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isatuximab用于异基因造血细胞移植后红细胞延迟植入

Isatuximab for Delayed Red Cell Engraftment after Allogeneic Hematopoietic Cell Transplantation.

作者信息

Nauffal Mary, Eng Stephen, Lin Andrew, Chan Alexander, Mazzerella Kathryn, Giralt Sergio, Perales Miguel-Angel, Gyurkocza Boglarka

机构信息

Department of Pharmacy Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Department of Pathology Hematopathology Service Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Case Rep Hematol. 2024 Aug 30;2024:5790011. doi: 10.1155/2024/5790011. eCollection 2024.

DOI:10.1155/2024/5790011
PMID:39246802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11379505/
Abstract

Isatuximab is an IgG1-derived monoclonal antibody against CD38 approved for the treatment of adult patients with multiple myeloma. Here we describe the successful treatment of a therapy-refractory pure red cell aplasia case following ABO-mismatched allogeneic stem cell transplantation with isatuximab. Our patient was a 75-year-old female with acute myeloid leukemia who received an HLA-B antigen mismatched, unrelated peripheral blood stem cell transplant with a major ABO incompatibility (blood group A+ in the donor and blood group O+ in the recipient). The patient developed persistent red cell aplasia and anti-A antibodies for more than 500 days from transplant. She received therapy with rituximab, bortezomib, prednisone, and darbepoetin alfa with partial to no response. After repeated insurance denials for daratumumab, isatuximab was obtained from the manufacturer through their CareASSIST program. Following the completion of 2 cycles of isatuximab (8 doses), significant and sustained red cell recovery was observed.

摘要

isatuximab是一种抗CD38的IgG1衍生单克隆抗体,已被批准用于治疗成年多发性骨髓瘤患者。在此,我们描述了1例难治性纯红细胞再生障碍性贫血病例在ABO血型不匹配的异基因干细胞移植后使用isatuximab成功治疗的情况。我们的患者是一名75岁的急性髓系白血病女性,接受了HLA - B抗原不匹配的无关供者外周血干细胞移植,存在主要ABO血型不合(供者血型为A +,受者血型为O +)。该患者自移植后500多天出现持续性红细胞再生障碍和抗A抗体。她接受了利妥昔单抗、硼替佐米、泼尼松和达贝泊汀α治疗,部分缓解或无反应。在反复被保险公司拒绝使用达雷妥尤单抗后,通过制造商的CareASSIST项目获得了isatuximab。在完成2个周期的isatuximab(8剂)治疗后,观察到红细胞显著且持续恢复。

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Isatuximab for Delayed Red Cell Engraftment after Allogeneic Hematopoietic Cell Transplantation.isatuximab用于异基因造血细胞移植后红细胞延迟植入
Case Rep Hematol. 2024 Aug 30;2024:5790011. doi: 10.1155/2024/5790011. eCollection 2024.
2
Daratumumab for Delayed Red-Cell Engraftment after Allogeneic Transplantation.达雷妥尤单抗治疗异基因移植后红细胞植入延迟。
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Successful treatment of refractory red cell aplasia after allogeneic hematopoietic cell transplantation with daratumumab.达雷妥尤单抗治疗异基因造血细胞移植后难治性红细胞再生障碍的疗效。
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Pure Red Cell Aplasia following ABO-Mismatched Allogeneic Hematopoietic Stem Cell Transplantation: Resolution with Daratumumab Treatment.ABO 血型不合异基因造血干细胞移植后纯红细胞再生障碍:达妥木单抗治疗后缓解。
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本文引用的文献

1
Isatuximab: A Review of Its Use in Multiple Myeloma.依沙妥昔单抗:在多发性骨髓瘤中的应用评价。
Target Oncol. 2021 Sep;16(5):675-686. doi: 10.1007/s11523-021-00827-0. Epub 2021 Aug 5.
2
Treatment for pure red cell aplasia after major ABO-incompatible allogeneic stem cell transplantation: a multicentre study.主要 ABO 不相容异基因干细胞移植后纯红细胞再生障碍的治疗:一项多中心研究。
Br J Haematol. 2021 May;193(4):814-826. doi: 10.1111/bjh.17463. Epub 2021 Apr 12.
3
Crystal structure of CD38 in complex with daratumumab, a first-in-class anti-CD38 antibody drug for treating multiple myeloma.
CD38 复合物的晶体结构,其中 daratumumab 是一种治疗多发性骨髓瘤的首创抗 CD38 抗体药物。
Biochem Biophys Res Commun. 2021 Jan 15;536:26-31. doi: 10.1016/j.bbrc.2020.12.048. Epub 2020 Dec 22.
4
Pure red cell aplasia after major or bidirectional ABO incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question.主要或双向 ABO 不相容造血干细胞移植后纯红细胞再生障碍:治疗还是不治疗,这是个问题。
Bone Marrow Transplant. 2021 Apr;56(4):769-778. doi: 10.1038/s41409-020-01124-6. Epub 2020 Nov 14.
5
Successful treatment of thrombocytopenia with daratumumab after allogeneic transplant: a case report and literature review.异基因移植后使用达雷妥尤单抗成功治疗血小板减少症:一例病例报告及文献综述
Blood Adv. 2020 Mar 10;4(5):815-818. doi: 10.1182/bloodadvances.2019001215.
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Therapeutic Opportunities with Pharmacological Inhibition of CD38 with Isatuximab.Isatuximab 抑制 CD38 的治疗机会。
Cells. 2019 Nov 26;8(12):1522. doi: 10.3390/cells8121522.
7
Rational management approach to pure red cell aplasia.纯红细胞再生障碍性贫血的合理治疗方法。
Haematologica. 2018 Feb;103(2):221-230. doi: 10.3324/haematol.2017.175810. Epub 2017 Dec 7.