含氟达拉滨方案治疗血液病癌症的未来前景。

Peter Hillmen
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引用次数: 5

摘要

在过去十年中,对疾病生物学和治疗方法的理解的发展未能改变许多人类血液系统恶性肿瘤的自然历史,包括慢性淋巴细胞白血病(CLL)。尽管对这些癌症的分子基础和表型特征有了更好的认识,疾病分类和预后有所改善,发现了更有效的细胞毒性和生物制剂,但这些疾病在很大程度上仍然无法治愈。20世纪80年代,一类新的细胞毒性药物,即嘌呤类似物的发展,预示着治疗惰性淋巴样白血病和淋巴瘤的新乐观时期。最近,选择性靶向细胞表面蛋白的单克隆抗体和靶向细胞周期或凋亡途径的药物已经被开发出来,它们单独或联合使用有望对这些疾病的治疗产生重大影响。其中,抗cd52抗体阿仑妥珠单抗和抗cd20抗体利妥昔单抗已被证明最有潜力治疗CLL。此外,由于与传统细胞毒性药物相比,它们的作用方式不同,在早期试验中,涉及氟达拉滨和这些抗体的联合治疗方案显示出特别的希望。这些联合治疗的令人鼓舞的发现正在将治疗的意图从缓解转向治愈。本文综述了目前和未来含氟达拉滨方法的治疗应用。讨论的策略包括氟达拉滨与阿仑单抗、利妥昔单抗或其他单克隆抗体联合使用,以及氟达拉滨与更多实验性药物(如反义寡核苷酸、免疫毒素或放射免疫偶联物)联合使用的潜在益处。氟达拉滨加阿仑单抗的成功应用,或氟达拉滨与其他细胞毒性药物的联合,作为干细胞移植技术的准备方案也被涵盖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future prospects for fludarabine-containing regimens in the treatment of hematological cancers.

Developments in the understanding of disease biology and in therapeutic approaches during the last decade have failed to alter the natural history of many human hematological malignancies, including chronic lymphocytic leukemia (CLL). Despite better appreciation of the molecular foundations and phenotypic characteristics of these cancers, improvements to disease classification and prognosis, and the discovery of more effective cytotoxic and biological agents, these disorders remain largely incurable. The development of a new class of cytotoxic agents in the 1980 s, namely the purine analogs, heralded a period of renewed optimism in the treatment of indolent lymphoid leukemias and lymphomas. More recently, monoclonal antibodies that selectively target cell-surface proteins, and agents that target cell-cycle or apoptotic pathways, have been developed and their use alone or in combination promise to have a major impact on the treatment of these conditions. Of these, the anti-CD52 antibody alemtuzumab and the anti-CD20 antibody rituximab have demonstrated the most potential for the treatment of CLL. Further, because of their different mode of action in comparison to conventional cytotoxic agents, combination regimens involving fludarabine and these antibodies are showing particular promise in early trials. The encouraging findings with these combination therapies are moving the intent of therapy from palliation towards cure. This paper reviews the therapeutic application of present and future fludarabine-containing approaches. The strategies that are discussed include fludarabine given with alemtuzumab, rituximab, or other monoclonal antibodies, and the potential benefits of combining fludarabine with more experimental agents such as antisense oligonucleotides, immunotoxins, or radioimmunoconjugates. The successful application of fludarabine plus alemtuzumab, or fludarabine in combination with other cytotoxic agents, as preparative regimens for stem cell transplantation techniques is also covered.

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