Treatment of bullous pemphigoid with low-dose oral cyclophosphamide: a case series of 20 patients
Background Cyclophosphamide has been commonly used for the treatment of pemphigus vulgaris and mucous membrane pemphigoid with satisfactory results. Published data of this therapeutic approach for bullous pemphigoid are scant and showed significant morbidity and mortality. Objective To assess the cl...
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Veröffentlicht in: | Journal of the European Academy of Dermatology and Venereology 2014-06, Vol.28 (6), p.814-818 |
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creator | Gual, A. Iranzo, P. Mascaró Jr, J.M. |
description | Background
Cyclophosphamide has been commonly used for the treatment of pemphigus vulgaris and mucous membrane pemphigoid with satisfactory results. Published data of this therapeutic approach for bullous pemphigoid are scant and showed significant morbidity and mortality.
Objective
To assess the clinical efficacy and safety of low‐dose oral cyclophosphamide (CFM) (50–100 mg/day) in patients with refractory bullous pemphigoid.
Methods
We conducted a retrospective study including patients with bullous pemphigoid treated with CFM in the department of Dermatology in the Hospital Clínic of Barcelona, Spain.
Results
Complete response was observed in 11 (58%) over 19 evaluable patients. Cyclophosphamide at 50 mg/day was enough to achieve clinical remission in eight of these patients. Partial response was observed in four (21%) more patients. Bone marrow suppression appeared in 12 (60%) patients, but treatment discontinuation was only required in three (15%) cases. Gastrointestinal intolerance occurred in one (5%) patient. One patient died during therapy from heart failure (not attributed to CFM) and another patient developed acute myeloid leukaemia 1.5 years after CFM therapy.
Conclusions
In our series, CFM had a marked therapeutic effect in bullous pemphigoid. These results of efficacy are similar to those described in other autoimmune blistering skin diseases. Only a few patients had to discontinue their treatment due to adverse effects. Therefore, we consider that low‐dose oral CFM can be valuable therapeutic alternative in elderly patients with moderate‐to‐severe bullous pemphigoid. |
doi_str_mv | 10.1111/jdv.12155 |
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Cyclophosphamide has been commonly used for the treatment of pemphigus vulgaris and mucous membrane pemphigoid with satisfactory results. Published data of this therapeutic approach for bullous pemphigoid are scant and showed significant morbidity and mortality.
Objective
To assess the clinical efficacy and safety of low‐dose oral cyclophosphamide (CFM) (50–100 mg/day) in patients with refractory bullous pemphigoid.
Methods
We conducted a retrospective study including patients with bullous pemphigoid treated with CFM in the department of Dermatology in the Hospital Clínic of Barcelona, Spain.
Results
Complete response was observed in 11 (58%) over 19 evaluable patients. Cyclophosphamide at 50 mg/day was enough to achieve clinical remission in eight of these patients. Partial response was observed in four (21%) more patients. Bone marrow suppression appeared in 12 (60%) patients, but treatment discontinuation was only required in three (15%) cases. Gastrointestinal intolerance occurred in one (5%) patient. One patient died during therapy from heart failure (not attributed to CFM) and another patient developed acute myeloid leukaemia 1.5 years after CFM therapy.
Conclusions
In our series, CFM had a marked therapeutic effect in bullous pemphigoid. These results of efficacy are similar to those described in other autoimmune blistering skin diseases. Only a few patients had to discontinue their treatment due to adverse effects. Therefore, we consider that low‐dose oral CFM can be valuable therapeutic alternative in elderly patients with moderate‐to‐severe bullous pemphigoid.</description><identifier>ISSN: 0926-9959</identifier><identifier>EISSN: 1468-3083</identifier><identifier>DOI: 10.1111/jdv.12155</identifier><identifier>PMID: 23581830</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Aged ; Aged, 80 and over ; Cyclophosphamide - administration & dosage ; Female ; Humans ; Immunosuppressive Agents - administration & dosage ; Male ; Pemphigoid, Bullous - drug therapy ; Retrospective Studies</subject><ispartof>Journal of the European Academy of Dermatology and Venereology, 2014-06, Vol.28 (6), p.814-818</ispartof><rights>2013 The Authors Journal of the European Academy of Dermatology and Venereology © 2013 European Academy of Dermatology and Venereology</rights><rights>2013 The Authors Journal of the European Academy of Dermatology and Venereology © 2013 European Academy of Dermatology and Venereology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3965-bf248e7c59a23a798eb19a8a78353d86b19a307c6c3b1ffa31d6caeb406da3923</citedby><cites>FETCH-LOGICAL-c3965-bf248e7c59a23a798eb19a8a78353d86b19a307c6c3b1ffa31d6caeb406da3923</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%2Fjdv.12155$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjdv.12155$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23581830$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gual, A.</creatorcontrib><creatorcontrib>Iranzo, P.</creatorcontrib><creatorcontrib>Mascaró Jr, J.M.</creatorcontrib><title>Treatment of bullous pemphigoid with low-dose oral cyclophosphamide: a case series of 20 patients</title><title>Journal of the European Academy of Dermatology and Venereology</title><addtitle>J Eur Acad Dermatol Venereol</addtitle><description>Background
Cyclophosphamide has been commonly used for the treatment of pemphigus vulgaris and mucous membrane pemphigoid with satisfactory results. Published data of this therapeutic approach for bullous pemphigoid are scant and showed significant morbidity and mortality.
Objective
To assess the clinical efficacy and safety of low‐dose oral cyclophosphamide (CFM) (50–100 mg/day) in patients with refractory bullous pemphigoid.
