{"id":381347,"date":"2024-08-24T00:01:00","date_gmt":"2024-08-23T22:01:00","guid":{"rendered":"https:\/\/medizinonline.com\/current-analyses-of-the-pioneer-among-the-jak-i\/"},"modified":"2024-09-02T14:49:53","modified_gmt":"2024-09-02T12:49:53","slug":"current-analyses-of-the-pioneer-among-the-jak-i","status":"publish","type":"post","link":"https:\/\/medizinonline.com\/en\/current-analyses-of-the-pioneer-among-the-jak-i\/","title":{"rendered":"Current analyses of the pioneer among the JAK-i"},"content":{"rendered":"\n<p><strong>The first representative of the Janus kinase (JAK) inhibitor class to be approved for atopic dermatitis was baricitinib. In an extensive study program, this selective and reversible inhibitor of JAK-1 and JAK-2 has demonstrated rapid relief of itching and skin lesions &#8211; even in areas of the body that are often difficult to treat. Real-world data is now available that confirms this positive balance.<\/strong><\/p>\n\n<!--more-->\n\n<p>Pruritogenic cytokines that are involved in the pathogenesis of atopic dermatitis (AD) and trigger their cytokine response via the JAK-STAT signaling pathway are interleukin (IL)-4, IL-13 and IL-31 [1]. Upadacitinib and abrocitinib selectively inhibit JAK-1, whereas baricitinib has an equally high specificity for JAK-1 and -2 [2,3]. All three oral JAK inhibitors (JAK-i) are characterized by a rapid onset of action and often lead to a reduction in itching within a short period of time, as post-hoc analyses of the BREEZE study program on baricitinib show <strong>(box)<\/strong> [4\u20136].  <\/p>\n\n<figure style=\"font-size:15px\" class=\"wp-block-table\"><table class=\"has-background\" style=\"background-color:#8dd2fc5e\"><tbody><tr><td><strong>Significant reduction in itching as early as week 2 <\/strong><br\/>In the BREEZE-AD1 and BREEZE-AD2 phase III trials, monotherapy with baricitinib and in BREEZE-AD7 a combination therapy of baricitinib with topical corticosteroids (TCS) was investigated [4,5].\nPost-hoc analyses of pooled data from the BREEZE-AD1\/AD2 studies show that a significantly higher proportion of study participants receiving baricitinib 4 mg daily (n=248) compared to placebo (n=493) achieved an <sup>NRS\u00a3<\/sup> score of 0\/1 at week 2 (8.9% vs. 1.6%; p&lt;0.0001) and that these effects persisted or intensified up to week 16 (14.1% vs. 3.9%; p&lt;0.0001) [6].  Even when combined with TCS, the differences between baricitinib 4 mg (n=111) vs. placebo (n=109) were already significant at week 2 (16.2% vs. 2.8%; p=0.0064) and this continued until week 16 (22.5% vs. 8.3%; p=0.0287) [6]. However, there is now also interesting new data on the question of how baricitinib performs in AD patients in everyday life, e.g. from registry studies and patient surveys.  <\/td><\/tr><tr><td><em><sup>\u00a3<\/sup> NRS = numerical rating scale; 0=no itching, 10=worst imaginable itching<\/em><\/td><\/tr><\/tbody><\/table><\/figure>\n\n<h3 id=\"treatgermany-register-study\" class=\"wp-block-heading\">TREATgermany register study  <\/h3>\n\n<p>TREATgermany is one of the largest AD registries with over 1600 patients currently included. In a recent analysis, data from 81 adult patients with moderate to severe AD who received baricitinib between October 2020 and August 2022 were evaluated [7]. The data from the initial examination and the three-month follow-up were analyzed with regard to various outcome parameters. The mean objective SCORAD** value changed from 45.9 at the beginning of the study to 28.2. In terms of EASI, the mean value decreased from 21.5 to 9.3. The <sup> EASI$-50<\/sup> and EASI-75 rates rose to 60% and 44% respectively. Subjective symptoms, including itching and quality of life (DLQI<sup>&amp;)<\/sup>, also improved significantly. In summary, baricitinib showed good efficacy and tolerability in this interim analysis of the TREATgermany population. Data on long-term efficacy and safety are expected in the further course of the registry study. Compared to biologics, closer monitoring is required during therapy with JAK-i. Since Janus kinases mediate the effect of several inflammatory cytokines, JAK inhibition is associated with an increased risk of infection [1].  <\/p>\n\n<p class=\"has-small-font-size\"><em>** SCORAD = SCORing Atopic Dermatitis (25-60 points=moderate; &gt;60 points=severe; maximum score=103)<\/em><br\/><em><sup>$<\/sup> EASI = Eczema Area and Severity Index<\/em><br\/><em><sup>&amp;<\/sup> DLQI = Dermatology Life Quality Index<\/em><\/p>\n\n<h3 id=\"multinational-patient-survey\" class=\"wp-block-heading\">Multinational patient survey<\/h3>\n\n<p>A cross-national online questionnaire study investigated satisfaction with baricitinib therapy in patients with moderate to severe AD using a four-point Likert scale [8]. Adult AD patients who had been treated with baricitinib for \u22654 weeks in routine clinical practice in France (n=48), Germany (n=53) or the UK (n=69) were surveyed. The average age was 39.3 years, 59% were female and the mean time since AD diagnosis was 20.9 years. At the start of baricitinib therapy, at least 10% of the body surface was affected by AD in 28% and the mean pruritus NRS was 6.8 (SD 2.0), which corresponds to significant pruritus. 19% classified their AD as moderately severe, 79% as severe. After treatment with baricitinib, which lasted a median of 4 months (range: 1-24), the patients reported an improvement, with 56% stating that the AD was only mild or had almost disappeared. It was found that most patients were either satisfied (n=58; 34%) or very satisfied (n=53; 31%) with baricitinib therapy. High rates of &#8216;very satisfied&#8217; and &#8216;satisfied&#8217; were recorded for the control of AD, including a reduction in itching (36% and 56%), a reduction in pain in the skin area (26% and 51%) and an improvement in sleep quality (16% and 55%). 63% and 19% of patients stated that the pruritus had &#8216;greatly improved&#8217; and &#8216;very greatly improved&#8217; respectively since the start of treatment. This reflects the overall high level of patient satisfaction, particularly with regard to itching relief. This is a significant finding considering that one of the main goals of AD is to treat pruritus quickly and effectively.  <\/p>\n\n<p><em>Congress: Dermatologie kompakt  praxisnah <\/em><\/p>\n\n<p>Literature:<\/p>\n\n<ol class=\"wp-block-list\">\n<li>Klein B, Treudler R, Simon JC: JAK-Inhibitoren in der Dermatologie \u2013 kleine Molek\u00fcle, grosse Wirkung? \u00dcbersicht \u00fcber Wirkmechanismus, Studienergebnisse und m\u00f6gliche unerw\u00fcnschte Wirkungen. JDDG 2022; 20(1): 19-25. <\/li>\n\n\n\n<li>Bonnekoh H, Butze M, Metz M: Charakterisierung der Effekte von neuen Therapien zur Behandlung der atopischen Dermatitis auf den Pruritus. JDDG 2022; 20(2): 150-156.  <\/li>\n\n\n\n<li>Nezamololama N, et al: Emerging systemic JAK inhibitors in the treatment of atopic dermatitis: a review of abrocitinib, baricitinib, and upadacitinib. Drugs Context. 2020 Nov 16;9:2020-8-5. doi: 10.7573\/dic.2020-8-5.  <\/li>\n\n\n\n<li>Simpson EL, et al: Baricitinib in patients with moderate-to-severe atopic dermatitis and inadequate response to topical corticosteroids: results from two randomized monotherapy phase III trials. Br J Dermatol 2020; 183(2): 242-255.<\/li>\n\n\n\n<li>Reich K, et al: Efficacy and safety of baricitinib combined with topical corticosteroids for treatment of moderate to severe atopic dermatitis: a randomized clinical trial. JAMA Dermatol 2020; 156(12): 1333-1343.<\/li>\n\n\n\n<li>Schl\u00f6be A, et al: Minimal-To-No-Itch with Baricitinib in Patients With Moderate to Severe Atopic Dermatitis: Results From Three Randomized, Phase 3 Clinical Trials, P038. JDDG 2024; 22, Issue S1: 1-40.