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      Matched related transplantation versus immunosuppressive therapy plus eltrombopag for first-line treatment of severe aplastic anemia: a multicenter, prospective study

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          Abstract

          This study prospectively compared the efficacy and safety between matched related donor-hematopoietic stem cell transplantation (MRD-HSCT) ( n = 108) and immunosuppressive therapy (IST) plus eltrombopag (EPAG) (IST + EPAG) ( n = 104) to determine whether MRD-HSCT was still superior as a front-line treatment for patients with severe aplastic anemia (SAA). Compared with IST + EPAG group, patients in the MRD-HSCT achieved faster transfusion independence, absolute neutrophil count ≥ 1.0 × 10 9/L ( P < 0.05), as well as high percentage of normal blood routine at 6-month (86.5% vs. 23.7%, P < 0.001). In the MRD-HSCT and IST + EPAG groups, 3-year overall survival (OS) was 84.2 ± 3.5% and 89.7 ± 3.1% ( P = 0.164), whereas 3-year failure-free survival (FFS) was 81.4 ± 4.0% and 59.1 ± 4.9% ( P = 0.002), respectively. Subgroup analysis indicated that the FFS of the MRD-HSCT was superior to that of the IST + EPAG among patients aged < 40 years old (81.0 ± 4.6% vs. 63.7 ± 6.5%, P = 0.033), and among patients with vSAA (86.1 ± 5.9% vs. 54.9 ± 7.9%, P = 0.003), while the 3-year OS of the IST + EPAG was higher than that of the MRD-HSCT among the patient aged ≥ 40 years old (100.0 ± 0.0% vs. 77.8 ± 9.8%, P = 0.036). Multivariate analysis showed that first-line MRD-HSCT treatment was associated favorably with normal blood results at 6-month and FFS ( P < 0.05). These outcomes suggest that MRD-HSCT remains the preferred first-line option for SAA patients aged < 40 years old or with vSAA even in the era of EPAG.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s13045-022-01324-1.

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          Eltrombopag Added to Standard Immunosuppression for Aplastic Anemia.

          Acquired aplastic anemia results from immune-mediated destruction of bone marrow. Immunosuppressive therapies are effective, but reduced numbers of residual stem cells may limit their efficacy. In patients with aplastic anemia that was refractory to immunosuppression, eltrombopag, a synthetic thrombopoietin-receptor agonist, led to clinically significant increases in blood counts in almost half the patients. We combined standard immunosuppressive therapy with eltrombopag in previously untreated patients with severe aplastic anemia.
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            How I treat acquired aplastic anemia

            Acquired severe aplastic anemia (SAA) is a rare hematologic disease associated with significant morbidity and mortality. Immune destruction of hemopoietic stem cells plays an important role in pathogenesis, as shown by successful treatment with immunosuppressive agents, leading to transfusion independence or complete recovery of peripheral blood counts in a proportion of patients. Growth factors can be combined with immunosuppressive therapy (IST) and may improve response rates, as recently shown with thrombopoietin analogs. Anabolic steroids may still play a role in combination with IST. The problem with IST is failure to respond and the development of late clonal disorders. Bone marrow transplantation (BMT) is the other therapeutic option: a matched sibling donor remains the best choice. For patients lacking a matched family donor, unrelated donors can be readily found, although mostly for patients of Caucasian origin. Other BMT options include unrelated cord blood or mismatched family donors. Acute and chronic graft-versus-host disease remain important complications of BMT. Patient age is a strong predictor of outcome for both IST and BMT, and must be considered when designing therapeutic strategies. Early diagnosis and treatment, as well as long-term monitoring, remain crucial steps for successful treatment of SAA.
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              Eltrombopag and improved hematopoiesis in refractory aplastic anemia.

