The Prognostic Impact of CD163-Positive Macrophages in Follicular Lymphoma: A Study from the BC Cancer Agency and the Lymphoma Study Association
We aimed to assess the prognostic significance of follicular lymphoma-associated macrophages in the era of rituximab treatment and maintenance. We applied immunohistochemistry for CD68 and CD163 to two large tissue microarrays (TMA). The first TMA included samples from 186 patients from the BC Cance...
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creator | Kridel, Robert Xerri, Luc Gelas-Dore, Bénédicte Tan, King Feugier, Pierre Vawda, Ayesha Canioni, Danielle Farinha, Pedro Boussetta, Sami Moccia, Alden A Brice, Pauline Chavez, Elizabeth A Kyle, Alastair H Scott, David W Sanders, Ashley D Fabiani, Bettina Slack, Graham W Minchinton, Andrew I Haioun, Corinne Connors, Joseph M Sehn, Laurie H Steidl, Christian Gascoyne, Randy D Salles, Gilles |
description | We aimed to assess the prognostic significance of follicular lymphoma-associated macrophages in the era of rituximab treatment and maintenance.
We applied immunohistochemistry for CD68 and CD163 to two large tissue microarrays (TMA). The first TMA included samples from 186 patients from the BC Cancer Agency (BCCA) who had been treated with first-line systemic treatment including rituximab, cyclophosphamide, vincristine, and prednisone. The second contained 395 samples from PRIMA trial patients treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone, and randomized to rituximab maintenance or observation. Macrophage infiltration was assessed using Aperio image analysis. Each of the two cohorts was randomly split into training/validation sets.
An increased CD163-positive pixel count was predictive of adverse outcome in the BCCA dataset [5-year progression-free survival (PFS) 38% vs. 72%, respectively, P = 0.004 in the training cohort and 5-year PFS 29% vs. 61%, respectively, P = 0.004 in the validation cohort]. In the PRIMA trial, an increased CD163 pixel count was associated with favorable outcome (5-year PFS 60% vs. 44%, respectively, P = 0.011 in the training cohort and 5-year PFS 55% vs. 37%, respectively, P = 0.030 in the validation cohort).
CD163-positive macrophages predict outcome in follicular lymphoma, but their prognostic impact is highly dependent on treatment received. |
doi_str_mv | 10.1158/1078-0432.CCR-14-3253 |
format | Article |
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We applied immunohistochemistry for CD68 and CD163 to two large tissue microarrays (TMA). The first TMA included samples from 186 patients from the BC Cancer Agency (BCCA) who had been treated with first-line systemic treatment including rituximab, cyclophosphamide, vincristine, and prednisone. The second contained 395 samples from PRIMA trial patients treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone, and randomized to rituximab maintenance or observation. Macrophage infiltration was assessed using Aperio image analysis. Each of the two cohorts was randomly split into training/validation sets.
An increased CD163-positive pixel count was predictive of adverse outcome in the BCCA dataset [5-year progression-free survival (PFS) 38% vs. 72%, respectively, P = 0.004 in the training cohort and 5-year PFS 29% vs. 61%, respectively, P = 0.004 in the validation cohort]. In the PRIMA trial, an increased CD163 pixel count was associated with favorable outcome (5-year PFS 60% vs. 44%, respectively, P = 0.011 in the training cohort and 5-year PFS 55% vs. 37%, respectively, P = 0.030 in the validation cohort).
