Bone marrow biopsy superiority over PET/CT in predicting progression‐free survival in a homogeneously‐treated cohort of diffuse large B‐cell lymphoma

Several studies have reported uneven results when evaluating the prognostic value of bone marrow biopsy (BMB) and PET/CT as part of the staging of diffuse large B‐cell lymphoma (DLBCL). The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the a...

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Veröffentlicht in:Cancer medicine (Malden, MA) MA), 2017-11, Vol.6 (11), p.2507-2514
Hauptverfasser: Chen‐Liang, Tzu‐Hua, Martín‐Santos, Taida, Jerez, Andrés, Rodríguez‐García, Guillermo, Senent, Leonor, Martínez‐Millán, Cristina, Muiña, Begoña, Orero, Mayte, Teruel, Anabel, Martín, Alejandro, Gómez‐Espuch, Joaquín, Kennedy, Kyra, Benet, Carmen, Raya, José María, Fernández‐González, Marta, Cruz, Fátima, Guinot, Marta, Villegas, Carolina, Ballester, Isabel, Baile, Mónica, Moya, María, López‐Jiménez, Javier, Frutos, Laura, Navarro, José Luis, Uña, Jon, Fernández‐López, Rosa, Igua, Carolina, Contreras, José, Sánchez‐Vañó, Raquel, Cozar, María del Puig, Tamayo, Pilar, Mucientes, Jorge, Sánchez‐Blanco, José Javier, Pérez‐Ceballos, Elena, Ortuño, Francisco José
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container_end_page 2514
container_issue 11
container_start_page 2507
container_title Cancer medicine (Malden, MA)
container_volume 6
creator Chen‐Liang, Tzu‐Hua
Martín‐Santos, Taida
Jerez, Andrés
Rodríguez‐García, Guillermo
Senent, Leonor
Martínez‐Millán, Cristina
Muiña, Begoña
Orero, Mayte
Teruel, Anabel
Martín, Alejandro
Gómez‐Espuch, Joaquín
Kennedy, Kyra
Benet, Carmen
Raya, José María
Fernández‐González, Marta
Cruz, Fátima
Guinot, Marta
Villegas, Carolina
Ballester, Isabel
Baile, Mónica
Moya, María
López‐Jiménez, Javier
Frutos, Laura
Navarro, José Luis
Uña, Jon
Fernández‐López, Rosa
Igua, Carolina
Contreras, José
Sánchez‐Vañó, Raquel
Cozar, María del Puig
Tamayo, Pilar
Mucientes, Jorge
Sánchez‐Blanco, José Javier
Pérez‐Ceballos, Elena
Ortuño, Francisco José
description Several studies have reported uneven results when evaluating the prognostic value of bone marrow biopsy (BMB) and PET/CT as part of the staging of diffuse large B‐cell lymphoma (DLBCL). The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the analysis models might explain part of these discrepancies. To address this issue we have carried a retrospective multicenter study including 268 DLBCL patients with a BMB and a PET/CT available at diagnosis where we estimated both the prognosis impact and the diagnostic accuracy of each technique. Only patients treated with R‐CHOP/21 as first line (n = 203) were included in the survival analysis. With a median follow‐up of 25 months the estimated 3‐year progression‐free survival (PFS) and overall survival (OS) were 76.3% and 82.7% respectively. In a multivariate analysis designed to avoid a collinearity bias with IPI categories, BMB‐BMI [bone marrow involvement](+) (HR: 3.6) and ECOG PS > 1 (HR: 2.9) were independently associated with a shorter PFS and three factors, age >60 years old (HR: 2.4), ECOG PS >1 (HR: 2.4), and abnormally elevated B2‐microglobulin levels (HR: 2.2) were independently associated with a shorter OS. In our DLBCL cohort, treated with a uniform first‐line chemotherapy regimen, BMI by BMB complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort BMI by PET/CT could not independently predict a shorter PFS and/or OS. Bone marrow involvement by biopsy complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort, bone marrow involvement by PET/CT could not independently predict a shorter PFS and/or OS.
