Enhanced Efficacy of Dust Mite Sublingual Immunotherapy in Low-Response Allergic Rhinitis Patients after Dose Increment at 6 Months: A Prospective Study

Background: Several studies have suggested that sublingual immunotherapy (SLIT) involves a dose-response relationship and inadequate dosage might not achieve a favorable clinical effect. Objective: The aim of this prospective study was to investigate the efficacy and safety of increasing SLIT dosage...

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Veröffentlicht in:International archives of allergy and immunology 2020-04, Vol.181 (4), p.311-319
Hauptverfasser: Gao, Yingqin, Lin, Xia, Ma, Jing, Wei, Xin, Wang, Qiuju, Wang, Meilan
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container_issue 4
container_start_page 311
container_title International archives of allergy and immunology
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creator Gao, Yingqin
Lin, Xia
Ma, Jing
Wei, Xin
Wang, Qiuju
Wang, Meilan
description Background: Several studies have suggested that sublingual immunotherapy (SLIT) involves a dose-response relationship and inadequate dosage might not achieve a favorable clinical effect. Objective: The aim of this prospective study was to investigate the efficacy and safety of increasing SLIT dosage at 6 months in patients with house dust mite-induced allergic rhinitis (AR) who had low response to treatment. Methods: A total of 157 AR participants aged 4–60 years were enrolled and received SLIT with Dermatophagoides farinae drops. After 6 months of SLIT, patients were interviewed and then classified into a high-response (HR) group and a low-response (LR) group based on the combined symptom and medication score (CSMS) reduction rate. Patients with a CSMS reduction rate over 50% were defined as HR and continued the original dose, while patients with a CSMS reduction rate ranging from 20 to 50% were defined as LR and received an increased dose (percentage of dosage increment, 33.33% for patients aged 0.05). The improvement of adults in the LR group was significantly lower than that of children at 6 months (p < 0.05), but there was no difference in later follow-ups (p > 0.05). There was no difference in CSMS or VAS in patients with monosensitization and polysensitization in the same treatment group at 1 year and in subsequent visits (p> 0.05). Overall, 47 patients withdrew from this study due to NR (n = 22) and other reasons (n = 25). Conclusions: Six months might be a critical time point for efficacy assessment and dosage adjustment for AR patients after SLIT. In patients with low response, dosage enhancement within a certain range may enhance the effectiveness of SLIT.
doi_str_mv 10.1159/000505746
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Objective: The aim of this prospective study was to investigate the efficacy and safety of increasing SLIT dosage at 6 months in patients with house dust mite-induced allergic rhinitis (AR) who had low response to treatment. Methods: A total of 157 AR participants aged 4–60 years were enrolled and received SLIT with Dermatophagoides farinae drops. After 6 months of SLIT, patients were interviewed and then classified into a high-response (HR) group and a low-response (LR) group based on the combined symptom and medication score (CSMS) reduction rate. Patients with a CSMS reduction rate over 50% were defined as HR and continued the original dose, while patients with a CSMS reduction rate ranging from 20 to 50% were defined as LR and received an increased dose (percentage of dosage increment, 33.33% for patients aged &lt;14 years and 50% for patients aged ≥14 years). Patients with a CSMS reduction rate below 20% were considered nonresponse (NR) and recommended to withdraw from SLIT. CSMS, visual analog scale (VAS), and adverse events were assessed at 0.5, 1, 2, and 3 years during the 3-year treatment. Results: A total of 54 and 56 patients completed the treatment in the HR and LR groups, respectively. The CSMS and VAS of both groups decreased significantly at 6 months (p &lt; 0.05). Significant differences between the two groups were found in CSMS and VAS at 6 months and 1 year (p &lt; 0.05), but not in later follow-ups (p &gt; 0.05). The improvement of adults in the LR group was significantly lower than that of children at 6 months (p &lt; 0.05), but there was no difference in later follow-ups (p &gt; 0.05). There was no difference in CSMS or VAS in patients with monosensitization and polysensitization in the same treatment group at 1 year and in subsequent visits (p&gt; 0.05). Overall, 47 patients withdrew from this study due to NR (n = 22) and other reasons (n = 25). Conclusions: Six months might be a critical time point for efficacy assessment and dosage adjustment for AR patients after SLIT. In patients with low response, dosage enhancement within a certain range may enhance the effectiveness of SLIT.