Locally advanced breast cancer: MR imaging for prediction of response to neoadjuvant chemotherapy - Results from ACRIN 6657/I-SPY TRIAL Journal Article


Authors: Hylton, N. M.; Blume, J. D.; Bernreuter, W. K.; Pisano, E. D.; Rosen, M. A.; Morris, E. A.; Weatherall, P. T.; Lehman, C. D.; Newstead, G. M.; Polin, S.; Marques, H. S.; Esserman, L. J.; Schnall, M. D.
Article Title: Locally advanced breast cancer: MR imaging for prediction of response to neoadjuvant chemotherapy - Results from ACRIN 6657/I-SPY TRIAL
Abstract: Purpose: To compare magnetic resonance (MR) imaging findings and clinical assessment for prediction of pathologic response to neoadjuvant chemotherapy (NACT) in patients with stage II or III breast cancer. Materials and Methods: The HIPAA-compliant protocol and the informed consent process were approved by the American College of Radiology Institutional Review Board and local-site institutional review boards. Women with invasive breast cancer of 3 cm or greater undergoing NACT with an anthracycline-based regimen, with or without a taxane, were enrolled between May 2002 and March 2006. MR imaging was performed before NACT (first examination), after one cycle of anthracyline-based treatment (second examination), between the anthracycline-based regimen and taxane (third examination), and after all chemotherapy and prior to surgery (fourth examination). MR imaging assessment included measurements of tumor longest diameter and volume and peak signal enhancement ratio. Clinical size was also recorded at each time point. Change in clinical and MR imaging predictor variables were compared for the ability to predict pathologic complete response (pCR) and residual cancer burden (RCB). Univariate and multivariate random-effects logistic regression models were used to characterize the ability of tumor response measurements to predict pathologic outcome, with area under the receiver operating characteristic curve (AUC) used as a summary statistic. Results: Data in 216 women (age range, 26-68 years) with two or more imaging time points were analyzed. For prediction of both pCR and RCB, MR imaging size measurements were superior to clinical examination at all time points, with tumor volume change showing the greatest relative benefit at the second MR imaging examination. AUC differences between MR imaging volume and clinical size predictors at the early, mid-, and posttreatment time points, respectively, were 0.14, 0.09, and 0.02 for prediction of pCR and 0.09, 0.07, and 0.05 for prediction of RCB. In multivariate analysis, the AUC for predicting pCR at the second imaging examination increased from 0.70 for volume alone to 0.73 when all four predictor variables were used. Additional predictive value was gained with adjustments for age and race. Conclusion: MR imaging findings are a stronger predictor of pathologic response to NACT than clinical assessment, with the greatest advantage observed with the use of volumetric measurement of tumor response early in treatment. © RSNA, 2012.
Keywords: adult; controlled study; human tissue; treatment outcome; aged; middle aged; major clinical study; histopathology; cancer localization; advanced cancer; cancer combination chemotherapy; clinical trials as topic; cancer adjuvant therapy; neoadjuvant therapy; nuclear magnetic resonance imaging; outcome assessment; magnetic resonance imaging; neoplasm staging; diagnostic accuracy; prospective studies; multiple cycle treatment; breast cancer; image analysis; tumor volume; antineoplastic combined chemotherapy protocols; logistic models; clinical assessment; breast neoplasms; neoplasm, residual; contrast enhancement; image quality; drug response; predictive value of tests; area under curve; neoplasm invasiveness; taxane derivative; anthracycline; predictive value; roc curve; receiver operating characteristic; volumetry
Journal Title: Radiology
Volume: 263
Issue: 3
ISSN: 0033-8419
Publisher: Radiological Society of North America, Inc.  
Date Published: 2012-06-01
Start Page: 663
End Page: 672
Language: English
DOI: 10.1148/radiol.12110748
PROVIDER: scopus
PMCID: PMC3359517
PUBMED: 22623692
DOI/URL:
Notes: --- - "Export Date: 2 July 2012" - "CODEN: RADLA" - "Source: Scopus"
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  1. Elizabeth A Morris
    336 Morris