<\/li>\n\n\n\n<li>Traidl S, et al: Treatment of moderate-to-severe atopic dermatitis with baricitinib &#8211; results from an interim analysis of the TREATgermany registry, P024. JDDG 2024; 22, Issue S1: 1-40.<\/li>\n\n\n\n<li>Augustin M, et al: Treatment satisfaction of adult patients with moderate-to-severe atopic dermatitis treated with baricitinib in France, Germany, and the United Kingdom: final results from a cross-sectional patient survey, P039. JDDG 2024; 22, Issue S1: 1-40.<\/li>\n<\/ol>\n\n<p><\/p>\n\n<p class=\"has-small-font-size\"><em>DERMATOLOGIE PRAXIS 2024; 34(3): 41 (published on 17.6.24, ahead of print)<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The first representative of the Janus kinase (JAK) inhibitor class to be approved for atopic dermatitis was baricitinib. In an extensive study program, this selective and reversible inhibitor of JAK-1&hellip;<\/p>\n","protected":false},"author":7,"featured_media":381356,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"pmpro_default_level":"","cat_1_feature_home_top":false,"cat_2_editor_pick":false,"csco_eyebrow_text":"\"Small Molecules\" at AD  ","footnotes":""},"category":[11513,11340,11548,11503],"tags":[12624,17420,65710,37603,15545,75917],"powerkit_post_featured":[],"class_list":["post-381347","post","type-post","status-publish","format-standard","has-post-thumbnail","category-congress-reports","category-dermatology-and-venereology","category-rx-en","category-studies","tag-atopic-dermatitis-en","tag-baricitinib-en","tag-jak-i-en","tag-real-world-data","tag-small-molecules-en","tag-special-localizations","pmpro-has-access"],"acf":[],"publishpress_future_action":{"enabled":false,"date":"2026-04-20 23:34:36","action":"change-status","newStatus":"draft","terms":[],"taxonomy":"category","extraData":[]},"publishpress_future_workflow_manual_trigger":{"enabledWorkflows":[]},"wpml_current_locale":"en_US","wpml_translations":{"fr_FR":{"locale":"fr_FR","id":381349,"slug":"dernieres-analyses-sur-le-pionnier-des-jak-i","post_title":"Derni\u00e8res analyses sur le pionnier des JAK-i","href":"https:\/\/medizinonline.com\/fr\/dernieres-analyses-sur-le-pionnier-des-jak-i\/"},"it_IT":{"locale":"it_IT","id":381350,"slug":"le-analisi-attuali-del-pioniere-tra-le-jak-i","post_title":"Le analisi attuali del pioniere tra le JAK-i","href":"https:\/\/medizinonline.com\/it\/le-analisi-attuali-del-pioniere-tra-le-jak-i\/"},"pt_PT":{"locale":"pt_PT","id":381348,"slug":"as-analises-actuais-do-pioneiro-entre-os-genes-jak-i","post_title":"As an\u00e1lises actuais do pioneiro entre os genes JAK-i","href":"https:\/\/medizinonline.com\/pt-pt\/as-analises-actuais-do-pioneiro-entre-os-genes-jak-i\/"},"es_ES":{"locale":"es_ES","id":381351,"slug":"los-analisis-actuales-del-pionero-entre-los-jak-i","post_title":"Los an\u00e1lisis actuales del pionero entre los JAK-i","href":"https:\/\/medizinonline.com\/es\/los-analisis-actuales-del-pionero-entre-los-jak-i\/"}},"_links":{"self":[{"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/posts\/381347","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/users\/7"}],"replies":[{"embeddable":true,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/comments?post=381347"}],"version-history":[{"count":2,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/posts\/381347\/revisions"}],"predecessor-version":[{"id":385172,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/posts\/381347\/revisions\/385172"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/media\/381356"}],"wp:attachment":[{"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/media?parent=381347"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/category?post=381347"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/tags?post=381347"},{"taxonomy":"powerkit_post_featured","embeddable":true,"href":"https:\/\/medizinonline.com\/en\/wp-json\/wp\/v2\/powerkit_post_featured?post=381347"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}