CD163-positive macrophages predict outcome in follicular lymphoma, but their prognostic impact is highly dependent on treatment received.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-14-3253</identifier><identifier>PMID: 25869385</identifier><language>eng</language><publisher>United States</publisher><subject>Aged ; Antigens, CD - biosynthesis ; Antigens, CD - genetics ; Antigens, Differentiation, Myelomonocytic - biosynthesis ; Antigens, Differentiation, Myelomonocytic - genetics ; Cyclophosphamide - administration & dosage ; Disease-Free Survival ; Doxorubicin - administration & dosage ; Female ; Humans ; Lymphoma, Follicular - drug therapy ; Lymphoma, Follicular - genetics ; Lymphoma, Follicular - pathology ; Macrophages - drug effects ; Macrophages - metabolism ; Male ; Middle Aged ; Prognosis ; Receptors, Cell Surface - biosynthesis ; Receptors, Cell Surface - genetics ; Rituximab - administration & dosage ; Tissue Array Analysis ; Treatment Outcome ; Tumor Microenvironment - drug effects ; Vincristine - administration & dosage</subject><ispartof>Clinical cancer research, 2015-08, Vol.21 (15), p.3428-3435</ispartof><rights>2015 American Association for Cancer Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-3b4c28464003903f20c0995e5f34ba4d3c98a5361cbb72f5efea49b420437b3c3</citedby><cites>FETCH-LOGICAL-c507t-3b4c28464003903f20c0995e5f34ba4d3c98a5361cbb72f5efea49b420437b3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3343,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25869385$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kridel, Robert</creatorcontrib><creatorcontrib>Xerri, Luc</creatorcontrib><creatorcontrib>Gelas-Dore, Bénédicte</creatorcontrib><creatorcontrib>Tan, King</creatorcontrib><creatorcontrib>Feugier, Pierre</creatorcontrib><creatorcontrib>Vawda, Ayesha</creatorcontrib><creatorcontrib>Canioni, Danielle</creatorcontrib><creatorcontrib>Farinha, Pedro</creatorcontrib><creatorcontrib>Boussetta, Sami</creatorcontrib><creatorcontrib>Moccia, Alden A</creatorcontrib><creatorcontrib>Brice, Pauline</creatorcontrib><creatorcontrib>Chavez, Elizabeth A</creatorcontrib><creatorcontrib>Kyle, Alastair H</creatorcontrib><creatorcontrib>Scott, David W</creatorcontrib><creatorcontrib>Sanders, Ashley D</creatorcontrib><creatorcontrib>Fabiani, Bettina</creatorcontrib><creatorcontrib>Slack, Graham W</creatorcontrib><creatorcontrib>Minchinton, Andrew I</creatorcontrib><creatorcontrib>Haioun, Corinne</creatorcontrib><creatorcontrib>Connors, Joseph M</creatorcontrib><creatorcontrib>Sehn, Laurie H</creatorcontrib><creatorcontrib>Steidl, Christian</creatorcontrib><creatorcontrib>Gascoyne, Randy D</creatorcontrib><creatorcontrib>Salles, Gilles</creatorcontrib><title>The Prognostic Impact of CD163-Positive Macrophages in Follicular Lymphoma: A Study from the BC Cancer Agency and the Lymphoma Study Association</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>We aimed to assess the prognostic significance of follicular lymphoma-associated macrophages in the era of rituximab treatment and maintenance.
We applied immunohistochemistry for CD68 and CD163 to two large tissue microarrays (TMA). The first TMA included samples from 186 patients from the BC Cancer Agency (BCCA) who had been treated with first-line systemic treatment including rituximab, cyclophosphamide, vincristine, and prednisone. The second contained 395 samples from PRIMA trial patients treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone, and randomized to rituximab maintenance or observation. Macrophage infiltration was assessed using Aperio image analysis. Each of the two cohorts was randomly split into training/validation sets.
An increased CD163-positive pixel count was predictive of adverse outcome in the BCCA dataset [5-year progression-free survival (PFS) 38% vs. 72%, respectively, P = 0.004 in the training cohort and 5-year PFS 29% vs. 61%, respectively, P = 0.004 in the validation cohort]. In the PRIMA trial, an increased CD163 pixel count was associated with favorable outcome (5-year PFS 60% vs. 44%, respectively, P = 0.011 in the training cohort and 5-year PFS 55% vs. 37%, respectively, P = 0.030 in the validation cohort).
