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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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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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><identifier>ISSN: 2045-7634</identifier><identifier>EISSN: 2045-7634</identifier><identifier>DOI: 10.1002/cam4.1205</identifier><identifier>PMID: 28960797</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>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</subject><ispartof>Cancer medicine (Malden, MA), 2017-11, Vol.6 (11), p.2507-2514</ispartof><rights>2017 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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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 > 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.</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 & dosage</subject><subject>Survival analysis</subject><subject>Survival Rate</subject><subject>Vincristine - therapeutic use</subject><subject>Young 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Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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 & 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 > 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.</abstract><cop>United States</cop><pub>John Wiley & 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> |
fulltext | fulltext |
identifier | ISSN: 2045-7634 |
ispartof | Cancer medicine (Malden, MA), 2017-11, Vol.6 (11), p.2507-2514 |
issn | 2045-7634 2045-7634 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5673915 |
source | MEDLINE; Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-20T02%3A45%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bone%20marrow%20biopsy%20superiority%20over%20PET/CT%20in%20predicting%20progression%E2%80%90free%20survival%20in%20a%20homogeneously%E2%80%90treated%20cohort%20of%20diffuse%20large%20B%E2%80%90cell%20lymphoma&rft.jtitle=Cancer%20medicine%20(Malden,%20MA)&rft.au=Chen%E2%80%90Liang,%20Tzu%E2%80%90Hua&rft.date=2017-11&rft.volume=6&rft.issue=11&rft.spage=2507&rft.epage=2514&rft.pages=2507-2514&rft.issn=2045-7634&rft.eissn=2045-7634&rft_id=info:doi/10.1002/cam4.1205&rft_dat=%3Cproquest_pubme%3E1960910458%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1960910458&rft_id=info:pmid/28960797&rfr_iscdi=true |