Sampaio Mariana Miranda, Santos Maria Luísa Cordeiro, Marques Hanna Santos, Gonçalves Vinícius Lima de Souza, Araújo Glauber Rocha Lima, Lopes Luana Weber, Apolonio Jonathan Santos, Silva Camilo Santana, Santos Luana Kauany de Sá, Cuzzuol Beatriz Rocha, Guimarães Quézia Estéfani Silva, Santos Mariana Novaes, de Brito Breno Bittencourt, da Silva Filipe Antônio França, Oliveira Márcio Vasconcelos, Souza Cláudio Lima, de Melo Fabrício Freire
Instituto Multidisciplinar em Saúde, Universidade Federal da Bahia, Vitória da Conquista 45029-094, Bahia, Brazil.
Campus Vitória da Conquista, Universidade Estadual do Sudoeste da Bahia, Vitória da Conquista 45083-900, Bahia, Brazil.
World J Clin Oncol. 2021 Feb 24;12(2):69-94. doi: 10.5306/wjco.v12.i2.69.
Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm and was the first neoplastic disease associated with a well-defined genotypic anomaly - the presence of the Philadelphia chromosome. The advances in cytogenetic and molecular assays are of great importance to the diagnosis, prognosis, treatment, and monitoring of CML. The discovery of the fusion oncogene has revolutionized the treatment of CML patients by allowing the development of targeted drugs that inhibit the tyrosine kinase activity of the BCR-ABL oncoprotein. Tyrosine kinase inhibitors (known as TKIs) are the standard therapy for CML and greatly increase the survival rates, despite adverse effects and the odds of residual disease after discontinuation of treatment. As therapeutic alternatives, the subsequent TKIs lead to faster and deeper molecular remissions; however, with the emergence of resistance to these drugs, immunotherapy appears as an alternative, which may have a cure potential in these patients. Against this background, this article aims at providing an overview on CML clinical management and a summary on the main targeted drugs available in that context.
慢性髓性白血病(CML)是一种骨髓增殖性肿瘤,是第一种与明确的基因型异常——费城染色体的存在相关的肿瘤性疾病。细胞遗传学和分子检测的进展对CML的诊断、预后、治疗和监测具有重要意义。融合致癌基因的发现彻底改变了CML患者的治疗方式,使得能够开发出抑制BCR-ABL癌蛋白酪氨酸激酶活性的靶向药物。酪氨酸激酶抑制剂(称为TKIs)是CML的标准治疗方法,尽管存在不良反应和停药后残留疾病的几率,但能大大提高生存率。作为治疗选择,后续的TKIs可导致更快、更深的分子缓解;然而,随着对这些药物耐药性的出现,免疫疗法成为一种替代选择,可能对这些患者具有治愈潜力。在此背景下,本文旨在概述CML的临床管理,并总结该背景下可用的主要靶向药物。