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用于实体瘤的新一代铂类药物。

New-generation platinum agents for solid tumors.

作者信息

Shah Neel, Dizon Don S

机构信息

The Warren Alpert Medical School of Brown University, Providence, RI 02912, USA.

出版信息

Future Oncol. 2009 Feb;5(1):33-42. doi: 10.2217/14796694.5.1.33.

Abstract

Cisplatin was one of the first chemotherapeutic agents to exhibit broad efficacy in solid tumors and it remains among the most widely used agents in the treatment of cancer. Its introduction inspired great efforts to design similarly effective platinum agents that overcome the three main limitations of cisplatin: toxicity, tumor resistance and poor oral bioavailability. However, 40 years after the initial discovery of cisplatin, only two platinum agents have garnered US FDA approval: carboplatin and oxaliplatin. Although hundreds of promising agents were tested in clinical trials during the 1990s, only oxaliplatin made it past clinical development. For a brief period, the economic cost of these unsuccessful efforts retarded further efforts to develop new agents. However, two exciting platinum agents have been brought to Phase III trials: satraplatin in hormone-refractory prostate cancer and picoplatin in small-cell lung cancer. If successful, they may inspire a new effort to bring better-designed platinum agents to market. This article reviews the clinical development of platinum agents to date and speculates on the role of platinum agents in the near future.

摘要

顺铂是最早在实体瘤中展现出广泛疗效的化疗药物之一,至今仍是治疗癌症最常用的药物之一。它的问世促使人们付出巨大努力来设计同样有效的铂类药物,以克服顺铂的三个主要局限性:毒性、肿瘤耐药性和口服生物利用度差。然而,在顺铂首次被发现40年后,仅有两种铂类药物获得了美国食品药品监督管理局(FDA)的批准:卡铂和奥沙利铂。尽管在20世纪90年代有数百种有前景的药物进入临床试验,但只有奥沙利铂通过了临床研发。在一段短暂时期内,这些未成功尝试的经济成本阻碍了进一步开发新药的努力。然而,有两种令人振奋的铂类药物已进入III期试验:用于激素难治性前列腺癌的沙铂和用于小细胞肺癌的匹铂。如果试验成功,它们可能会激发新一轮将设计更优的铂类药物推向市场的努力。本文回顾了迄今为止铂类药物的临床研发情况,并推测了铂类药物在不久的将来所扮演的角色。

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