Methods
We conducted a retrospective study including patients with bullous pemphigoid treated with CFM in the department of Dermatology in the Hospital Clínic of Barcelona, Spain.
Results
Complete response was observed in 11 (58%) over 19 evaluable patients. Cyclophosphamide at 50 mg/day was enough to achieve clinical remission in eight of these patients. Partial response was observed in four (21%) more patients. Bone marrow suppression appeared in 12 (60%) patients, but treatment discontinuation was only required in three (15%) cases. Gastrointestinal intolerance occurred in one (5%) patient. One patient died during therapy from heart failure (not attributed to CFM) and another patient developed acute myeloid leukaemia 1.5 years after CFM therapy.
Conclusions
In our series, CFM had a marked therapeutic effect in bullous pemphigoid. These results of efficacy are similar to those described in other autoimmune blistering skin diseases. Only a few patients had to discontinue their treatment due to adverse effects. Therefore, we consider that low‐dose oral CFM can be valuable therapeutic alternative in elderly patients with moderate‐to‐severe bullous pemphigoid.</description><subject>Administration, Oral</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Male</subject><subject>Pemphigoid, Bullous - drug therapy</subject><subject>Retrospective Studies</subject><issn>0926-9959</issn><issn>1468-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1v1DAQhi1URJfCoX8A-VgOaf0RJza3tkChWgESBXqzJs6EdXHWwc6y7L8n2217q8RcRqN55pHmJeSQs2M-1clN--eYC67UEzLjZaULybTcIzNmRFUYo8w-eZ7zDWOMc6WfkX0hleZashmBq4Qw9rgcaexoswohrjIdsB8W_mf0LV37cUFDXBdtzEhjgkDdxoU4LGIeFtD7Ft9QoA6mbcbkMW9FgtEBRj9p8wvytIOQ8eVdPyDf3r-7Ov9QzD9ffDw_nRdOmkoVTSdKjbVTBoSE2mhsuAENtZZKtrraTpLVrnKy4V0HkreVA2xKVrUgjZAH5GjnHVL8vcI82t5nhyHAEqefLFey1FyUhv0HKkpel-bW-nqHuhRzTtjZIfke0sZyZrfh2yl8exv-xL66066aHtsH8j7tCTjZAWsfcPO4yV6-_X6vLHYXPo_49-EC0i9b1bJW9senC6u-fBXzs_raXsp_lbqdJg</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Gual, A.</creator><creator>Iranzo, P.</creator><creator>Mascaró Jr, J.M.</creator><general>Blackwell Publishing Ltd</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>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201406</creationdate><title>Treatment of bullous pemphigoid with low-dose oral cyclophosphamide: a case series of 20 patients</title><author>Gual, A. ; Iranzo, P. ; Mascaró Jr, J.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3965-bf248e7c59a23a798eb19a8a78353d86b19a307c6c3b1ffa31d6caeb406da3923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Administration, Oral</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Male</topic><topic>Pemphigoid, Bullous - drug therapy</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gual, A.</creatorcontrib><creatorcontrib>Iranzo, P.</creatorcontrib><creatorcontrib>Mascaró Jr, J.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>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of the European Academy of Dermatology and Venereology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gual, A.</au><au>Iranzo, P.</au><au>Mascaró Jr, J.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of bullous pemphigoid with low-dose oral cyclophosphamide: a case series of 20 patients</atitle><jtitle>Journal of the European Academy of Dermatology and Venereology</jtitle><addtitle>J Eur Acad Dermatol Venereol</addtitle><date>2014-06</date><risdate>2014</risdate><volume>28</volume><issue>6</issue><spage>814</spage><epage>818</epage><pages>814-818</pages><issn>0926-9959</issn><eissn>1468-3083</eissn><abstract>Background
Cyclophosphamide has been commonly used for the treatment of pemphigus vulgaris and mucous membrane pemphigoid with satisfactory results. Published data of this therapeutic approach for bullous pemphigoid are scant and showed significant morbidity and mortality.
Objective
To assess the clinical efficacy and safety of low‐dose oral cyclophosphamide (CFM) (50–100 mg/day) in patients with refractory bullous pemphigoid.
Methods
We conducted a retrospective study including patients with bullous pemphigoid treated with CFM in the department of Dermatology in the Hospital Clínic of Barcelona, Spain.
Results
Complete response was observed in 11 (58%) over 19 evaluable patients. Cyclophosphamide at 50 mg/day was enough to achieve clinical remission in eight of these patients. Partial response was observed in four (21%) more patients. Bone marrow suppression appeared in 12 (60%) patients, but treatment discontinuation was only required in three (15%) cases. Gastrointestinal intolerance occurred in one (5%) patient. One patient died during therapy from heart failure (not attributed to CFM) and another patient developed acute myeloid leukaemia 1.5 years after CFM therapy.
Conclusions
In our series, CFM had a marked therapeutic effect in bullous pemphigoid. These results of efficacy are similar to those described in other autoimmune blistering skin diseases. Only a few patients had to discontinue their treatment due to adverse effects. Therefore, we consider that low‐dose oral CFM can be valuable therapeutic alternative in elderly patients with moderate‐to‐severe bullous pemphigoid.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23581830</pmid><doi>10.1111/jdv.12155</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Administration, Oral Aged Aged, 80 and over Cyclophosphamide - administration & dosage Female Humans Immunosuppressive Agents - administration & dosage Male Pemphigoid, Bullous - drug therapy Retrospective Studies |
title | Treatment of bullous pemphigoid with low-dose oral cyclophosphamide: a case series of 20 patients |
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