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Belatacept rescue conversion in kidney transplant recipients with vascular lesions (Banff cv score >2): a retrospective cohort study
Immunosuppression in kidney transplant recipients with decreased graft function and histological vascular changes can be particularly challenging. The impact of a late rescue conversion to belatacept on kidney graft survival in this context has never been studied. We report a bicentric retrospective...
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Published in: | Nephrology, dialysis, transplantation dialysis, transplantation, 2023-02, Vol.38 (2), p.481-490 |
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creator | Bertrand, Dominique Matignon, Marie Morel, Antoine Ludivine, Lebourg Lemoine, Mathilde Hanoy, Mélanie Roy, Frank Le Nezam, Dorian Hamzaoui, Mouad de Nattes, Tristan Moktefi, Anissa François, Arnaud Laurent, Charlotte Etienne, Isabelle Guerrot, Dominique |
description | Immunosuppression in kidney transplant recipients with decreased graft function and histological vascular changes can be particularly challenging. The impact of a late rescue conversion to belatacept on kidney graft survival in this context has never been studied.
We report a bicentric retrospective cohort study comparing a calcineurin inhibitor (CNI) to belatacept switch versus CNI continuation in 139 kidney transplant recipients with histological kidney vascular damage (cv ≥2, g + cpt ≤1, i + t ≤1) and low estimated glomerular filtration rate (≤40 mL/min/1.73 m²). Primary outcome was death-censored graft survival.
During the study follow-up, 10 graft losses (14.5%) occurred in the belatacept group (n = 69) versus 26 (37.1%) in the matched CNI group (n = 70) (P = .005). Death-censored graft survival was significantly higher in the belatacept group (P = .001). At 3 years, graft survival was 84.0% in the belatacept group compared with 65.1% in the control group. Continuing CNI was an independent risk factor for graft loss [hazard ratio (HR) 3.46; P |
doi_str_mv | 10.1093/ndt/gfac178 |
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We report a bicentric retrospective cohort study comparing a calcineurin inhibitor (CNI) to belatacept switch versus CNI continuation in 139 kidney transplant recipients with histological kidney vascular damage (cv ≥2, g + cpt ≤1, i + t ≤1) and low estimated glomerular filtration rate (≤40 mL/min/1.73 m²). Primary outcome was death-censored graft survival.
During the study follow-up, 10 graft losses (14.5%) occurred in the belatacept group (n = 69) versus 26 (37.1%) in the matched CNI group (n = 70) (P = .005). Death-censored graft survival was significantly higher in the belatacept group (P = .001). At 3 years, graft survival was 84.0% in the belatacept group compared with 65.1% in the control group. Continuing CNI was an independent risk factor for graft loss [hazard ratio (HR) 3.46; P < .005]. The incidence of cellular rejection after the conversion was low (4.3% in both groups) and not significantly different between groups (P = .84). Patients switched to belatacept developed significantly less donor-specific antibodies de novo. Belatacept was an independent risk factor for the occurrence of opportunistic infections (HR 4.84; P < .005).
The replacement of CNI with belatacept in patients with decreased allograft function and vascular lesions is associated with an improvement in graft survival and represents a valuable option in a context of organ shortage. Caution should be exercised regarding the increased risk of opportunistic infection.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfac178</identifier><identifier>PMID: 35544123</identifier><language>eng</language><publisher>England</publisher><subject>Abatacept - therapeutic use ; Calcineurin Inhibitors - therapeutic use ; Graft Rejection - etiology ; Graft Rejection - prevention & control ; Graft Survival ; Humans ; Immunosuppressive Agents - therapeutic use ; Kidney Transplantation - adverse effects ; Retrospective Studies ; Transplant Recipients</subject><ispartof>Nephrology, dialysis, transplantation, 2023-02, Vol.38 (2), p.481-490</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the ERA.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c289t-890b6b712232dffb4beae8952a2f36cd1541b632700e5ae7a0f31cbb6310d26c3</citedby><cites>FETCH-LOGICAL-c289t-890b6b712232dffb4beae8952a2f36cd1541b632700e5ae7a0f31cbb6310d26c3</cites><orcidid>0000-0002-3714-8768 ; 0000-0002-5953-5785 ; 0000-0002-6015-3979 ; 0000-0002-3443-5024</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35544123$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bertrand, Dominique</creatorcontrib><creatorcontrib>Matignon, Marie</creatorcontrib><creatorcontrib>Morel, Antoine</creatorcontrib><creatorcontrib>Ludivine, Lebourg</creatorcontrib><creatorcontrib>Lemoine, Mathilde</creatorcontrib><creatorcontrib>Hanoy, Mélanie</creatorcontrib><creatorcontrib>Roy, Frank Le</creatorcontrib><creatorcontrib>Nezam, Dorian</creatorcontrib><creatorcontrib>Hamzaoui, Mouad</creatorcontrib><creatorcontrib>de Nattes, Tristan</creatorcontrib><creatorcontrib>Moktefi, Anissa</creatorcontrib><creatorcontrib>François, Arnaud</creatorcontrib><creatorcontrib>Laurent, Charlotte</creatorcontrib><creatorcontrib>Etienne, Isabelle</creatorcontrib><creatorcontrib>Guerrot, Dominique</creatorcontrib><title>Belatacept rescue conversion in kidney transplant recipients with vascular lesions (Banff cv score >2): a retrospective cohort study</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Immunosuppression in kidney transplant recipients with decreased graft function and histological vascular changes can be particularly challenging. The impact of a late rescue conversion to belatacept on kidney graft survival in this context has never been studied.
