Mycophenolate mofetil (MMF) for the treatment of steroid-resistant idiopathic thrombocytopenic purpura
: The treatment of chronic idiopathic thrombocytopenic purpura (ITP) is difficult in those unresponsive to corticosteroids and/or splenectomy. We attempted to induce durable response in 21 patients with refractory ITP by applying mycophenolate mofetil (MMF) (1.5–2.0 g/d), a novel immunosuppressive a...
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Veröffentlicht in: | European journal of haematology 2003-06, Vol.70 (6), p.353-357 |
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creator | Hou, Ming Peng, Jun Shi, Yan Zhang, Chunqing Qin, Ping Zhao, Chuanli Ji, Xuebin Wang, Xueyong Zhang, Maohong |
description | : The treatment of chronic idiopathic thrombocytopenic purpura (ITP) is difficult in those unresponsive to corticosteroids and/or splenectomy. We attempted to induce durable response in 21 patients with refractory ITP by applying mycophenolate mofetil (MMF) (1.5–2.0 g/d), a novel immunosuppressive agent. Overall response rate was 62% (13 of 21), including 24% (five of 21) in complete response (CR), 29% (six of 21) in partial response (PR), and 10% (two of 21) in minor response (MR). The response rates for non‐splenectomized and splenectomized ITP patients were 64% (nine of 14) and 57% (four of seven), respectively (P > 0.05). 39% (five of 13) responders relapsed as a result of dose reduction or withdraw of MMF, and 61% (eight of 13) responders maintained their effectiveness for a median of 24 wk. Sustained response was observed in three patients in whom MMF was withdrawn. MMF was well tolerated with only slight nausea and diarrhea recorded in 3 of 21 cases. No premature withdrawal was found in this study. CD3+ peripheral blood mononuclear cells (PBMC) and CD19+ PBMC were significantly reduced 12 wk after MMF administration in the responders. Platelet‐associated antibodies against glycoproteins GPIIb/IIIa were detected in 13 of 21 (62%) patients before MMF treatment, and antibody levels were significantly decreased in responders 12 wk after MMF administration. This suggested that MMF might correct the immunologic abnormalities underlying the destruction of circulating platelets in ITP. We conclude that MMF could be used as a second‐line agent for the treatment of steroid‐resistant ITP before or after splenectomy and thereby is worth of further evaluation in randomized studies. |
doi_str_mv | 10.1034/j.1600-0609.2003.00076.x |
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We attempted to induce durable response in 21 patients with refractory ITP by applying mycophenolate mofetil (MMF) (1.5–2.0 g/d), a novel immunosuppressive agent. Overall response rate was 62% (13 of 21), including 24% (five of 21) in complete response (CR), 29% (six of 21) in partial response (PR), and 10% (two of 21) in minor response (MR). The response rates for non‐splenectomized and splenectomized ITP patients were 64% (nine of 14) and 57% (four of seven), respectively (P > 0.05). 39% (five of 13) responders relapsed as a result of dose reduction or withdraw of MMF, and 61% (eight of 13) responders maintained their effectiveness for a median of 24 wk. Sustained response was observed in three patients in whom MMF was withdrawn. MMF was well tolerated with only slight nausea and diarrhea recorded in 3 of 21 cases. No premature withdrawal was found in this study. CD3+ peripheral blood mononuclear cells (PBMC) and CD19+ PBMC were significantly reduced 12 wk after MMF administration in the responders. Platelet‐associated antibodies against glycoproteins GPIIb/IIIa were detected in 13 of 21 (62%) patients before MMF treatment, and antibody levels were significantly decreased in responders 12 wk after MMF administration. This suggested that MMF might correct the immunologic abnormalities underlying the destruction of circulating platelets in ITP. We conclude that MMF could be used as a second‐line agent for the treatment of steroid‐resistant ITP before or after splenectomy and thereby is worth of further evaluation in randomized studies.