Impact of Initial FDG-PET/CT and Serum-Free Light Chain on Transformation of Conventionally Defined Solitary Plasmacytoma to Multiple Myeloma
Solitary plasmacytoma (SP) is a localized proliferation of monoclonal plasma cells in either bone or soft tissue, without evidence of multiple myeloma (MM), and whose prognosis is marked by a high risk of transformation to MM. We studied the impact of FDG-PET/CT (2[18F]fluoro-2-deoxy-D-glucose posit...
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creator | FOUQUET, Guillemette GUIDEZ, Stéphanie BERTHON, Céline TERRIOU, Louis COITEUX, Valérie MACRO, Margaret DECAUX, Olivier FACON, Thierry HUGLO, Damien LELEU, Xavier HERBAUX, Charles VAN DE WYNGAERT, Zoé BONNET, Sarah BEAUVAIS, David DEMARQUETTE, Hélène ADIB, Salim HIVERT, Bénédicte WEMEAU, Mathieu |
description | Solitary plasmacytoma (SP) is a localized proliferation of monoclonal plasma cells in either bone or soft tissue, without evidence of multiple myeloma (MM), and whose prognosis is marked by a high risk of transformation to MM.
We studied the impact of FDG-PET/CT (2[18F]fluoro-2-deoxy-D-glucose positron emission tomography-computed tomography) on the risk of transformation of SP to overt MM among other markers in a series of 43 patients diagnosed with SP.
Median age was 57.5 years; 48% of patients had an abnormal involved serum-free light chain (sFLC) value, and 64% had an abnormal sFLC ratio at diagnosis. Thirty-three percent had two or more hypermetabolic lesions on initial PET/CT, and 20% had two or more focal lesions on initial MRI. With a median follow-up of 50 months, 14 patients transformed to MM with a median time (TTMM) of 71 months. The risk factors that significantly shortened TTMM at diagnosis were two or more hypermetabolic lesions on PET/CT, abnormal sFLC ratio and involved sFLC, and to a lesser extent at completion of treatment, absence of normalized involved sFLC and PET/CT or MRI. In a multivariate analysis, abnormal initial involved sFLC [OR = 10; 95% confidence interval (CI), 1-87; P = 0.008] and PET/CT (OR = 5; 95% CI, 0-9; P = 0.032) independently shortened TTMM.
An abnormal involved sFLC value and the presence of at least two hypermetabolic lesions on PET/CT at diagnosis of SP were the two predictors of early evolution to myeloma in our series. This data analysis will need confirmation in a larger study, and the study of these two risk factors may lead to a different management of patients with SP in the future. . |
doi_str_mv | 10.1158/1078-0432.ccr-13-2910 |
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We studied the impact of FDG-PET/CT (2[18F]fluoro-2-deoxy-D-glucose positron emission tomography-computed tomography) on the risk of transformation of SP to overt MM among other markers in a series of 43 patients diagnosed with SP.
Median age was 57.5 years; 48% of patients had an abnormal involved serum-free light chain (sFLC) value, and 64% had an abnormal sFLC ratio at diagnosis. Thirty-three percent had two or more hypermetabolic lesions on initial PET/CT, and 20% had two or more focal lesions on initial MRI. With a median follow-up of 50 months, 14 patients transformed to MM with a median time (TTMM) of 71 months. The risk factors that significantly shortened TTMM at diagnosis were two or more hypermetabolic lesions on PET/CT, abnormal sFLC ratio and involved sFLC, and to a lesser extent at completion of treatment, absence of normalized involved sFLC and PET/CT or MRI. In a multivariate analysis, abnormal initial involved sFLC [OR = 10; 95% confidence interval (CI), 1-87; P = 0.008] and PET/CT (OR = 5; 95% CI, 0-9; P = 0.032) independently shortened TTMM.
