clinical outcomes in the patients who will receive NAC especially in countries with limited resource for high-cost gene expression assays.
The authors gratefully acknowledge the patients who generously participated in this study. We are grateful to Mr. Suthipol Udompunturak (Faculty of Medicine, Siriraj Hospital) for helping with statistical analysis and appreciated the help from Miss Surat Phumphuang (Department of Surgery, Siriraj Hospital) for coordination of research work and data collection.
The authors report no conflicts of interest in this work.
The abstract of this paper was presented at the 16th St. Gallen International Breast Cancer Conference as an abstract presentation with interim findings. The poster’s abstract was published in “Poster Abstracts” in The Breast: https://doi.org/10.1016/S0960-9776(19)30270-X.
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