Bernardi Chiara, Beauverd Yan, Tran Thien An, Maulini Marie, Mappoura Maria, Morin Sarah, Simonetta Federico, Cairoli Anne, Auner Holger W, Samii Kaveh, Chalandon Yves, de Ramon Ortiz Carmen
Division of Haematology, Department of Oncology, Geneva University Hospitals, Geneva, Switzerland.
Translational Research Center for Oncohematology, Department of Medicine and Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Front Immunol. 2024 Nov 29;15:1495233. doi: 10.3389/fimmu.2024.1495233. eCollection 2024.
Plasma cell leukemia (PCL) is an aggressive and high-risk variant of multiple myeloma (MM) with a very poor prognosis. Given its rarity and aggressiveness, there is a lack of clinical trials testing the efficacity of novel therapies in these patients. New immune approaches such as B-cell maturation antigen (BCMA) and G protein-coupled receptor, family C, group 5, member D (GPRC5D) -targeting agents, including chimeric antigen receptor (CAR) T-cells and bispecific antibodies could play a role in PCL treatment. However, PCL patients were excluded from recent pivotal clinical trials testing those agents and only some case reports have been published. We present here the clinical course of a patient with relapsed/refractory (R/R) primary (p) PCL who was treated with anti-BCMA and anti-GPRC5D bispecific antibodies at our center.
浆细胞白血病(PCL)是多发性骨髓瘤(MM)的一种侵袭性高风险变异型,预后极差。鉴于其罕见性和侵袭性,缺乏针对这些患者测试新型疗法疗效的临床试验。新的免疫疗法,如靶向B细胞成熟抗原(BCMA)和G蛋白偶联受体C族第5组成员D(GPRC5D)的药物,包括嵌合抗原受体(CAR)T细胞和双特异性抗体,可能在PCL治疗中发挥作用。然而,PCL患者被排除在近期测试这些药物的关键临床试验之外,仅有一些病例报告发表。我们在此介绍一名复发/难治性(R/R)原发性(p)PCL患者在我们中心接受抗BCMA和抗GPRC5D双特异性抗体治疗的临床过程。