Association between serial dynamic contrast-enhanced MRI and dynamic 18F-FDG PET measures in patients undergoing neoadjuvant chemotherapy for locally advanced breast cancer

Purpose To investigate the relationship between changes in vascularity and metabolic activity measured by dynamic contrast‐enhanced magnetic resonance imaging (DCE‐MRI) and dynamic 18F‐FDG‐positron emission tomography (PET) in breast tumors undergoing neoadjuvant chemotherapy. Materials and Methods...

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Veröffentlicht in:Journal of magnetic resonance imaging 2010-11, Vol.32 (5), p.1124-1131
Hauptverfasser: Partridge, Savannah C., Vanantwerp, Risa K., Doot, Robert K., Chai, Xiaoyu, Kurland, Brenda F., Eby, Peter R., Specht, Jennifer M., Dunnwald, Lisa K., Schubert, Erin K., Lehman, Constance D., Mankoff, David A.
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container_end_page 1131
container_issue 5
container_start_page 1124
container_title Journal of magnetic resonance imaging
container_volume 32
creator Partridge, Savannah C.
Vanantwerp, Risa K.
Doot, Robert K.
Chai, Xiaoyu
Kurland, Brenda F.
Eby, Peter R.
Specht, Jennifer M.
Dunnwald, Lisa K.
Schubert, Erin K.
Lehman, Constance D.
Mankoff, David A.
description Purpose To investigate the relationship between changes in vascularity and metabolic activity measured by dynamic contrast‐enhanced magnetic resonance imaging (DCE‐MRI) and dynamic 18F‐FDG‐positron emission tomography (PET) in breast tumors undergoing neoadjuvant chemotherapy. Materials and Methods PET and MRI examinations were performed in 14 patients with locally advanced breast cancer (LABC) before and after chemotherapy. Dynamic 18F‐FDG PET measures included 18F‐FDG transport rate constant from blood to tissue (K1) and metabolism flux constant (Ki). DCE‐MRI measures included initial peak enhancement (PE), signal enhancement ratio (SER), and tumor volume. Spearman rank‐order correlations were assessed between changes in PET and MRI parameters, and measures were compared between patients with and without pathologic complete response (pCR) by Mann–Whitney U‐test. Results Changes in glucose delivery (PET K1) were closely correlated with changes in tumor vascularity as reflected by DCE‐MRI SER (r = 0.83, P < 0.001). Metabolic changes in PET Ki showed moderate correlations with vascularity changes as reflected by SER (r = 0.71) and PE (r = 0.76), and correlated closely with MRI tumor volume (r = 0.79, P < 0.001). Decreases in K1, Ki, SER, and PE were greater for patients with pCR compared to those with residual disease (P < 0.05). Conclusion Dynamic 18F‐FDG PET and DCE‐MRI tumor measures of tumor metabolism, vascularity, and volume were well correlated for assessing LABC response to neoadjuvant chemotherapy and significantly discriminated pathologic complete responders. Further work is necessary to assess the value of combined PET and MRI for evaluating tumor pharmacodynamics in response to novel therapy. J. Magn. Reson. Imaging 2010;32:1124–1131. © 2010 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jmri.22362
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Materials and Methods PET and MRI examinations were performed in 14 patients with locally advanced breast cancer (LABC) before and after chemotherapy. Dynamic 18F‐FDG PET measures included 18F‐FDG transport rate constant from blood to tissue (K1) and metabolism flux constant (Ki). DCE‐MRI measures included initial peak enhancement (PE), signal enhancement ratio (SER), and tumor volume. Spearman rank‐order correlations were assessed between changes in PET and MRI parameters, and measures were compared between patients with and without pathologic complete response (pCR) by Mann–Whitney U‐test. Results Changes in glucose delivery (PET K1) were closely correlated with changes in tumor vascularity as reflected by DCE‐MRI SER (r = 0.83, P &lt; 0.001). Metabolic