</description><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1034/j.1600-0609.2003.00076.x</identifier><identifier>PMID: 12756016</identifier><identifier>CODEN: EJHAEC</identifier><language>eng</language><publisher>Oxford, UK: Munksgaard International Publishers</publisher><subject>Adult ; Aged ; Autoantibodies - analysis ; autoimmunity ; Biological and medical sciences ; Blood. Blood coagulation. Reticuloendothelial system ; Drug Resistance ; Female ; Hematologic and hematopoietic diseases ; Humans ; immunosuppression ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - pharmacology ; Leukocytes - drug effects ; Male ; Medical sciences ; Middle Aged ; mycophenolate mofetil ; Mycophenolic Acid - administration & dosage ; Mycophenolic Acid - analogs & derivatives ; Mycophenolic Acid - pharmacology ; Pharmacology. Drug treatments ; Platelet diseases and coagulopathies ; Platelet Glycoprotein GPIIb-IIIa Complex - immunology ; Prednisone - therapeutic use ; Purpura, Thrombocytopenic, Idiopathic - drug therapy ; Purpura, Thrombocytopenic, Idiopathic - surgery ; Remission Induction ; Splenectomy ; thrombocytopenia</subject><ispartof>European journal of haematology, 2003-06, Vol.70 (6), p.353-357</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4326-e4b424060e668cf93ef44d56c264de2da301c1e8a355be7adb9d3f0a03d1596d3</citedby><cites>FETCH-LOGICAL-c4326-e4b424060e668cf93ef44d56c264de2da301c1e8a355be7adb9d3f0a03d1596d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1034%2Fj.1600-0609.2003.00076.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14769314$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12756016$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hou, Ming</creatorcontrib><creatorcontrib>Peng, Jun</creatorcontrib><creatorcontrib>Shi, Yan</creatorcontrib><creatorcontrib>Zhang, Chunqing</creatorcontrib><creatorcontrib>Qin, Ping</creatorcontrib><creatorcontrib>Zhao, Chuanli</creatorcontrib><creatorcontrib>Ji, Xuebin</creatorcontrib><creatorcontrib>Wang, Xueyong</creatorcontrib><creatorcontrib>Zhang, Maohong</creatorcontrib><title>Mycophenolate mofetil (MMF) for the treatment of steroid-resistant idiopathic thrombocytopenic purpura</title><title>European journal of haematology</title><addtitle>Eur J Haematol</addtitle><description>: The treatment of chronic idiopathic thrombocytopenic purpura (ITP) is difficult in those unresponsive to corticosteroids and/or splenectomy. We attempted to induce durable response in 21 patients with refractory ITP by applying mycophenolate mofetil (MMF) (1.5–2.0 g/d), a novel immunosuppressive agent. Overall response rate was 62% (13 of 21), including 24% (five of 21) in complete response (CR), 29% (six of 21) in partial response (PR), and 10% (two of 21) in minor response (MR). The response rates for non‐splenectomized and splenectomized ITP patients were 64% (nine of 14) and 57% (four of seven), respectively (P > 0.05). 39% (five of 13) responders relapsed as a result of dose reduction or withdraw of MMF, and 61% (eight of 13) responders maintained their effectiveness for a median of 24 wk. Sustained response was observed in three patients in whom MMF was withdrawn. MMF was well tolerated with only slight nausea and diarrhea recorded in 3 of 21 cases. No premature withdrawal was found in this study. CD3+ peripheral blood mononuclear cells (PBMC) and CD19+ PBMC were significantly reduced 12 wk after MMF administration in the responders. Platelet‐associated antibodies against glycoproteins GPIIb/IIIa were detected in 13 of 21 (62%) patients before MMF treatment, and antibody levels were significantly decreased in responders 12 wk after MMF administration. This suggested that MMF might correct the immunologic abnormalities underlying the destruction of circulating platelets in ITP. We conclude that MMF could be used as a second‐line agent for the treatment of steroid‐resistant ITP before or after splenectomy and thereby is worth of further evaluation in randomized studies.