干扰素:辅助治疗的潜在药物:过去的成就和未来的挑战

Eric M. Bonnem
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引用次数: 13

摘要

本文旨在总结目前α干扰素的研究经验,为今后的研究提供方向。α干扰素已被证实或具有潜在活性的领域有四个:抗病毒、癌前病变、辅助和晚期疾病。干扰素α -2b已被证明有活性的三种主要病毒性疾病是慢性病毒性肝炎、获得性免疫缺陷综合征和人乳头状瘤病毒感染。体外研究表明,α干扰素可能抑制某些癌前病变向恶性疾病的转化;例如,阴道上皮内瘤变。在辅助治疗中,生物反应调节剂,如α -干扰素,可能在帮助免疫系统摧毁放疗或化疗后肿瘤体积缩小后残留的肿瘤细胞方面发挥作用。与肿瘤体积大的患者相比,肿瘤体积小的患者(如恶性黑色素瘤、卵巢癌)和早期而非晚期疾病患者(如慢性骨髓性白血病、毛细胞白血病、多发性骨髓瘤、非霍奇金淋巴瘤)的反应率更高。这可能是由于对小肿瘤的疗效或由于免疫佐剂的作用。在晚期疾病中,问题是如何最好地利用干扰素和其他治疗方式之间可能的协同效应。联合治疗的最佳剂量、方案和患者群体尚未确定。本文的主要目的是确定如何最好地利用当前的知识状态来构建α干扰素的未来试验,并确定现有数据是否表明干扰素在初始肿瘤消退后具有辅助作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alpha interferon: The potential drug of adjuvant therapy: Past achievements and future challenges

This paper aims to summarize current experience with alpha interferon and provide direction for future study. There are four areas in which alpha interferon has proven or potential activity: antiviral, premalignant, adjuvant and advanced disease settings. The three main viral diseases in which interferon alfa-2b has been shown to have activity are chronic viral hepatitis, acquired immunodeficiency syndrome, and human papilloma virus infections. In vitro studies suggest that alpha interferon may inhibit transformation of some premalignant conditions into malignant disease; e.g., vaginal intraepithelial neoplasia. In the adjuvant setting, it is possible that a biological response modifier, such as alpha interferon, may have a role in helping the immune system to destroy residual tumour cells following tumour bulk reduction with radiation or chemotherapy. A higher response rate has been seen in patients with small tumour bulk compared to those with large tumour bulk (e.g., malignant melanoma, ovarian carcinoma), and in patients with early, rather than late, disease (e.g., chronic myelogenous leukaemia, hairy cell leukaemia, multiple myeloma, non-Hodgkin's lymphoma). This may be due to efficacy in a small tumour bulk setting or due to an immunoadjuvant role. In advanced disease, the question is how best to exploit the possible synergistic effects between alpha interferon and other therapeutic modalities. The optimum dose, schedule and patient populations for combined treatment have yet to be determined. The major objective of this paper is to determine how best to capitalize upon the current state of knowledge to build for future trials of alpha interferon, and to determine whether the existing data suggest an adjuvant role for interferon after initial tumour regression.

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