Romiplostim with ciclosporin A in patients with aplastic anaemia naïve to immunosuppressive therapy: A phase 2/3 study
- PMID: 40639944
- PMCID: PMC12378949
- DOI: 10.1111/bjh.20206
Romiplostim with ciclosporin A in patients with aplastic anaemia naïve to immunosuppressive therapy: A phase 2/3 study
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.
Keywords: aplastic anaemia; ciclosporin; immunosuppressive therapy; romiplostim; thrombopoietin.
© 2025 The Author(s). British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
Conflict of interest statement
JWL received grants or contracts from Alexion Pharmaceuticals, Inc. and Kyowa Kirin Co., Ltd.; consulting fees from Alexion Pharmaceuticals, Inc., Kyowa Kirin Co., Ltd. and Sanofi K.K.; and payment or honoraria from Alexion Pharmaceuticals, Inc., Kyowa Kirin Co., Ltd. and Sanofi K.K. SC received grants or contracts from Kyowa Kirin Co., Ltd., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Astellas Pharma Inc. and Thyas Co., Ltd.; payment or honoraria from Sanofi K.K., Kyowa Kirin Co., Ltd., AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Meiji Seika Pharma Co., Ltd., Nippon Kayaku Co., Ltd., Astellas Pharma Inc., Novartis Pharma K.K., PharmaEssentia Japan K.K., Takeda Pharmaceutical Co., Ltd., Nippon Shinyaku Co., Ltd. and Asahi Kasei Pharma Corporation; and support for attending meetings and/or travel from Kyowa Kirin Co., Ltd. KU received grants or contracts from Astellas Pharma Inc., AbbVie G.K., Bristol‐Myers Squibb K.K., Ono Pharmaceutical Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., Apellis Pharmaceuticals, Inc., Yakult Honsha Co., Ltd., MSD K.K., Alexion Pharmaceuticals, Inc., Incyte Biosciences Japan G.K., Eisai Co., Ltd., Kyowa Kirin Co., Ltd., Sanofi K.K., Celgene K.K., Daiichi Sankyo Co., Ltd., Nippon Shinyaku Co., Ltd., Novartis Pharma K.K., Takeda Pharmaceutical Co., Ltd., Ohara Pharmaceutical Co., Ltd., and Pfizer Japan Inc.; consulting fees from Alnylam Japan K.K., Chugai Pharmaceutical Co., Ltd., Ohara Pharmaceutical Co., Ltd., and SobiTM Japan; and payment or honoraria from Novartis Pharma K.K., AbbVie G.K., Alexion Pharmaceuticals, Inc., Incyte Biosciences Japan G.K., Ono Pharmaceutical Co., Ltd., Kyowa Kirin Co., Ltd., Sanofi K.K., Takeda Pharmaceutical Co., Ltd., Nippon Shinyaku Co., Ltd., Bristol‐Myers Squibb K.K., Amgen K.K., Asahi Kasei Pharma Corporation, AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Meiji Seika Pharma Co., Ltd., Otsuka Pharmaceutical Co., Ltd., PharmaEssentia Japan K.K. and Janssen Pharmaceutical K.K. KI received payment or honoraria from Meiji Seika Pharma Co. Ltd., Janssen Pharmaceutical K.K., Towa Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co. Ltd., Alexion Pharmaceuticals, Inc., AbbVie G.K., Astellas Pharma Inc., Amgen K.K., AstraZeneca K.K., Daiichi Sankyo Co., Ltd., Gilead Sciences K.K., PharmaEssentia Japan K.K., Kyowa Kirin Co., Ltd., Novartis Pharma K.K., Sanofi K.K., Asahi Kasei Pharma Corporation, Nippon Kayaku Co., Ltd., Nippon Shinyaku Co., Ltd., Eisai Co., Ltd., Genmab K.K., Chugai Pharmaceutical Co., Ltd., Bristol‐Myers Squibb K.K., Ono Pharmaceutical Co. Ltd., and Otsuka Pharmaceutical Co. Ltd. MN is an employee of Kyowa Kirin Co., Ltd. AM received consulting fees from Kyowa Kirin Co., Ltd.; payments or honoraria from Alexion Pharmaceuticals, Inc., Nippon Shinyaku Co., Ltd., Sumitomo Dainippon Pharma Co., Ltd., Novartis Pharma K.K. and Chugai Pharma Co., Ltd.; and participation on a Data Safety Monitoring Board or Advisory Board from Kyowa Kirin Co., Ltd. KO received consulting fees from Kyowa Kirin Co., Ltd. KM received grants or contracts from Kyowa Kirin Co., Ltd., Chugai Pharmaceutical Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Taiho Pharmaceutical Co., Ltd., Sumitomo Pharma Co., Ltd.; consulting fees from Bristol‐Myers Squibb K.K., Kyowa Kirin Co., Ltd., and Otsuka Pharmaceutical Co., Ltd.; payment or honoraria from Bristol‐Myers Squibb K.K., and Kyowa Kirin Co., Ltd.; and participation on a Data Safety Monitoring Board or Advisory Board from Novartis Pharma K.K., and Ono Pharmaceutical Co., Ltd. YK received payment or honoraria from Novartis Pharma K.K., Kyowa Kirin Co., Ltd., Sanofi K.K., and Pfizer Japan Inc.; support for attending meetings and/or travel from Pfizer Japan Inc.; and participation on a Data Safety Monitoring Board or Advisory Board from Kyowa Kirin Co., Ltd. SN received payment or honoraria from Kyowa Kirin Co., Ltd. JHJ, S‐SY, GO, Y‐CM, TK and J‐WC report no competing interests.
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