changes in PET Ki showed moderate correlations with vascularity changes as reflected by SER (r = 0.71) and PE (r = 0.76), and correlated closely with MRI tumor volume (r = 0.79, P &lt; 0.001). Decreases in K1, Ki, SER, and PE were greater for patients with pCR compared to those with residual disease (P &lt; 0.05). Conclusion Dynamic 18F‐FDG PET and DCE‐MRI tumor measures of tumor metabolism, vascularity, and volume were well correlated for assessing LABC response to neoadjuvant chemotherapy and significantly discriminated pathologic complete responders. Further work is necessary to assess the value of combined PET and MRI for evaluating tumor pharmacodynamics in response to novel therapy. J. Magn. Reson. Imaging 2010;32:1124–1131. © 2010 Wiley‐Liss, Inc.</description><identifier>ISSN: 1053-1807</identifier><identifier>EISSN: 1522-2586</identifier><identifier>DOI: 10.1002/jmri.22362</identifier><identifier>PMID: 21031518</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Breast Neoplasms - blood supply ; Breast Neoplasms - diagnosis ; Breast Neoplasms - diagnostic imaging ; Breast Neoplasms - pathology ; Contrast Media ; dynamic 18F-FDG positron emission tomography (PET) ; dynamic contrast-enhanced MRI (DCE-MRI) ; Female ; Fluorodeoxyglucose F18 ; Gadolinium DTPA ; Humans ; locally advanced breast cancer ; Magnetic Resonance Imaging ; Middle Aged ; Neoadjuvant Therapy ; pathologic response ; Positron-Emission Tomography ; Radiopharmaceuticals ; treatment</subject><ispartof>Journal of magnetic resonance imaging, 2010-11, Vol.32 (5), p.1124-1131</ispartof><rights>Copyright © 2010 Wiley‐Liss, Inc.</rights><rights>2010 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmri.22362$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmri.22362$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21031518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Partridge, Savannah C.</creatorcontrib><creatorcontrib>Vanantwerp, Risa K.</creatorcontrib><creatorcontrib>Doot, Robert K.</creatorcontrib><creatorcontrib>Chai, Xiaoyu</creatorcontrib><creatorcontrib>Kurland, Brenda F.</creatorcontrib><creatorcontrib>Eby, Peter R.</creatorcontrib><creatorcontrib>Specht, Jennifer M.</creatorcontrib><creatorcontrib>Dunnwald, Lisa K.</creatorcontrib><creatorcontrib>Schubert, Erin K.</creatorcontrib><creatorcontrib>Lehman, Constance D.</creatorcontrib><creatorcontrib>Mankoff, David A.</creatorcontrib><title>Association between serial dynamic contrast-enhanced MRI and dynamic 18F-FDG PET measures in patients undergoing neoadjuvant chemotherapy for locally advanced breast cancer</title><title>Journal of magnetic resonance imaging</title><addtitle>J. Magn. Reson. Imaging</addtitle><description>Purpose To investigate the relationship between changes in vascularity and metabolic activity measured by dynamic contrast‐enhanced magnetic resonance imaging (DCE‐MRI) and dynamic 18F‐FDG‐positron emission tomography (PET) in breast tumors undergoing neoadjuvant chemotherapy. Materials and Methods PET and MRI examinations were performed in 14 patients with locally advanced breast cancer (LABC) before and after chemotherapy. Dynamic 18F‐FDG PET measures included 18F‐FDG transport rate constant from blood to tissue (K1) and metabolism flux constant (Ki). DCE‐MRI measures included initial peak enhancement (PE), signal enhancement ratio (SER), and tumor volume. Spearman rank‐order correlations were assessed between changes in PET and MRI parameters, and measures were compared between patients with and without pathologic complete response (pCR) by Mann–Whitney U‐test. Results Changes in glucose delivery (PET K1) were closely correlated with changes in tumor vascularity as reflected by DCE‐MRI SER (r = 0.83, P &lt; 0.001). Metabolic changes in PET Ki showed moderate correlations with vascularity changes as reflected by SER (r = 0.71) and PE (r = 0.76), and correlated closely with