Improved survival with combined modality therapy in the modern era for primary mediastinal B‐cell lymphoma
Primary mediastinal B‐cell lymphoma (PMBCL) is an uncommon lymphoma for which existing data is limited. We utilized the National Cancer Database (NCDB) to evaluate PMBCL and the impact of radiotherapy (RT) on outcomes in the years following FDA approval of rituximab. We queried the NCDB for patients...
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Veröffentlicht in: | American journal of hematology 2016-05, Vol.91 (5), p.476-480 |
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description | Primary mediastinal B‐cell lymphoma (PMBCL) is an uncommon lymphoma for which existing data is limited. We utilized the National Cancer Database (NCDB) to evaluate PMBCL and the impact of radiotherapy (RT) on outcomes in the years following FDA approval of rituximab. We queried the NCDB for patients with PMBCL diagnosed from 2006 to 2011 and treated with multiagent chemotherapy. Kaplan–Meier overall survival (OS) estimates, univariate (UVA), and multivariate (MVA) Cox proportional hazards regression analyses were performed. Propensity score matched analysis (PSMA) was performed to account for indication bias and mitigate heterogeneity between treatment groups. 465 patients were identified with a median follow‐up of 36 months. Median age was 36 years; 43% received RT. 5‐year OS for the entire cohort was 87%, and for the no‐RT and RT groups, 83% versus 93%, respectively. On UVA, OS was improved with RT (HR 0.34, P = 0.002). On MVA, RT remained significantly associated with improved OS (HR 0.44, P = 0.028) while Medicaid insurance status and increasing stage remained significantly associated with OS decrement. PSMA confirmed the OS benefit associated with RT. This analysis is the largest PMBCL dataset to date and demonstrates a significant survival benefit associated with RT in patients receiving multiagent chemotherapy in the rituximab era. More than half of patients treated in the United States during this time period did not receive RT. In the absence of phase III data to support omission, combined modality therapy with its associated survival benefit should be the benchmark against which other therapies are compared. Am. J. Hematol. 91:476–480, 2016. © 2016 Wiley Periodicals, Inc. |
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We utilized the National Cancer Database (NCDB) to evaluate PMBCL and the impact of radiotherapy (RT) on outcomes in the years following FDA approval of rituximab. We queried the NCDB for patients with PMBCL diagnosed from 2006 to 2011 and treated with multiagent chemotherapy. Kaplan–Meier overall survival (OS) estimates, univariate (UVA), and multivariate (MVA) Cox proportional hazards regression analyses were performed. Propensity score matched analysis (PSMA) was performed to account for indication bias and mitigate heterogeneity between treatment groups. 465 patients were identified with a median follow‐up of 36 months. Median age was 36 years; 43% received RT. 5‐year OS for the entire cohort was 87%, and for the no‐RT and RT groups, 83% versus 93%, respectively. On UVA, OS was improved with RT (HR 0.34, P = 0.002). On MVA, RT remained significantly associated with improved OS (HR 0.44, P = 0.028) while Medicaid insurance status and increasing stage remained significantly associated with OS decrement. PSMA confirmed the OS benefit associated with RT. This analysis is the largest PMBCL dataset to date and demonstrates a significant survival benefit associated with RT in patients receiving multiagent chemotherapy in the rituximab era. More than half of patients treated in the United States during this time period did not receive RT. In the absence of phase III data to support omission, combined modality therapy with its associated survival benefit should be the benchmark against which other therapies are compared. Am. J. Hematol. 91:476–480, 2016. © 2016 Wiley Periodicals, Inc.