CP-174 Successful desensitisation in a patient with lenalidomide hypersensitivity

BackgroundA man with relapsed and refractory myeloma and previous neuropathy to intravenous chemotherapy (CyBorD) was treated with daily lenalidomide 25 mg orally plus dexamethasone. On the third day of treatment, more than 12 hours after taking the last lenalidomide pill, the patient presented with...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of hospital pharmacy. Science and practice 2017-03, Vol.24 (Suppl 1), p.A78-A78
Hauptverfasser: Baptista, M, Oliveira, R, Barreto, P, Fagundes, J, Cardoso, J, Guerra, J, Pité, H, Bernardo, M, Morais-Almeida, M, Chambel, M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page A78
container_issue Suppl 1
container_start_page A78
container_title European journal of hospital pharmacy. Science and practice
container_volume 24
creator Baptista, M
Oliveira, R
Barreto, P
Fagundes, J
Cardoso, J
Guerra, J
Pité, H
Bernardo, M
Morais-Almeida, M
Chambel, M
description BackgroundA man with relapsed and refractory myeloma and previous neuropathy to intravenous chemotherapy (CyBorD) was treated with daily lenalidomide 25 mg orally plus dexamethasone. On the third day of treatment, more than 12 hours after taking the last lenalidomide pill, the patient presented with generalised macular erythema, periocular oedema, scalp pruritus and fever (38.0°C). Lenalidomide treatment was discontinued and he was successfully treated with systemic corticosteroids and antihistamines. The patient was subsequently referred to the allergy centre for desensitisation.PurposeLenalidomide plus dexamethasone is a highly effective regimen that has significantly improved outcomes in patients with multiple myeloma. Hypersensitivity reactions to lenalidomide may preclude its use in patients who would otherwise benefit from this treatment. We report a successful oral desensitisation protocol for lenalidomide in a patient with relapsed and refractory myeloma with hypersensitivity reaction to this drug.Material and methodsIn brief, lenalidomide was dissolved in isotonic sodium chloride and diluted to concentrations of 0.0025 mg/mL (solution A), 0.025 mg/mL (solution B) and 1 mg/mL (solution C). After pretreatment with dexamethasone, he was gradually given increasing lenalidomide doses to take orally at 15–60 min intervals (cumulative dose 25.2415 mg). The patient tolerated the escalating doses with no reaction and subsequently begun lenalidomide 15 mg daily, plus 8 mg dexamethasone 3 times per week. He tolerated continuous lenalidomide dosing with no evidence of recurrent hypersensitivity for 21 days.ResultsThis protocol was repeated on a monthly basis, and the patient has successfully completed 13 cycles of lenalidomide plus dexamethasone. During the desensitisation, he was monitored for any symptoms, skin or mucosal lesions, and had his blood pressure, heart rate, temperature and pulse oximetry regularly checked.ConclusionThe patient remains asymptomatic and free from any evidence of multiple myeloma progression. Limited literature exists on drug desensitisation with lenalidomide. This is a successful report of a lenalidomide desensitisation protocol. It supports the utility of adapted drug desensitisation in the oncology setting for lenalidomide administration in patients with drug hypersensitivity and without effective treatment alternatives.References and/or acknowledgementsAcknowledgements to all of the team.No conflict of interest
doi_str_mv 10.1136/ejhpharm-2017-000640.172
format Article
fullrecord <record><control><sourceid>proquest_bmj_p</sourceid><recordid>TN_cdi_proquest_journals_2552763958</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4317854181</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1008-5d721ba9dabd931d7e4a1d57cc04034216d703385dca58244881b0f76ef1fbda3</originalsourceid><addsrcrecordid>eNp9kMtKxDAUhoMoOIzzDgHX1ZNbkyxl8AYDCqPrkDYpzdCbTat058YX9UnsMKNLV-eH853Dz4cQJnBFCEuv_a7sStvXCQUiEwBI-byR9AQtKHCZaJ3y078s0nO0ijFkIBhTmjO9QNv1c0Ik__782o557mMsxgo7H30TwxCiHULb4NBgi7s5-2bAH2EoceUbWwXX1sF5XE6d748X72GYLtBZYavoV8e5RK93ty_rh2TzdP-4vtkkGQFQiXCSksxqZzOnGXHSc0uckHkOHBinJHUS5qLC5VYoyrlSJINCpr4gReYsW6LLw9-ub99GHweza8d-LhYNFYLKlGmh_qOIkowxqjTMFDtQWb0zXR9q20-GgNlrNr-azV6zOWg2s2b2A59rcwk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1873332890</pqid></control><display><type>article</type><title>CP-174 