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Lymphocyte subsets and assessment of cancer risk in renal transplant recipients
Renal transplant recipients have a well‐recognized increased risk of de novo neoplasia. In this study, we investigated whether lymphocyte subset count could predict the risk of developing noncutaneous neoplasia (NCSC) in renal transplant recipients (RTR). Between January 1995 and December 1995, lymp...
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Published in: | Transplant international 2002-09, Vol.15 (8), p.393-396 |
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creator | Ducloux, Didier Carron, Pierre‐Louis Motte, Gerard Ab, Abdelfatah Rebibou, Jean‐Michel Bresson‐Vautrin, Catherine Tiberghien, Pierre Saint‐Hillier, Yves Chalopin, Jean‐Marc |
description | Renal transplant recipients have a well‐recognized increased risk of de novo neoplasia. In this study, we investigated whether lymphocyte subset count could predict the risk of developing noncutaneous neoplasia (NCSC) in renal transplant recipients (RTR). Between January 1995 and December 1995, lymphocyte subsets (CD4, CD8, CD19) were measured in 281 RTR. This population was studied until November 1999 for the development of NCSC. The mean follow‐up was 42±9 months. Neoplasm was diagnosed in 22 patients (7.9%). Patients who developed a cancer were significantly older (53.8±6 years vs 38±16 years, P |
doi_str_mv | 10.1111/j.1432-2277.2002.tb00187.x |
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In this study, we investigated whether lymphocyte subset count could predict the risk of developing noncutaneous neoplasia (NCSC) in renal transplant recipients (RTR). Between January 1995 and December 1995, lymphocyte subsets (CD4, CD8, CD19) were measured in 281 RTR. This population was studied until November 1999 for the development of NCSC. The mean follow‐up was 42±9 months. Neoplasm was diagnosed in 22 patients (7.9%). Patients who developed a cancer were significantly older (53.8±6 years vs 38±16 years, P<0.0001), had lower CD4 (234±126/mm3 vs 543±214/mm3, P<0.005) and CD19 (19±9/mm3 vs 51±22/mm3, P<0.0001) levels, and more frequently had past histories of skin cancer (24% vs 4%, P<0.01). Cox regression revealed that high CD4 levels (RR 0.73, 95% CI 0.62–0.89 for each 100/mm3 increase in CD4 cell count) were associated with decreased risk of NCSC, whereas age (RR 2.49, 95% CI 1.12–5.92 for each 10‐year increase in age) was predictive of the subsequent development of NCSC. To conclude, CD4 cell depletion is associated with the development of solid cancers and lymphoma in RTR.</description><identifier>ISSN: 0934-0874</identifier><identifier>EISSN: 1432-2277</identifier><identifier>DOI: 10.1111/j.1432-2277.2002.tb00187.x</identifier><identifier>PMID: 12221457</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Antigens, CD19 - analysis ; Biological and medical sciences ; Cancer ; Carcinogenesis, carcinogens and anticarcinogens ; CD4 Lymphocyte Count ; Female ; General aspects ; Humans ; Immunosuppression ; Kidney Transplantation - adverse effects ; Kidney Transplantation - immunology ; Lymphocyte subsets ; Male ; Medical sciences ; Middle Aged ; Neoplasms - etiology ; Renal transplantation ; Risk ; Tumors</subject><ispartof>Transplant international, 2002-09, Vol.15 (8), p.393-396</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4003-27037b4540b8873e6c87769522932e6b4c805af71422a317cd2b00e8fba7d6c13</citedby><cites>FETCH-LOGICAL-c4003-27037b4540b8873e6c87769522932e6b4c805af71422a317cd2b00e8fba7d6c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13927159$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12221457$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ducloux, Didier</creatorcontrib><creatorcontrib>Carron, Pierre‐Louis</creatorcontrib><creatorcontrib>Motte, Gerard</creatorcontrib><creatorcontrib>Ab, Abdelfatah</creatorcontrib><creatorcontrib>Rebibou, Jean‐Michel</creatorcontrib><creatorcontrib>Bresson‐Vautrin, Catherine</creatorcontrib><creatorcontrib>Tiberghien, Pierre</creatorcontrib><creatorcontrib>Saint‐Hillier, Yves</creatorcontrib><creatorcontrib>Chalopin, Jean‐Marc</creatorcontrib><title>Lymphocyte