Johnson Melissa D, Perfect John R
Division of Infectious Diseases and International Health, Duke University Medical Center, Box 3306 DUMC, Durham, NC 27710, USA.
Expert Opin Pharmacother. 2003 May;4(5):807-23. doi: 10.1517/14656566.4.5.807.
Caspofungin (Cancidas, Merck & Co. Inc.) is the first echinocandin antifungal agent to gain FDA-approval for use in the US. It has excellent clinical activity against Candida spp. and Aspergillus spp. but lacks significant activity against Cryptococcus neoformans. Caspofungin may have some activity against dimorphic fungi such as Histoplasma capsulatum and Coccidioides immitis, but no clinical data is available for treatment of these infections. Caspofungin has demonstrated poor activity against most filamentous fungi in vitro. Several clinical trials have demonstrated its efficacy in the treatment of oropharyngeal, oesophageal and invasive candidiasis, as well as invasive aspergillosis. As a result of caspofungin's unique mechanism of action, and the high morbidity and mortality of invasive fungal infections, there is considerable interest in using this new antifungal agent as part of a combination antifungal therapy. In vitro studies and small case series indicate that caspofungin does not appear to be antagonistic when combined with other antifungals, such as itraconazole, voriconazole or amphotericin B against Aspergillus spp. Caspofungin exerts concentration-dependent killing effects in many different in vitro and animal models of disseminated fungal infection. The usual daily dose is 50 mg/day i.v. following a 70 mg i.v. loading dose. However, higher caspofungin doses have been safely administered and up to 70 mg/day can be administered for patients who fail to respond to lower doses. Caspofungin has an excellent safety profile with reduced toxicities, compared to other licensed antifungal agents. Fever, thrombophlebitis, headache and liver enzyme elevations were the most common drug-related side effects reported in clinical trials so far. Additional data are needed to document its safety in long-term use, and with higher doses in patients with invasive fungal infections. Caspofungin is a promising agent as first-line therapy for invasive candidiasis, and as salvage therapy for invasive aspergillosis. However, more clinical data are needed to define its role as primary therapy for invasive aspergillosis, and its role in combination antifungal therapy.
卡泊芬净(科赛斯,默克公司)是首个获美国食品药品监督管理局(FDA)批准在美国使用的棘白菌素类抗真菌药物。它对念珠菌属和曲霉菌属具有出色的临床活性,但对新型隐球菌缺乏显著活性。卡泊芬净可能对双相真菌如荚膜组织胞浆菌和粗球孢子菌有一定活性,但尚无用于治疗这些感染的临床数据。卡泊芬净在体外对大多数丝状真菌显示出较差的活性。多项临床试验已证明其在治疗口咽、食管和侵袭性念珠菌病以及侵袭性曲霉病方面的疗效。由于卡泊芬净独特的作用机制,以及侵袭性真菌感染的高发病率和死亡率,人们对将这种新型抗真菌药物作为联合抗真菌治疗的一部分有着浓厚兴趣。体外研究和小病例系列表明,卡泊芬净与其他抗真菌药物如伊曲康唑、伏立康唑或两性霉素B联合用于曲霉菌属时似乎并无拮抗作用。在许多不同的播散性真菌感染体外和动物模型中,卡泊芬净发挥浓度依赖性杀菌作用。通常的每日剂量是静脉注射70mg负荷剂量后,50mg/天。然而,已安全给予更高剂量的卡泊芬净,对于低剂量治疗无反应的患者,可给予高达70mg/天的剂量。与其他已获许可的抗真菌药物相比,卡泊芬净具有出色的安全性,毒性降低。发热、血栓性静脉炎、头痛和肝酶升高是迄今为止临床试验中报告的最常见的药物相关副作用。需要更多数据来证明其长期使用的安全性,以及在侵袭性真菌感染患者中高剂量使用的安全性。卡泊芬净作为侵袭性念珠菌病的一线治疗药物以及侵袭性曲霉病的挽救治疗药物是一种有前景的药物。然而,需要更多临床数据来确定其作为侵袭性曲霉病一线治疗的作用,以及其在联合抗真菌治疗中的作用。