</description><identifier>ISSN: 1018-2438</identifier><identifier>EISSN: 1423-0097</identifier><identifier>DOI: 10.1159/000505746</identifier><identifier>PMID: 32069460</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Care and treatment ; Clinical Immunology – Research Article ; Complications and side effects ; Hay-fever ; Health aspects ; House-dust mite ; Immunotherapy ; Patient outcomes</subject><ispartof>International archives of allergy and immunology, 2020-04, Vol.181 (4), p.311-319</ispartof><rights>2020 S. Karger AG, Basel</rights><rights>2020 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2020 S. Karger AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-85e480819a78b5ff819c52720047bd97c23bc10d0d0b8646aaf4fe73c30afb043</citedby><cites>FETCH-LOGICAL-c432t-85e480819a78b5ff819c52720047bd97c23bc10d0d0b8646aaf4fe73c30afb043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32069460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Yingqin</creatorcontrib><creatorcontrib>Lin, Xia</creatorcontrib><creatorcontrib>Ma, Jing</creatorcontrib><creatorcontrib>Wei, Xin</creatorcontrib><creatorcontrib>Wang, Qiuju</creatorcontrib><creatorcontrib>Wang, Meilan</creatorcontrib><title>Enhanced Efficacy of Dust Mite Sublingual Immunotherapy in Low-Response Allergic Rhinitis Patients after Dose Increment at 6 Months: A Prospective Study</title><title>International archives of allergy and immunology</title><addtitle>Int Arch Allergy Immunol</addtitle><description>Background: Several studies have suggested that sublingual immunotherapy (SLIT) involves a dose-response relationship and inadequate dosage might not achieve a favorable clinical effect. Objective: The aim of this prospective study was to investigate the efficacy and safety of increasing SLIT dosage at 6 months in patients with house dust mite-induced allergic rhinitis (AR) who had low response to treatment. Methods: A total of 157 AR participants aged 4–60 years were enrolled and received SLIT with Dermatophagoides farinae drops. After 6 months of SLIT, patients were interviewed and then classified into a high-response (HR) group and a low-response (LR) group based on the combined symptom and medication score (CSMS) reduction rate. Patients with a CSMS reduction rate over 50% were defined as HR and continued the original dose, while patients with a CSMS reduction rate ranging from 20 to 50% were defined as LR and received an increased dose (percentage of dosage increment, 33.33% for patients aged &lt;14 years and 50% for patients aged ≥14 years). Patients with a CSMS reduction rate below 20% were considered nonresponse (NR) and recommended to withdraw from SLIT. CSMS, visual analog scale (VAS), and adverse events were assessed at 0.5, 1, 2, and 3 years during the 3-year treatment. Results: A total of 54 and 56 patients completed the treatment in the HR and LR groups, respectively. The CSMS and VAS of both groups decreased significantly at 6 months (p &lt; 0.05). Significant differences between the two groups were found in CSMS and VAS at 6 months and 1 year (p &lt; 0.05), but not in later follow-ups (p &gt; 0.05). The improvement of adults in the LR group was significantly lower than that of children at 6 months (p &lt; 0.05), but there was no difference in later follow-ups (p &gt; 0.05). There was no difference in CSMS or VAS in patients with monosensitization and polysensitization in the same treatment group at 1 year and in subsequent visits (p&gt; 0.05). Overall, 47 patients withdrew from this study due to NR (n = 22) and other reasons (n = 25). Conclusions: Six months might be a critical time point for efficacy assessment and dosage adjustment for AR patients after SLIT. 