We report a bicentric retrospective cohort study comparing a calcineurin inhibitor (CNI) to belatacept switch versus CNI continuation in 139 kidney transplant recipients with histological kidney vascular damage (cv ≥2, g + cpt ≤1, i + t ≤1) and low estimated glomerular filtration rate (≤40 mL/min/1.73 m²). Primary outcome was death-censored graft survival.
During the study follow-up, 10 graft losses (14.5%) occurred in the belatacept group (n = 69) versus 26 (37.1%) in the matched CNI group (n = 70) (P = .005). Death-censored graft survival was significantly higher in the belatacept group (P = .001). At 3 years, graft survival was 84.0% in the belatacept group compared with 65.1% in the control group. Continuing CNI was an independent risk factor for graft loss [hazard ratio (HR) 3.46; P < .005]. The incidence of cellular rejection after the conversion was low (4.3% in both groups) and not significantly different between groups (P = .84). Patients switched to belatacept developed significantly less donor-specific antibodies de novo. Belatacept was an independent risk factor for the occurrence of opportunistic infections (HR 4.84; P < .005).
The replacement of CNI with belatacept in patients with decreased allograft function and vascular lesions is associated with an improvement in graft survival and represents a valuable option in a context of organ shortage. Caution should be exercised regarding the increased risk of opportunistic infection.</description><subject>Abatacept - therapeutic use</subject><subject>Calcineurin Inhibitors - therapeutic use</subject><subject>Graft Rejection - etiology</subject><subject>Graft Rejection - prevention & control</subject><subject>Graft Survival</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Retrospective Studies</subject><subject>Transplant Recipients</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNo9kMlOwzAQhi0EgrKcuCMfQSjUS5yFAxJFbFIlLnCOHGcMhtQJtlPUJ-A1eBaeDEcUTiPNfP-M_SF0SMkZJSWf2iZMn7VUNC820ISmGUkYL8QmmsQpTYgg5Q7a9f6VEFKyPN9GO1yINKWMT9DnDFoZpII-YAdeDYBVZ5fgvOksNha_mcbCCgcnre9baUdMmd6ADR5_mPCClzLGWulwC2PI4-OZtFpjtcRedQ6-vy7YyTn-_pIxGlzne1DBLMdDL50L2IehWe2jLS1bDwfruoeebq4fr-6S-cPt_dXlPFGsKENSlKTO6pwyxlmjdZ3WIKEoBZNM80w1VKS0zjjLCQEhIZdEc6rq2KKkYZnie-j4d2_vuvcBfKgWxito48-gG3zFsoyNboSI6OkvquKbvQNd9c4spFtVlFSj-Sqar9bmI320XjzUC2j-2T_V_AeOB4Qm</recordid><startdate>20230213</startdate><enddate>20230213</enddate><creator>Bertrand, Dominique</creator><creator>Matignon, Marie</creator><creator>Morel, Antoine</creator><creator>Ludivine, Lebourg</creator><creator>Lemoine, Mathilde</creator><creator>Hanoy, Mélanie</creator><creator>Roy, Frank Le</creator><creator>Nezam, Dorian</creator><creator>Hamzaoui, Mouad</creator><creator>de Nattes, Tristan</creator><creator>Moktefi, Anissa</creator><creator>François, Arnaud</creator><creator>Laurent, Charlotte</creator><creator>Etienne, Isabelle</creator><creator>Guerrot, Dominique</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><orcidid>https://orcid.org/0000-0002-3714-8768</orcidid><orcidid>https://orcid.org/0000-0002-5953-5785</orcidid><orcidid>https://orcid.org/0000-0002-6015-3979</orcidid><orcidid>https://orcid.org/0000-0002-3443-5024</orcidid></search><sort><creationdate>20230213</creationdate><title>Belatacept rescue conversion in kidney transplant recipients with vascular lesions (Banff cv score >2): a retrospective cohort study</title><author>Bertrand, Dominique ; Matignon, Marie ; Morel, Antoine ; Ludivine, Lebourg ; Lemoine, Mathilde ; Hanoy, Mélanie ; Roy, Frank Le ; Nezam, Dorian ; Hamzaoui, Mouad ; de Nattes, Tristan ; Moktefi, Anissa ; François, Arnaud ; Laurent, Charlotte ; Etienne, Isabelle ; Guerrot, Dominique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-890b6b712232dffb4beae8952a2f36cd1541b632700e5ae7a0f31cbb6310d26c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abatacept - therapeutic use</topic><topic>Calcineurin Inhibitors - therapeutic use</topic><topic>Graft Rejection - etiology</topic><topic>Graft Rejection - prevention & control</topic><topic>Graft Survival</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Retrospective Studies</topic><topic>Transplant