Serum amyloid A is not a marker for relapse of multicentric lymphoma in dogs

Background: Serum amyloid A (SAA) is an acute phase protein whose concentration increases in inflammatory, infectious, and neoplastic conditions in animals and human beings. Multicentric lymphoma is a common cancer in dogs, and chemotherapy is indicated to attain long‐term survival. However, frequen...

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Veröffentlicht in:Veterinary clinical pathology 2008-03, Vol.37 (1), p.79-85
Hauptverfasser: Merlo, A, Rezende, B.C.G, Franchini, M.L, Monteiro, P.R.G, Lucas, S.R.R
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container_end_page 85
container_issue 1
container_start_page 79
container_title Veterinary clinical pathology
container_volume 37
creator Merlo, A
Rezende, B.C.G
Franchini, M.L
Monteiro, P.R.G
Lucas, S.R.R
description Background: Serum amyloid A (SAA) is an acute phase protein whose concentration increases in inflammatory, infectious, and neoplastic conditions in animals and human beings. Multicentric lymphoma is a common cancer in dogs, and chemotherapy is indicated to attain long‐term survival. However, frequent relapses lead to changes in chemotherapeutic protocols. Objectives: The aims of this study were to evaluate SAA as a marker for relapse of multicentric lymphoma in dogs and to determine whether chemotherapy induces changes in the concentration of SAA during treatment. Methods: SAA was measured by an ELISA test in healthy control dogs (n=20), in healthy dogs receiving chemotherapy (n=8), and in dogs with lymphoma (n=20). All dogs receiving chemotherapy were randomly assigned to 2 treatment groups, one receiving cyclophosphamide, vincristine, and prednisone (CVP) and the other receiving vincristine, cyclophosphamide, methotrexate, and l‐asparaginase (VCMA) protocols. SAA concentration was determined before chemotherapy at weeks 1–4 in healthy dogs receiving chemotherapy and in dogs with lymphoma, then every 3 weeks for 4 months in healthy dogs, and at relapse and in the sample prior to relapse in dogs with lymphoma. SAA was measured only once in the healthy control dogs. Results were analyzed using repeated measures ANOVA followed by Tukey multiple comparison tests to compare groups and weeks of treatment. Results: Mean SAA concentration was significantly higher in dogs with lymphoma before chemotherapy compared with healthy and chemotherapy control dogs. No increase in SAA concentration was found at relapse. No differences were observed in SAA concentration based on type of chemotherapy protocol. Conclusions: SAA is not a marker of relapse in dogs with multicentric lymphoma, nor does chemotherapy regimen affect SAA concentration.
doi_str_mv 10.1111/j.1939-165X.2008.00016.x
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Multicentric lymphoma is a common cancer in dogs, and chemotherapy is indicated to attain long‐term survival. However, frequent relapses lead to changes in chemotherapeutic protocols. Objectives: The aims of this study were to evaluate SAA as a marker for relapse of multicentric lymphoma in dogs and to determine whether chemotherapy induces changes in the concentration of SAA during treatment. Methods: SAA was measured by an ELISA test in healthy control dogs (n=20), in healthy dogs receiving chemotherapy (n=8), and in dogs with lymphoma (n=20). All dogs receiving chemotherapy were randomly assigned to 2 treatment groups, one receiving cyclophosphamide, vincristine, and prednisone (CVP) and the other receiving vincristine, cyclophosphamide, methotrexate, and l‐asparaginase (VCMA) protocols. SAA concentration was determined before chemotherapy at weeks 1–4 in healthy dogs receiving chemotherapy and in dogs with lymphoma, then every 3 weeks for 4 months in healthy dogs, and at relapse and in the sample prior to relapse in dogs with lymphoma. SAA was measured only once in the healthy control dogs. Results were analyzed using repeated measures ANOVA followed by Tukey multiple comparison tests to compare groups and weeks of treatment. Results: Mean SAA concentration was significantly higher in dogs with lymphoma before chemotherapy compared with healthy and chemotherapy control dogs. No increase in SAA concentration was found at relapse. No differences were observed in SAA concentration based on type of chemotherapy protocol. 