An abnormal involved sFLC value and the presence of at least two hypermetabolic lesions on PET/CT at diagnosis of SP were the two predictors of early evolution to myeloma in our series. This data analysis will need confirmation in a larger study, and the study of these two risk factors may lead to a different management of patients with SP in the future. .</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.ccr-13-2910</identifier><identifier>PMID: 24714772</identifier><identifier>CODEN: CCREF4</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Aged ; Antineoplastic agents ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Bone Neoplasms - metabolism ; Bone Neoplasms - mortality ; Bone Neoplasms - pathology ; Cell Transformation, Neoplastic - metabolism ; Cell Transformation, Neoplastic - pathology ; Female ; Fluorodeoxyglucose F18 ; Follow-Up Studies ; Genetics ; Hematologic and hematopoietic diseases ; Humans ; Immunodeficiencies. Immunoglobulinopathies ; Immunoglobulin Light Chains - metabolism ; Immunoglobulinopathies ; Immunopathology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Life Sciences ; Male ; Medical sciences ; Middle Aged ; Multiple Myeloma - metabolism ; Multiple Myeloma - mortality ; Multiple Myeloma - pathology ; Neoplasm Staging ; Pharmacology. Drug treatments ; Plasmacytoma - metabolism ; Plasmacytoma - mortality ; Plasmacytoma - pathology ; Positron-Emission Tomography - methods ; Prognosis ; Radiopharmaceuticals ; Retrospective Studies ; Survival Rate ; Tomography, X-Ray Computed - methods</subject><ispartof>Clinical cancer research, 2014-06, Vol.20 (12), p.3254-3260</ispartof><rights>2015 INIST-CNRS</rights><rights>2014 American Association for Cancer Research.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-5115e232041dc31ba202a28be3741d97f58b6c6d2517f47dc07a4e1b1ed9ca6c3</citedby><cites>FETCH-LOGICAL-c486t-5115e232041dc31ba202a28be3741d97f58b6c6d2517f47dc07a4e1b1ed9ca6c3</cites><orcidid>0009-0008-2320-6729 ; 0000-0002-9822-4170 ; 0000-0002-3474-2577 ; 0000-0001-7705-8460 ; 0000-0003-4910-476X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3343,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28538906$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24714772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01064578$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>FOUQUET, Guillemette</creatorcontrib><creatorcontrib>GUIDEZ, Stéphanie</creatorcontrib><creatorcontrib>BERTHON, Céline</creatorcontrib><creatorcontrib>TERRIOU, Louis</creatorcontrib><creatorcontrib>COITEUX, Valérie</creatorcontrib><creatorcontrib>MACRO, Margaret</creatorcontrib><creatorcontrib>DECAUX, Olivier</creatorcontrib><creatorcontrib>FACON, Thierry</creatorcontrib><creatorcontrib>HUGLO, Damien</creatorcontrib><creatorcontrib>LELEU, Xavier</creatorcontrib><creatorcontrib>HERBAUX, Charles</creatorcontrib><creatorcontrib>VAN DE WYNGAERT, Zoé</creatorcontrib><creatorcontrib>BONNET, Sarah</creatorcontrib><creatorcontrib>BEAUVAIS, David</creatorcontrib><creatorcontrib>DEMARQUETTE, Hélène</creatorcontrib><creatorcontrib>ADIB, Salim</creatorcontrib><creatorcontrib>HIVERT, Bénédicte</creatorcontrib><creatorcontrib>WEMEAU, Mathieu</creatorcontrib><title>Impact of Initial FDG-PET/CT and Serum-Free Light Chain on Transformation of Conventionally Defined Solitary Plasmacytoma to Multiple Myeloma</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Solitary plasmacytoma (SP) is a localized proliferation of monoclonal plasma cells in either bone or soft tissue, without evidence of multiple myeloma (MM), and whose prognosis is marked by a high risk of transformation to MM.
We studied the impact of FDG-PET/CT (2[18F]fluoro-2-deoxy-D-glucose positron emission tomography-computed tomography) on the risk of transformation of SP to overt MM among other markers in a series of 43 patients diagnosed with SP.
Median age was 57.5 years; 48% of patients had an abnormal involved serum-free light chain (sFLC) value, and 64% had an abnormal sFLC ratio at diagnosis. Thirty-three percent had two or more hypermetabolic lesions on initial PET/CT, and 20% had two or more focal lesions on initial MRI. With a median follow-up of 50 months, 14 patients transformed to MM with a median time (TTMM) of 71 months. The risk factors that significantly shortened TTMM at diagnosis were two or more hypermetabolic lesions on PET/CT, abnormal sFLC ratio and involved sFLC, and to a lesser extent at completion of treatment, absence of normalized involved sFLC and PET/CT or MRI. In a multivariate analysis, abnormal initial involved sFLC [OR = 10; 95% confidence interval (CI), 1-87; P = 0.008] and PET/CT (OR = 5; 95% CI, 0-9; P = 0.032) independently shortened TTMM.
