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 |
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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 |
format | Article |
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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.</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. In practice, romiplostim was generally not continued long term and was cost neutral for overall ITP management.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Chronic Disease</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunologic Factors - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Purpura, Thrombocytopenic, Idiopathic - drug therapy</subject><subject>Receptors, Fc - therapeutic use</subject><subject>Receptors, Thrombopoietin - agonists</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Thrombopoietin - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0041-1132</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFO3DAQhi3UCra0B14AWeqJQ8ATx05yRIiFSohK7VaVerEc7wQMGzu1HWD79DXdXW4dWePL938j_YQcATuFPGcp9KfAOZd7ZAaC10XZtuIdmTFWQQHAywPyIcYHxljZMtgnB6WsGGvKakb-XPY9mkR9TzVN98EPnR-9xWQdDWhwTD5QfeedjRlydIr4ylqXgn5C56dI7TBMDundynfTKsfyG3Wy6FKkzzbd74Ct3ayTH9FZ_ZG87_Uq4qftf0h-zC8XF9fFzderLxfnN4WpJMii77A0WnSNqFH3dWegEthoIThIgx3m3UDTganKEiWKVsslq-rWCN0uOW_4Ifm88Y7B_54wJvXgp-DySQW1EK0EJqpMnWwoE3yMAXs1BjvosFbA1GvLKres_rWc2eOtceoGXL6Ru1ozcLYBnu0K1_83qcW3-U5ZbBK5Z3x5S-jwqGTNa6F-3l6p69tf3yUs5mrO_wKijJiP</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Zeller, Michelle P.</creator><creator>Heddle, Nancy M.</creator><creator>Kelton, John G.</creator><creator>Hamilton, Korinne</creator><creator>Wang, Grace</creator><creator>Sholapur, Naushin</creator><creator>Carruthers, Julie</creator><creator>Hsia, Cyrus</creator><creator>Blais, Normand</creator><creator>Toltl, Lisa</creator><creator>Hamm, Caroline</creator><creator>Pearson, Marc-André</creator><creator>Arnold, Donald M.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope></search><sort><creationdate>201601</creationdate><title>Effect of a thrombopoietin receptor agonist on use of intravenous immune globulin in patients with immune thrombocytopenia</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4616-fbe2ca5b857eaf7bc145e8a55316cebe16c818b1c422e6e59a6d0479c5a9d3383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Chronic Disease</topic><topic>Drug Administration Schedule</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Immunologic Factors - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Purpura, Thrombocytopenic, Idiopathic - drug therapy</topic><topic>Receptors, Fc - therapeutic use</topic><topic>Receptors, Thrombopoietin - agonists</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Thrombopoietin - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & 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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