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dc.contributor.authorThaci, Diamant
dc.contributor.authorTziotzios, Christos
dc.contributor.authorIto, Taisuke
dc.contributor.authorKo, Justin
dc.contributor.authorKaradag, Ayse Serap
dc.contributor.authorFang, Hong
dc.contributor.authorEdwards, Roger A.
dc.contributor.authorBonfanti, Gianluca
dc.contributor.authorWolk, Robert
dc.contributor.authorTran, Helen
dc.contributor.authorLaw, Ernest
dc.contributor.authorKaradag, Ayse Serap
dc.date.accessioned2023-11-06T08:36:58Z
dc.date.available2023-11-06T08:36:58Z
dc.date.issued2023en_US
dc.identifier.citationThaçi, D., Tziotzios, C., Ito, T., Ko, J., Karadağ, A. S., Fang, H., ... & Law, E. (2023). Hair loss profiles and ritlecitinib efficacy in patients with alopecia areata: post hoc analysis of the ALLEGRO phase 2b/3 study. Dermatology and Therapy, 1-14.en_US
dc.identifier.issn21938210
dc.identifier.urihttps://doi.org/10.1007/s13555-023-00997
dc.identifier.urihttps://hdl.handle.net/20.500.12294/3959
dc.description.abstractIntroductionRitlecitinib demonstrated efficacy in patients with alopecia areata (AA) in the ALLEGRO phase 2b/3 study (NCT03732807). However, hair loss presentation may vary based on location (e.g., scalp, eyebrow/eyelash, body). Here, we sought to identify distinct hair loss profiles at baseline and evaluate whether they affected the efficacy of ritlecitinib.MethodsPatients with AA aged & GE; 12 years with & GE; 50% scalp hair loss were randomized to daily ritlecitinib 10 mg (assessed for dose ranging only), 30 or 50 mg (& PLUSMN; 4-week, 200-mg loading dose), or placebo for 24 weeks. Latent class analysis (LCA) identified hair loss profiles based on four baseline measurements: clinician-reported extent of scalp (Severity of Alopecia Tool score), eyebrow hair loss, eyelash hair loss, and patient-reported body hair loss. Logistic regression evaluated ritlecitinib (50 and 30 mg) efficacy vs placebo using Patient Global Impression of Change (PGI-C) and Patient Satisfaction with Hair Growth (P-Sat; amount, quality, and overall satisfaction) responses at Week 24, adjusting for key covariates, including latent class membership.ResultsLCA identified five latent classes: (1) primarily non-alopecia totalis (AT; complete loss of scalp hair); (2) non-AT with moderate non-scalp involvement; (3) extensive scalp, eyebrow, and eyelash involvement; (4) AT with moderate non-scalp involvement; and (5) primarily alopecia universalis (complete scalp, face, and body hair loss). Adjusting for latent class membership, patients receiving ritlecitinib 30 or 50 mg were significantly more likely to achieve PGI-C response (30 mg: odds ratio, 8.62 [95% confidence interval, 4.42-18.08]; 50 mg: 12.29 [6.29-25.85]) and P-Sat quality of hair regrowth (30 mg: 6.71 [3.53-13.51]; 50 mg: 8.17 [4.30-16.46]) vs placebo at Week 24. Results were similar for P-Sat overall satisfaction and amount of hair regrowth.ConclusionDistinct and clinically relevant hair loss profiles were identified in ALLEGRO-2b/3 participants. Ritlecitinib was efficacious compared with placebo, independent of hair loss profile at baseline.Trial registrationClinicalTrials.gov identifier, NCT03732807.en_US
dc.language.isoengen_US
dc.publisherADIS INT LTDen_US
dc.relation.ispartofDERMATOLOGY AND THERAPYen_US
dc.identifier.doi10.1007/s13555-023-00997en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRitlecitiniben_US
dc.subjectLatent Class Analysisen_US
dc.subjectHair Lossen_US
dc.subjectAlopecia Areataen_US
dc.titleHair Loss Profiles and Ritlecitinib Efficacy in Patients with Alopecia Areata: Post Hoc Analysis of the ALLEGRO Phase 2b/3 Studyen_US
dc.typearticleen_US
dc.departmentTıp Fakültesi, Dahili Tıp Bölümüen_US
dc.authorid0000-0003-4232-5906en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.institutionauthorKaradag, Ayse Serap
dc.authorwosidIXJ-3667-2023en_US
dc.identifier.wosqualityQ2en_US
dc.identifier.wosWOS:001068045700003en_US


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