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Plasma fibrinogen level as possible prognostic biomarker in diffuse large B-cell lymphoma

Objectives: Although many studies have assessed numerous molecular and immunohistochemical prognostic markers for diffuse large Bcell lymphoma (DLBCL), there is always a need for simple widely available markers. This study was planned to illustrate the clinical significance of baseline plasma fibrin...

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Published in:Hematology (Luxembourg) 2019-01, Vol.24 (1), p.103-107
Main Authors: Shehata, Amira Mohamed Foad, Aldesoky, Amira I., Gohar, Suzy F.
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description Objectives: Although many studies have assessed numerous molecular and immunohistochemical prognostic markers for diffuse large Bcell lymphoma (DLBCL), there is always a need for simple widely available markers. This study was planned to illustrate the clinical significance of baseline plasma fibrinogen levels in DLBCL patients. Methods: We prospectively investigated 76 DLBCL patients treated with rituximab plus cyclophosphamide, vincristine, doxorubicin and hostacortine between August 2015 and February 2018. Baseline plasma fibrinogen level was measured and correlated with patients' clinical features, laboratory parameters, response to therapy, progression-free survival and overall survival. Results: Significant association between fibrinogen level and clinical features such as the presence of B symptoms (P 
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This study was planned to illustrate the clinical significance of baseline plasma fibrinogen levels in DLBCL patients. Methods: We prospectively investigated 76 DLBCL patients treated with rituximab plus cyclophosphamide, vincristine, doxorubicin and hostacortine between August 2015 and February 2018. Baseline plasma fibrinogen level was measured and correlated with patients' clinical features, laboratory parameters, response to therapy, progression-free survival and overall survival. Results: Significant association between fibrinogen level and clinical features such as the presence of B symptoms (P &lt; .001) and clinical stage (P &lt; .001) was observed while no association with age, gender, number of involved extranodal sites, performance status and international prognostic index (IPI) was found. Baseline fibrinogen level was significantly related to laboratory parameters including red cell distribution width (RDW) (P &lt; .001), platelet count (P = .02), serum lactate dehydrogenase (LDH) (P = .009) and B2-microglobulin (P = .008). No statistically significant correlations were detected between baseline fibrinogen levels; and response to therapy, progression-free survival and overall survival. Conclusion: Baseline plasma fibrinogen level did not show prognostic significance for DLBCL patients, although it was associated with patients' clinical features and laboratory parameters. 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This study was planned to illustrate the clinical significance of baseline plasma fibrinogen levels in DLBCL patients. Methods: We prospectively investigated 76 DLBCL patients treated with rituximab plus cyclophosphamide, vincristine, doxorubicin and hostacortine between August 2015 and February 2018. Baseline plasma fibrinogen level was measured and correlated with patients' clinical features, laboratory parameters, response to therapy, progression-free survival and overall survival. Results: Significant association between fibrinogen level and clinical features such as the presence of B symptoms (P &lt; .001) and clinical stage (P &lt; .001) was observed while no association with age, gender, number of involved extranodal sites, performance status and international prognostic index (IPI) was found. Baseline fibrinogen level was significantly related to laboratory parameters including red cell distribution width (RDW) (P &lt; .001), platelet count (P = .02), serum lactate dehydrogenase (LDH) (P = .009) and B2-microglobulin (P = .008). No statistically significant correlations were detected between baseline fibrinogen levels; and response to therapy, progression-free survival and overall survival. Conclusion: Baseline plasma fibrinogen level did not show prognostic significance for DLBCL patients, although it was associated with patients' clinical features and laboratory parameters. 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Aldesoky, Amira I. ; Gohar, Suzy F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-566816f8c42380291b25276b23a4ddd3000198fb3e299454cb6823a8ca68e8ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - blood</topic><topic>CAV protocol</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>diffuse large B-cell lymphoma</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - administration &amp; dosage</topic><topic>Female</topic><topic>fibrinogen</topic><topic>Fibrinogen - metabolism</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>lactate dehydrogenases</topic><topic>Lymphoma, Large B-Cell, Diffuse - blood</topic><topic>Lymphoma, Large B-Cell, Diffuse - drug therapy</topic><topic>Lymphoma, Large B-Cell, Diffuse - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>prognosis</topic><topic>progression-free survival</topic><topic>Prospective Studies</topic><topic>rituximab</topic><topic>Rituximab - administration &amp; dosage</topic><topic>Survival Rate</topic><topic>Vincristine - administration &amp; dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shehata, Amira Mohamed Foad</creatorcontrib><creatorcontrib>Aldesoky, Amira I.</creatorcontrib><creatorcontrib>Gohar, Suzy F.</creatorcontrib><collection>Taylor &amp; Francis 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>MEDLINE - Academic</collection><jtitle>Hematology (Luxembourg)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shehata, Amira Mohamed Foad</au><au>Aldesoky, Amira I.</au><au>Gohar, Suzy F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma fibrinogen level as possible prognostic biomarker in diffuse large B-cell lymphoma</atitle><jtitle>Hematology (Luxembourg)</jtitle><addtitle>Hematology</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>24</volume><issue>1</issue><spage>103</spage><epage>107</epage><pages>103-107</pages><issn>1607-8454</issn><eissn>1607-8454</eissn><abstract>Objectives: Although many studies have assessed numerous molecular and immunohistochemical prognostic markers for diffuse large Bcell lymphoma (DLBCL), there is always a need for simple widely available markers. This study was planned to illustrate the clinical significance of baseline plasma fibrinogen levels in DLBCL patients. Methods: We prospectively investigated 76 DLBCL patients treated with rituximab plus cyclophosphamide, vincristine, doxorubicin and hostacortine between August 2015 and February 2018. Baseline plasma fibrinogen level was measured and correlated with patients' clinical features, laboratory parameters, response to therapy, progression-free survival and overall survival. Results: Significant association between fibrinogen level and clinical features such as the presence of B symptoms (P &lt; .001) and clinical stage (P &lt; .001) was observed while no association with age, gender, number of involved extranodal sites, performance status and international prognostic index (IPI) was found. 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subjects Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Biomarkers
Biomarkers, Tumor - blood
CAV protocol
Cyclophosphamide - administration & dosage
diffuse large B-cell lymphoma
Disease-Free Survival
Doxorubicin - administration & dosage
Female
fibrinogen
Fibrinogen - metabolism
Follow-Up Studies
Humans
lactate dehydrogenases
Lymphoma, Large B-Cell, Diffuse - blood
Lymphoma, Large B-Cell, Diffuse - drug therapy
Lymphoma, Large B-Cell, Diffuse - mortality
Male
Middle Aged
prognosis
progression-free survival
Prospective Studies
rituximab
Rituximab - administration & dosage
Survival Rate
Vincristine - administration & dosage
title Plasma fibrinogen level as possible prognostic biomarker in diffuse large B-cell lymphoma
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