Rheumatologic complications of CAR-T Cell therapy. Experience of a single center
Chimeric Antigen Receptor T-cell (CAR-T) therapy has emerged as a promising treatment for hematological malignancies. However, its association with immune-related complications such as rheumatic complications, is not well defined. We conducted a retrospective study to analyze rheumatic complications...
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Veröffentlicht in: | Seminars in arthritis and rheumatism 2025-04, Vol.71, p.152610, Article 152610 |
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creator | Gómez-Puerta, José A Monegal, Ana Ponce, Andrés Peris, Pilar Martínez-Cibrian, Nuria Sarmiento-Monroy, Juan Camilo Ortiz-Maldonado, Valentin Triguero, Ana Fernández de Larrea, Carlos Delgado, Julio García-Herrera, Adriana Albero-González, Raquel Bosch-Amate, Xavier Español-Rego, Marta González, Azucena Sanmartí, Raimon Juan, Manel |
description | Chimeric Antigen Receptor T-cell (CAR-T) therapy has emerged as a promising treatment for hematological malignancies. However, its association with immune-related complications such as rheumatic complications, is not well defined.
We conducted a retrospective study to analyze rheumatic complications in 310 patients treated with CAR-T therapy at a single center from January 2020 to May 2024.
We identified six patients (1.9 %) who developed rheumatic complications, including rheumatoid arthritis (RA)-like manifestations with biopsy-proven nodules, palindromic rheumatism, myositis, necrotizing fasciitis, and osteonecrosis (ON). Symptoms appeared between 2 to 11 weeks after therapy, with inflammatory arthritis manifesting later. Notably, 2 patients developed RA-like arthritis with subcutaneous nodulosis, while others presented with transient arthritis flares, severe soft tissue and joint involvement, such as pseudo-podagra and ON. Imaging findings and biopsies confirmed the diagnoses. Treatment included glucocorticoids, hydroxychloroquine, and nonsteroidal anti-inflammatory drugs, with variable responses.
Clinicians should be aware of these potential complications to ensure prompt diagnosis and management. Further research is needed to elucidate the mechanisms underlying these autoimmune phenomena and to establish standardized treatment protocols. |
doi_str_mv | 10.1016/j.semarthrit.2024.152610 |
format | Article |
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We conducted a retrospective study to analyze rheumatic complications in 310 patients treated with CAR-T therapy at a single center from January 2020 to May 2024.
We identified six patients (1.9 %) who developed rheumatic complications, including rheumatoid arthritis (RA)-like manifestations with biopsy-proven nodules, palindromic rheumatism, myositis, necrotizing fasciitis, and osteonecrosis (ON). Symptoms appeared between 2 to 11 weeks after therapy, with inflammatory arthritis manifesting later. Notably, 2 patients developed RA-like arthritis with subcutaneous nodulosis, while others presented with transient arthritis flares, severe soft tissue and joint involvement, such as pseudo-podagra and ON. Imaging findings and biopsies confirmed the diagnoses. Treatment included glucocorticoids, hydroxychloroquine, and nonsteroidal anti-inflammatory drugs, with variable responses.
Clinicians should be aware of these potential complications to ensure prompt diagnosis and management. Further research is needed to elucidate the mechanisms underlying these autoimmune phenomena and to establish standardized treatment protocols.</description><identifier>ISSN: 0049-0172</identifier><identifier>ISSN: 1532-866X</identifier><identifier>EISSN: 1532-866X</identifier><identifier>DOI: 10.1016/j.semarthrit.2024.152610</identifier><identifier>PMID: 39754918</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>CAR-T therapy ; immune-mediated complications ; osteonecrosis ; palindromic rheumatism ; rheumatic complications ; rheumatoid arthritis</subject><ispartof>Seminars in arthritis and rheumatism, 2025-04, Vol.71, p.152610, Article 152610</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1648-5625ff7e72a4c97989b86c0a87143e71d0957029d1005fce30f076c62e8724ff3</cites><orcidid>0000-0001-8177-702X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0049017224002506$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39754918$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gómez-Puerta, José A</creatorcontrib><creatorcontrib>Monegal, Ana</creatorcontrib><creatorcontrib>Ponce, Andrés</creatorcontrib><creatorcontrib>Peris, Pilar</creatorcontrib><creatorcontrib>Martínez-Cibrian, Nuria</creatorcontrib><creatorcontrib>Sarmiento-Monroy, Juan Camilo</creatorcontrib><creatorcontrib>Ortiz-Maldonado, Valentin</creatorcontrib><creatorcontrib>Triguero, Ana</creatorcontrib><creatorcontrib>Fernández de Larrea, Carlos</creatorcontrib><creatorcontrib>Delgado, Julio</creatorcontrib><creatorcontrib>García-Herrera, Adriana</creatorcontrib><creatorcontrib>Albero-González, Raquel</creatorcontrib><creatorcontrib>Bosch-Amate, Xavier</creatorcontrib><creatorcontrib>Español-Rego, Marta</creatorcontrib><creatorcontrib>González, Azucena</creatorcontrib><creatorcontrib>Sanmartí, Raimon</creatorcontrib><creatorcontrib>Juan, Manel</creatorcontrib><title>Rheumatologic complications of CAR-T Cell therapy. Experience of a single center</title><title>Seminars in arthritis and rheumatism</title><addtitle>Semin Arthritis Rheum</addtitle><description>Chimeric Antigen Receptor T-cell (CAR-T) therapy has emerged as a promising treatment for hematological malignancies. However, its association with immune-related complications such as rheumatic complications, is not well defined.
