Personalized patient care with aggressive hematological malignancies in non-responders to first-line treatment

IF 1 Q4 PHARMACOLOGY & PHARMACY
K. Miura, N. Iriyama, Y. Hatta, M. Takei
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引用次数: 1

Abstract

ABSTRACT Introduction Whereas most patients with aggressive hematological malignancies can achieve disease remission after receiving current standard first-line chemotherapies, the prognosis of those with primary refractory disease remains poor. Conventional salvage chemotherapies are usually unsuccessful, but significant advances have been achieved in precision medicine for these patients in recent years. Areas covered This article presents a comprehensive review of current personalized care for patients with primary refractory aggressive hematological malignancies, focusing on acute leukemias and aggressive non-Hodgkin lymphomas. Expert opinions Salvage treatment for refractory acute myeloid leukemia (AML) should be personalized by the FMS-like tyrosine kinase 3 (FLT3) mutation status. Additionally, treatment for isocitrate dehydrogenase 1 or 2 (IDH1/2)-mutated refractory AML can be specified. Inotuzumab ozogamicin and blinatumomab are essential drugs for refractory B-cell acute lymphoblastic leukemia. These antibodies can be selected based on the disease status, such as measurable residual disease. For refractory diffuse large B-cell lymphoma, treatment options are different according to the cell-of-origin. Finally, accurate pathological phenotyping is an essential first step to optimize refractory peripheral T-cell lymphoma treatment. Although novel personalized approaches have improved the clinical outcomes of these patients, consolidation with hematopoietic stem cell transplantation has a vital role in most cases.
对一线治疗无反应的侵袭性血液恶性肿瘤患者的个性化护理
虽然大多数侵袭性血液系统恶性肿瘤患者在接受目前标准的一线化疗后可以达到疾病缓解,但原发性难治性疾病患者的预后仍然很差。传统的挽救性化疗通常是不成功的,但近年来在这些患者的精准医疗方面取得了重大进展。本文全面回顾了目前针对原发性难治性侵袭性血液系统恶性肿瘤患者的个性化护理,重点是急性白血病和侵袭性非霍奇金淋巴瘤。专家意见:难治性急性髓性白血病(AML)的抢救治疗应根据fms样酪氨酸激酶3 (FLT3)突变状态进行个体化治疗。此外,可以指定异柠檬酸脱氢酶1或2 (IDH1/2)突变的难治性AML的治疗。Inotuzumab ozogamicin和blinatumumab是治疗难治性b细胞急性淋巴母细胞白血病的必需药物。这些抗体可以根据疾病状态来选择,例如可测量的残留疾病。对于难治性弥漫性大b细胞淋巴瘤,治疗方案根据细胞来源不同而不同。最后,准确的病理表型是优化难治性外周t细胞淋巴瘤治疗必不可少的第一步。虽然新的个性化方法改善了这些患者的临床结果,但在大多数情况下,巩固造血干细胞移植具有至关重要的作用。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
9
期刊介绍: Expert Review of Precision Medicine and Drug Development publishes primarily review articles covering the development and clinical application of medicine to be used in a personalized therapy setting; in addition, the journal also publishes original research and commentary-style articles. In an era where medicine is recognizing that a one-size-fits-all approach is not always appropriate, it has become necessary to identify patients responsive to treatments and treat patient populations using a tailored approach. Areas covered include: Development and application of drugs targeted to specific genotypes and populations, as well as advanced diagnostic technologies and significant biomarkers that aid in this. Clinical trials and case studies within personalized therapy and drug development. Screening, prediction and prevention of disease, prediction of adverse events, treatment monitoring, effects of metabolomics and microbiomics on treatment. Secondary population research, genome-wide association studies, disease–gene association studies, personal genome technologies. Ethical and cost–benefit issues, the impact to healthcare and business infrastructure, and regulatory issues.
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