doi_str_mv 10.1002/cam4.1205
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The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the analysis models might explain part of these discrepancies. To address this issue we have carried a retrospective multicenter study including 268 DLBCL patients with a BMB and a PET/CT available at diagnosis where we estimated both the prognosis impact and the diagnostic accuracy of each technique. Only patients treated with R‐CHOP/21 as first line (n = 203) were included in the survival analysis. With a median follow‐up of 25 months the estimated 3‐year progression‐free survival (PFS) and overall survival (OS) were 76.3% and 82.7% respectively. In a multivariate analysis designed to avoid a collinearity bias with IPI categories, BMB‐BMI [bone marrow involvement](+) (HR: 3.6) and ECOG PS &gt; 1 (HR: 2.9) were independently associated with a shorter PFS and three factors, age &gt;60 years old (HR: 2.4), ECOG PS &gt;1 (HR: 2.4), and abnormally elevated B2‐microglobulin levels (HR: 2.2) were independently associated with a shorter OS. In our DLBCL cohort, treated with a uniform first‐line chemotherapy regimen, BMI by BMB complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort BMI by PET/CT could not independently predict a shorter PFS and/or OS. Bone marrow involvement by biopsy complemented performance status in predicting those patients with a higher risk for relapse or progression. 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The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the analysis models might explain part of these discrepancies. To address this issue we have carried a retrospective multicenter study including 268 DLBCL patients with a BMB and a PET/CT available at diagnosis where we estimated both the prognosis impact and the diagnostic accuracy of each technique. Only patients treated with R‐CHOP/21 as first line (n = 203) were included in the survival analysis. With a median follow‐up of 25 months the estimated 3‐year progression‐free survival (PFS) and overall survival (OS) were 76.3% and 82.7% respectively. In a multivariate analysis designed to avoid a collinearity bias with IPI categories, BMB‐BMI [bone marrow involvement](+) (HR: 3.6) and ECOG PS &gt; 1 (HR: 2.9) were independently associated with a shorter PFS and three factors, age &gt;60 years old (HR: 2.4), ECOG PS &gt;1 (HR: 2.4), and abnormally elevated B2‐microglobulin levels (HR: 2.2) were independently associated with a shorter OS. In our DLBCL cohort, treated with a uniform first‐line chemotherapy regimen, BMI by BMB complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort BMI by PET/CT could not independently predict a shorter PFS and/or OS. Bone marrow involvement by biopsy complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort, bone marrow involvement by PET/CT could not independently predict a shorter PFS and/or OS.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies, Monoclonal, Murine-Derived - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>B-cell lymphoma</subject><subject>beta 2-Microglobulin - blood</subject><subject>Biopsy</subject><subject>Bone marrow</subject><subject>Bone Marrow - diagnostic imaging</subject><subject>Bone Marrow - pathology</subject><subject>Bone marrow biopsy</subject><subject>Chemotherapy</subject><subject>Clinical Cancer Research</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>diffuse large B‐cell lymphoma</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health Status</subject><subject>Humans</subject><subject>Lymphocytes B</subject><subject>Lymphoma</subject><subject>Lymphoma, Large B-Cell, Diffuse - diagnostic imaging</subject><subject>Lymphoma, Large B-Cell, Diffuse - drug therapy</subject><subject>Lymphoma, Large B-Cell, Diffuse - pathology</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Original Research</subject><subject>outcomes research</subject><subject>PET/CT</subject><subject>Positron Emission Tomography Computed Tomography</subject><subject>Predictive Value of Tests</subject><subject>Prednisone - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Rituximab - administration &amp; 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Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2079-6638</orcidid></search><sort><creationdate>201711</creationdate><title>Bone