</description><subject>Adult</subject><subject>Aged</subject><subject>Autoantibodies - analysis</subject><subject>autoimmunity</subject><subject>Biological and medical sciences</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Drug Resistance</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>immunosuppression</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Immunosuppressive Agents - pharmacology</subject><subject>Leukocytes - drug effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>mycophenolate mofetil</subject><subject>Mycophenolic Acid - administration & dosage</subject><subject>Mycophenolic Acid - analogs & derivatives</subject><subject>Mycophenolic Acid - pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Platelet diseases and coagulopathies</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - immunology</subject><subject>Prednisone - therapeutic use</subject><subject>Purpura, Thrombocytopenic, Idiopathic - drug therapy</subject><subject>Purpura, Thrombocytopenic, Idiopathic - surgery</subject><subject>Remission Induction</subject><subject>Splenectomy</subject><subject>thrombocytopenia</subject><issn>0902-4441</issn><issn>1600-0609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkdGKEzEUhoMobl19BZkbRS9mPJlkMh3wZll3u0qrIIrehUxyQlNnmjFJsX17U1t2b4VAwsn3nxy-EFJQqCgw_m5TUQFQgoCuqgFYBQCtqPaPyOz-4jGZQQd1yTmnF-RZjJsM1R1tn5ILWreNACpmxK4O2k9r3PpBJSxGbzG5oXizWt2-LawPRVpjkQKqNOI2Fd4WMWHwzpQBo4tJ5aIzzk8qrZ3OdPBj7_Uh-Qm3uTDtQl7qOXli1RDxxXm_JN9vb75d35XLL4uP11fLUnNWixJ5z2uep0ch5tp2DC3nphG6FtxgbRQDqinOFWuaHltl-s4wCwqYoU0nDLskr099p-B_7zAmObqocRjUFv0uypaxGlqgGZyfQB18jAGtnIIbVThICvLoWG7kUaU8qpRHx_KfY7nP0ZfnN3b9iOYheJaagVdnQEWtBhvUVrv4wPFWdIzyzL0_cX_cgIf_HkDefLrLhxwvT_H8Dbi_j6vwS4qWtY388Xkhf9L5h6-sW8oF-wv3BKex</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Hou, Ming</creator><creator>Peng, Jun</creator><creator>Shi, Yan</creator><creator>Zhang, Chunqing</creator><creator>Qin, Ping</creator><creator>Zhao, Chuanli</creator><creator>Ji, Xuebin</creator><creator>Wang, Xueyong</creator><creator>Zhang, Maohong</creator><general>Munksgaard International Publishers</general><general>Blackwell</general><scope>BSCLL</scope><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>200306</creationdate><title>Mycophenolate mofetil (MMF) for the treatment of steroid-resistant idiopathic thrombocytopenic purpura</title><author>Hou, Ming ; Peng, Jun ; Shi, Yan ; Zhang, Chunqing ; Qin, Ping ; Zhao, Chuanli ; Ji, Xuebin ; Wang, Xueyong ; Zhang, Maohong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4326-e4b424060e668cf93ef44d56c264de2da301c1e8a355be7adb9d3f0a03d1596d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Autoantibodies - analysis</topic><topic>autoimmunity</topic><topic>Biological and medical sciences</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Drug Resistance</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>immunosuppression</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Immunosuppressive Agents - pharmacology</topic><topic>Leukocytes - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>mycophenolate mofetil</topic><topic>Mycophenolic Acid - administration & dosage</topic><topic>Mycophenolic Acid - analogs & derivatives</topic><topic>Mycophenolic Acid - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Platelet diseases and coagulopathies</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - immunology</topic><topic>Prednisone - therapeutic use</topic><topic>Purpura, Thrombocytopenic, Idiopathic - drug therapy</topic><topic>Purpura, Thrombocytopenic, Idiopathic - surgery</topic><topic>Remission