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Treatment of Chronic Pulmonary Aspergillosis: Current Standards and Future Perspectives.

Identifieur interne : 000432 ( Main/Exploration ); précédent : 000431; suivant : 000433

Treatment of Chronic Pulmonary Aspergillosis: Current Standards and Future Perspectives.

Auteurs : Ana Alastruey-Izquierdo [Espagne] ; Jacques Cadranel [France] ; Holger Flick [Autriche] ; Cendrine Godet [France] ; Christophe Hennequin [France] ; Martin Hoenigl [États-Unis, Autriche] ; Chris Kosmidis [Royaume-Uni] ; Christoph Lange [Allemagne, Suède] ; Oxana Munteanu ; Iain Page [Royaume-Uni] ; Helmut J F. Salzer [Allemagne]

Source :

RBID : pubmed:29982245

Descripteurs français

English descriptors

Abstract

Chronic pulmonary aspergillosis (CPA) complicates conditions including tuberculosis, chronic obstructive pulmonary disease and sarcoidosis, and is associated with high morbidity and mortality. Surgical cure should be considered where feasible; however, many patients are unsuitable for surgery due to extensive disease or poor respiratory function. Azoles are the only oral drug with anti-Aspergillus activity and itraconazole and voriconazole are considered as first-line drugs. A randomized controlled trial demonstrated improvement or stability in three-quarters of patients given 6 months of itraconazole, but a quarter relapsed on stopping therapy. Long-term treatment may therefore be required in some cases. Itraconazole, voriconazole and posaconazole require therapeutic drug monitoring. No published data are yet available for isavuconazole. Adverse drug effects of azoles are common, including peripheral neuropathy, heart failure, elevated liver enzymes, QTc prolongation and sun sensitivity. Many serious drug-drug interactions occur, including major interactions with rifamycins, simvastatin, warfarin, clopidogrel, immunosuppressant drugs like sirolimus. Furthermore, drug resistance occurs, including cross-resistance to all azoles, but the true prevalence is not yet determined. Intravenous therapy is possible with echinocandins or amphotericin B, but long-term use is challenging. Hemoptysis complicates CPA and can be fatal. Tranexamic acid should be given acutely to reduce bleeding. Bronchial artery embolization can stop acute bleeds. In some circumstances, emergency surgery may be necessary to resect the source of the bleed. Current CPA treatments can be beneficial but have many drawbacks. New oral anti-Aspergillus agents are needed, along with optimization of currently available treatments.

DOI: 10.1159/000489474
PubMed: 29982245


Affiliations:


