Effect of a thrombopoietin receptor agonist on use of intravenous immune globulin in patients with immune thrombocytopenia

BACKGROUND Thrombopoietin receptor agonists are new treatments for patients with chronic immune thrombocytopenia (ITP). How one of these agent, romiplostim, has impacted practice patterns, especially the use of intravenous immune globulin (IVIG), has not been evaluated outside of clinical trials. ST...

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Veröffentlicht in:Transfusion (Philadelphia, Pa.) Pa.), 2016-01, Vol.56 (1), p.73-79
Hauptverfasser: Zeller, Michelle P., Heddle, Nancy M., Kelton, John G., Hamilton, Korinne, Wang, Grace, Sholapur, Naushin, Carruthers, Julie, Hsia, Cyrus, Blais, Normand, Toltl, Lisa, Hamm, Caroline, Pearson, Marc-André, Arnold, Donald M.
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container_end_page 79
container_issue 1
container_start_page 73
container_title Transfusion (Philadelphia, Pa.)
container_volume 56
creator Zeller, Michelle P.
Heddle, Nancy M.
Kelton, John G.
Hamilton, Korinne
Wang, Grace
Sholapur, Naushin
Carruthers, Julie
Hsia, Cyrus
Blais, Normand
Toltl, Lisa
Hamm, Caroline
Pearson, Marc-André
Arnold, Donald M.
description BACKGROUND Thrombopoietin receptor agonists are new treatments for patients with chronic immune thrombocytopenia (ITP). How one of these agent, romiplostim, has impacted practice patterns, especially the use of intravenous immune globulin (IVIG), has not been evaluated outside of clinical trials. STUDY DESIGN AND METHODS This was a retrospective cohort study of adult ITP patients treated with romiplostim in four Canadian centers. Patients had primary or secondary ITP and were followed for 1 year before starting weekly romiplostim treatment. We compared IVIG use, clinical outcomes, and cost before and after romiplostim. RESULTS Twenty‐nine patients with ITP received romiplostim. Median age was 54 years (interquartile range [IQR], 45‐63 years) and patients had a median of two prior ITP treatments (IQR, 1‐4) including splenectomy (n = 7). Median platelet (PLT) count was 23 × 109 before and 124 × 109 after romiplostim. Median duration of romiplostim treatment was 3.7 months. Patients used a median of two IVIG infusions per year before and 0.7 per year after starting romiplostim (p = 0.16). For patients who received weekly romiplostim for at least 1 month (n = 19), IVIG infusions were three (IQR, 1‐5) per year before and 0.7 (IQR, 0.4‐1.6) per year after romiplostim. Results were squewed by two high IVIG users. Nineteen (66%) patients discontinued romiplostim treatment during follow‐up because of lack of response (n = 8), sustained response (n = 5), toxicities (n = 4), or response to splenectomy (n = 2). Overall health care costs were similar before and after romiplostim when concomitant treatments, nursing resources, and hospitalizations were considered. CONCLUSIONS Romiplostim was associated with improved PLT counts and fewer IVIG infusions for most ITP patients. In practice, romiplostim was generally not continued long term and was cost neutral for overall ITP management.