An abnormal involved sFLC value and the presence of at least two hypermetabolic lesions on PET/CT at diagnosis of SP were the two predictors of early evolution to myeloma in our series. This data analysis will need confirmation in a larger study, and the study of these two risk factors may lead to a different management of patients with SP in the future. .</description><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Bone Neoplasms - metabolism</subject><subject>Bone Neoplasms - mortality</subject><subject>Bone Neoplasms - pathology</subject><subject>Cell Transformation, Neoplastic - metabolism</subject><subject>Cell Transformation, Neoplastic - pathology</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18</subject><subject>Follow-Up Studies</subject><subject>Genetics</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunoglobulin Light Chains - metabolism</subject><subject>Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple Myeloma - metabolism</subject><subject>Multiple Myeloma - mortality</subject><subject>Multiple Myeloma - pathology</subject><subject>Neoplasm Staging</subject><subject>Pharmacology. Drug treatments</subject><subject>Plasmacytoma - metabolism</subject><subject>Plasmacytoma - mortality</subject><subject>Plasmacytoma - pathology</subject><subject>Positron-Emission Tomography - methods</subject><subject>Prognosis</subject><subject>Radiopharmaceuticals</subject><subject>Retrospective Studies</subject><subject>Survival Rate</subject><subject>Tomography, X-Ray Computed - methods</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcFu1DAQhiMEoqXwCCBfkOCQ1mPHcfZYpd12pa2oYDlbE8dhjZx4sb2V9iF4Zxzttpxm5tc3v635i-Ij0EsA0VwBlU1JK84utQ4l8JItgL4qzkEIWXJWi9e5f2bOincx_qYUKqDV2-KMVRIqKdl58Xc17lAn4geymmyy6Mjy5q58vN1ctRuCU09-mLAfy2Uwhqztr20i7RbtRPxENgGnOPgwYrJ5zBatn57MNE_o3IHcmMFOJlt4ZxOGA3l0GEfUh-RHJMmTh71LducMeTgYl7X3xZsBXTQfTvWi-Lm83bT35frb3aq9Xpe6aupUinwBwzijFfSaQ4eMMmRNZ7jMykIOoulqXfdMgBwq2WsqsTLQgekXGmvNL4qvR98tOrULdsyfUx6tur9eq1mjQOtKyOYJMvvlyO6C_7M3ManRRm2cw8n4fVQguKgZiJpnVBxRHXyMwQwv3kDVnJqaE1FzIqptvyvgak4t7306PbHvRtO_bD3HlIHPJwCjRjfkw2sb_3ON4M2C1vwfyo6fsQ</recordid><startdate>20140615</startdate><enddate>20140615</enddate><creator>FOUQUET, Guillemette</creator><creator>GUIDEZ, Stéphanie</creator><creator>BERTHON, Céline</creator><creator>TERRIOU, Louis</creator><creator>COITEUX, Valérie</creator><creator>MACRO, Margaret</creator><creator>DECAUX, Olivier</creator><creator>FACON, Thierry</creator><creator>HUGLO, Damien</creator><creator>LELEU, Xavier</creator><creator>HERBAUX, Charles</creator><creator>VAN DE WYNGAERT, Zoé</creator><creator>BONNET, Sarah</creator><creator>BEAUVAIS, David</creator><creator>DEMARQUETTE, Hélène</creator><creator>ADIB, Salim</creator><creator>HIVERT, Bénédicte</creator><creator>WEMEAU, Mathieu</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0009-0008-2320-6729</orcidid><orcidid>https://orcid.org/0000-0002-9822-4170</orcidid><orcidid>https://orcid.org/0000-0002-3474-2577</orcidid><orcidid>https://orcid.org/0000-0001-7705-8460</orcidid><orcidid>https://orcid.org/0000-0003-4910-476X</orcidid></search><sort><creationdate>20140615</creationdate><title>Impact of Initial FDG-PET/CT and Serum-Free Light Chain on Transformation of Conventionally Defined Solitary Plasmacytoma to Multiple Myeloma</title><author>FOUQUET, Guillemette ; GUIDEZ, Stéphanie ; BERTHON, Céline ; TERRIOU, Louis ; COITEUX, Valérie ; MACRO, Margaret ; DECAUX, Olivier ; FACON, Thierry ; HUGLO, Damien ; LELEU, Xavier ; HERBAUX, Charles ; VAN DE WYNGAERT, Zoé ; BONNET, Sarah ; BEAUVAIS, David ; DEMARQUETTE, Hélène ; ADIB, Salim ; HIVERT, Bénédicte ; WEMEAU, Mathieu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-5115e232041dc31ba202a28be3741d97f58b6c6d2517f47dc07a4e1b1ed9ca6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Bone Neoplasms - metabolism</topic><topic>Bone Neoplasms - mortality</topic><topic>Bone Neoplasms - pathology</topic><topic>Cell Transformation, Neoplastic - metabolism</topic><topic>Cell Transformation, Neoplastic - pathology</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>Follow-Up Studies</topic><topic>Genetics</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunoglobulin Light Chains - metabolism</topic><topic>Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple Myeloma - metabolism</topic><topic>Multiple Myeloma - mortality</topic><topic>Multiple Myeloma - pathology</topic><topic>Neoplasm Staging</topic><topic>Pharmacology. Drug treatments</topic><topic>Plasmacytoma - metabolism</topic><topic>Plasmacytoma - mortality</topic><topic>Plasmacytoma - pathology</topic><topic>Positron-Emission Tomography - methods</topic><topic>Prognosis</topic><topic>Radiopharmaceuticals</topic><topic>Retrospective Studies</topic><topic>Survival Rate</topic><topic>Tomography, X-Ray Computed - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FOUQUET, Guillemette</creatorcontrib><creatorcontrib>GUIDEZ, Stéphanie</creatorcontrib><creatorcontrib>BERTHON, Céline</creatorcontrib><creatorcontrib>TERRIOU, Louis</creatorcontrib><creatorcontrib>COITEUX, Valérie</creatorcontrib><creatorcontrib>MACRO, Margaret</creatorcontrib><creatorcontrib>DECAUX, Olivier</creatorcontrib><creatorcontrib>FACON, Thierry</creatorcontrib><creatorcontrib>HUGLO, Damien</creatorcontrib><creatorcontrib>LELEU, Xavier</creatorcontrib><creatorcontrib>HERBAUX, Charles</creatorcontrib><creatorcontrib>VAN DE WYNGAERT, Zoé</creatorcontrib><creatorcontrib>BONNET, Sarah</creatorcontrib><creatorcontrib>BEAUVAIS, David</creatorcontrib><creatorcontrib>DEMARQUETTE, Hélène</creatorcontrib><creatorcontrib>ADIB, Salim</creatorcontrib><creatorcontrib>HIVERT, Bénédicte</creatorcontrib><creatorcontrib>WEMEAU, Mathieu</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FOUQUET, Guillemette</au><au>GUIDEZ, Stéphanie</au><au>BERTHON, Céline</au><au>TERRIOU, Louis</au><au>COITEUX, Valérie</au><au>MACRO, Margaret</au><au>DECAUX, Olivier</au><au>FACON, Thierry</au><au>HUGLO, Damien</au><au>LELEU, Xavier</au><au>HERBAUX, Charles</au><au>VAN DE WYNGAERT, Zoé</au><au>BONNET, Sarah</au><au>BEAUVAIS, David</au><au>DEMARQUETTE, Hélène</au><au>ADIB, Salim</au><au>HIVERT, Bénédicte</au><au>WEMEAU, Mathieu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Initial FDG-PET/CT and Serum-Free Light Chain on Transformation of Conventionally Defined Solitary Plasmacytoma to Multiple Myeloma</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2014-06-15</date><risdate>2014</risdate><volume>20</volume><issue>12</issue><spage>3254</spage><epage>3260</epage><pages>3254-3260</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><coden>CCREF4</coden><abstract>Solitary plasmacytoma (SP) is a localized proliferation of monoclonal plasma cells in either bone or soft tissue, without evidence of multiple myeloma (MM), and whose prognosis is marked by a high risk of transformation to MM.