</description><identifier>ISSN: 0361-8609</identifier><identifier>EISSN: 1096-8652</identifier><identifier>DOI: 10.1002/ajh.24325</identifier><identifier>PMID: 26852276</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Combined Modality Therapy ; Datasets as Topic ; Female ; Follow-Up Studies ; Hematology ; Humans ; Immunotherapy ; Insurance Coverage - statistics & numerical data ; Kaplan-Meier Estimate ; Lymphoma, B-Cell - drug therapy ; Lymphoma, B-Cell - radiotherapy ; Male ; Mediastinal Neoplasms - drug therapy ; Mediastinal Neoplasms - radiotherapy ; Middle Aged ; Neoplasm Staging ; Prognosis ; Propensity Score ; Proportional Hazards Models ; Registries ; Risk Factors ; Rituximab - administration & dosage ; Treatment Outcome ; United States ; Young Adult</subject><ispartof>American journal of hematology, 2016-05, Vol.91 (5), p.476-480</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3885-7735bb7397965ae5c19a456e818fdfe73c8bf0d4fd2437023767d5608153bd623</citedby><cites>FETCH-LOGICAL-c3885-7735bb7397965ae5c19a456e818fdfe73c8bf0d4fd2437023767d5608153bd623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fajh.24325$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fajh.24325$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26852276$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jackson, Matthew W.</creatorcontrib><creatorcontrib>Rusthoven, Chad G.</creatorcontrib><creatorcontrib>Jones, Bernard L.</creatorcontrib><creatorcontrib>Kamdar, Manali</creatorcontrib><creatorcontrib>Rabinovitch, Rachel</creatorcontrib><title>Improved survival with combined modality therapy in the modern era for primary mediastinal B‐cell lymphoma</title><title>American journal of hematology</title><addtitle>Am J Hematol</addtitle><description>Primary mediastinal B‐cell lymphoma (PMBCL) is an uncommon lymphoma for which existing data is limited. We utilized the National Cancer Database (NCDB) to evaluate PMBCL and the impact of radiotherapy (RT) on outcomes in the years following FDA approval of rituximab. We queried the NCDB for patients with PMBCL diagnosed from 2006 to 2011 and treated with multiagent chemotherapy. Kaplan–Meier overall survival (OS) estimates, univariate (UVA), and multivariate (MVA) Cox proportional hazards regression analyses were performed. Propensity score matched analysis (PSMA) was performed to account for indication bias and mitigate heterogeneity between treatment groups. 465 patients were identified with a median follow‐up of 36 months. Median age was 36 years; 43% received RT. 5‐year OS for the entire cohort was 87%, and for the no‐RT and RT groups, 83% versus 93%, respectively. On UVA, OS was improved with RT (HR 0.34, P = 0.002). On MVA, RT remained significantly associated with improved OS (HR 0.44, P = 0.028) while Medicaid insurance status and increasing stage remained significantly associated with OS decrement. PSMA confirmed the OS benefit associated with RT. This analysis is the largest PMBCL dataset to date and demonstrates a significant survival benefit associated with RT in patients receiving multiagent chemotherapy in the rituximab era. More than half of patients treated in the United States during this time period did not receive RT. In the absence of phase III data to support omission, combined modality therapy with its associated survival benefit should be the benchmark against which other therapies are compared. Am. J. Hematol. 91:476–480, 2016. © 2016 Wiley Periodicals, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Combined Modality Therapy</subject><subject>Datasets as Topic</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Insurance Coverage - statistics & numerical data</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymphoma, B-Cell - drug therapy</subject><subject>Lymphoma, B-Cell - radiotherapy</subject><subject>Male</subject><subject>Mediastinal Neoplasms - drug therapy</subject><subject>Mediastinal Neoplasms - radiotherapy</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Prognosis</subject><subject>Propensity Score</subject><subject>Proportional Hazards Models</subject><subject>Registries</subject><subject>Risk Factors</subject><subject>Rituximab - administration & dosage</subject><subject>Treatment Outcome</subject><subject>United States</subject><subject>Young Adult</subject><issn>0361-8609</issn><issn>1096-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kbtOwzAYhS0EoqUw8ALIEgsMpb7El4ylAlpUiQXmyEkcxVUuxU5aZeMReEaeBKctDEhM_nX0-eg__wHgEqM7jBCZqFV-RwJK2BEYYhTyseSMHIMhohz7GYUDcObcCiGMA4lOwYBwyQgRfAiKRbm29Uan0LV2YzaqgFvT5DCpy9hUXi7rVBWm6WCTa6vWHTRVP_a6thX0GsxqC9fWlMp2sNSpUa4xlTe6__r4THRRwKIr13ldqnNwkqnC6YvDOwJvjw-vs_l4-fK0mE2X44RKycZCUBbHgoYi5ExpluBQBYxriWWWZlrQRMYZSoMs9aEFIlRwkTKOJGY0TjmhI3Cz9_XR3lvtmqg0rt9EVbpuXYSFpLT_RT16_Qdd1a312-8oghhCjHnqdk8ltnbO6iw65I0wivoKIl9BtKvAs1cHxzb21_glf27ugcke2JpCd_87RdPn-d7yG9UukKI</recordid><startdate>201605</startdate><enddate>201605</enddate><creator>Jackson, Matthew W.</creator><creator>Rusthoven, Chad G.</creator><creator>Jones, Bernard L.