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Karger AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200401</creationdate><title>Enhanced Efficacy of Dust Mite Sublingual Immunotherapy in Low-Response Allergic Rhinitis Patients after Dose Increment at 6 Months: A Prospective Study</title><author>Gao, Yingqin ; Lin, Xia ; Ma, Jing ; Wei, Xin ; Wang, Qiuju ; Wang, Meilan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-85e480819a78b5ff819c52720047bd97c23bc10d0d0b8646aaf4fe73c30afb043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Care and treatment</topic><topic>Clinical Immunology – Research Article</topic><topic>Complications and side effects</topic><topic>Hay-fever</topic><topic>Health aspects</topic><topic>House-dust mite</topic><topic>Immunotherapy</topic><topic>Patient outcomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Yingqin</creatorcontrib><creatorcontrib>Lin, Xia</creatorcontrib><creatorcontrib>Ma, Jing</creatorcontrib><creatorcontrib>Wei, Xin</creatorcontrib><creatorcontrib>Wang, Qiuju</creatorcontrib><creatorcontrib>Wang, Meilan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International archives of allergy and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Yingqin</au><au>Lin, Xia</au><au>Ma, Jing</au><au>Wei, Xin</au><au>Wang, Qiuju</au><au>Wang, Meilan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhanced Efficacy of Dust Mite Sublingual Immunotherapy in Low-Response Allergic Rhinitis Patients after Dose Increment at 6 Months: A Prospective Study</atitle><jtitle>International archives of allergy and immunology</jtitle><addtitle>Int Arch Allergy Immunol</addtitle><date>2020-04-01</date><risdate>2020</risdate><volume>181</volume><issue>4</issue><spage>311</spage><epage>319</epage><pages>311-319</pages><issn>1018-2438</issn><eissn>1423-0097</eissn><abstract>Background: Several studies have suggested that sublingual immunotherapy (SLIT) involves a dose-response relationship and inadequate dosage might not achieve a favorable clinical effect. Objective: The aim of this prospective study was to investigate the efficacy and safety of increasing SLIT dosage at 6 months in patients with house dust mite-induced allergic rhinitis (AR) who had low response to treatment. Methods: A total of 157 AR participants aged 4–60 years were enrolled and received SLIT with Dermatophagoides farinae drops. After 6 months of SLIT, patients were interviewed and then classified into a high-response (HR) group and a low-response (LR) group based on the combined symptom and medication score (CSMS) reduction rate. Patients with a CSMS reduction rate over 50% were defined as HR and continued the original dose, while patients with a CSMS reduction rate ranging from 20 to 50% were defined as LR and received an increased dose (percentage of dosage increment, 33.33% for patients aged &lt;14 years and 50% for patients aged ≥14 years). Patients with a CSMS reduction rate below 20% were considered nonresponse (NR) and recommended to withdraw from SLIT. CSMS, visual analog scale (VAS), and adverse events were assessed at 0.5, 1, 2, and 3 years during the 3-year treatment. Results: A total of 54 and 56 patients completed the treatment in the HR and LR groups, respectively. The CSMS and VAS of both groups decreased significantly at 6 months (p &lt; 0.05). Significant differences between the two groups were found in CSMS and VAS at 6 months and 1 year (p &lt; 0.05), but not in later follow-ups (p &gt; 0.05). The improvement of adults in the LR group was significantly lower than that of children at 6 months (p &lt; 0.05), but there was no difference in later follow-ups (p &gt; 0.05). There was no difference in CSMS or VAS in patients with monosensitization and polysensitization in the same treatment group at 1 year and in subsequent visits (p&gt; 0.05). Overall, 47 patients withdrew from this study due to NR (n = 22) and other reasons (n = 25). Conclusions: Six months might be a critical time point for efficacy assessment and dosage adjustment for AR patients after SLIT. In patients with low response, dosage enhancement within a certain range may enhance the effectiveness of SLIT.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>32069460</pmid><doi>10.1159/000505746</doi><tpages>9</tpages></addata></record>
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source Karger Journals; Alma/SFX Local Collection
subjects Care and treatment
Clinical Immunology – Research Article
Complications and side effects
Hay-fever
Health aspects
House-dust mite
Immunotherapy
Patient outcomes
title Enhanced Efficacy of Dust Mite Sublingual Immunotherapy in Low-Response Allergic Rhinitis Patients after Dose Increment at 6 Months: A Prospective Study
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