We studied the impact of FDG-PET/CT (2[18F]fluoro-2-deoxy-D-glucose positron emission tomography-computed tomography) on the risk of transformation of SP to overt MM among other markers in a series of 43 patients diagnosed with SP.
Median age was 57.5 years; 48% of patients had an abnormal involved serum-free light chain (sFLC) value, and 64% had an abnormal sFLC ratio at diagnosis. Thirty-three percent had two or more hypermetabolic lesions on initial PET/CT, and 20% had two or more focal lesions on initial MRI. With a median follow-up of 50 months, 14 patients transformed to MM with a median time (TTMM) of 71 months. The risk factors that significantly shortened TTMM at diagnosis were two or more hypermetabolic lesions on PET/CT, abnormal sFLC ratio and involved sFLC, and to a lesser extent at completion of treatment, absence of normalized involved sFLC and PET/CT or MRI. In a multivariate analysis, abnormal initial involved sFLC [OR = 10; 95% confidence interval (CI), 1-87; P = 0.008] and PET/CT (OR = 5; 95% CI, 0-9; P = 0.032) independently shortened TTMM.
An abnormal involved sFLC value and the presence of at least two hypermetabolic lesions on PET/CT at diagnosis of SP were the two predictors of early evolution to myeloma in our series. This data analysis will need confirmation in a larger study, and the study of these two risk factors may lead to a different management of patients with SP in the future. .</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>24714772</pmid><doi>10.1158/1078-0432.ccr-13-2910</doi><tpages>7</tpages><orcidid>https://orcid.org/0009-0008-2320-6729</orcidid><orcidid>https://orcid.org/0000-0002-9822-4170</orcidid><orcidid>https://orcid.org/0000-0002-3474-2577</orcidid><orcidid>https://orcid.org/0000-0001-7705-8460</orcidid><orcidid>https://orcid.org/0000-0003-4910-476X</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Aged Antineoplastic agents Biological and medical sciences Biomarkers, Tumor - analysis Bone Neoplasms - metabolism Bone Neoplasms - mortality Bone Neoplasms - pathology Cell Transformation, Neoplastic - metabolism Cell Transformation, Neoplastic - pathology Female Fluorodeoxyglucose F18 Follow-Up Studies Genetics Hematologic and hematopoietic diseases Humans Immunodeficiencies. Immunoglobulinopathies Immunoglobulin Light Chains - metabolism Immunoglobulinopathies Immunopathology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Life Sciences Male Medical sciences Middle Aged Multiple Myeloma - metabolism Multiple Myeloma - mortality Multiple Myeloma - pathology Neoplasm Staging Pharmacology. Drug treatments Plasmacytoma - metabolism Plasmacytoma - mortality Plasmacytoma - pathology Positron-Emission Tomography - methods Prognosis Radiopharmaceuticals Retrospective Studies Survival Rate Tomography, X-Ray Computed - methods |
title | Impact of Initial FDG-PET/CT and Serum-Free Light Chain on Transformation of Conventionally Defined Solitary Plasmacytoma to Multiple Myeloma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T14%3A28%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Impact%20of%20Initial%20FDG-PET/CT%20and%20Serum-Free%20Light%20Chain%20on%20Transformation%20of%20Conventionally%20Defined%20Solitary%20Plasmacytoma%20to%20Multiple%20Myeloma&rft.jtitle=Clinical%20cancer%20research&rft.au=FOUQUET,%20Guillemette&rft.date=2014-06-15&rft.volume=20&rft.issue=12&rft.spage=3254&rft.epage=3260&rft.pages=3254-3260&rft.issn=1078-0432&rft.eissn=1557-3265&rft.coden=CCREF4&rft_id=info:doi/10.1158/1078-0432.ccr-13-2910&rft_dat=%3Cproquest_hal_p%3E1535621563%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1535621563&rft_id=info:pmid/24714772&rfr_iscdi=true |