We conducted a retrospective study to analyze rheumatic complications in 310 patients treated with CAR-T therapy at a single center from January 2020 to May 2024.
We identified six patients (1.9 %) who developed rheumatic complications, including rheumatoid arthritis (RA)-like manifestations with biopsy-proven nodules, palindromic rheumatism, myositis, necrotizing fasciitis, and osteonecrosis (ON). Symptoms appeared between 2 to 11 weeks after therapy, with inflammatory arthritis manifesting later. Notably, 2 patients developed RA-like arthritis with subcutaneous nodulosis, while others presented with transient arthritis flares, severe soft tissue and joint involvement, such as pseudo-podagra and ON. Imaging findings and biopsies confirmed the diagnoses. Treatment included glucocorticoids, hydroxychloroquine, and nonsteroidal anti-inflammatory drugs, with variable responses.
Clinicians should be aware of these potential complications to ensure prompt diagnosis and management. Further research is needed to elucidate the mechanisms underlying these autoimmune phenomena and to establish standardized treatment protocols.</description><subject>CAR-T therapy</subject><subject>immune-mediated complications</subject><subject>osteonecrosis</subject><subject>palindromic rheumatism</subject><subject>rheumatic complications</subject><subject>rheumatoid arthritis</subject><issn>0049-0172</issn><issn>1532-866X</issn><issn>1532-866X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhi0EotvCX0A-ckmYceKPHMuqfEiVQFWRuFmuM-56lcTBziL678myLRw5zeV55515GOMINQKqd_u60OjysstxqQWItkYpFMIztkHZiMoo9f052wC0XQWoxRk7L2UPgKhAv2RnTadl26HZsK83OzqMbklDuo-e-zTOQ_RuiWkqPAW-vbypbvmWhoEvO8pufqj51a-ZcqTJ05FwvMTpfiDuaVoov2IvghsKvX6cF-zbh6vb7afq-svHz9vL68qjak0llZAhaNLCtb7TnenujPLgjMa2IY09dFKD6HoEkMFTAwG08kqQ0aINoblgb09755x-HKgsdozFr3e6idKh2AYlSiPXn1fUnFCfUymZgp1zXPU9WAR79Gn39p9Pe_RpTz7X6JvHlsPdSP3f4JPAFXh_Amj99WekbIv_o6aPmfxi-xT_3_IbGP-Kcw</recordid><startdate>202504</startdate><enddate>202504</enddate><creator>Gómez-Puerta, José A</creator><creator>Monegal, Ana</creator><creator>Ponce, Andrés</creator><creator>Peris, Pilar</creator><creator>Martínez-Cibrian, Nuria</creator><creator>Sarmiento-Monroy, Juan Camilo</creator><creator>Ortiz-Maldonado, Valentin</creator><creator>Triguero, Ana</creator><creator>Fernández de Larrea, Carlos</creator><creator>Delgado, Julio</creator><creator>García-Herrera, Adriana</creator><creator>Albero-González, Raquel</creator><creator>Bosch-Amate, Xavier</creator><creator>Español-Rego, Marta</creator><creator>González, Azucena</creator><creator>Sanmartí, Raimon</creator><creator>Juan, Manel</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8177-702X</orcidid></search><sort><creationdate>202504</creationdate><title>Rheumatologic complications of CAR-T Cell therapy. Experience of a single center</title><author>Gómez-Puerta, José A ; Monegal, Ana ; Ponce, Andrés ; Peris, Pilar ; Martínez-Cibrian, Nuria ; Sarmiento-Monroy, Juan Camilo ; Ortiz-Maldonado, Valentin ; Triguero, Ana ; Fernández de Larrea, Carlos ; Delgado, Julio ; García-Herrera, Adriana ; Albero-González, Raquel ; Bosch-Amate, Xavier ; Español-Rego, Marta ; González, Azucena ; Sanmartí, Raimon ; Juan, Manel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1648-5625ff7e72a4c97989b86c0a87143e71d0957029d1005fce30f076c62e8724ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>CAR-T therapy</topic><topic>immune-mediated complications</topic><topic>osteonecrosis</topic><topic>palindromic rheumatism</topic><topic>rheumatic complications</topic><topic>rheumatoid arthritis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gómez-Puerta, José