CD163-positive macrophages predict outcome in follicular lymphoma, but their prognostic impact is highly dependent on treatment received.</description><subject>Aged</subject><subject>Antigens, CD - biosynthesis</subject><subject>Antigens, CD - genetics</subject><subject>Antigens, Differentiation, Myelomonocytic - biosynthesis</subject><subject>Antigens, Differentiation, Myelomonocytic - genetics</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Lymphoma, Follicular - drug therapy</subject><subject>Lymphoma, Follicular - genetics</subject><subject>Lymphoma, Follicular - pathology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Receptors, Cell Surface - biosynthesis</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Rituximab - administration & dosage</subject><subject>Tissue Array Analysis</subject><subject>Treatment Outcome</subject><subject>Tumor Microenvironment - drug effects</subject><subject>Vincristine - administration & dosage</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFOwzAQRC0EoqXwCSAfuaTYsZ043EqgUKmICsrZclynNUriYCdI_Qs-mYS2XDntSDuzK80D4BKjMcaM32AU8wBREo7T9DXANCAhI0dgiBmLOx2x404fPANw5v0HQphiRE_BIGQ8SghnQ_C93Gi4cHZdWd8YBWdlLVUDbQ7TexyRYGG9acyXhs9SOVtv5Fp7aCo4tUVhVFtIB-fbst7YUt7CCXxr2tUW5s6WsOkO36UwlZXSDk7WulJbKKvV7-KQ2Qcm3ltlZGNsdQ5Ocll4fbGfI_A-fVimT8H85XGWTuaBYihuApJRFXIaUYRIgkgeIoWShGmWE5pJuiIq4ZKRCKssi8Oc6VxLmmQ07OqIM6LICFzv7tbOfrbaN6I0XumikJW2rReYIx5h3Pf0rzVGmCeEhr2V7axdWd47nYvamVK6rcBI9NxEz0T0TETHTWAqem5d7mr_os1KvfpLHUCRH-vWktY</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Kridel, Robert</creator><creator>Xerri, Luc</creator><creator>Gelas-Dore, Bénédicte</creator><creator>Tan, King</creator><creator>Feugier, Pierre</creator><creator>Vawda, Ayesha</creator><creator>Canioni, Danielle</creator><creator>Farinha, Pedro</creator><creator>Boussetta, Sami</creator><creator>Moccia, Alden A</creator><creator>Brice, Pauline</creator><creator>Chavez, Elizabeth A</creator><creator>Kyle, Alastair H</creator><creator>Scott, David W</creator><creator>Sanders, Ashley D</creator><creator>Fabiani, Bettina</creator><creator>Slack, Graham W</creator><creator>Minchinton, Andrew I</creator><creator>Haioun, Corinne</creator><creator>Connors, Joseph M</creator><creator>Sehn, Laurie H</creator><creator>Steidl, Christian</creator><creator>Gascoyne, Randy D</creator><creator>Salles, Gilles</creator><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><scope>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope></search><sort><creationdate>20150801</creationdate><title>The Prognostic Impact of CD163-Positive Macrophages in Follicular Lymphoma: A Study from the BC Cancer Agency and the Lymphoma Study Association</title><author>Kridel, Robert ; Xerri, Luc ; Gelas-Dore, Bénédicte ; Tan, King ; Feugier, Pierre ; Vawda, Ayesha ; Canioni, Danielle ; Farinha, Pedro ; Boussetta, Sami ; Moccia, Alden A ; Brice, Pauline ; Chavez, Elizabeth A ; Kyle, Alastair H ; Scott, David W ; Sanders, Ashley D ; Fabiani, Bettina ; Slack, Graham W ; Minchinton, Andrew I ; Haioun, Corinne ; Connors, Joseph M ; Sehn, Laurie H ; Steidl, Christian ; Gascoyne, Randy D ; Salles, Gilles</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-3b4c28464003903f20c0995e5f34ba4d3c98a5361cbb72f5efea49b420437b3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Antigens, CD - biosynthesis</topic><topic>Antigens, CD - genetics</topic><topic>Antigens, Differentiation, Myelomonocytic - biosynthesis</topic><topic>Antigens, Differentiation, Myelomonocytic - genetics</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Lymphoma, Follicular - drug therapy</topic><topic>Lymphoma, Follicular - genetics</topic><topic>Lymphoma, Follicular - pathology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Receptors, Cell Surface - biosynthesis</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Rituximab - administration & dosage</topic><topic>Tissue Array Analysis</topic><topic>Treatment Outcome</topic><topic>Tumor Microenvironment - drug effects</topic><topic>Vincristine - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kridel, Robert</creatorcontrib><creatorcontrib>Xerri, Luc</creatorcontrib><creatorcontrib>Gelas-Dore, Bénédicte</creatorcontrib><creatorcontrib>Tan, King</creatorcontrib><creatorcontrib>Feugier, Pierre</creatorcontrib><creatorcontrib>Vawda, Ayesha</creatorcontrib><creatorcontrib>Canioni, Danielle</creatorcontrib><creatorcontrib>Farinha, Pedro</creatorcontrib><creatorcontrib>Boussetta, Sami</creatorcontrib><creatorcontrib>Moccia, Alden