</creator><creator>Kamdar, Manali</creator><creator>Rabinovitch, Rachel</creator><general>Wiley Subscription Services, Inc</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>201605</creationdate><title>Improved survival with combined modality therapy in the modern era for primary mediastinal B‐cell lymphoma</title><author>Jackson, Matthew W. ; Rusthoven, Chad G. ; Jones, Bernard L. ; Kamdar, Manali ; Rabinovitch, Rachel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3885-7735bb7397965ae5c19a456e818fdfe73c8bf0d4fd2437023767d5608153bd623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Combined Modality Therapy</topic><topic>Datasets as Topic</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hematology</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Insurance Coverage - statistics & numerical data</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymphoma, B-Cell - drug therapy</topic><topic>Lymphoma, B-Cell - radiotherapy</topic><topic>Male</topic><topic>Mediastinal Neoplasms - drug therapy</topic><topic>Mediastinal Neoplasms - radiotherapy</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Prognosis</topic><topic>Propensity Score</topic><topic>Proportional Hazards Models</topic><topic>Registries</topic><topic>Risk Factors</topic><topic>Rituximab - administration & dosage</topic><topic>Treatment Outcome</topic><topic>United States</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jackson, Matthew W.</creatorcontrib><creatorcontrib>Rusthoven, Chad G.</creatorcontrib><creatorcontrib>Jones, Bernard L.</creatorcontrib><creatorcontrib>Kamdar, Manali</creatorcontrib><creatorcontrib>Rabinovitch, Rachel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jackson, Matthew W.</au><au>Rusthoven, Chad G.</au><au>Jones, Bernard L.</au><au>Kamdar, Manali</au><au>Rabinovitch, Rachel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved survival with combined modality therapy in the modern era for primary mediastinal B‐cell lymphoma</atitle><jtitle>American journal of hematology</jtitle><addtitle>Am J Hematol</addtitle><date>2016-05</date><risdate>2016</risdate><volume>91</volume><issue>5</issue><spage>476</spage><epage>480</epage><pages>476-480</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><abstract>Primary mediastinal B‐cell lymphoma (PMBCL) is an uncommon lymphoma for which existing data is limited. We utilized the National Cancer Database (NCDB) to evaluate PMBCL and the impact of radiotherapy (RT) on outcomes in the years following FDA approval of rituximab. We queried the NCDB for patients with PMBCL diagnosed from 2006 to 2011 and treated with multiagent chemotherapy. Kaplan–Meier overall survival (OS) estimates, univariate (UVA), and multivariate (MVA) Cox proportional hazards regression analyses were performed. Propensity score matched analysis (PSMA) was performed to account for indication bias and mitigate heterogeneity between treatment groups. 465 patients were identified with a median follow‐up of 36 months. Median age was 36 years; 43% received RT. 5‐year OS for the entire cohort was 87%, and for the no‐RT and RT groups, 83% versus 93%, respectively. On UVA, OS was improved with RT (HR 0.34, P = 0.002). On MVA, RT remained significantly associated with improved OS (HR 0.44, P = 0.028) while Medicaid insurance status and increasing stage remained significantly associated with OS decrement. PSMA confirmed the OS benefit associated with RT. This analysis is the largest PMBCL dataset to date and demonstrates a significant survival benefit associated with RT in patients receiving multiagent chemotherapy in the rituximab era. More than half of patients treated in the United States during this time period did not receive RT. In the absence of phase III data to support omission, combined modality therapy with its associated survival benefit should be the benchmark against which other therapies are compared. Am. J. Hematol. 91:476–480, 2016. © 2016 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>26852276</pmid><doi>10.1002/ajh.24325</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols - therapeutic use Combined Modality Therapy Datasets as Topic Female Follow-Up Studies Hematology Humans Immunotherapy Insurance Coverage - statistics & numerical data Kaplan-Meier Estimate Lymphoma, B-Cell - drug therapy Lymphoma, B-Cell - radiotherapy Male Mediastinal Neoplasms - drug therapy Mediastinal Neoplasms - radiotherapy Middle Aged Neoplasm Staging Prognosis Propensity Score Proportional Hazards Models Registries Risk Factors Rituximab - administration & dosage Treatment Outcome United States Young Adult |
title | Improved survival with combined modality therapy in the modern era for primary mediastinal B‐cell lymphoma |
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