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<term>Antifungal Agents (therapeutic use)</term>
<term>Humans (MeSH)</term>
<term>Lung (diagnostic imaging)</term>
<term>Lung (pathology)</term>
<term>Lung (surgery)</term>
<term>Practice Guidelines as Topic (MeSH)</term>
<term>Pulmonary Aspergillosis (diagnostic imaging)</term>
<term>Pulmonary Aspergillosis (drug therapy)</term>
<term>Pulmonary Aspergillosis (surgery)</term>
</keywords>
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<term>Antifongiques (usage thérapeutique)</term>
<term>Aspergillose pulmonaire (chirurgie)</term>
<term>Aspergillose pulmonaire (imagerie diagnostique)</term>
<term>Aspergillose pulmonaire (traitement médicamenteux)</term>
<term>Guides de bonnes pratiques cliniques comme sujet (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Poumon (anatomopathologie)</term>
<term>Poumon (chirurgie)</term>
<term>Poumon (imagerie diagnostique)</term>
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<term>Poumon</term>
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<term>Aspergillose pulmonaire</term>
<term>Poumon</term>
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<term>Lung</term>
<term>Pulmonary Aspergillosis</term>
</keywords>
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<term>Pulmonary Aspergillosis</term>
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<term>Aspergillose pulmonaire</term>
<term>Poumon</term>
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<term>Lung</term>
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<keywords scheme="MESH" qualifier="surgery" xml:lang="en">
<term>Lung</term>
<term>Pulmonary Aspergillosis</term>
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<term>Aspergillose pulmonaire</term>
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<term>Antifongiques</term>
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<term>Practice Guidelines as Topic</term>
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<term>Guides de bonnes pratiques cliniques comme sujet</term>
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<div type="abstract" xml:lang="en">Chronic pulmonary aspergillosis (CPA) complicates conditions including tuberculosis, chronic obstructive pulmonary disease and sarcoidosis, and is associated with high morbidity and mortality. Surgical cure should be considered where feasible; however, many patients are unsuitable for surgery due to extensive disease or poor respiratory function. Azoles are the only oral drug with anti-Aspergillus activity and itraconazole and voriconazole are considered as first-line drugs. A randomized controlled trial demonstrated improvement or stability in three-quarters of patients given 6 months of itraconazole, but a quarter relapsed on stopping therapy. Long-term treatment may therefore be required in some cases. Itraconazole, voriconazole and posaconazole require therapeutic drug monitoring. No published data are yet available for isavuconazole. Adverse drug effects of azoles are common, including peripheral neuropathy, heart failure, elevated liver enzymes, QTc prolongation and sun sensitivity. Many serious drug-drug interactions occur, including major interactions with rifamycins, simvastatin, warfarin, clopidogrel, immunosuppressant drugs like sirolimus. Furthermore, drug resistance occurs, including cross-resistance to all azoles, but the true prevalence is not yet determined. Intravenous therapy is possible with echinocandins or amphotericin B, but long-term use is challenging. Hemoptysis complicates CPA and can be fatal. Tranexamic acid should be given acutely to reduce bleeding. Bronchial artery embolization can stop acute bleeds. In some circumstances, emergency surgery may be necessary to resect the source of the bleed. Current CPA treatments can be beneficial but have many drawbacks. New oral anti-Aspergillus agents are needed, along with optimization of currently available treatments.</div>
</front>
</TEI>
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<DateCompleted>
<Year>2018</Year>
<Month>12</Month>
<Day>21</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>12</Month>
<Day>21</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1423-0356</ISSN>
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<Volume>96</Volume>
<Issue>2</Issue>
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<MedlineDate>2018</MedlineDate>
</PubDate>
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<Title>Respiration; international review of thoracic diseases</Title>
<ISOAbbreviation>Respiration</ISOAbbreviation>
</Journal>
<ArticleTitle>Treatment of Chronic Pulmonary Aspergillosis: Current Standards and Future Perspectives.</ArticleTitle>
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<Abstract>
<AbstractText>Chronic pulmonary aspergillosis (CPA) complicates conditions including tuberculosis, chronic obstructive pulmonary disease and sarcoidosis, and is associated with high morbidity and mortality. Surgical cure should be considered where feasible; however, many patients are unsuitable for surgery due to extensive disease or poor respiratory function. Azoles are the only oral drug with anti-Aspergillus activity and itraconazole and voriconazole are considered as first-line drugs. A randomized controlled trial demonstrated improvement or stability in three-quarters of patients given 6 months of itraconazole, but a quarter relapsed on stopping therapy. Long-term treatment may therefore be required in some cases. Itraconazole, voriconazole and posaconazole require therapeutic drug monitoring. No published data are yet available for isavuconazole. Adverse drug effects of azoles are common, including peripheral neuropathy, heart failure, elevated liver enzymes, QTc prolongation and sun sensitivity. Many serious drug-drug interactions occur, including major interactions with rifamycins, simvastatin, warfarin, clopidogrel, immunosuppressant drugs like sirolimus. Furthermore, drug resistance occurs, including cross-resistance to all azoles, but the true prevalence is not yet determined. Intravenous therapy is possible with echinocandins or amphotericin B, but long-term use is challenging. Hemoptysis complicates CPA and can be fatal. Tranexamic acid should be given acutely to reduce bleeding. Bronchial artery embolization can stop acute bleeds. In some circumstances, emergency surgery may be necessary to resect the source of the bleed. Current CPA treatments can be beneficial but have many drawbacks. New oral anti-Aspergillus agents are needed, along with optimization of currently available treatments.</AbstractText>
<CopyrightInformation>© 2018 S. Karger AG, Basel.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Alastruey-Izquierdo</LastName>
<ForeName>Ana</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Mycology Reference Laboratory, National Centre for Microbiology, Instituto de Salud Carlos III, Madrid, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cadranel</LastName>
<ForeName>Jacques</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Service de Pneumologie, AP-HP, Hôpital Tenon, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Sorbonne Université, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Flick</LastName>
<ForeName>Holger</ForeName>
<Initials>H</Initials>
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<Affiliation>Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Godet</LastName>
<ForeName>Cendrine</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Service des Maladies Infectieuses et Tropicales, CHU de Poitiers, Poitiers, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hennequin</LastName>
<ForeName>Christophe</ForeName>
<Initials>C</Initials>
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<Affiliation>Sorbonne Universités, UPMC Univ Paris 06, INSERM, Centre de Recherche Saint-Antoine (CRSA), Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Service de Parasitologie-Mycologie, AP-HP, Hôpital Saint-Antoine, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hoenigl</LastName>
<ForeName>Martin</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases, University of California, San Diego, California, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Section of Infectious Diseases and Tropical Medicine and Division of Pulmonology, Medical University of Graz, Graz, Austria.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Kosmidis</LastName>
<ForeName>Chris</ForeName>
<Initials>C</Initials>
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<Affiliation>National Aspergillosis Center, Manchester University Foundation Trust, UK, and Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Lange</LastName>
<ForeName>Christoph</ForeName>
<Initials>C</Initials>
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<Affiliation>Division of Clinical Infectious Diseases, Research Center Borstel, Leibniz Lung Center, Borstel, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Center for Infection Research, Clinical Tuberculosis Center, Borstel, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>International Health/Infectious Diseases, University of Lübeck, Lübeck, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Medicine, Karolinska Institutet, Stockholm, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Munteanu</LastName>
<ForeName>Oxana</ForeName>
<Initials>O</Initials>
<AffiliationInfo>
<Affiliation>Division of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine and Pharmacy Nicolae Testemitanu, Chisinau, Moldova.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Page</LastName>
<ForeName>Iain</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>National Aspergillosis Center, Manchester University Foundation Trust, UK, and Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom.</Affiliation>
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<Author ValidYN="Y">
<LastName>Salzer</LastName>
<ForeName>Helmut J F</ForeName>
<Initials>HJF</Initials>
<AffiliationInfo>
<Affiliation>Division of Clinical Infectious Diseases, Research Center Borstel, Leibniz Lung Center, Borstel, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Center for Infection Research, Clinical Tuberculosis Center, Borstel, Germany.</Affiliation>
</AffiliationInfo>
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<CollectiveName>on behalf of CPAnet</CollectiveName>
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<Language>eng</Language>
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<Keyword MajorTopicYN="N">Management</Keyword>
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<Month>12</Month>
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<li>Californie</li>
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<name sortKey="Lange, Christoph" sort="Lange, Christoph" uniqKey="Lange C" first="Christoph" last="Lange">Christoph Lange</name>
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