Induction</topic><topic>Splenectomy</topic><topic>thrombocytopenia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hou, Ming</creatorcontrib><creatorcontrib>Peng, Jun</creatorcontrib><creatorcontrib>Shi, Yan</creatorcontrib><creatorcontrib>Zhang, Chunqing</creatorcontrib><creatorcontrib>Qin, Ping</creatorcontrib><creatorcontrib>Zhao, Chuanli</creatorcontrib><creatorcontrib>Ji, Xuebin</creatorcontrib><creatorcontrib>Wang, Xueyong</creatorcontrib><creatorcontrib>Zhang, Maohong</creatorcontrib><collection>Istex</collection><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>European journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hou, Ming</au><au>Peng, Jun</au><au>Shi, Yan</au><au>Zhang, Chunqing</au><au>Qin, Ping</au><au>Zhao, Chuanli</au><au>Ji, Xuebin</au><au>Wang, Xueyong</au><au>Zhang, Maohong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mycophenolate mofetil (MMF) for the treatment of steroid-resistant idiopathic thrombocytopenic purpura</atitle><jtitle>European journal of haematology</jtitle><addtitle>Eur J Haematol</addtitle><date>2003-06</date><risdate>2003</risdate><volume>70</volume><issue>6</issue><spage>353</spage><epage>357</epage><pages>353-357</pages><issn>0902-4441</issn><eissn>1600-0609</eissn><coden>EJHAEC</coden><abstract>: The treatment of chronic idiopathic thrombocytopenic purpura (ITP) is difficult in those unresponsive to corticosteroids and/or splenectomy. We attempted to induce durable response in 21 patients with refractory ITP by applying mycophenolate mofetil (MMF) (1.5–2.0 g/d), a novel immunosuppressive agent. Overall response rate was 62% (13 of 21), including 24% (five of 21) in complete response (CR), 29% (six of 21) in partial response (PR), and 10% (two of 21) in minor response (MR). The response rates for non‐splenectomized and splenectomized ITP patients were 64% (nine of 14) and 57% (four of seven), respectively (P > 0.05). 39% (five of 13) responders relapsed as a result of dose reduction or withdraw of MMF, and 61% (eight of 13) responders maintained their effectiveness for a median of 24 wk. Sustained response was observed in three patients in whom MMF was withdrawn. MMF was well tolerated with only slight nausea and diarrhea recorded in 3 of 21 cases. No premature withdrawal was found in this study. CD3+ peripheral blood mononuclear cells (PBMC) and CD19+ PBMC were significantly reduced 12 wk after MMF administration in the responders. Platelet‐associated antibodies against glycoproteins GPIIb/IIIa were detected in 13 of 21 (62%) patients before MMF treatment, and antibody levels were significantly decreased in responders 12 wk after MMF administration. This suggested that MMF might correct the immunologic abnormalities underlying the destruction of circulating platelets in ITP. We conclude that MMF could be used as a second‐line agent for the treatment of steroid‐resistant ITP before or after splenectomy and thereby is worth of further evaluation in randomized studies.</abstract><cop>Oxford, UK</cop><pub>Munksgaard International Publishers</pub><pmid>12756016</pmid><doi>10.1034/j.1600-0609.2003.00076.x</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Autoantibodies - analysis autoimmunity Biological and medical sciences Blood. Blood coagulation. Reticuloendothelial system Drug Resistance Female Hematologic and hematopoietic diseases Humans immunosuppression Immunosuppressive Agents - administration & dosage Immunosuppressive Agents - pharmacology Leukocytes - drug effects Male Medical sciences Middle Aged mycophenolate mofetil Mycophenolic Acid - administration & dosage Mycophenolic Acid - analogs & derivatives Mycophenolic Acid - pharmacology Pharmacology. Drug treatments Platelet diseases and coagulopathies Platelet Glycoprotein GPIIb-IIIa Complex - immunology Prednisone - therapeutic use Purpura, Thrombocytopenic, Idiopathic - drug therapy Purpura, Thrombocytopenic, Idiopathic - surgery Remission Induction Splenectomy thrombocytopenia |
title | Mycophenolate mofetil (MMF) for the treatment of steroid-resistant idiopathic thrombocytopenic purpura |
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