Successful desensitisation in a patient with lenalidomide hypersensitivity</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Baptista, M ; Oliveira, R ; Barreto, P ; Fagundes, J ; Cardoso, J ; Guerra, J ; Pité, H ; Bernardo, M ; Morais-Almeida, M ; Chambel, M</creator><creatorcontrib>Baptista, M ; Oliveira, R ; Barreto, P ; Fagundes, J ; Cardoso, J ; Guerra, J ; Pité, H ; Bernardo, M ; Morais-Almeida, M ; Chambel, M</creatorcontrib><description>BackgroundA man with relapsed and refractory myeloma and previous neuropathy to intravenous chemotherapy (CyBorD) was treated with daily lenalidomide 25 mg orally plus dexamethasone. On the third day of treatment, more than 12 hours after taking the last lenalidomide pill, the patient presented with generalised macular erythema, periocular oedema, scalp pruritus and fever (38.0°C). Lenalidomide treatment was discontinued and he was successfully treated with systemic corticosteroids and antihistamines. The patient was subsequently referred to the allergy centre for desensitisation.PurposeLenalidomide plus dexamethasone is a highly effective regimen that has significantly improved outcomes in patients with multiple myeloma. Hypersensitivity reactions to lenalidomide may preclude its use in patients who would otherwise benefit from this treatment. We report a successful oral desensitisation protocol for lenalidomide in a patient with relapsed and refractory myeloma with hypersensitivity reaction to this drug.Material and methodsIn brief, lenalidomide was dissolved in isotonic sodium chloride and diluted to concentrations of 0.0025 mg/mL (solution A), 0.025 mg/mL (solution B) and 1 mg/mL (solution C). After pretreatment with dexamethasone, he was gradually given increasing lenalidomide doses to take orally at 15–60 min intervals (cumulative dose 25.2415 mg). The patient tolerated the escalating doses with no reaction and subsequently begun lenalidomide 15 mg daily, plus 8 mg dexamethasone 3 times per week. He tolerated continuous lenalidomide dosing with no evidence of recurrent hypersensitivity for 21 days.ResultsThis protocol was repeated on a monthly basis, and the patient has successfully completed 13 cycles of lenalidomide plus dexamethasone. During the desensitisation, he was monitored for any symptoms, skin or mucosal lesions, and had his blood pressure, heart rate, temperature and pulse oximetry regularly checked.ConclusionThe patient remains asymptomatic and free from any evidence of multiple myeloma progression. Limited literature exists on drug desensitisation with lenalidomide. This is a successful report of a lenalidomide desensitisation protocol. It supports the utility of adapted drug desensitisation in the oncology setting for lenalidomide administration in patients with drug hypersensitivity and without effective treatment alternatives.References and/or acknowledgementsAcknowledgements to all of the team.No conflict of interest</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2017-000640.172</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Drug dosages ; Immunotherapy ; Multiple myeloma ; Patients ; Targeted cancer therapy</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A78-A78</ispartof><rights>2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2017 (c) 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2017 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids></links><search><creatorcontrib>Baptista, M</creatorcontrib><creatorcontrib>Oliveira, R</creatorcontrib><creatorcontrib>Barreto, P</creatorcontrib><creatorcontrib>Fagundes, J</creatorcontrib><creatorcontrib>Cardoso, J</creatorcontrib><creatorcontrib>Guerra, J</creatorcontrib><creatorcontrib>Pité, H</creatorcontrib><creatorcontrib>Bernardo, M</creatorcontrib><creatorcontrib>Morais-Almeida, M</creatorcontrib><creatorcontrib>Chambel, M</creatorcontrib><title>CP-174 Successful desensitisation in a patient with lenalidomide hypersensitivity</title><title>European journal of hospital pharmacy. Science and practice</title><description>BackgroundA man with relapsed and refractory myeloma and previous neuropathy to intravenous chemotherapy (CyBorD) was treated with daily lenalidomide 25 mg orally plus dexamethasone. On the third day of treatment, more than 12 hours after taking the last