A</creatorcontrib><creatorcontrib>Brice, Pauline</creatorcontrib><creatorcontrib>Chavez, Elizabeth A</creatorcontrib><creatorcontrib>Kyle, Alastair H</creatorcontrib><creatorcontrib>Scott, David W</creatorcontrib><creatorcontrib>Sanders, Ashley D</creatorcontrib><creatorcontrib>Fabiani, Bettina</creatorcontrib><creatorcontrib>Slack, Graham W</creatorcontrib><creatorcontrib>Minchinton, Andrew I</creatorcontrib><creatorcontrib>Haioun, Corinne</creatorcontrib><creatorcontrib>Connors, Joseph M</creatorcontrib><creatorcontrib>Sehn, Laurie H</creatorcontrib><creatorcontrib>Steidl, Christian</creatorcontrib><creatorcontrib>Gascoyne, Randy D</creatorcontrib><creatorcontrib>Salles, Gilles</creatorcontrib><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><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kridel, Robert</au><au>Xerri, Luc</au><au>Gelas-Dore, Bénédicte</au><au>Tan, King</au><au>Feugier, Pierre</au><au>Vawda, Ayesha</au><au>Canioni, Danielle</au><au>Farinha, Pedro</au><au>Boussetta, Sami</au><au>Moccia, Alden A</au><au>Brice, Pauline</au><au>Chavez, Elizabeth A</au><au>Kyle, Alastair H</au><au>Scott, David W</au><au>Sanders, Ashley D</au><au>Fabiani, Bettina</au><au>Slack, Graham W</au><au>Minchinton, Andrew I</au><au>Haioun, Corinne</au><au>Connors, Joseph M</au><au>Sehn, Laurie H</au><au>Steidl, Christian</au><au>Gascoyne, Randy D</au><au>Salles, Gilles</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Prognostic Impact of CD163-Positive Macrophages in Follicular Lymphoma: A Study from the BC Cancer Agency and the Lymphoma Study Association</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>21</volume><issue>15</issue><spage>3428</spage><epage>3435</epage><pages>3428-3435</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>We aimed to assess the prognostic significance of follicular lymphoma-associated macrophages in the era of rituximab treatment and maintenance.
We applied immunohistochemistry for CD68 and CD163 to two large tissue microarrays (TMA). The first TMA included samples from 186 patients from the BC Cancer Agency (BCCA) who had been treated with first-line systemic treatment including rituximab, cyclophosphamide, vincristine, and prednisone. The second contained 395 samples from PRIMA trial patients treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone, and randomized to rituximab maintenance or observation. Macrophage infiltration was assessed using Aperio image analysis. Each of the two cohorts was randomly split into training/validation sets.
An increased CD163-positive pixel count was predictive of adverse outcome in the BCCA dataset [5-year progression-free survival (PFS) 38% vs. 72%, respectively, P = 0.004 in the training cohort and 5-year PFS 29% vs. 61%, respectively, P = 0.004 in the validation cohort]. In the PRIMA trial, an increased CD163 pixel count was associated with favorable outcome (5-year PFS 60% vs. 44%, respectively, P = 0.011 in the training cohort and 5-year PFS 55% vs. 37%, respectively, P = 0.030 in the validation cohort).
CD163-positive macrophages predict outcome in follicular lymphoma, but their prognostic impact is highly dependent on treatment received.</abstract><cop>United States</cop><pmid>25869385</pmid><doi>10.1158/1078-0432.CCR-14-3253</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antigens, CD - biosynthesis Antigens, CD - genetics Antigens, Differentiation, Myelomonocytic - biosynthesis Antigens, Differentiation, Myelomonocytic - genetics Cyclophosphamide - administration & dosage Disease-Free Survival Doxorubicin - administration & dosage Female Humans Lymphoma, Follicular - drug therapy Lymphoma, Follicular - genetics Lymphoma, Follicular - pathology Macrophages - drug effects Macrophages - metabolism Male Middle Aged Prognosis Receptors, Cell Surface - biosynthesis Receptors, Cell Surface - genetics Rituximab - administration & dosage Tissue Array Analysis Treatment Outcome Tumor Microenvironment - drug effects Vincristine - administration & dosage |
title | The Prognostic Impact of CD163-Positive Macrophages in Follicular Lymphoma: A Study from the BC Cancer Agency and the Lymphoma Study Association |
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