doi_str_mv 10.1111/trf.13336
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How one of these agent, romiplostim, has impacted practice patterns, especially the use of intravenous immune globulin (IVIG), has not been evaluated outside of clinical trials. STUDY DESIGN AND METHODS This was a retrospective cohort study of adult ITP patients treated with romiplostim in four Canadian centers. Patients had primary or secondary ITP and were followed for 1 year before starting weekly romiplostim treatment. We compared IVIG use, clinical outcomes, and cost before and after romiplostim. RESULTS Twenty‐nine patients with ITP received romiplostim. Median age was 54 years (interquartile range [IQR], 45‐63 years) and patients had a median of two prior ITP treatments (IQR, 1‐4) including splenectomy (n = 7). Median platelet (PLT) count was 23 × 109 before and 124 × 109 after romiplostim. Median duration of romiplostim treatment was 3.7 months. Patients used a median of two IVIG infusions per year before and 0.7 per year after starting romiplostim (p = 0.16). For patients who received weekly romiplostim for at least 1 month (n = 19), IVIG infusions were three (IQR, 1‐5) per year before and 0.7 (IQR, 0.4‐1.6) per year after romiplostim. Results were squewed by two high IVIG users. Nineteen (66%) patients discontinued romiplostim treatment during follow‐up because of lack of response (n = 8), sustained response (n = 5), toxicities (n = 4), or response to splenectomy (n = 2). Overall health care costs were similar before and after romiplostim when concomitant treatments, nursing resources, and hospitalizations were considered. CONCLUSIONS Romiplostim was associated with improved PLT counts and fewer IVIG infusions for most ITP patients. In practice, romiplostim was generally not continued long term and was cost neutral for overall ITP management.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/trf.13336</identifier><identifier>PMID: 26400824</identifier><identifier>CODEN: TRANAT</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Chronic Disease ; Drug Administration Schedule ; Drug Therapy, Combination ; Female ; Follow-Up Studies ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Immunologic Factors - therapeutic use ; Male ; Middle Aged ; Purpura, Thrombocytopenic, Idiopathic - drug therapy ; Receptors, Fc - therapeutic use ; Receptors, Thrombopoietin - agonists ; Recombinant Fusion Proteins - therapeutic use ; Retrospective Studies ; Thrombopoietin - therapeutic use ; Treatment Outcome ; Young Adult</subject><ispartof>Transfusion (Philadelphia, Pa.), 2016-01, Vol.56 (1), p.73-79</ispartof><rights>2015 AABB</rights><rights>2015 AABB.</rights><rights>2016 AABB</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4616-fbe2ca5b857eaf7bc145e8a55316cebe16c818b1c422e6e59a6d0479c5a9d3383</citedby><cites>FETCH-LOGICAL-c4616-fbe2ca5b857eaf7bc145e8a55316cebe16c818b1c422e6e59a6d0479c5a9d3383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftrf.13336$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftrf.13336$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26400824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeller, Michelle P.</creatorcontrib><creatorcontrib>Heddle, Nancy M.</creatorcontrib><creatorcontrib>Kelton, John G.</creatorcontrib><creatorcontrib>Hamilton, Korinne</creatorcontrib><creatorcontrib>Wang, Grace</creatorcontrib><creatorcontrib>Sholapur, Naushin</creatorcontrib><creatorcontrib>Carruthers, Julie</creatorcontrib><creatorcontrib>Hsia, Cyrus</creatorcontrib><creatorcontrib>Blais, Normand</creatorcontrib><creatorcontrib>Toltl, Lisa</creatorcontrib><creatorcontrib>Hamm, Caroline</creatorcontrib><creatorcontrib>Pearson, Marc-André</creatorcontrib><creatorcontrib>Arnold, Donald M.</creatorcontrib><title>Effect of a thrombopoietin receptor agonist on use of intravenous immune globulin in patients with immune thrombocytopenia</title><title>Transfusion (Philadelphia, Pa.)</title><addtitle>Transfusion</addtitle><description>BACKGROUND Thrombopoietin receptor agonists are new treatments for patients with chronic immune thrombocytopenia (ITP). How one of these agent, romiplostim, has impacted practice patterns, especially the use of intravenous immune globulin (IVIG), has not been evaluated outside of clinical trials. STUDY DESIGN AND METHODS This was a retrospective cohort study of adult ITP patients treated with romiplostim in four Canadian centers. Patients had primary or secondary ITP and were followed for 1 year before starting weekly romiplostim treatment. We compared IVIG use, clinical outcomes, and cost before and after romiplostim. RESULTS Twenty‐nine patients