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Gallium nitrate for the treatment of non-Hodgkin's lymphoma.

机译:硝酸镓用于治疗非霍奇金淋巴瘤。

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Mortality from non-Hodgkin's lymphoma (NHL) is high, thus defining the need for additional therapeutic agents for this disease. Gallium nitrate is a metal compound that is presently approved for the treatment of hypercalcaemia associated with malignancy. In clinical trials first conducted over two decades ago, this drug was found to have antineoplastic activity in NHL. However, its development as an antineoplastic agent for the treatment of NHL was never rigorously pursued. Gallium has unique mechanisms of action that include its binding to transferrin in the circulation and targeting transferrin receptors present on lymphoma cells. As it shares chemical properties with iron, gallium can disrupt critical steps in iron homeostasis that are essential for tumour cell viability and growth and can inhibit the iron-dependent activity of ribonucleotide reductase. The drug may also target other cellular processes unrelated to iron. Phase I/II studies have shown that gallium nitrate displays the most efficacy and lowest toxicity in NHL when administered as a continuous intravenous infusion, producing response rates of 43% in patients with relapsed or refractory NHL. It does not suppress the white blood cells or platelets and does not share cross-resistance with other chemotherapeutic drugs. These characteristics make it particularly attractive for the treatment of myelosuppressed patients and for incorporation into combination therapy. Multi-institutional Phase II clinical trials are in progress to evaluate gallium nitrate as a single agent or in combination. These studies will help define its role in the current treatment of NHL.
机译:非霍奇金淋巴瘤(NHL)造成的死亡率很高,因此需要针对该疾病的其他治疗药物。硝酸镓是一种金属化合物,目前被批准用于治疗与恶性肿瘤有关的高钙血症。在二十多年前首次进行的临床试验中,发现该药物在NHL中具有抗肿瘤活性。然而,从未严格追求将其开发为用于治疗NHL的抗肿瘤药。镓具有独特的作用机制,包括与循环中的转铁蛋白结合以及靶向淋巴瘤细胞上存在的转铁蛋白受体。镓与铁具有相同的化学性质,因此它可以破坏铁稳态的关键步骤,这对于肿瘤细胞的生存能力和生长至关重要,并且可以抑制核糖核苷酸还原酶的铁依赖性活性。该药物还可靶向与铁无关的其他细胞过程。 I / II期研究表明,以连续静脉滴注方式给药时,硝酸镓在NHL中显示出最高的功效和最低的毒性,对于复发性或难治性NHL患者,其应答率达到43%。它不抑制白细胞或血小板,并且不与其他化学治疗药物共享交叉耐药性。这些特性使其对于骨髓抑制患者的治疗以及与联合疗法的结合特别有吸引力。目前正在进行多机构II期临床试验,以评估硝酸镓作为单药还是联合用药。这些研究将有助于确定其在目前NHL治疗中的作用。

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