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dc.contributor.author문영철*
dc.date.accessioned2025-10-29T16:30:05Z-
dc.date.available2025-10-29T16:30:05Z-
dc.date.issued2025*
dc.identifier.issn1365-2141*
dc.identifier.otherOAK-38090*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/273184-
dc.description.abstractRomiplostim has been shown to restore multi-lineage haematopoiesis and is effective in patients with aplastic anaemia (AA) refractory to immunosuppressive therapy (IST). This open-label, phase 2/3 study (NCT04095936) recruited adult AA patients in Japan and Korea who had not received prior IST and evaluated the efficacy and safety of romiplostim plus ciclosporin A (CsA). Romiplostim was initiated at 10 μg/kg once weekly through Week 4 and adjusted between 0 and 20 μg/kg from Week 5 onwards. CsA was administered at 5–6 mg/kg/day in two divided doses through Week 26. A total of 24 patients (median [range] age, 52 [19–80] years) were enrolled, and 22 (91.7%) completed the study. Four patients (16.7%) had very severe AA (VSAA), 13 (54.2%) had severe AA (SAA) and seven (29.2%) had transfusion-dependent non-severe AA (NSAA). A haematological response at Week 27 was observed in 10/24 patients (overall response, 41.7%; 95% confidence interval, 22.1%–63.4%). At Week 27, the subgroup overall response rates were 0.0% in VSAA, 46.2% in SAA and 57.1% in NSAA. Nearly 92% of patients experienced at least one treatment-emergent adverse event (TEAE), but no drug-related Grade ≥3 TEAEs were reported. One patient developed myelodysplastic syndromes. Treatment with romiplostim plus CsA was effective and well tolerated in patients with AA who had not previously received IST. © 2025 Elsevier B.V., All rights reserved.*
dc.languageEnglish*
dc.publisherJohn Wiley and Sons Inc*
dc.subjectAplastic Anaemia*
dc.subjectCiclosporin*
dc.subjectImmunosuppressive Therapy*
dc.subjectRomiplostim*
dc.subjectThrombopoietin*
dc.subjectAzathioprine*
dc.subjectCyclosporine*
dc.subjectDexamethasone*
dc.subjectEltrombopag*
dc.subjectErythropoietin*
dc.subjectHemoglobin*
dc.subjectPrednisolone*
dc.subjectPrednisone*
dc.subjectImmunosuppressive Agents*
dc.subjectReceptors, Fc*
dc.subjectRecombinant Fusion Proteins*
dc.subjectCorticosteroid*
dc.subjectFc Receptor*
dc.subjectFusion Protein*
dc.subjectImmunosuppressive Agent*
dc.subjectAdult*
dc.subjectAged*
dc.subjectAnemia*
dc.subjectAplastic Anemia*
dc.subjectArticle*
dc.subjectBleeding*
dc.subjectCytogenetics*
dc.subjectDrug Efficacy*
dc.subjectDrug Safety*
dc.subjectErythrocyte Transfusion*
dc.subjectFemale*
dc.subjectFollow Up*
dc.subjectHuman*
dc.subjectImmunosuppressive Treatment*
dc.subjectLeukocyte Count*
dc.subjectMajor Clinical Study*
dc.subjectMale*
dc.subjectNeutropenia*
dc.subjectNeutrophil Count*
dc.subjectOutcome Assessment*
dc.subjectOverall Response Rate*
dc.subjectPhase 2 Clinical Trial*
dc.subjectPhase 3 Clinical Trial*
dc.subjectPlatelet Count*
dc.subjectRelapse*
dc.subjectSplenectomy*
dc.subjectStatistical Analysis*
dc.subjectThrombocytopenia*
dc.subjectClinical Trial*
dc.subjectCombination Drug Therapy*
dc.subjectDrug Therapy*
dc.subjectMiddle Aged*
dc.subjectMulticenter Study*
dc.subjectTreatment Outcome*
dc.subjectVery Elderly*
dc.subjectYoung Adult*
dc.subjectAged, 80 And Over*
dc.subjectAnemia, Aplastic*
dc.subjectDrug Therapy, Combination*
dc.subjectHumans*
dc.titleRomiplostim with ciclosporin A in patients with aplastic anaemia naïve to immunosuppressive therapy: A phase 2/3 study*
dc.typeArticle*
dc.relation.issue2*
dc.relation.volume207*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage582*
dc.relation.lastpage590*
dc.relation.journaltitleBritish Journal of Haematology*
dc.identifier.doi10.1111/bjh.20206*
dc.identifier.wosidWOS:001525566100001*
dc.identifier.scopusid2-s2.0-105010577046*
dc.author.googleLee J.*
dc.author.googleJang J.*
dc.author.googleChiba S.*
dc.author.googleYoon S.*
dc.author.googleOshikawa G.*
dc.author.googleUsuki K.*
dc.author.googleMun Y.C.*
dc.author.googleKawakita T.*
dc.author.googleImada K.*
dc.author.googleCheong J.*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20260622150610*


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