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The rate of in vitro fludarabine-induced peripheral blood and bone marrow cell apoptosis may predict the chemotherapy outcome in patients with chronic lymphocytic leukemia

机译:氟达拉滨体外诱导的外周血和骨髓细胞凋亡的发生率可能预示着慢性淋巴细胞白血病患者的化疗结果

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摘要

The problem of drug sensitivity and predicting the outcome of chemotherapy seems to be of great importance in hemato-oncological disorders. There are some factors that can help to predict effects of chemotherapy in chronic lymphocytic leukemia (CLL), such as presence of del17p, del11q, or TP53 gene mutations, which result in resistance to purine analogues and alkylating drugs. Despite the new therapeutic options introduced recently, purine analogues in combination with cyclophosphamide and the monoclonal antibody rituximab is still the gold standard for the first-line treatment of fit patients with CLL. The aim of this study was to assess whether the rate of apoptosis caused by one of purine analogues-fludarabine in cell cultures differs between patients who clinically respond to fludarabine-based chemotherapy and those who do not respond.
机译:在血液肿瘤疾病中,药物敏感性和预测化疗结果的问题似乎非常重要。有一些因素可以帮助预测化学疗法对慢性淋巴细胞性白血病(CLL)的作用,例如del17p,del11q或TP53基因突变的存在,这些突变导致对嘌呤类似物和烷基化药物的耐药性。尽管最近引入了新的治疗选择,嘌呤类似物与环磷酰胺和单克隆抗体利妥昔单抗的结合仍是适合CLL的一线治疗的金标准。这项研究的目的是评估在临床上对基于氟达拉滨的化疗有反应的患者和对化疗无反应的患者中,嘌呤类似物氟达拉滨之一在细胞培养物中引起的凋亡率是否存在差异。

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