with ITP received romiplostim. Median age was 54 years (interquartile range [IQR], 45‐63 years) and patients had a median of two prior ITP treatments (IQR, 1‐4) including splenectomy (n = 7). Median platelet (PLT) count was 23 × 109 before and 124 × 109 after romiplostim. Median duration of romiplostim treatment was 3.7 months. Patients used a median of two IVIG infusions per year before and 0.7 per year after starting romiplostim (p = 0.16). For patients who received weekly romiplostim for at least 1 month (n = 19), IVIG infusions were three (IQR, 1‐5) per year before and 0.7 (IQR, 0.4‐1.6) per year after romiplostim. Results were squewed by two high IVIG users. Nineteen (66%) patients discontinued romiplostim treatment during follow‐up because of lack of response (n = 8), sustained response (n = 5), toxicities (n = 4), or response to splenectomy (n = 2). Overall health care costs were similar before and after romiplostim when concomitant treatments, nursing resources, and hospitalizations were considered. CONCLUSIONS Romiplostim was associated with improved PLT counts and fewer IVIG infusions for most ITP patients. 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Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeller, Michelle P.</au><au>Heddle, Nancy M.</au><au>Kelton, John G.</au><au>Hamilton, Korinne</au><au>Wang, Grace</au><au>Sholapur, Naushin</au><au>Carruthers, Julie</au><au>Hsia, Cyrus</au><au>Blais, Normand</au><au>Toltl, Lisa</au><au>Hamm, Caroline</au><au>Pearson, Marc-André</au><au>Arnold, Donald M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of a thrombopoietin receptor agonist on use of intravenous immune globulin in patients with immune thrombocytopenia</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2016-01</date><risdate>2016</risdate><volume>56</volume><issue>1</issue><spage>73</spage><epage>79</epage><pages>73-79</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><coden>TRANAT</coden><abstract>BACKGROUND Thrombopoietin receptor agonists are new treatments for patients with chronic immune thrombocytopenia (ITP). How one of these agent, romiplostim, has impacted practice patterns, especially the use of intravenous immune globulin (IVIG), has not been evaluated outside of clinical trials. STUDY DESIGN AND METHODS This was a retrospective cohort study of adult ITP patients treated with romiplostim in four Canadian centers. Patients had primary or secondary ITP and were followed for 1 year before starting weekly romiplostim treatment. We compared IVIG use, clinical outcomes, and cost before and after romiplostim. RESULTS Twenty‐nine patients with ITP received romiplostim. Median age was 54 years (interquartile range [IQR], 45‐63 years) and patients had a median of two prior ITP treatments (IQR, 1‐4) including splenectomy (n = 7). Median platelet (PLT) count was 23 × 109 before and 124 × 109 after romiplostim. Median duration of romiplostim treatment was 3.7 months. Patients used a median of two IVIG infusions per year before and 0.7 per year after starting romiplostim (p = 0.16). For patients who received weekly romiplostim for at least 1 month (n = 19), IVIG infusions were three (IQR, 1‐5) per year before and 0.7 (IQR, 0.4‐1.6) per year after romiplostim. Results were squewed by two high IVIG users. Nineteen (66%) patients discontinued romiplostim treatment during follow‐up because of lack of response (n = 8), sustained response (n = 5), toxicities (n = 4), or response to splenectomy (n = 2). Overall health care costs were similar before and after romiplostim when concomitant treatments, nursing resources, and hospitalizations were considered. CONCLUSIONS Romiplostim was associated with improved PLT counts and fewer IVIG infusions for most ITP patients. In practice, romiplostim was generally not continued long term and was cost neutral for overall ITP management.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26400824</pmid><doi>10.1111/trf.13336</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Chronic Disease
Drug Administration Schedule
Drug Therapy, Combination
Female
Follow-Up Studies
Humans
Immunoglobulins, Intravenous - therapeutic use
Immunologic Factors - therapeutic use
Male
Middle Aged
Purpura, Thrombocytopenic, Idiopathic - drug therapy
Receptors, Fc - therapeutic use
Receptors, Thrombopoietin - agonists
Recombinant Fusion Proteins - therapeutic use
Retrospective Studies
Thrombopoietin - therapeutic use
Treatment Outcome
Young Adult
title Effect of a thrombopoietin receptor agonist on use of intravenous immune globulin in patients with immune thrombocytopenia
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