marrow biopsy superiority over PET/CT in predicting progression‐free survival in a homogeneously‐treated cohort of diffuse large B‐cell lymphoma</title><author>Chen‐Liang, Tzu‐Hua ; Martín‐Santos, Taida ; Jerez, Andrés ; Rodríguez‐García, Guillermo ; Senent, Leonor ; Martínez‐Millán, Cristina ; Muiña, Begoña ; Orero, Mayte ; Teruel, Anabel ; Martín, Alejandro ; Gómez‐Espuch, Joaquín ; Kennedy, Kyra ; Benet, Carmen ; Raya, José María ; Fernández‐González, Marta ; Cruz, Fátima ; Guinot, Marta ; Villegas, Carolina ; Ballester, Isabel ; Baile, Mónica ; Moya, María ; López‐Jiménez, Javier ; Frutos, Laura ; Navarro, José Luis ; Uña, Jon ; Fernández‐López, Rosa ; Igua, Carolina ; Contreras, José ; Sánchez‐Vañó, Raquel ; Cozar, María del Puig ; Tamayo, Pilar ; Mucientes, Jorge ; Sánchez‐Blanco, José Javier ; Pérez‐Ceballos, Elena ; Ortuño, Francisco José</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5095-bdb8acdf23678bc1dd018f944125befc1ea439c0c0932b056386f946d018ba4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibodies, Monoclonal, Murine-Derived - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>B-cell lymphoma</topic><topic>beta 2-Microglobulin - blood</topic><topic>Biopsy</topic><topic>Bone marrow</topic><topic>Bone Marrow - diagnostic imaging</topic><topic>Bone Marrow - pathology</topic><topic>Bone marrow biopsy</topic><topic>Chemotherapy</topic><topic>Clinical Cancer Research</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>diffuse large B‐cell lymphoma</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - therapeutic use</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health Status</topic><topic>Humans</topic><topic>Lymphocytes B</topic><topic>Lymphoma</topic><topic>Lymphoma, Large B-Cell, Diffuse - diagnostic imaging</topic><topic>Lymphoma, Large B-Cell, Diffuse - drug therapy</topic><topic>Lymphoma, Large B-Cell, Diffuse - pathology</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Original Research</topic><topic>outcomes research</topic><topic>PET/CT</topic><topic>Positron Emission Tomography Computed Tomography</topic><topic>Predictive Value of Tests</topic><topic>Prednisone - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Rituximab - administration &amp; dosage</topic><topic>Survival analysis</topic><topic>Survival Rate</topic><topic>Vincristine - therapeutic use</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen‐Liang, Tzu‐Hua</creatorcontrib><creatorcontrib>Martín‐Santos, Taida</creatorcontrib><creatorcontrib>Jerez, Andrés</creatorcontrib><creatorcontrib>Rodríguez‐García, Guillermo</creatorcontrib><creatorcontrib>Senent, Leonor</creatorcontrib><creatorcontrib>Martínez‐Millán, Cristina</creatorcontrib><creatorcontrib>Muiña, Begoña</creatorcontrib><creatorcontrib>Orero, Mayte</creatorcontrib><creatorcontrib>Teruel, Anabel</creatorcontrib><creatorcontrib>Martín, Alejandro</creatorcontrib><creatorcontrib>Gómez‐Espuch, Joaquín</creatorcontrib><creatorcontrib>Kennedy, Kyra</creatorcontrib><creatorcontrib>Benet, Carmen</creatorcontrib><creatorcontrib>Raya, José María</creatorcontrib><creatorcontrib>Fernández‐González, Marta</creatorcontrib><creatorcontrib>Cruz, Fátima</creatorcontrib><creatorcontrib>Guinot, Marta</creatorcontrib><creatorcontrib>Villegas, Carolina</creatorcontrib><creatorcontrib>Ballester, Isabel</creatorcontrib><creatorcontrib>Baile, Mónica</creatorcontrib><creatorcontrib>Moya, María</creatorcontrib><creatorcontrib>López‐Jiménez, Javier</creatorcontrib><creatorcontrib>Frutos, Laura</creatorcontrib><creatorcontrib>Navarro, José Luis</creatorcontrib><creatorcontrib>Uña, Jon</creatorcontrib><creatorcontrib>Fernández‐López, Rosa</creatorcontrib><creatorcontrib>Igua, Carolina</creatorcontrib><creatorcontrib>Contreras, José</creatorcontrib><creatorcontrib>Sánchez‐Vañó, Raquel</creatorcontrib><creatorcontrib>Cozar, María del Puig</creatorcontrib><creatorcontrib>Tamayo, Pilar</creatorcontrib><creatorcontrib>Mucientes, Jorge</creatorcontrib><creatorcontrib>Sánchez‐Blanco, José Javier</creatorcontrib><creatorcontrib>Pérez‐Ceballos, Elena</creatorcontrib><creatorcontrib>Ortuño, Francisco José</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer medicine (Malden, MA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen‐Liang, Tzu‐Hua</au><au>Martín‐Santos, Taida</au><au>Jerez, Andrés</au><au>Rodríguez‐García, Guillermo</au><au>Senent, Leonor</au><au>Martínez‐Millán, Cristina</au><au>Muiña, Begoña</au><au>Orero, Mayte</au><au>Teruel, Anabel</au><au>Martín, Alejandro</au><au>Gómez‐Espuch, Joaquín</au><au>Kennedy, Kyra</au><au>Benet, Carmen</au><au>Raya, José María</au><au>Fernández‐González, Marta</au><au>Cruz, Fátima</au><au>Guinot, Marta</au><au>Villegas, Carolina</au><au>Ballester, Isabel</au><au>Baile, Mónica</au><au>Moya, María</au><au>López‐Jiménez, Javier</au><au>Frutos, Laura</au><au>Navarro, José Luis</au><au>Uña, Jon</au><au>Fernández‐López, Rosa</au><au>Igua, Carolina</au><au>Contreras, José</au><au>Sánchez‐Vañó, Raquel</au><au>Cozar, María del Puig</au><au>Tamayo, Pilar</au><au>Mucientes, Jorge</au><au>Sánchez‐Blanco, José Javier</au><au>Pérez‐Ceballos, Elena</au><au>Ortuño, Francisco José</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone marrow biopsy superiority over PET/CT in predicting progression‐free survival in a homogeneously‐treated cohort of diffuse large B‐cell lymphoma</atitle><jtitle>Cancer medicine (Malden, MA)</jtitle><addtitle>Cancer Med</addtitle><date>2017-11</date><risdate>2017</risdate><volume>6</volume><issue>11</issue><spage>2507</spage><epage>2514</epage><pages>2507-2514</pages><issn>2045-7634</issn><eissn>2045-7634</eissn><abstract>Several studies have reported uneven results when evaluating the prognostic value of bone marrow biopsy (BMB) and PET/CT as part of the staging of diffuse large B‐cell lymphoma (DLBCL). The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the analysis models might explain part of these discrepancies. To address this issue we have carried a retrospective multicenter study including 268 DLBCL patients with a BMB and a PET/CT available at diagnosis where we estimated both the prognosis impact and the diagnostic accuracy of each technique. Only patients treated with R‐CHOP/21 as first line (n = 203) were included in the survival analysis. With a median follow‐up of 25 months the estimated 3‐year progression‐free survival (PFS) and overall survival (OS) were 76.3% and 82.7% respectively. In a multivariate analysis designed to avoid a collinearity bias with IPI categories, BMB‐BMI [bone marrow involvement](+) (HR: 3.6) and ECOG PS &gt; 1 (HR: 2.9) were independently associated with a shorter PFS and three factors, age &gt;60 years old (HR: 2.4), ECOG PS &gt;1 (HR: 2.4), and abnormally elevated B2‐microglobulin levels (HR: 2.2) were independently associated with a shorter OS. In our DLBCL cohort, treated with a uniform first‐line chemotherapy regimen, BMI by BMB complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort BMI by PET/CT could not independently predict a shorter PFS and/or OS. Bone marrow involvement by biopsy complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort, bone marrow involvement by PET/CT could not independently predict a shorter PFS and/or OS.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>28960797</pmid><doi>10.1002/cam4.1205</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2079-6638</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Antibodies, Monoclonal, Murine-Derived - therapeutic use
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
B-cell lymphoma
beta 2-Microglobulin - blood
Biopsy
Bone marrow
Bone Marrow - diagnostic imaging
Bone Marrow - pathology
Bone marrow biopsy
Chemotherapy
Clinical Cancer Research
Cyclophosphamide - therapeutic use
diffuse large B‐cell lymphoma
Disease-Free Survival
Doxorubicin - therapeutic use
Female
Follow-Up Studies
Health Status
Humans
Lymphocytes B
Lymphoma
Lymphoma, Large B-Cell, Diffuse - diagnostic imaging
Lymphoma, Large B-Cell, Diffuse - drug therapy
Lymphoma, Large B-Cell, Diffuse - pathology
Male
Medical prognosis
Middle Aged
Multivariate Analysis
Original Research
outcomes research
PET/CT
Positron Emission Tomography Computed Tomography
Predictive Value of Tests
Prednisone - therapeutic use
Retrospective Studies
Rituximab - administration & dosage
Survival analysis
Survival Rate
Vincristine - therapeutic use
Young Adult
title Bone marrow biopsy superiority over PET/CT in predicting progression‐free survival in a homogeneously‐treated cohort of diffuse large B‐cell lymphoma
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