A Real-World Study of Achievement Rate and Predictive Factors of Clinical and Deep Remission to Biologics in Patients with Severe Asthma

Recent advances in biologics have provided new insights into the clinical course of asthma, including disease modification, clinical remission (CR), and deep remission (DR). However, the extent to which biologics achieve CR and DR in severe asthma patients is poorly understood. To assess the achieve...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical medicine 2023-04, Vol.12 (8), p.2900
Hauptverfasser: Oishi, Keiji, Hamada, Kazuki, Murata, Yoriyuki, Matsuda, Kazuki, Ohata, Syuichiro, Yamaji, Yoshikazu, Asami-Noyama, Maki, Edakuni, Nobutaka, Kakugawa, Tomoyuki, Hirano, Tsunahiko, Matsunaga, Kazuto
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 8
container_start_page 2900
container_title Journal of clinical medicine
container_volume 12
creator Oishi, Keiji
Hamada, Kazuki
Murata, Yoriyuki
Matsuda, Kazuki
Ohata, Syuichiro
Yamaji, Yoshikazu
Asami-Noyama, Maki
Edakuni, Nobutaka
Kakugawa, Tomoyuki
Hirano, Tsunahiko
Matsunaga, Kazuto
description Recent advances in biologics have provided new insights into the clinical course of asthma, including disease modification, clinical remission (CR), and deep remission (DR). However, the extent to which biologics achieve CR and DR in severe asthma patients is poorly understood. To assess the achievement rate and predictors of CR and DR using long-term biologics, we retrospectively evaluated 54 severe asthma patients recently started on biologics. "CR" denotes the achievement of all three criteria: (1) absence of asthma symptoms, (2) no asthma exacerbations, and (3) no use of oral corticosteroids. DR denoted CR plus (4) normalized pulmonary function and (5) suppressed type 2 inflammation. CR and DR achievement rates were 68.5% and 31.5%, respectively. Compared with the non-deep remission group, the DR group had higher adult-onset asthma rates (94.1% vs. 70.3%, = 0.078), shorter asthma duration (5 vs. 19 years, = 0.006), and higher FEV (91.5% vs. 71.5%, < 0.001). There were no significant differences in the Asthma Control Questionnaire scores, exacerbation frequency, or type 2 inflammation at baseline between groups. Asthma duration combined with FEV can stratify the achievement rates of CR and DR. the early introduction of biologics in severe asthma patients may help achieve CR and DR.
doi_str_mv 10.3390/jcm12082900
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10142972</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A750301971</galeid><sourcerecordid>A750301971</sourcerecordid><originalsourceid>FETCH-LOGICAL-c438t-6f009c7cfb40f9aaa7bc54809c59d268d59b22643247ecf8f89bd133fbdb181d3</originalsourceid><addsrcrecordid>eNpdkl1rFDEUhoMottReeS8BbwQZm4-ZTXIl42q1ULC0ipchk4_dLJnJmmRW-g_82WZtrau5SUgennNecgB4jtEbSgU62-gRE8SJQOgROCaIsQZRTh8fnI_Aac4bVBfnLcHsKTiiDCNBKDsGP3t4bVVovsUUDLwps7mF0cFer73d2dFOBV6rYqGaDLxK1nhd_M7Cc6VLTHmPLoOfvFbhN_Le2m0Vjj5nHydYInznY4grrzP0E7xSxVdlhj98WcObWiFZ2OeyHtUz8MSpkO3p_X4Cvp5_-LL81Fx-_nix7C8b3VJemoVDSGim3dAiJ5RSbNBdy-tdJwxZcNOJgZBFS0nLrHbccTEYTKkbzIA5NvQEvL3zbudhtEbXdpIKcpv8qNKtjMrLf18mv5aruJMY4ZYIRqrh1b0hxe-zzUXWuNqGoCYb5ywJR0zg2m1b0Zf_oZs4p6nm21OLru044n-plQpW-snFWljvpbJnHaIIC4Yr9fqO0inmnKx76BkjuZ8FeTALlX5xGPOB_fPz9Bc-Kq7g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2806545808</pqid></control><display><type>article</type><title>A Real-World Study of Achievement Rate and Predictive Factors of Clinical and Deep Remission to Biologics in Patients with Severe Asthma</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Oishi, Keiji ; Hamada, Kazuki ; Murata, Yoriyuki ; Matsuda, Kazuki ; Ohata, Syuichiro ; Yamaji, Yoshikazu ; Asami-Noyama, Maki ; Edakuni, Nobutaka ; Kakugawa, Tomoyuki ; Hirano, Tsunahiko ; Matsunaga, Kazuto</creator><creatorcontrib>Oishi, Keiji ; Hamada, Kazuki ; Murata, Yoriyuki ; Matsuda, Kazuki ; Ohata, Syuichiro ; Yamaji, Yoshikazu ; Asami-Noyama, Maki ; Edakuni, Nobutaka ; Kakugawa, Tomoyuki ; Hirano, Tsunahiko ; Matsunaga, Kazuto</creatorcontrib><description>Recent advances in biologics have provided new insights into the clinical course of asthma, including disease modification, clinical remission (CR), and deep remission (DR). However, the extent to which biologics achieve CR and DR in severe asthma patients is poorly understood. To assess the achievement rate and predictors of CR and DR using long-term biologics, we retrospectively evaluated 54 severe asthma patients recently started on biologics. "CR" denotes the achievement of all three criteria: (1) absence of asthma symptoms, (2) no asthma exacerbations, and (3) no use of oral corticosteroids. DR denoted CR plus (4) normalized pulmonary function and (5) suppressed type 2 inflammation. CR and DR achievement rates were 68.5% and 31.5%, respectively. Compared with the non-deep remission group, the DR group had higher adult-onset asthma rates (94.1% vs. 70.3%, = 0.078), shorter asthma duration (5 vs. 19 years, = 0.006), and higher FEV (91.5% vs. 71.5%, &lt; 0.001). There were no significant differences in the Asthma Control Questionnaire scores, exacerbation frequency, or type 2 inflammation at baseline between groups. Asthma duration combined with FEV can stratify the achievement rates of CR and DR. the early introduction of biologics in severe asthma patients may help achieve CR and DR.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm12082900</identifier><identifier>PMID: 37109237</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Asthma ; Biological products ; Blood ; Clinical medicine ; Disease ; Drug therapy ; Hospitals ; Immunology ; Immunotherapy ; Inflammation ; Monoclonal antibodies ; Patient outcomes ; Patients ; Regression (Disease) ; Regression analysis ; Remission (Medicine) ; Statistics ; Steroids</subject><ispartof>Journal of clinical medicine, 2023-04, Vol.12 (8), p.2900</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-6f009c7cfb40f9aaa7bc54809c59d268d59b22643247ecf8f89bd133fbdb181d3</citedby><cites>FETCH-LOGICAL-c438t-6f009c7cfb40f9aaa7bc54809c59d268d59b22643247ecf8f89bd133fbdb181d3</cites><orcidid>0000-0002-5475-0806 ; 0000-0002-0514-3241 ; 0000-0003-4230-0450 ; 0000-0002-5082-1486 ; 0000-0003-1339-1031</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142972/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142972/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37109237$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oishi, Keiji</creatorcontrib><creatorcontrib>Hamada, Kazuki</creatorcontrib><creatorcontrib>Murata, Yoriyuki</creatorcontrib><creatorcontrib>Matsuda, Kazuki</creatorcontrib><creatorcontrib>Ohata, Syuichiro</creatorcontrib><creatorcontrib>Yamaji, Yoshikazu</creatorcontrib><creatorcontrib>Asami-Noyama, Maki</creatorcontrib><creatorcontrib>Edakuni, Nobutaka</creatorcontrib><creatorcontrib>Kakugawa, Tomoyuki</creatorcontrib><creatorcontrib>Hirano, Tsunahiko</creatorcontrib><creatorcontrib>Matsunaga, Kazuto</creatorcontrib><title>A Real-World Study of Achievement Rate and Predictive Factors of Clinical and Deep Remission to Biologics in Patients with Severe Asthma</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>Recent advances in biologics have provided new insights into the clinical course of asthma, including disease modification, clinical remission (CR), and deep remission (DR). However, the extent to which biologics achieve CR and DR in severe asthma patients is poorly understood. To assess the achievement rate and predictors of CR and DR using long-term biologics, we retrospectively evaluated 54 severe asthma patients recently started on biologics. "CR" denotes the achievement of all three criteria: (1) absence of asthma symptoms, (2) no asthma exacerbations, and (3) no use of oral corticosteroids. DR denoted CR plus (4) normalized pulmonary function and (5) suppressed type 2 inflammation. CR and DR achievement rates were 68.5% and 31.5%, respectively. Compared with the non-deep remission group, the DR group had higher adult-onset asthma rates (94.1% vs. 70.3%, = 0.078), shorter asthma duration (5 vs. 19 years, = 0.006), and higher FEV (91.5% vs. 71.5%, &lt; 0.001). There were no significant differences in the Asthma Control Questionnaire scores, exacerbation frequency, or type 2 inflammation at baseline between groups. Asthma duration combined with FEV can stratify the achievement rates of CR and DR. the early introduction of biologics in severe asthma patients may help achieve CR and DR.