subsets and assessment of cancer risk in renal transplant recipients</title><title>Transplant international</title><addtitle>Transpl Int</addtitle><description>Renal transplant recipients have a well‐recognized increased risk of de novo neoplasia. In this study, we investigated whether lymphocyte subset count could predict the risk of developing noncutaneous neoplasia (NCSC) in renal transplant recipients (RTR). Between January 1995 and December 1995, lymphocyte subsets (CD4, CD8, CD19) were measured in 281 RTR. This population was studied until November 1999 for the development of NCSC. The mean follow‐up was 42±9 months. Neoplasm was diagnosed in 22 patients (7.9%). Patients who developed a cancer were significantly older (53.8±6 years vs 38±16 years, P<0.0001), had lower CD4 (234±126/mm3 vs 543±214/mm3, P<0.005) and CD19 (19±9/mm3 vs 51±22/mm3, P<0.0001) levels, and more frequently had past histories of skin cancer (24% vs 4%, P<0.01). Cox regression revealed that high CD4 levels (RR 0.73, 95% CI 0.62–0.89 for each 100/mm3 increase in CD4 cell count) were associated with decreased risk of NCSC, whereas age (RR 2.49, 95% CI 1.12–5.92 for each 10‐year increase in age) was predictive of the subsequent development of NCSC. To conclude, CD4 cell depletion is associated with the development of solid cancers and lymphoma in RTR.</description><subject>Adult</subject><subject>Aged</subject><subject>Antigens, CD19 - analysis</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>CD4 Lymphocyte Count</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>Immunosuppression</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Kidney Transplantation - immunology</subject><subject>Lymphocyte subsets</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasms - etiology</subject><subject>Renal transplantation</subject><subject>Risk</subject><subject>Tumors</subject><issn>0934-0874</issn><issn>1432-2277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqVkEtr3DAQgEVJaDZp_0IRhfRmRxrJKzmHQAl5wUIgJGcha8fUW7-q8ZLsv4-WNc05c5nDfPP6GPspRS5TXGxyqRVkAMbkIATkUyWEtCZ_-8IW_0tHbCFKpTNhjT5hp0QbkVhbiK_sRAKA1IVZsMfVrhv_DGE3IadtRTgR9_2aeyIk6rCf-FDz4PuAkceG_vKm5xF73_Ip-p7G1ickYmjGJsH0jR3XviX8Pucz9nJ783x9n60e7x6uf6-yoIVQGRihTKULLSprjcJlsMYsywKgVIDLSgcrCl8bqQG8kiasIf2Itq68WS-DVGfs12HuGId_W6TJdQ0FbNM5OGzJGRBWWgUJvDyAIQ5EEWs3xqbzceekcHudbuP2ztzemdvrdLNO95aaf8xbtlWH64_W2V8CzmfAU_BtnZSEhj44VYKRRZm4qwP32rS4-8QJ7vnpQZVKvQPEUpF7</recordid><startdate>200209</startdate><enddate>200209</enddate><creator>Ducloux, Didier</creator><creator>Carron, Pierre‐Louis</creator><creator>Motte, Gerard</creator><creator>Ab, Abdelfatah</creator><creator>Rebibou, Jean‐Michel</creator><creator>Bresson‐Vautrin, Catherine</creator><creator>Tiberghien, Pierre</creator><creator>Saint‐Hillier, Yves</creator><creator>Chalopin, Jean‐Marc</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Publishing</general><scope>IQODW</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>200209</creationdate><title>Lymphocyte subsets and assessment of cancer risk in renal transplant recipients</title><author>Ducloux, Didier ; Carron, Pierre‐Louis ; Motte, Gerard ; Ab, Abdelfatah ; Rebibou, Jean‐Michel ; Bresson‐Vautrin, Catherine ; Tiberghien, Pierre ; Saint‐Hillier, Yves ; Chalopin, Jean‐Marc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4003-27037b4540b8873e6c87769522932e6b4c805af71422a317cd2b00e8fba7d6c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antigens, CD19 - analysis</topic><topic>Biological and medical sciences</topic><topic>Cancer</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>CD4 Lymphocyte Count</topic><topic>Female</topic><topic>General aspects</topic><topic>Humans</topic><topic>Immunosuppression</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Kidney Transplantation - immunology</topic><topic>Lymphocyte subsets</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasms - etiology</topic><topic>Renal transplantation</topic><topic>Risk</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ducloux, Didier</creatorcontrib><creatorcontrib>Carron, Pierre‐Louis</creatorcontrib><creatorcontrib>Motte, Gerard</creatorcontrib><creatorcontrib>Ab, Abdelfatah</creatorcontrib><creatorcontrib>Rebibou, Jean‐Michel</creatorcontrib><creatorcontrib>Bresson‐Vautrin, Catherine</creatorcontrib><creatorcontrib>Tiberghien, Pierre</creatorcontrib><creatorcontrib>Saint‐Hillier, Yves</creatorcontrib><creatorcontrib>Chalopin, Jean‐Marc</creatorcontrib><collection>Pascal-Francis</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>Transplant international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ducloux, Didier</au><au>Carron, Pierre‐Louis</au><au>Motte, Gerard</au><au>Ab, Abdelfatah</au><au>Rebibou, Jean‐Michel</au><au>Bresson‐Vautrin, Catherine</au><au>Tiberghien, Pierre</au><au>Saint‐Hillier, Yves</au><au>Chalopin, Jean‐Marc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lymphocyte subsets and assessment of cancer risk in renal transplant recipients</atitle><jtitle>Transplant international</jtitle><addtitle>Transpl Int</addtitle><date>2002-09</date><risdate>2002</risdate><volume>15</volume><issue>8</issue><spage>393</spage><epage>396</epage><pages>393-396</pages><issn>0934-0874</issn><eissn>1432-2277</eissn><abstract>Renal transplant recipients have a well‐recognized increased risk of de novo neoplasia. In this study, we investigated whether lymphocyte subset count could predict the risk of developing noncutaneous neoplasia (NCSC) in renal transplant recipients (RTR). Between January 1995 and December 1995, lymphocyte subsets (CD4, CD8, CD19) were measured in 281 RTR. This population was studied until November 1999 for the development of NCSC. The mean follow‐up was 42±9 months. Neoplasm was diagnosed in 22 patients (7.9%). Patients who developed a cancer were significantly older (53.8±6 years vs 38±16 years, P<0.0001), had lower CD4 (234±126/mm3 vs 543±214/mm3, P<0.005) and CD19 (19±9/mm3 vs 51±22/mm3, P<0.0001) levels, and more frequently had past histories of skin cancer (24% vs 4%, P<0.01). Cox regression revealed that high CD4 levels (RR 0.73, 95% CI 0.62–0.89 for each 100/mm3 increase in CD4 cell count) were associated with decreased risk of NCSC, whereas age (RR 2.49, 95% CI 1.12–5.92 for each 10‐year increase in age) was predictive of the subsequent development of NCSC. To conclude, CD4 cell depletion is associated with the development of solid cancers and lymphoma in RTR.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12221457</pmid><doi>10.1111/j.1432-2277.2002.tb00187.x</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Aged Antigens, CD19 - analysis Biological and medical sciences Cancer Carcinogenesis, carcinogens and anticarcinogens CD4 Lymphocyte Count Female General aspects Humans Immunosuppression Kidney Transplantation - adverse effects Kidney Transplantation - immunology Lymphocyte subsets Male Medical sciences Middle Aged Neoplasms - etiology Renal transplantation Risk Tumors |
title | Lymphocyte subsets and assessment of cancer risk in renal transplant recipients |
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