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Treatment and monitoring of Philadelphia chromosome-positive leukemia patients: recent advances and remaining challenges

机译:费城染色体阳性白血病患者的治疗和监测:最新进展和尚存的挑战

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摘要

The Philadelphia (Ph) chromosome, resulting from the t(9;22)(q34;q11) translocation, can be found in chronic myeloid leukemia (CML) as well as in a subset of acute lymphoblastic leukemias (ALL). The deregulated BCR-ABL1 tyrosine kinase encoded by the fusion gene resulting from the translocation is considered the pathogenetic driver and can be therapeutically targeted. In both CML and Ph-positive (Ph+) ALL, tyrosine kinase inhibitors (TKIs) have significantly improved outcomes. In the TKI era, testing for BCR-ABL1 transcript levels by real-time quantitative polymerase chain reaction (RQ-PCR) has become the gold standard to monitor patient response, anticipate relapse, and guide therapeutic decisions. In CML, key molecular response milestones have been defined that draw the ideal trajectory towards optimal long-term outcomes. Treatment discontinuation (treatment-free remission, TFR) has proven feasible in a proportion of patients, and clinical efforts are now focused on how to increase this proportion and how to best select TFR candidates. In Ph+ ALL, results of trials with second- and third-generation TKIs are challenging the role of intensive chemotherapy and even that of allogeneic stem cell transplantation. Additional weapons are offered by the recently introduced monoclonal antibodies. In patients harboring mutations in the BCR-ABL1 kinase domain, prompt therapeutic reassessment and individualization based on mutation status are important to regain response and prevent disease progression. Next-generation sequencing is likely to become a precious tool for mutation testing because of the greater sensitivity and the possibility to discriminate between compound and polyclonal mutations. In this review, we discuss the latest advances in treatment and monitoring of CML and Ph+ ALL and the issues that still need to be addressed to make the best use of the therapeutic armamentarium and molecular testing technologies currently at our disposal.
机译:由t(9; 22)(q34; q11)易位产生的费城(Ph)染色体可以在慢性粒细胞白血病(CML)以及急性淋巴细胞性白血病(ALL)的子集中找到。由易位导致的融合基因编码的BCR-ABL1酪氨酸激酶失控被认为是致病性驱动因素,可以作为治疗靶标。在CML和Ph阳性(Ph +)ALL中,酪氨酸激酶抑制剂(TKIs)均能显着改善结局。在TKI时代,通过实时定量聚合酶链反应(RQ-PCR)测试BCR-ABL1转录水平已成为监测患者反应,预测复发并指导治疗决策的金标准。在CML中,已定义了关键的分子响应里程碑,这些里程碑将理想轨迹引向了最佳的长期结果。停药治疗(无治疗缓解,TFR)已被证明对一定比例的患者是可行的,现在的临床工作集中在如何增加这一比例以及如何最好地选择TFR候选者上。在Ph + ALL中,第二代和第三代TKI的试验结果正在挑战强化化学疗法甚至同种异体干细胞移植的作用。最近推出的单克隆抗体可提供其他武器。对于在BCR-ABL1激酶结构域中存在突变的患者,及时进行治疗性重新评估和基于突变状态的个体化对于重新获得应答并预防疾病进展很重要。由于更高的灵敏度以及区分化合物和多克隆突变的可能性,下一代测序可能会成为突变测试的宝贵工具。在这篇综述中,我们讨论了CML和Ph + ALL的治疗和监测方面的最新进展,以及为充分利用当前可供使用的治疗性武器库和分子测试技术仍需要解决的问题。

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