lenalidomide pill, the patient presented with generalised macular erythema, periocular oedema, scalp pruritus and fever (38.0°C). Lenalidomide treatment was discontinued and he was successfully treated with systemic corticosteroids and antihistamines. The patient was subsequently referred to the allergy centre for desensitisation.PurposeLenalidomide plus dexamethasone is a highly effective regimen that has significantly improved outcomes in patients with multiple myeloma. Hypersensitivity reactions to lenalidomide may preclude its use in patients who would otherwise benefit from this treatment. We report a successful oral desensitisation protocol for lenalidomide in a patient with relapsed and refractory myeloma with hypersensitivity reaction to this drug.Material and methodsIn brief, lenalidomide was dissolved in isotonic sodium chloride and diluted to concentrations of 0.0025 mg/mL (solution A), 0.025 mg/mL (solution B) and 1 mg/mL (solution C). After pretreatment with dexamethasone, he was gradually given increasing lenalidomide doses to take orally at 15–60 min intervals (cumulative dose 25.2415 mg). The patient tolerated the escalating doses with no reaction and subsequently begun lenalidomide 15 mg daily, plus 8 mg dexamethasone 3 times per week. He tolerated continuous lenalidomide dosing with no evidence of recurrent hypersensitivity for 21 days.ResultsThis protocol was repeated on a monthly basis, and the patient has successfully completed 13 cycles of lenalidomide plus dexamethasone. During the desensitisation, he was monitored for any symptoms, skin or mucosal lesions, and had his blood pressure, heart rate, temperature and pulse oximetry regularly checked.ConclusionThe patient remains asymptomatic and free from any evidence of multiple myeloma progression. Limited literature exists on drug desensitisation with lenalidomide. This is a successful report of a lenalidomide desensitisation protocol. It supports the utility of adapted drug desensitisation in the oncology setting for lenalidomide administration in patients with drug hypersensitivity and without effective treatment alternatives.References and/or acknowledgementsAcknowledgements to all of the team.No conflict of interest</description><subject>Drug dosages</subject><subject>Immunotherapy</subject><subject>Multiple myeloma</subject><subject>Patients</subject><subject>Targeted cancer therapy</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kMtKxDAUhoMoOIzzDgHX1ZNbkyxl8AYDCqPrkDYpzdCbTat058YX9UnsMKNLV-eH853Dz4cQJnBFCEuv_a7sStvXCQUiEwBI-byR9AQtKHCZaJ3y078s0nO0ijFkIBhTmjO9QNv1c0Ik__782o557mMsxgo7H30TwxCiHULb4NBgi7s5-2bAH2EoceUbWwXX1sF5XE6d748X72GYLtBZYavoV8e5RK93ty_rh2TzdP-4vtkkGQFQiXCSksxqZzOnGXHSc0uckHkOHBinJHUS5qLC5VYoyrlSJINCpr4gReYsW6LLw9-ub99GHweza8d-LhYNFYLKlGmh_qOIkowxqjTMFDtQWb0zXR9q20-GgNlrNr-azV6zOWg2s2b2A59rcwk</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Baptista, M</creator><creator>Oliveira, R</creator><creator>Barreto, P</creator><creator>Fagundes, J</creator><creator>Cardoso, J</creator><creator>Guerra, J</creator><creator>Pité, H</creator><creator>Bernardo, M</creator><creator>Morais-Almeida, M</creator><creator>Chambel, M</creator><general>BMJ Publishing Group LTD</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201703</creationdate><title>CP-174 Successful desensitisation in a patient with lenalidomide hypersensitivity</title><author>Baptista, M ; Oliveira, R ; Barreto, P ; Fagundes, J ; Cardoso, J ; Guerra, J ; Pité, H ; Bernardo, M ; Morais-Almeida, M ; Chambel, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1008-5d721ba9dabd931d7e4a1d57cc04034216d703385dca58244881b0f76ef1fbda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Drug dosages</topic><topic>Immunotherapy</topic><topic>Multiple myeloma</topic><topic>Patients</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baptista, M</creatorcontrib><creatorcontrib>Oliveira, R</creatorcontrib><creatorcontrib>Barreto, P</creatorcontrib><creatorcontrib>Fagundes, J</creatorcontrib><creatorcontrib>Cardoso, J</creatorcontrib><creatorcontrib>Guerra, J</creatorcontrib><creatorcontrib>Pité, H</creatorcontrib><creatorcontrib>Bernardo, M</creatorcontrib><creatorcontrib>Morais-Almeida, M</creatorcontrib><creatorcontrib>Chambel, M</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>European journal of hospital pharmacy. Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baptista, M</au><au>Oliveira, R</au><au>Barreto, P</au><au>Fagundes, J</au><au>Cardoso, J</au><au>Guerra, J</au><au>Pité, H</au><au>Bernardo, M</au><au>Morais-Almeida, M</au><au>Chambel, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CP-174 Successful desensitisation in a patient with lenalidomide hypersensitivity</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2017-03</date><risdate>2017</risdate><volume>24</volume><issue>Suppl 1</issue><spage>A78</spage><epage>A78</epage><pages>A78-A78</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>BackgroundA man with relapsed and refractory myeloma and previous neuropathy to intravenous chemotherapy (CyBorD) was treated with daily lenalidomide 25 mg orally plus dexamethasone. On the third day of treatment, more than 12 hours after taking the last lenalidomide pill, the patient presented with generalised macular erythema, periocular oedema, scalp pruritus and fever (38.0°C). Lenalidomide treatment was discontinued and he was successfully treated with systemic corticosteroids and antihistamines. The patient was subsequently referred to the allergy centre for desensitisation.PurposeLenalidomide plus dexamethasone is a highly effective regimen that has significantly improved outcomes in patients with multiple myeloma. Hypersensitivity reactions to lenalidomide may preclude its use in patients who would otherwise benefit from this treatment. We report a successful oral desensitisation protocol for lenalidomide in a patient with relapsed and refractory myeloma with hypersensitivity reaction to this drug.Material and methodsIn brief, lenalidomide was dissolved in isotonic sodium chloride and diluted to concentrations of 0.0025 mg/mL (solution A), 0.025 mg/mL (solution B) and 1 mg/mL (solution C). After pretreatment with dexamethasone, he was gradually given increasing lenalidomide doses to take orally at 15–60 min intervals (cumulative dose 25.2415 mg). The patient tolerated the escalating doses with no reaction and subsequently begun lenalidomide 15 mg daily, plus 8 mg dexamethasone 3 times per week. He tolerated continuous lenalidomide dosing with no evidence of recurrent hypersensitivity for 21 days.ResultsThis protocol was repeated on a monthly basis, and the patient has successfully completed 13 cycles of lenalidomide plus dexamethasone. During the desensitisation, he was monitored for any symptoms, skin or mucosal lesions, and had his blood pressure, heart rate, temperature and pulse oximetry regularly checked.ConclusionThe patient remains asymptomatic and free from any evidence of multiple myeloma progression. Limited literature exists on drug desensitisation with lenalidomide. This is a successful report of a lenalidomide desensitisation protocol. It supports the utility of adapted drug desensitisation in the oncology setting for lenalidomide administration in patients with drug hypersensitivity and without effective treatment alternatives.References and/or acknowledgementsAcknowledgements to all of the team.No conflict of interest</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2017-000640.172</doi></addata></record>
fulltext fulltext
identifier ISSN: 2047-9956
ispartof European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A78-A78
issn 2047-9956
2047-9964
language eng
recordid cdi_proquest_journals_2552763958
source EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Drug dosages
Immunotherapy
Multiple myeloma
Patients
Targeted cancer therapy
title CP-174 Successful desensitisation in a patient with lenalidomide hypersensitivity
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T07%3A12%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_bmj_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CP-174%E2%80%85Successful%20desensitisation%20in%20a%20patient%20with%20lenalidomide%20hypersensitivity&rft.jtitle=European%20journal%20of%20hospital%20pharmacy.%20Science%20and%20practice&rft.au=Baptista,%20M&rft.date=2017-03&rft.volume=24&rft.issue=Suppl%201&rft.spage=A78&rft.epage=A78&rft.pages=A78-A78&rft.issn=2047-9956&rft.eissn=2047-9964&rft_id=info:doi/10.1136/ejhpharm-2017-000640.172&rft_dat=%3Cproquest_bmj_p%3E4317854181%3C/proquest_bmj_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1873332890&rft_id=info:pmid/&rfr_iscdi=true