Wadler S, Schwartz E L
Department of Oncology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY 10467.
Semin Oncol. 1992 Apr;19(2 Suppl 3):45-8.
The interferons (IFNs) were identified as novel, endogenous antiviral agents in 1957. Shortly thereafter, antiproliferative and immunostimulatory activities were identified for these compounds. Based on these observations, partially purified IFNs entered clinical trials in the 1970s and recombinant IFNs in 1980. IFNs have demonstrated important clinical activity in hairy cell leukemia, melanoma, renal cell carcinoma, and Kaposi's sarcoma as monotherapy. Shortly after their introduction into clinical trials, however, preclinical studies demonstrated synergistic interactions between IFNs and cytotoxic drugs. Numerous preclinical trials have demonstrated a broad spectrum of interactions between IFNs and at least 20 cytotoxic agents both in vitro and in vivo. Early clinical trials suggest a benefit to combinations of fluorouracil and recombinant interferon alfa in refractory gastrointestinal malignancies. Combinations of IFNs and cytotoxic agents deserve further investigations; however, different principles apply for combining IFNs with cytotoxic drugs than for the design of combination chemotherapy regimens.
1957年,干扰素被确认为新型内源性抗病毒剂。此后不久,人们发现这些化合物具有抗增殖和免疫刺激活性。基于这些观察结果,部分纯化的干扰素于20世纪70年代进入临床试验,重组干扰素于1980年进入临床试验。干扰素作为单一疗法,已在毛细胞白血病、黑色素瘤、肾细胞癌和卡波西肉瘤中显示出重要的临床活性。然而,在它们被引入临床试验后不久,临床前研究表明干扰素与细胞毒性药物之间存在协同相互作用。大量临床前试验已证明,干扰素与至少20种细胞毒性药物在体外和体内均存在广泛的相互作用。早期临床试验表明,氟尿嘧啶与重组干扰素α联合使用对难治性胃肠道恶性肿瘤有益。干扰素与细胞毒性药物的联合应用值得进一步研究;然而,将干扰素与细胞毒性药物联合使用的原则与联合化疗方案的设计原则不同。