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Romiplostim with ciclosporin A in patients with aplastic anaemia naïve to immunosuppressive therapy: A phase 2/3 study

Title
Romiplostim with ciclosporin A in patients with aplastic anaemia naïve to immunosuppressive therapy: A phase 2/3 study
Authors
Lee J.; Jang J.; Chiba S.; Yoon S.; Oshikawa G.; Usuki K.; Mun Y.C.; Kawakita T.; Imada K.; Cheong J.
Ewha Authors
문영철
SCOPUS Author ID
문영철scopus
Issue Date
2025
Journal Title
British Journal of Haematology
ISSN
1365-2141JCR Link
Citation
British Journal of Haematology vol. 207, no. 2, pp. 582 - 590
Keywords
Aplastic Anaemia; Ciclosporin; Immunosuppressive Therapy; Romiplostim; Thrombopoietin; Azathioprine; Cyclosporine; Dexamethasone; Eltrombopag; Erythropoietin; Hemoglobin; Prednisolone; Prednisone; Immunosuppressive Agents; Receptors, Fc; Recombinant Fusion Proteins; Corticosteroid; Fc Receptor; Fusion Protein; Immunosuppressive Agent; Adult; Aged; Anemia; Aplastic Anemia; Article; Bleeding; Cytogenetics; Drug Efficacy; Drug Safety; Erythrocyte Transfusion; Female; Follow Up; Human; Immunosuppressive Treatment; Leukocyte Count; Major Clinical Study; Male; Neutropenia; Neutrophil Count; Outcome Assessment; Overall Response Rate; Phase 2 Clinical Trial; Phase 3 Clinical Trial; Platelet Count; Relapse; Splenectomy; Statistical Analysis; Thrombocytopenia; Clinical Trial; Combination Drug Therapy; Drug Therapy; Middle Aged; Multicenter Study; Treatment Outcome; Very Elderly; Young Adult; Aged, 80 And Over; Anemia, Aplastic; Drug Therapy, Combination; Humans
Publisher
John Wiley and Sons Inc
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Romiplostim 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.
DOI
10.1111/bjh.20206
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의과대학 > 의학과 > Journal papers
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