Abstract

BackgroundTo better predict the likelihood of response to chemotherapy, we have conducted a study comparing the gene expression patterns of primary tumours with their corresponding response to systemic chemotherapy in the metastatic setting.MethodsmRNA expression profiles of breast carcinomas of patients that later developed distant metastases were analyzed using supervised and non-supervised classification techniques to identify predictors of response to chemotherapy. The top differentially expressed genes between the responders and non-responders were identified and further explored. An independent dataset which was generated to predict response to neo-adjuvant CT was utilized for the purpose of validation. Response to chemotherapy was also correlated to the clinicopathologic characteristics, molecular subtypes, metastatic behavior and survival outcomes.ResultsAnthracycline containing regimens were the most common first line treatment (58.4%), followed by non-anthracycline/non-taxane containing (25.8%) and taxane containing (15.7%) regimens. Response was achieved in 41.6% of the patients to the first line CT and in 21.8% to second line CT. Response was not found to be significantly correlated to tumour type, grade, lymph node status, ER and PR status. Patients with HER2+ tumours showed better response to anthracycline containing therapy (p: 0.002). Response to first and second line chemotherapy did not differ among gene expression based molecular subtypes (p: 0.236 and p: 0.20). Using supervised classification, a 14 gene response classifier was identified. This 14-gene predictor could successfully predict the likelihood of better response to first and second line CT (p: <.0001 and p: 0.761, respectively) in the training set. However, the predictive value of this gene set in data of response to neoadjuvant chemotherapy could not be validated.ConclusionsTo our knowledge, this is the first study revealing the relation between gene expression profiles of the primary tumours and their chemotherapy responsiveness in the metastatic setting. In contrast to the findings for neoadjuvant chemotherapy treatment, there was no association of molecular subtype with response to chemotherapy in the metastatic setting. Using supervised classification, we identified a classifier of chemotherapy response; however, we could not validate this classifier using neoadjuvant response data.Trial registrationNon applicable. Subjects were retrospectively registered.

Highlights

  • To better predict the likelihood of response to chemotherapy, we have conducted a study comparing the gene expression patterns of primary tumours with their corresponding response to systemic chemotherapy in the metastatic setting

  • In the current study we have shown that Estrogen receptor (ER)-positive/HER2negative tumours with high-risk recurrence scores had shorter time to develop metastatic disease and shorter overall survival, we were not able to confirm an association with chemotherapy response

  • We present a comprehensive study comparing the gene expression patterns of primary tumours from metastatic breast cancer patients according to their responsiveness of chemotherapy during their treatment of metastatic disease

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Summary

Introduction

To better predict the likelihood of response to chemotherapy, we have conducted a study comparing the gene expression patterns of primary tumours with their corresponding response to systemic chemotherapy in the metastatic setting. The main aim of treating metastatic breast cancer is to prolong survival of the patients with acceptable toxicity and to palliate the disease-related symptoms. Response to combined chemotherapy agents varies between 50 and 70% in the metastatic setting [1, 2]. The decision to treat patients with metastatic breast cancer with chemotherapy is usually taken depending on many factors such as patient age and performance status, site of metastasis, hormone receptor status and prior exposure to chemotherapy, [3, 4]. Used first-line therapeutic options in the metastatic setting include anthracycline- and/or taxane-based regimens [5]. In case of disease progression other cytotoxic agents may be applied to maximize the duration of quality time for these patients [6]

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