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      Dysmegakaryopoiesis and Transient Mild Increase in Bone Marrow Blasts in Patients With Aplastic Anemia Treated With Eltrombopag May Be Signs of Hematologic Improvement and Not Portend Clonal Evolution

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          Abstract

          Objectives

          Eltrombopag, a thrombopoietin-receptor agonist, stimulates hematopoiesis in patients with acquired aplastic anemia (AA). Cytomorphologic changes in bone marrow after eltrombopag administration are still unclear. This study examined the effect of eltrombopag on cytomorphologic findings using data from prior phase 2 studies (E1201 and E1202).

          Methods

          Microscopic examinations were performed in 31 patients with AA (E1201 [n = 21], E1202 [n = 10]). The relationship between hematologic improvement and morphologic findings was also investigated.

          Results

          In 5 patients (E1201 [n = 3], E1202 [n = 2]), the bone marrow blast count increased after initiation of eltrombopag treatment compared with screening values. The blast count was less than 5%, and the increase in bone marrow blasts was transient in all 4 patients who had bone marrow examinations at follow-up. In 8 patients (E1201 [n = 5], E1202 [n = 3]), dysplastic forms of megakaryocytes were found in the bone marrow following treatment initiation. Dysmegakaryopoiesis of 10% or more was found in 3 patients. None of the patients revealed micromegakaryocytes. Ten patients showed an increase in bone marrow blasts and/or dysmegakaryopoiesis following treatment initiation. Nine of 10 patients showed hematologic improvement in 1 or more lineages.

          Conclusions

          Dysmegakaryopoiesis without micromegakaryocytes and a transient increase of less than 5% in bone marrow blast count may be signs of hematologic improvement with eltrombopag for patients with AA.

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          Most cited references26

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          Guidelines for the diagnosis and management of adult aplastic anaemia.

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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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              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
                Journal
                Am J Clin Pathol
                Am J Clin Pathol
                ajcp
                American Journal of Clinical Pathology
                Oxford University Press (US )
                0002-9173
                1943-7722
                November 2022
                26 August 2022
                26 August 2022
                : 158
                : 5
                : 604-615
                Affiliations
                Department of Hemato-Oncology and Medical Education, Saitama International Medical Center, Saitama Medical University , SaitamaJapan
                Department of Hematology, Japanese Red Cross Osaka Hospital , Osaka, Japan
                Department of Hematology, University of Tsukuba , Tsukuba, Japan
                Department of Hematology, National Hospital Organization Nagoya Medical Center , Nagoya, Japan
                Division of Transfusion Medicine, Kanazawa University Hospital , Kanazawa, Japan
                Department of Hematology and Oncology, Osaka University Hospital , Osaka, Japan
                Department of Hematology, Japanese Red Cross Nagoya Daiichi Hospital , Nagoya, Japan
                Department of Hematology, Miyagi Cancer Center , Natori, Japan
                Department of Hematology, Suita Municipal Hospital , Suita, Japan
                Hematology Ohta Clinic , Shinsaibashi, Japan
                Department of Hematology, NTT Medical Center Tokyo , Tokyo, Japan
                Department of Hematology, Itami City Hospital , Itami, Japan
                Department of Hematology, Okayama City Hospital , Okayama, Japan
                Novartis Pharma , Tokyo, Japan
                Novartis Pharma , Tokyo, Japan
                Kanazawa University Institute of Medical Pharmaceutical and Health Sciences , Kanazawa, Japan
                Author notes
                Corresponding author: Akira Matsuda; amatsu@ 123456saitama-med.ac.jp .
                Article
                aqac094
                10.1093/ajcp/aqac094
                9631234
                36018052
                89933b45-d1b7-4b29-bd02-3d70edb2c22c
                © American Society for Clinical Pathology, 2022.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 November 2021
                : 24 June 2022
                Page count
                Pages: 12
                Funding
                Funded by: GlaxoSmithKline, DOI 10.13039/100004330;
                Categories
                Original Articles
                AcademicSubjects/MED00690

                aplastic anemia,blast count,bone marrow,eltrombopag,hematologic improvement,dysmegakaryopoiesis

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