MRI tumor volume (r = 0.79, P &lt; 0.001). Decreases in K1, Ki, SER, and PE were greater for patients with pCR compared to those with residual disease (P &lt; 0.05). Conclusion Dynamic 18F‐FDG PET and DCE‐MRI tumor measures of tumor metabolism, vascularity, and volume were well correlated for assessing LABC response to neoadjuvant chemotherapy and significantly discriminated pathologic complete responders. Further work is necessary to assess the value of combined PET and MRI for evaluating tumor pharmacodynamics in response to novel therapy. J. Magn. Reson. Imaging 2010;32:1124–1131. © 2010 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Breast Neoplasms - blood supply</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - diagnostic imaging</subject><subject>Breast Neoplasms - pathology</subject><subject>Contrast Media</subject><subject>dynamic 18F-FDG positron emission tomography (PET)</subject><subject>dynamic contrast-enhanced MRI (DCE-MRI)</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18</subject><subject>Gadolinium DTPA</subject><subject>Humans</subject><subject>locally advanced breast cancer</subject><subject>Magnetic Resonance Imaging</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>pathologic response</subject><subject>Positron-Emission Tomography</subject><subject>Radiopharmaceuticals</subject><subject>treatment</subject><issn>1053-1807</issn><issn>1522-2586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUctu1DAUjRCIlsKGD0DesUrrxzhONkildIai4VFUxNJy7JsZD4k9tZMp-ad-JE6njGB179U9Dx2dLHtN8CnBmJ5tumBPKWUFfZIdE05pTnlZPE075iwnJRZH2YsYNxjjqprx59kRJZgRTsrj7P48Rq-t6q13qIb-DsChCMGqFpnRqc5qpL3rg4p9Dm6tnAaDPn-_QsqZA4KU83z-YYG-Xd6gDlQcAkRkHdomXXB9RIMzEFbeuhVy4JXZDDvleqTX0Pl-DUFtR9T4gFqvVduOSJnd3qkOSS4Bpyu8zJ41qo3w6nGeZD_mlzcXH_Pl18XVxfkyt0wImteMF4zTFLDCxhAgVW2M0nXDTVk0qiCaamxq0eiZKKGqSgDKaKMrVTd1TTk7yd7tdbdD3YHRMOVv5TbYToVRemXl_x9n13Lld5JWhZiRSeDto0DwtwPEXnY2amhbldIPUYqCJmsiWEK--dfq4PG3oQQge8CdbWE8_AmWU_dy6l4-dC8_pVYetsTJ9xwbe_h94KjwSxaCCS5_flnI6pqK5fvrpeTsD1UZtng</recordid><startdate>201011</startdate><enddate>201011</enddate><creator>Partridge, Savannah C.</creator><creator>Vanantwerp, Risa K.</creator><creator>Doot, Robert K.</creator><creator>Chai, Xiaoyu</creator><creator>Kurland, Brenda F.</creator><creator>Eby, Peter R.</creator><creator>Specht, Jennifer M.</creator><creator>Dunnwald, Lisa K.</creator><creator>Schubert, Erin K.</creator><creator>Lehman, Constance D.</creator><creator>Mankoff, David A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201011</creationdate><title>Association between serial dynamic contrast-enhanced MRI and dynamic 18F-FDG PET measures in patients undergoing neoadjuvant chemotherapy for locally advanced breast cancer</title><author>Partridge, Savannah C. ; Vanantwerp, Risa K. ; Doot, Robert K. ; Chai, Xiaoyu ; Kurland, Brenda F. ; Eby, Peter R. ; Specht, Jennifer M. ; Dunnwald, Lisa K. ; Schubert, Erin K. ; Lehman, Constance D. ; Mankoff, David A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3772-b35635215190dd1e19bddacbf5d86fa61c2c0db7fc478e998ee232fc9abfbb253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Breast Neoplasms - blood supply</topic><topic>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - diagnostic imaging</topic><topic>Breast Neoplasms - pathology</topic><topic>Contrast Media</topic><topic>dynamic 18F-FDG positron emission tomography (PET)</topic><topic>dynamic contrast-enhanced MRI (DCE-MRI)</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>Gadolinium DTPA</topic><topic>Humans</topic><topic>locally advanced breast cancer</topic><topic>Magnetic Resonance Imaging</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>pathologic response</topic><topic>Positron-Emission Tomography</topic><topic>Radiopharmaceuticals</topic><topic>treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Partridge, Savannah C.</creatorcontrib><creatorcontrib>Vanantwerp, Risa K.