</description><subject>Asthma</subject><subject>Biological products</subject><subject>Blood</subject><subject>Clinical medicine</subject><subject>Disease</subject><subject>Drug therapy</subject><subject>Hospitals</subject><subject>Immunology</subject><subject>Immunotherapy</subject><subject>Inflammation</subject><subject>Monoclonal antibodies</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Regression (Disease)</subject><subject>Regression analysis</subject><subject>Remission (Medicine)</subject><subject>Statistics</subject><subject>Steroids</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkl1rFDEUhoMottReeS8BbwQZm4-ZTXIl42q1ULC0ipchk4_dLJnJmmRW-g_82WZtrau5SUgennNecgB4jtEbSgU62-gRE8SJQOgROCaIsQZRTh8fnI_Aac4bVBfnLcHsKTiiDCNBKDsGP3t4bVVovsUUDLwps7mF0cFer73d2dFOBV6rYqGaDLxK1nhd_M7Cc6VLTHmPLoOfvFbhN_Le2m0Vjj5nHydYInznY4grrzP0E7xSxVdlhj98WcObWiFZ2OeyHtUz8MSpkO3p_X4Cvp5_-LL81Fx-_nix7C8b3VJemoVDSGim3dAiJ5RSbNBdy-tdJwxZcNOJgZBFS0nLrHbccTEYTKkbzIA5NvQEvL3zbudhtEbXdpIKcpv8qNKtjMrLf18mv5aruJMY4ZYIRqrh1b0hxe-zzUXWuNqGoCYb5ywJR0zg2m1b0Zf_oZs4p6nm21OLru044n-plQpW-snFWljvpbJnHaIIC4Yr9fqO0inmnKx76BkjuZ8FeTALlX5xGPOB_fPz9Bc-Kq7g</recordid><startdate>20230416</startdate><enddate>20230416</enddate><creator>Oishi, Keiji</creator><creator>Hamada, Kazuki</creator><creator>Murata, Yoriyuki</creator><creator>Matsuda, Kazuki</creator><creator>Ohata, Syuichiro</creator><creator>Yamaji, Yoshikazu</creator><creator>Asami-Noyama, Maki</creator><creator>Edakuni, Nobutaka</creator><creator>Kakugawa, Tomoyuki</creator><creator>Hirano, Tsunahiko</creator><creator>Matsunaga, Kazuto</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><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>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5475-0806</orcidid><orcidid>https://orcid.org/0000-0002-0514-3241</orcidid><orcidid>https://orcid.org/0000-0003-4230-0450</orcidid><orcidid>https://orcid.org/0000-0002-5082-1486</orcidid><orcidid>https://orcid.org/0000-0003-1339-1031</orcidid></search><sort><creationdate>20230416</creationdate><title>A Real-World Study of Achievement Rate and Predictive Factors of Clinical and Deep Remission to Biologics in Patients with Severe Asthma</title><author>Oishi, Keiji ; Hamada, Kazuki ; Murata, Yoriyuki ; Matsuda, Kazuki ; Ohata, Syuichiro ; Yamaji, Yoshikazu ; Asami-Noyama, Maki ; Edakuni, Nobutaka ; Kakugawa, Tomoyuki ; Hirano, Tsunahiko ; Matsunaga, Kazuto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-6f009c7cfb40f9aaa7bc54809c59d268d59b22643247ecf8f89bd133fbdb181d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Asthma</topic><topic>Biological products</topic><topic>Blood</topic><topic>Clinical medicine</topic><topic>Disease</topic><topic>Drug therapy</topic><topic>Hospitals</topic><topic>Immunology</topic><topic>Immunotherapy</topic><topic>Inflammation</topic><topic>Monoclonal antibodies</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>Regression (Disease)</topic><topic>Regression analysis</topic><topic>Remission (Medicine)</topic><topic>Statistics</topic><topic>Steroids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oishi, Keiji</creatorcontrib><creatorcontrib>Hamada, Kazuki</creatorcontrib><creatorcontrib>Murata, Yoriyuki</creatorcontrib><creatorcontrib>Matsuda, Kazuki</creatorcontrib><creatorcontrib>Ohata, Syuichiro</creatorcontrib><creatorcontrib>Yamaji, Yoshikazu</creatorcontrib><creatorcontrib>Asami-Noyama, Maki</creatorcontrib><creatorcontrib>Edakuni, Nobutaka</creatorcontrib><creatorcontrib>Kakugawa, Tomoyuki</creatorcontrib><creatorcontrib>Hirano, Tsunahiko</creatorcontrib><creatorcontrib>Matsunaga, Kazuto</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><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 Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oishi, Keiji</au><au>Hamada, Kazuki</au><au>Murata, Yoriyuki</au><au>Matsuda, Kazuki</au><au>Ohata, Syuichiro</au><au>Yamaji, Yoshikazu</au><au>Asami-Noyama, Maki</au><au>Edakuni, Nobutaka</au><au>Kakugawa, Tomoyuki</au><au>Hirano, Tsunahiko</au><au>Matsunaga, Kazuto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Real-World Study of Achievement Rate and Predictive Factors of Clinical and Deep Remission to Biologics in Patients with Severe Asthma</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2023-04-16</date><risdate>2023</risdate><volume>12</volume><issue>8</issue><spage>2900</spage><pages>2900-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>Recent advances in biologics have provided new insights into the clinical course of asthma, including disease modification, clinical remission (CR), and deep remission (DR). However, the extent to which biologics achieve CR and DR in severe asthma patients is poorly understood. To assess the achievement rate and predictors of CR and DR using long-term biologics, we retrospectively evaluated 54 severe asthma patients recently started on biologics. "CR" denotes the achievement of all three criteria: (1) absence of asthma symptoms, (2) no asthma exacerbations, and (3) no use of oral corticosteroids. DR denoted CR plus (4) normalized pulmonary function and (5) suppressed type 2 inflammation. CR and DR achievement rates were 68.5% and 31.5%, respectively. Compared with the non-deep remission group, the DR group had higher adult-onset asthma rates (94.1% vs. 70.3%, = 0.078), shorter asthma duration (5 vs. 19 years, = 0.006), and higher FEV (91.5% vs. 71.5%, &lt; 0.001). There were no significant differences in the Asthma Control Questionnaire scores, exacerbation frequency, or type 2 inflammation at baseline between groups. Asthma duration combined with FEV can stratify the achievement rates of CR and DR. the early introduction of biologics in severe asthma patients may help achieve CR and DR.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37109237</pmid><doi>10.3390/jcm12082900</doi><orcidid>https://orcid.org/0000-0002-5475-0806</orcidid><orcidid>https://orcid.org/0000-0002-0514-3241</orcidid><orcidid>https://orcid.org/0000-0003-4230-0450</orcidid><orcidid>https://orcid.org/0000-0002-5082-1486</orcidid><orcidid>https://orcid.org/0000-0003-1339-1031</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2077-0383
ispartof Journal of clinical medicine, 2023-04, Vol.12 (8), p.2900
issn 2077-0383
2077-0383
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10142972
source MDPI - Multidisciplinary Digital Publishing Institute; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
subjects Asthma
Biological products
Blood
Clinical medicine
Disease
Drug therapy
Hospitals
Immunology
Immunotherapy
Inflammation
Monoclonal antibodies
Patient outcomes
Patients
Regression (Disease)
Regression analysis
Remission (Medicine)
Statistics
Steroids
title A Real-World Study of Achievement Rate and Predictive Factors of Clinical and Deep Remission to Biologics in Patients with Severe Asthma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T17%3A59%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Real-World%20Study%20of%20Achievement%20Rate%20and%20Predictive%20Factors%20of%20Clinical%20and%20Deep%20Remission%20to%20Biologics%20in%20Patients%20with%20Severe%20Asthma&rft.jtitle=Journal%20of%20clinical%20medicine&rft.au=Oishi,%20Keiji&rft.date=2023-04-16&rft.volume=12&rft.issue=8&rft.spage=2900&rft.pages=2900-&rft.issn=2077-0383&rft.eissn=2077-0383&rft_id=info:doi/10.3390/jcm12082900&rft_dat=%3Cgale_pubme%3EA750301971%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2806545808&rft_id=info:pmid/37109237&rft_galeid=A750301971&rfr_iscdi=true