              Severe aplastic anemia, which is characterized by immune-mediated bone marrow hypoplasia and pancytopenia, can be treated effectively with immunosuppressive therapy or allogeneic transplantation. One third of patients have disease that is refractory to immunosuppression, with persistent, severe cytopenia and a profound deficit in hematopoietic stem cells and progenitor cells. Thrombopoietin may increase the number of hematopoietic stem cells and progenitor cells. We conducted a phase 2 study involving patients with aplastic anemia that was refractory to immunosuppression to determine whether the oral thrombopoietin mimetic eltrombopag (Promacta) can improve blood counts. Twenty-five patients received eltrombopag at a dose of 50 mg, which could be increased, as needed, to a maximum dose of 150 mg daily, for a total of 12 weeks. Primary end points were clinically significant changes in blood counts or transfusion independence. Patients with a response continued to receive eltrombopag. Eleven of 25 patients (44%) had a hematologic response in at least one lineage at 12 weeks, with minimal toxic effects. Nine patients no longer needed platelet transfusions (median increase in platelet count, 44,000 per cubic millimeter). Six patients had improved hemoglobin levels (median increase, 4.4 g per deciliter); 3 of them were previously dependent on red-cell transfusions and no longer needed transfusions. Nine patients had increased neutrophil counts (median increase, 1350 per cubic millimeter). Serial bone marrow biopsies showed normalization of trilineage hematopoiesis in patients who had a response, without increased fibrosis. Monitoring of immune function revealed no consistent changes. Treatment with eltrombopag was associated with multilineage clinical responses in some patients with refractory severe aplastic anemia. (Funded by the National Heart, Lung, and Blood Institute; ClinicalTrials.gov number, NCT00922883.).
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                Author and article information

                Contributors
                kfzhang@ihcams.ac.cn
                zhanglsh@lzu.edu.cn
                wudepei@suda.edu.cn
                Journal
                J Hematol Oncol
                J Hematol Oncol
                Journal of Hematology & Oncology
                BioMed Central (London )
                1756-8722
                12 August 2022
                12 August 2022
                2022
                : 15
                : 105
                Affiliations
                [1 ]GRID grid.263761.7, ISNI 0000 0001 0198 0694, National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, , Institute of Blood and Marrow Transplantation of Soochow University, ; 188 Shizi Street, Suzhou, 215006 Jiangsu Province China
                [2 ]Department of Hematology, Haikou Municipal People’s Hospital, Affiliated Haikou Hospital Xiangya School of Medicine Central South University, Haikou, Hainan Province China
                [3 ]GRID grid.265021.2, ISNI 0000 0000 9792 1228, Department of Hematology, General Hospital, , Tianjin Medical University, ; Tianjin, China
                [4 ]GRID grid.506261.6, ISNI 0000 0001 0706 7839, Department of Hematology, Peking Union Medical College Hospital, , Chinese Academy of Medical Sciences and Peking Union Medical College, ; Beijing, China
                [5 ]GRID grid.506261.6, ISNI 0000 0001 0706 7839, State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood, Diseases, Anemia Therapeutic Center, Institute of Hematology & Blood Diseases Hospital, , Chinese Academy of Medical Sciences & Peking Union Medical College, ; Tianjin, China
                [6 ]GRID grid.412594.f, ISNI 0000 0004 1757 2961, Department of Hematology, , The First Affiliated Hospital of Guangxi Medical University, ; Nanning, China
                [7 ]GRID grid.470132.3, Department of Hematology, , The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, ; Huai’an, Jiangsu Province China
                [8 ]GRID grid.440299.2, Department of Hematology, , Xian Yang Central Hospital, ; Xianyang, Shanxi Province China
                [9 ]GRID grid.411294.b, ISNI 0000 0004 1798 9345, Department of Hematology, , The Second Hospital of Lanzhou University, ; Lanzhou, 730000 Gansu Province China
                Article
                1324
                10.1186/s13045-022-01324-1
                9373485
                35962406
                54cf5854-db61-4056-bc2d-bee2ce143476
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 22 May 2022
                : 27 July 2022
                Funding
                Funded by: This work was partly supported by grants from the National Natural Science Foundation of China
                Award ID: 81730003
                Award Recipient :
                Funded by: National Science and Technology Major Project
                Award ID: 2017ZX09304021
                Award Recipient :
                Funded by: National Key R&D Program of China
                Award ID: 2019YFC0840604, 2017YFA0104502
                Award Recipient :
                Funded by: Jiangsu Medical Outstanding Talents Project
                Award ID: JCRCA2016002
                Award Recipient :
                Funded by: Jiangsu Provincial Key Medical Center
                Award ID: YXZXA2016002
                Award Recipient :
                Categories
                Correspondence
                Custom metadata
                © The Author(s) 2022

                Oncology & Radiotherapy
                matched related transplantation,immunosuppressive therapy,eltrombopag,severe aplastic anemia

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