</creatorcontrib><creatorcontrib>Doot, Robert K.</creatorcontrib><creatorcontrib>Chai, Xiaoyu</creatorcontrib><creatorcontrib>Kurland, Brenda F.</creatorcontrib><creatorcontrib>Eby, Peter R.</creatorcontrib><creatorcontrib>Specht, Jennifer M.</creatorcontrib><creatorcontrib>Dunnwald, Lisa K.</creatorcontrib><creatorcontrib>Schubert, Erin K.</creatorcontrib><creatorcontrib>Lehman, Constance D.</creatorcontrib><creatorcontrib>Mankoff, David A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Partridge, Savannah C.</au><au>Vanantwerp, Risa K.</au><au>Doot, Robert K.</au><au>Chai, Xiaoyu</au><au>Kurland, Brenda F.</au><au>Eby, Peter R.</au><au>Specht, Jennifer M.</au><au>Dunnwald, Lisa K.</au><au>Schubert, Erin K.</au><au>Lehman, Constance D.</au><au>Mankoff, David A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between serial dynamic contrast-enhanced MRI and dynamic 18F-FDG PET measures in patients undergoing neoadjuvant chemotherapy for locally advanced breast cancer</atitle><jtitle>Journal of magnetic resonance imaging</jtitle><addtitle>J. Magn. Reson. Imaging</addtitle><date>2010-11</date><risdate>2010</risdate><volume>32</volume><issue>5</issue><spage>1124</spage><epage>1131</epage><pages>1124-1131</pages><issn>1053-1807</issn><eissn>1522-2586</eissn><abstract>Purpose To investigate the relationship between changes in vascularity and metabolic activity measured by dynamic contrast‐enhanced magnetic resonance imaging (DCE‐MRI) and dynamic 18F‐FDG‐positron emission tomography (PET) in breast tumors undergoing neoadjuvant chemotherapy. Materials and Methods PET and MRI examinations were performed in 14 patients with locally advanced breast cancer (LABC) before and after chemotherapy. Dynamic 18F‐FDG PET measures included 18F‐FDG transport rate constant from blood to tissue (K1) and metabolism flux constant (Ki). DCE‐MRI measures included initial peak enhancement (PE), signal enhancement ratio (SER), and tumor volume. Spearman rank‐order correlations were assessed between changes in PET and MRI parameters, and measures were compared between patients with and without pathologic complete response (pCR) by Mann–Whitney U‐test. Results Changes in glucose delivery (PET K1) were closely correlated with changes in tumor vascularity as reflected by DCE‐MRI SER (r = 0.83, P &lt; 0.001). Metabolic changes in PET Ki showed moderate correlations with vascularity changes as reflected by SER (r = 0.71) and PE (r = 0.76), and correlated closely with MRI tumor volume (r = 0.79, P &lt; 0.001). Decreases in K1, Ki, SER, and PE were greater for patients with pCR compared to those with residual disease (P &lt; 0.05). Conclusion Dynamic 18F‐FDG PET and DCE‐MRI tumor measures of tumor metabolism, vascularity, and volume were well correlated for assessing LABC response to neoadjuvant chemotherapy and significantly discriminated pathologic complete responders. Further work is necessary to assess the value of combined PET and MRI for evaluating tumor pharmacodynamics in response to novel therapy. J. Magn. Reson. Imaging 2010;32:1124–1131. © 2010 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21031518</pmid><doi>10.1002/jmri.22362</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Breast Neoplasms - blood supply
Breast Neoplasms - diagnosis
Breast Neoplasms - diagnostic imaging
Breast Neoplasms - pathology
Contrast Media
dynamic 18F-FDG positron emission tomography (PET)
dynamic contrast-enhanced MRI (DCE-MRI)
Female
Fluorodeoxyglucose F18
Gadolinium DTPA
Humans
locally advanced breast cancer
Magnetic Resonance Imaging
Middle Aged
Neoadjuvant Therapy
pathologic response
Positron-Emission Tomography
Radiopharmaceuticals
treatment
title Association between serial dynamic contrast-enhanced MRI and dynamic 18F-FDG PET measures in patients undergoing neoadjuvant chemotherapy for locally advanced breast cancer
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