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      Efficacy of Eltrombopag with Immunosuppressive Therapy Versus Immunosuppressive Therapy Alone on Severe Aplastic Anaemia: A Systematic Review and Meta-analysis

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          Abstract

          Background and Objective

          Severe aplastic anaemia (SAA) is a syndrome of bone marrow failure caused by T cell-mediated destruction of haematopoietic stem cells and progenitor cells. Whether patients with SAA should be treated with eltrombopag (EPAG) and immunosuppressive therapy (IST) or IST alone remains debatable. Therefore, we conducted this meta-analysis to compare the efficacy of eltrombopag + IST with that of IST alone in patients with SAA and to assess the difference in the efficacy of eltrombopag in adults and children.

          Methods

          We performed this meta-analysis by retrieving studies that met the inclusion and exclusion criteria from PubMed, EMBASE, and the Cochrane Library up to 1 January 2023. We used a random-effects model to calculate odds ratios (ORs) with 95% confidence intervals (CIs) for primary and secondary outcomes. I 2 statistics were used to evaluate the heterogeneity of the included studies.

          Results

          Six studies involving a total of 699 patients were included. In terms of the primary outcomes, our pooled results indicated that patients treated with EPAG + IST had a higher 6-month overall response rate (OR = 2.25; 95% CI, 1.60–3.16; p < 0.00001), a higher 6-month complete response rate (OR = 2.61; 95% CI, 1.82–3.74; p < 0.00001), and a lower 6-month nonresponse rate (OR = 0.32; 95% CI, 0.19–0.52; p < 0.00001). However, there was no significant difference in the rate of 6-month partial response (OR = 0.94; 95% CI, 0.49–1.81; p = 0.85).

          Conclusion

          This meta-analysis indicated that patients treated with additional eltrombopag for IST may have a higher rate of haematological response.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s40261-023-01266-7.

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          Most cited references39

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          The PRISMA 2020 statement: An updated guideline for reporting systematic reviews

          The Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement, published in 2009, was designed to help systematic reviewers transparently report why the review was done, what the authors did, and what they found. Over the past decade, advances in systematic review methodology and terminology have necessitated an update to the guideline. The PRISMA 2020 statement replaces the 2009 statement and includes new reporting guidance that reflects advances in methods to identify, select, appraise, and synthesise studies. The structure and presentation of the items have been modified to facilitate implementation. In this article, we present the PRISMA 2020 27-item checklist, an expanded checklist that details reporting recommendations for each item, the PRISMA 2020 abstract checklist, and the revised flow diagrams for original and updated reviews.
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            Aplastic Anemia

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              Current concepts in the pathophysiology and treatment of aplastic anemia.

              Aplastic anemia, an unusual hematologic disease, is the paradigm of the human bone marrow failure syndromes. Almost universally fatal just a few decades ago, aplastic anemia can now be cured or ameliorated by stem-cell transplantation or immunosuppressive drug therapy. The pathophysiology is immune mediated in most cases, with activated type 1 cytotoxic T cells implicated. The molecular basis of the aberrant immune response and deficiencies in hematopoietic cells is now being defined genetically; examples are telomere repair gene mutations in the target cells and dysregulated T-cell activation pathways. Immunosuppression with antithymocyte globulins and cyclosporine is effective at restoring blood-cell production in the majority of patients, but relapse and especially evolution of clonal hematologic diseases remain problematic. Allogeneic stem-cell transplant from histocompatible sibling donors is curative in the great majority of young patients with severe aplastic anemia; the major challenges are extending the benefits of transplantation to patients who are older or who lack family donors. Recent results with alternative sources of stem cells and a variety of conditioning regimens to achieve their engraftment have been promising, with survival in small pediatric case series rivaling conventional transplantation results.
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                Author and article information

                Contributors
                jjiefan@126.com
                hushaoyan@suda.edu.cn
                Journal
                Clin Drug Investig
                Clin Drug Investig
                Clinical Drug Investigation
                Springer International Publishing (Cham )
                1173-2563
                1179-1918
                11 May 2023
                11 May 2023
                2023
                : 43
                : 5
                : 315-324
                Affiliations
                [1 ]GRID grid.452253.7, ISNI 0000 0004 1804 524X, Department of Haematology and Oncology, Center of Jiangsu Pediatric Haematology and Oncology, , Children’s Hospital of Soochow University, ; No. 92, Zhongnan Street, Suzhou, 215000 China
                [2 ]GRID grid.33199.31, ISNI 0000 0004 0368 7223, Department of Nephrology, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), , Tongji Medical College, Huazhong University of Science and Technology, ; Wuhan, 430000 China
                Author information
                http://orcid.org/0000-0002-3386-6957
                Article
                1266
                10.1007/s40261-023-01266-7
                10198860
                37165250
                e77216e2-0994-4f80-893b-7ad7a4a914eb
                © The Author(s) 2023

                Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 2 April 2023
                Funding
                Funded by: the Translational Research Grant of NCRCH
                Award ID: 2020ZKPB02
                Award Recipient :
                Funded by: the Suzhou Health Talents Program
                Award ID: GSWS2020039
                Award Recipient :
                Funded by: the Suzhou Clinical Trial Institution Capacity Enhancement Program
                Award ID: SLT2021003
                Award Recipient :
                Categories
                Systematic Review
                Custom metadata
                © Springer Nature Switzerland AG 2023

                Pharmacology & Pharmaceutical medicine
                Pharmacology & Pharmaceutical medicine

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