Recipients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bertrand, Dominique</creatorcontrib><creatorcontrib>Matignon, Marie</creatorcontrib><creatorcontrib>Morel, Antoine</creatorcontrib><creatorcontrib>Ludivine, Lebourg</creatorcontrib><creatorcontrib>Lemoine, Mathilde</creatorcontrib><creatorcontrib>Hanoy, Mélanie</creatorcontrib><creatorcontrib>Roy, Frank Le</creatorcontrib><creatorcontrib>Nezam, Dorian</creatorcontrib><creatorcontrib>Hamzaoui, Mouad</creatorcontrib><creatorcontrib>de Nattes, Tristan</creatorcontrib><creatorcontrib>Moktefi, Anissa</creatorcontrib><creatorcontrib>François, Arnaud</creatorcontrib><creatorcontrib>Laurent, Charlotte</creatorcontrib><creatorcontrib>Etienne, Isabelle</creatorcontrib><creatorcontrib>Guerrot, Dominique</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><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bertrand, Dominique</au><au>Matignon, Marie</au><au>Morel, Antoine</au><au>Ludivine, Lebourg</au><au>Lemoine, Mathilde</au><au>Hanoy, Mélanie</au><au>Roy, Frank Le</au><au>Nezam, Dorian</au><au>Hamzaoui, Mouad</au><au>de Nattes, Tristan</au><au>Moktefi, Anissa</au><au>François, Arnaud</au><au>Laurent, Charlotte</au><au>Etienne, Isabelle</au><au>Guerrot, Dominique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Belatacept rescue conversion in kidney transplant recipients with vascular lesions (Banff cv score >2): a retrospective cohort study</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2023-02-13</date><risdate>2023</risdate><volume>38</volume><issue>2</issue><spage>481</spage><epage>490</epage><pages>481-490</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><abstract>Immunosuppression in kidney transplant recipients with decreased graft function and histological vascular changes can be particularly challenging. The impact of a late rescue conversion to belatacept on kidney graft survival in this context has never been studied.
We report a bicentric retrospective cohort study comparing a calcineurin inhibitor (CNI) to belatacept switch versus CNI continuation in 139 kidney transplant recipients with histological kidney vascular damage (cv ≥2, g + cpt ≤1, i + t ≤1) and low estimated glomerular filtration rate (≤40 mL/min/1.73 m²). Primary outcome was death-censored graft survival.
During the study follow-up, 10 graft losses (14.5%) occurred in the belatacept group (n = 69) versus 26 (37.1%) in the matched CNI group (n = 70) (P = .005). Death-censored graft survival was significantly higher in the belatacept group (P = .001). At 3 years, graft survival was 84.0% in the belatacept group compared with 65.1% in the control group. Continuing CNI was an independent risk factor for graft loss [hazard ratio (HR) 3.46; P < .005]. The incidence of cellular rejection after the conversion was low (4.3% in both groups) and not significantly different between groups (P = .84). Patients switched to belatacept developed significantly less donor-specific antibodies de novo. Belatacept was an independent risk factor for the occurrence of opportunistic infections (HR 4.84; P < .005).
The replacement of CNI with belatacept in patients with decreased allograft function and vascular lesions is associated with an improvement in graft survival and represents a valuable option in a context of organ shortage. Caution should be exercised regarding the increased risk of opportunistic infection.</abstract><cop>England</cop><pmid>35544123</pmid><doi>10.1093/ndt/gfac178</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3714-8768</orcidid><orcidid>https://orcid.org/0000-0002-5953-5785</orcidid><orcidid>https://orcid.org/0000-0002-6015-3979</orcidid><orcidid>https://orcid.org/0000-0002-3443-5024</orcidid></addata></record> |
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subjects | Abatacept - therapeutic use Calcineurin Inhibitors - therapeutic use Graft Rejection - etiology Graft Rejection - prevention & control Graft Survival Humans Immunosuppressive Agents - therapeutic use Kidney Transplantation - adverse effects Retrospective Studies Transplant Recipients |
title | Belatacept rescue conversion in kidney transplant recipients with vascular lesions (Banff cv score >2): a retrospective cohort study |
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