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
Hauptverfasser: Hou, Ming, Peng, Jun, Shi, Yan, Zhang, Chunqing, Qin, Ping, Zhao, Chuanli, Ji, Xuebin, Wang, Xueyong, Zhang, Maohong
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container_end_page 357
container_issue 6
container_start_page 353
container_title European journal of haematology
container_volume 70
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 Sustained response was observed in three patients in whom MMF was withdrawn.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 &gt; 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. 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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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14769314$$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 &gt; 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 &amp; 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 &amp; dosage</subject><subject>Mycophenolic Acid - analogs &amp; 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 &amp; 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 &amp; dosage</topic><topic>Mycophenolic Acid - analogs &amp; 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 &gt; 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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