DTT在解决达拉单抗在血库中产生的干扰中的应用

M.C. Barrientos-Soto , M. Castañeda-García , A. Herrera-García , S. Padilla-López , M.A. Dimas-Adame , R. Cazares-Tamez
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引用次数: 0

摘要

Daratumumab (DARA)是一种在2016年证明其治疗多发性骨髓瘤的有效性和安全性的药物。该产品以单克隆抗体为基础,在技术上对大多数血液相容性测试产生干扰,人为地产生高血液泛反应性和不相容性。寻找与患者血清相容的血液的困难也可能掩盖其他临床重要的同种抗体的存在,最重要的是,延迟红细胞浓缩物的及时递送,这显然危及患者的生命。在输血医学中,最近描述了解决这种技术干扰的非常不同的策略。我们采用二硫苏糖醇(DTT)对该患者可能的献血者的红细胞进行处理,从而消除了这一技术差异,使该血液成分得到充分、安全、及时的选择。在本文中,我们描述了第一例患者诊断多发性骨髓瘤用DARA治疗,其中该药物在输血前试验中引起的干扰被成功解决。沟通是管理这些病人的一个关键因素。医生应告知患者和血库在使用该药治疗时出现不相容交叉试验的风险。此外,建议所有多发性骨髓瘤患者在接受DARA治疗前进行红细胞表型分析,并携带卡片表明他们正在接受这种药物治疗。幸运的是,在本文发表时,这些类型的患者尚未报道溶血性输血反应。对于血库的工作人员来说,显然必须制定一项额外的操作程序,以描述从这些病人入院后必须遵循的技术和行政操作。从技术上讲,根据我们在本病例中报告的经验,我们建议使用DTT技术来解决DARA治疗患者输血前检测中的这种差异和技术困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of DTT in the resolution of the interferences generated by daratumumab in the blood bank

Daratumumab (DARA) is a medication that in 2016 proved its efficacy and safety in the treatment of multiple myeloma. This product, based on a monoclonal antibody, technically generates an interference in most blood compatibility tests, artificially producing high blood pan-reactivity and incompatibility. The difficulty in finding blood compatible with the patient's serum can also mask the presence of other clinically significant alloantibodies and, above all, delays the timely delivery of erythrocyte concentrate, which, obviously, endangers the patient's life.

In transfusion medicine, very different strategies have recently been described for the resolution of this technical interference. We adopted the use of dithiothreitol (or DTT) to treat the red blood cells of the possible blood donors for the patient, thus achieving the elimination of this technical discrepancy and the adequate, safe and timely selection of this blood component. In the present paper, we describe the first case of a patient with a diagnosis of multiple myeloma treated with DARA, in which the interference caused by this drug in pretransfusion tests was successfully resolved.

Communication is a key element in the management of these patients. The doctor should inform the patient and the blood bank about the risk of presenting incompatible cross-tests when they are being treated with this medication. It is additionally recommended that all patients with multiple myeloma should undergo an erythrocyte phenotyping before receiving their treatment with DARA, and carry a card indicating that they are receiving this medication. Fortunately, hemolytic transfusion reactions have not yet been reported in these types of patients at the time of this publication.

For the staff at blood banks, it is evident that an additional operating procedure must be in place to describe the technical and administrative operation that must be followed from the admission of these patients to the hospital.

Technically speaking, we recommend, based on our experience reported in this case, the use of the DTT technique to resolve this discrepancy and technical difficulty in pretransfusion testing in patients treated with DARA.

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