替法尼对血液恶性肿瘤的药物治疗

I. Kotsianidis, Evangelia Nakou, Irene Bouchliou
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引用次数: 0

摘要

对癌症细胞过程的阐明已经彻底改变了肿瘤药物的开发,导致了从非特异性化疗到选择性靶向致瘤性信号转导途径的转变。法尼基转移酶抑制剂(FTIs)靶向需要戊酰化才能发挥功能的蛋白质,从而抑制对细胞增殖和存活至关重要的各种分子靶标。Tipifarnib (R115777, Zarnestra®)是一种有效的特异性法尼基转移酶抑制剂,在临床前模型中可以获得很强的肿瘤生长抑制作用。作为单一药物,tipifarnib已被证明对几种血液系统恶性肿瘤有活性,即急性髓性白血病、骨髓增生异常综合征、慢性髓性白血病和多发性骨髓瘤。然而,考虑到血液肿瘤发病机制中涉及的分子畸变的复杂性,用替法尼单药治疗不太可能作为一种独立的治疗方法。事实上,通过将tipfarnib与其他抗癌药物联合使用,已经取得了更好的结果,而鉴定反应的分子预测因子的首次努力正在报告有趣的结果。正在进行的试验预计将确定蒂法尼在血液系统恶性肿瘤治疗中的确切作用。
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Pharmacotherapy of Hematologic Malignancies with Tipifarnib
The illumination of cellular processes in cancer has revolutionized oncology drug development leading to a shift from non-specific chemotherapy to the selective targeting of tumorigenic signal transduction pathways. Farnesyltransferase inhibitors (FTIs) target proteins needing prenylation for functioning, thus inhibiting a wide variety of molecular targets crucial for cell proliferation and survival. Tipifarnib (R115777, Zarnestra®), a potent and specific inhibitor of Farnesyltransferase, can attain strong inhibition of tumor growth in preclinical models. As a single agent, tipifarnib has demonstrated activity in several hematologic malignancies, namely acute myeloid leukemia, myelodysplastic syndrome, chronic myeloid leukemia and multiple myeloma. However, considering the complexity of the molecular aberrations implicated in the pathogenesis of hematologic neoplasms, it is rather unlikely that monotherapy with tipifarnib will serve as a stand-alone treatment approach. Indeed, improved results have been achieved by combining tipifarnib with other anticancer agents, whereas the first efforts for the identification of molecular predictors of response are reporting intriguing results. Ongoing trials are anticipated to define the exact role of tipifarnib in the treatment of hematologic malignancies.
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