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Multicentric lymphoma is a common cancer in dogs, and chemotherapy is indicated to attain long‐term survival. However, frequent relapses lead to changes in chemotherapeutic protocols. Objectives: The aims of this study were to evaluate SAA as a marker for relapse of multicentric lymphoma in dogs and to determine whether chemotherapy induces changes in the concentration of SAA during treatment. Methods: SAA was measured by an ELISA test in healthy control dogs (n=20), in healthy dogs receiving chemotherapy (n=8), and in dogs with lymphoma (n=20). All dogs receiving chemotherapy were randomly assigned to 2 treatment groups, one receiving cyclophosphamide, vincristine, and prednisone (CVP) and the other receiving vincristine, cyclophosphamide, methotrexate, and l‐asparaginase (VCMA) protocols. SAA concentration was determined before chemotherapy at weeks 1–4 in healthy dogs receiving chemotherapy and in dogs with lymphoma, then every 3 weeks for 4 months in healthy dogs, and at relapse and in the sample prior to relapse in dogs with lymphoma. SAA was measured only once in the healthy control dogs. Results were analyzed using repeated measures ANOVA followed by Tukey multiple comparison tests to compare groups and weeks of treatment. Results: Mean SAA concentration was significantly higher in dogs with lymphoma before chemotherapy compared with healthy and chemotherapy control dogs. No increase in SAA concentration was found at relapse. No differences were observed in SAA concentration based on type of chemotherapy protocol. Conclusions: SAA is not a marker of relapse in dogs with multicentric lymphoma, nor does chemotherapy regimen affect SAA concentration.</description><subject>Acute phase protein</subject><subject>acute phase proteins</subject><subject>Animals</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>biomarkers</subject><subject>Biomarkers, Tumor - blood</subject><subject>blood proteins</subject><subject>blood serum</subject><subject>chemotherapy</subject><subject>chemotherapy protocols</subject><subject>diagnostic techniques</subject><subject>disease diagnosis</subject><subject>dog</subject><subject>Dog Diseases - blood</subject><subject>Dogs</subject><subject>drugs</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>inflammation</subject><subject>lymphoma</subject><subject>Lymphoma - blood</subject><subject>Lymphoma - drug therapy</subject><subject>Lymphoma - veterinary</subject><subject>Male</subject><subject>prednisone</subject><subject>Recurrence</subject><subject>relapse</subject><subject>serum amyloid A</subject><subject>Serum Amyloid A Protein - metabolism</subject><issn>0275-6382</issn><issn>1939-165X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkF1v2yAUhtG0qk27_oWNq93Z48OA0a6qbGsnRd2krunuEMbQkdkhBVtL_v1wHXW3OxI6EjzvAR4AIEYlzvVhU2JJZYE5-1kShOoSIYR5uX8FFi8Hr8ECEcEKTmtyBs5T2iBEWd46BWe4ppyzSi7A6s7GsYe6P3TBt_AK-gS3YYAa9jr-thG6EGG0nd4lC4OD_dgN3tjtEL2B3aHf_Qq9hn4L2_CY3oATp7tkL4_9Atx_-fxjeVOsvl1_XV6tClMRwQvLuXUa166VXFcNF0ZSQawRxhFMOHWiFTKvhurG1cjUhLWNZQ3GqKGOanoB3s9zdzE8jTYNqvfJ2K7TWxvGpASqKsIYz2A9gyaGlKJ1ahd9_thBYaQmk2qjJmFqEqYmk-rZpNrn6NvjHWPT2_Zf8KguAx9n4I_v7OG_B6v18jueXlbMaZ8Gu39JZ-eKCyqYeri9Vg94vbyl8pNaZ_7dzDsdlH6MPqn7O4IwRUgSKrikfwFIwppe</recordid><startdate>200803</startdate><enddate>200803</enddate><creator>Merlo, A</creator><creator>Rezende, B.C.G</creator><creator>Franchini, M.L</creator><creator>Monteiro, P.R.G</creator><creator>Lucas, S.R.R</creator><general>Blackwell Publishing Inc</general><scope>FBQ</scope><scope>BSCLL</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></search><sort><creationdate>200803</creationdate><title>Serum amyloid A is not a marker for relapse of multicentric lymphoma in dogs</title><author>Merlo, A ; Rezende, B.C.G ; Franchini, M.L ; Monteiro, P.R.G ; Lucas, S.R.R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4276-e66efa18fd96a4b67c9372ec7cf21263f7d797d7b3abf80c825dbe5b110b3f3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acute phase protein</topic><topic>acute phase proteins</topic><topic>Animals</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>biomarkers</topic><topic>Biomarkers, Tumor - blood</topic><topic>blood proteins</topic><topic>blood serum</topic><topic>chemotherapy</topic><topic>chemotherapy protocols</topic><topic>diagnostic techniques</topic><topic>disease diagnosis</topic><topic>dog</topic><topic>Dog Diseases - blood</topic><topic>Dogs</topic><topic>drugs</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>inflammation</topic><topic>lymphoma</topic><topic>Lymphoma - blood</topic><topic>Lymphoma - drug therapy</topic><topic>Lymphoma - veterinary</topic><topic>Male</topic><topic>prednisone</topic><topic>Recurrence</topic><topic>relapse</topic><topic>serum amyloid A</topic><topic>Serum Amyloid A Protein - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Merlo, A</creatorcontrib><creatorcontrib>Rezende, B.C.G</creatorcontrib><creatorcontrib>Franchini, M.L</creatorcontrib><creatorcontrib>Monteiro, P.R.G</creatorcontrib><creatorcontrib>Lucas, S.R.R</creatorcontrib><collection>AGRIS</collection><collection>Istex</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>Veterinary clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Merlo, A</au><au>Rezende, B.C.G</au><au>Franchini, M.L</au><au>Monteiro, P.R.G</au><au>Lucas, S.R.R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum amyloid A is not a marker for relapse of multicentric lymphoma in dogs</atitle><jtitle>Veterinary clinical pathology</jtitle><addtitle>Vet Clin Pathol</addtitle><date>2008-03</date><risdate>2008</risdate><volume>37</volume><issue>1</issue><spage>79</spage><epage>85</epage><pages>79-85</pages><issn>0275-6382</issn><eissn>1939-165X</eissn><abstract>Background: Serum amyloid A (SAA) is an acute phase protein whose concentration increases in inflammatory, infectious, and neoplastic conditions in animals and human beings. Multicentric lymphoma is a common cancer in dogs, and chemotherapy is indicated to attain long‐term survival. However, frequent relapses lead to changes in chemotherapeutic protocols. Objectives: The aims of this study were to evaluate SAA as a marker for relapse of multicentric lymphoma in dogs and to determine whether chemotherapy induces changes in the concentration of SAA during treatment. Methods: SAA was measured by an ELISA test in healthy control dogs (n=20), in healthy dogs receiving chemotherapy (n=8), and in dogs with lymphoma (n=20). All dogs receiving chemotherapy were randomly assigned to 2 treatment groups, one receiving cyclophosphamide, vincristine, and prednisone (CVP) and the other receiving vincristine, cyclophosphamide, methotrexate, and l‐asparaginase (VCMA) protocols. SAA concentration was determined before chemotherapy at weeks 1–4 in healthy dogs receiving chemotherapy and in dogs with lymphoma, then every 3 weeks for 4 months in healthy dogs, and at relapse and in the sample prior to relapse in dogs with lymphoma. SAA was measured only once in the healthy control dogs. Results were analyzed using repeated measures ANOVA followed by Tukey multiple comparison tests to compare groups and weeks of treatment. Results: Mean SAA concentration was significantly higher in dogs with lymphoma before chemotherapy compared with healthy and chemotherapy control dogs. No increase in SAA concentration was found at relapse. No differences were observed in SAA concentration based on type of chemotherapy protocol. Conclusions: SAA is not a marker of relapse in dogs with multicentric lymphoma, nor does chemotherapy regimen affect SAA concentration.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>18366549</pmid><doi>10.1111/j.1939-165X.2008.00016.x</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Acute phase protein
acute phase proteins
Animals
Antineoplastic Agents - therapeutic use
biomarkers
Biomarkers, Tumor - blood
blood proteins
blood serum
chemotherapy
chemotherapy protocols
diagnostic techniques
disease diagnosis
dog
Dog Diseases - blood
Dogs
drugs
Enzyme-Linked Immunosorbent Assay
Female
inflammation
lymphoma
Lymphoma - blood
Lymphoma - drug therapy
Lymphoma - veterinary
Male
prednisone
Recurrence
relapse
serum amyloid A
Serum Amyloid A Protein - metabolism
title Serum amyloid A is not a marker for relapse of multicentric lymphoma in dogs
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