Bodet-Milin Caroline, Kraeber-Bodéré Françoise, Eugène Thomas, Guérard François, Gaschet Joëlle, Bailly Clément, Mougin Marie, Bourgeois Mickaël, Faivre-Chauvet Alain, Chérel Michel, Chevallier Patrice
CRCNA, INSERM U892, Nantes University, France; Department of Nuclear Medicine, Nantes University Hospital, France.
CRCNA, INSERM U892, Nantes University, France; Department of Nuclear Medicine, Nantes University Hospital, France; Department of Nuclear Medicine, ICO-René Gauducheau, Saint-Herblain, France.
Semin Nucl Med. 2016 Mar;46(2):135-46. doi: 10.1053/j.semnuclmed.2015.10.007.
Acute leukemias are characterized by accumulation of immature cells (blasts) and reduced production of healthy hematopoietic elements. According to the lineage origin, two major leukemias can be distinguished: acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL). Although the survival rate for pediatric ALL is close to 90%, half of the young adults with AML or ALL and approximately 90% of older patients with AML or ALL still die of their disease, raising the need for innovative therapeutic approaches. As almost all leukemic blasts express specific surface antigens, targeted immunotherapy appears to be particularly promising. However, published results of immunotherapy alone are generally modest. Radioimmunotherapy (RIT) brings additional therapeutic mechanisms using radiolabeled monoclonal antibodies (mAbs) directed to tumor antigens, thus adding radiobiological cytotoxicity to immunologic cytotoxicity. Because of the high radiosensitivity of tumor cells and the diffuse widespread nature of the disease, making it rapidly accessible to circulating radiolabeled mAbs, acute leukemias represent relevant indications for RIT. With the development of recombinant and humanized mAbs, innovative radionuclides, and more efficient radiolabeling and pretargeting techniques, RIT has significantly improved over the last 10 years. Different approaches of α and β RIT targeting CD22, CD33, CD45, or CD66 antigens have already been evaluated or are currently being developed in the treatment of acute leukemia. This review summarizes the preclinical and clinical studies demonstrating the potential of RIT in treatment of AML and ALL.
急性白血病的特征是未成熟细胞(原始细胞)积聚以及健康造血成分生成减少。根据谱系起源,可区分出两种主要的白血病:急性髓系白血病(AML)和急性淋巴细胞白血病(ALL)。尽管儿童ALL的生存率接近90%,但患有AML或ALL的年轻成年人中有一半以及患有AML或ALL的老年患者中约90%仍死于该病,因此需要创新的治疗方法。由于几乎所有白血病原始细胞都表达特定的表面抗原,靶向免疫疗法似乎特别有前景。然而,仅免疫疗法公布的结果通常并不理想。放射免疫疗法(RIT)利用针对肿瘤抗原的放射性标记单克隆抗体(mAb)带来额外的治疗机制,从而在免疫细胞毒性的基础上增加放射生物细胞毒性。由于肿瘤细胞的高放射敏感性以及疾病的广泛扩散性质,使得循环中的放射性标记mAb能够迅速到达肿瘤部位,急性白血病是RIT的相关适应症。随着重组和人源化mAb、创新放射性核素以及更高效的放射性标记和预靶向技术的发展,RIT在过去10年中有了显著改进。针对CD22、CD33、CD45或CD66抗原的α和β RIT的不同方法已在急性白血病治疗中得到评估或正在开发。本综述总结了证明RIT在治疗AML和ALL方面潜力的临床前和临床研究。