A</creatorcontrib><creatorcontrib>Monegal, Ana</creatorcontrib><creatorcontrib>Ponce, Andrés</creatorcontrib><creatorcontrib>Peris, Pilar</creatorcontrib><creatorcontrib>Martínez-Cibrian, Nuria</creatorcontrib><creatorcontrib>Sarmiento-Monroy, Juan Camilo</creatorcontrib><creatorcontrib>Ortiz-Maldonado, Valentin</creatorcontrib><creatorcontrib>Triguero, Ana</creatorcontrib><creatorcontrib>Fernández de Larrea, Carlos</creatorcontrib><creatorcontrib>Delgado, Julio</creatorcontrib><creatorcontrib>García-Herrera, Adriana</creatorcontrib><creatorcontrib>Albero-González, Raquel</creatorcontrib><creatorcontrib>Bosch-Amate, Xavier</creatorcontrib><creatorcontrib>Español-Rego, Marta</creatorcontrib><creatorcontrib>González, Azucena</creatorcontrib><creatorcontrib>Sanmartí, Raimon</creatorcontrib><creatorcontrib>Juan, Manel</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Seminars in arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gómez-Puerta, José A</au><au>Monegal, Ana</au><au>Ponce, Andrés</au><au>Peris, Pilar</au><au>Martínez-Cibrian, Nuria</au><au>Sarmiento-Monroy, Juan Camilo</au><au>Ortiz-Maldonado, Valentin</au><au>Triguero, Ana</au><au>Fernández de Larrea, Carlos</au><au>Delgado, Julio</au><au>García-Herrera, Adriana</au><au>Albero-González, Raquel</au><au>Bosch-Amate, Xavier</au><au>Español-Rego, Marta</au><au>González, Azucena</au><au>Sanmartí, Raimon</au><au>Juan, Manel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rheumatologic complications of CAR-T Cell therapy. Experience of a single center</atitle><jtitle>Seminars in arthritis and rheumatism</jtitle><addtitle>Semin Arthritis Rheum</addtitle><date>2025-04</date><risdate>2025</risdate><volume>71</volume><spage>152610</spage><pages>152610-</pages><artnum>152610</artnum><issn>0049-0172</issn><issn>1532-866X</issn><eissn>1532-866X</eissn><abstract>Chimeric Antigen Receptor T-cell (CAR-T) therapy has emerged as a promising treatment for hematological malignancies. However, its association with immune-related complications such as rheumatic complications, is not well defined.
We conducted a retrospective study to analyze rheumatic complications in 310 patients treated with CAR-T therapy at a single center from January 2020 to May 2024.
We identified six patients (1.9 %) who developed rheumatic complications, including rheumatoid arthritis (RA)-like manifestations with biopsy-proven nodules, palindromic rheumatism, myositis, necrotizing fasciitis, and osteonecrosis (ON). Symptoms appeared between 2 to 11 weeks after therapy, with inflammatory arthritis manifesting later. Notably, 2 patients developed RA-like arthritis with subcutaneous nodulosis, while others presented with transient arthritis flares, severe soft tissue and joint involvement, such as pseudo-podagra and ON. Imaging findings and biopsies confirmed the diagnoses. Treatment included glucocorticoids, hydroxychloroquine, and nonsteroidal anti-inflammatory drugs, with variable responses.
Clinicians should be aware of these potential complications to ensure prompt diagnosis and management. Further research is needed to elucidate the mechanisms underlying these autoimmune phenomena and to establish standardized treatment protocols.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39754918</pmid><doi>10.1016/j.semarthrit.2024.152610</doi><orcidid>https://orcid.org/0000-0001-8177-702X</orcidid></addata></record> |
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source | ScienceDirect Journals (5 years ago - present) |
subjects | CAR-T therapy immune-mediated complications osteonecrosis palindromic rheumatism rheumatic complications rheumatoid arthritis |
title | Rheumatologic complications of CAR-T Cell therapy. Experience of a single center |
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