2020
DOI: 10.3389/fonc.2020.00093
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The Diagnostic Performance of DCE-MRI in Evaluating the Pathological Response to Neoadjuvant Chemotherapy in Breast Cancer: A Meta-Analysis

Abstract: Background: Neoadjuvant chemotherapy (NAC) is commonly utilized in preoperative treatment for local breast cancer, and it gives high clinical response rates and can result in pathologic complete response (pCR) in 6-25% of patients. In recent years, dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) has been increasingly used to assess the pathological response of breast cancer to NAC. In present analysis, we assess the diagnostic performance of DCE-MRI in evaluating the pathological response of bre… Show more

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Cited by 48 publications
(40 citation statements)
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“…Meta-analysis showed that 18 F-FDG PET/CT had a moderate accuracy for the early prediction for pCR (sensitivity 85%, specificity 79% and diagnostic odds ratio 21.8), especially in HER2 positive and triple negative breast cancer 16 , 17 . DCE-MRI was also an effective method for early monitoring the efficacy during NAT (sensitivity 87%, specificity 82% and diagnostic odds ratio 30.3) 18 . However, both 18 F-FDG PET/CT and DCE-MRI require sophisticated imaging, additional radiation dose for patients, and less accessible compared with ultrasound.…”
Section: Discussionmentioning
confidence: 99%
“…Meta-analysis showed that 18 F-FDG PET/CT had a moderate accuracy for the early prediction for pCR (sensitivity 85%, specificity 79% and diagnostic odds ratio 21.8), especially in HER2 positive and triple negative breast cancer 16 , 17 . DCE-MRI was also an effective method for early monitoring the efficacy during NAT (sensitivity 87%, specificity 82% and diagnostic odds ratio 30.3) 18 . However, both 18 F-FDG PET/CT and DCE-MRI require sophisticated imaging, additional radiation dose for patients, and less accessible compared with ultrasound.…”
Section: Discussionmentioning
confidence: 99%
“…The quality of studies and the likelihood of bias were evaluated using Review Manager 5.3 software (Cochrane Collaboration, Oxford, UK), based on the Quality Assessment of Diagnostic Accuracy Studies-2 ( 18 ). We assessed the risk of bias and applicability concerns in four domains, including patient selection, index tests, reference standard, and flow, and timing ( 19 ).…”
Section: Methodsmentioning
confidence: 99%
“…The quality of studies and likelihood of bias were evaluated using Review Manager 5.3 software (Cochrane Collaboration, Oxford, UK), referring to the Quality Assessment of Diagnostic Accuracy Studies-2 (28). We assessed the risk of bias and applicability in four domains, including patient selection, index tests, reference standard, flow, and timing (29).…”
Section: Quality Assessmentmentioning
confidence: 99%