Dimopoulos Meletios A, Eleutherakis-Papaiakovou Vagelis
Department of Clinical Therapeutics, University of Athens School of Medicine, Athens, Greece.
Am J Med. 2004 Oct 1;117(7):508-15. doi: 10.1016/j.amjmed.2004.03.040.
Thalidomide, a glutamic acid derivative, was withdrawn from clinical use in 1962 due to its severe teratogenic effects. Its recent reinstitution in clinical practice was related to its benefits in leprosy and multiple myeloma. Moreover, the antiangiogenic and immunomodulatory properties of thalidomide have led to its evaluation in several malignant diseases, including myelofibrosis, renal cell cancer, prostate cancer, and Kaposi sarcoma. However, thalidomide use is associated with several side effects: somnolence and constipation are the most common, while deep vein thrombosis and peripheral neuropathy are the most serious. A combination of thalidomide with steroids or chemotherapy is being evaluated in several phase 2 studies. While it is not yet clear whether these combinations will enhance efficacy, they appear to increase the toxicity of thalidomide, and thalidomide analogs are being developed to minimize this toxicity. Ongoing studies will clarify the potential advantages of these agents in the treatment of neoplastic diseases.
沙利度胺是一种谷氨酸衍生物,因其严重的致畸作用于1962年被停止临床使用。它最近重新应用于临床实践与它在麻风病和多发性骨髓瘤治疗中的益处有关。此外,沙利度胺的抗血管生成和免疫调节特性已使其在多种恶性疾病中得到评估,包括骨髓纤维化、肾细胞癌、前列腺癌和卡波西肉瘤。然而,使用沙利度胺会伴随多种副作用:嗜睡和便秘最为常见,而深静脉血栓形成和周围神经病变最为严重。在多项2期研究中正在评估沙利度胺与类固醇或化疗的联合应用。虽然目前尚不清楚这些联合应用是否会提高疗效,但它们似乎会增加沙利度胺的毒性,因此正在研发沙利度胺类似物以尽量减少这种毒性。正在进行的研究将阐明这些药物在肿瘤疾病治疗中的潜在优势。