Lugović Liborija, Situm Mirna, Kos Liborka
University Department of Dermatology and Venereology Sestre Milosrdnice University Hospital, Vinogradska c. 29, HR-10000 Zagreb, Croatia.
Acta Dermatovenerol Croat. 2005;13(1):36-43.
As the incidence and already high mortality rates of malignant melanoma have been steadily increasing in recent decades, the early detection and excision of malignant melanoma have imposed as the most important task. Staging of malignant melanoma is determined according to the level of invasion (Clark level) and vertical thickness (Breslow scale). Besides operative therapy, which is the only effective treatment for malignant melanoma, postoperative adjuvant chemotherapy, immunotherapy, radiotherapy, and biologic therapy also are of great importance. In recent years, immunologic strategies including tumor vaccine and adjuvant therapy with interferon-alfa have been attempted to improve survival of patients with more advanced malignant melanoma. A recent melanoma research has focused on target therapy such as immunotherapy (vaccines, monoclonal antibodies, dendritic cells) and gene therapy. Genetic immunization has become an attractive strategy for the development of melanoma vaccines, because a number of antigens recognized by cellular components of the immune system have been identified at the molecular level. Numerous chemotherapeutic agents have shown activity in the treatment of metastatic malignant melanoma, such as dacarbazine (dimethyl triazene imidazole carboxamide); other agents have been used, however, with less success. However, a very modest effect was recorded in advanced malignant melanoma. There are many experimental trials using combined therapy for malignant melanoma, including chemotherapy (dimethyl triazene imidazole carboxamide) and biologic therapy (interleukin (IL)-2, interferon (IFN)-gamma, IFN-alfa). The results obtained open particularly interesting prospects in the field of malignant melanoma with high relevance for its development and progression. Molecular therapeutics and vaccine development will probably be an important focus for the future melanoma treatment.
近几十年来,恶性黑色素瘤的发病率和已然很高的死亡率一直在稳步上升,因此早期发现和切除恶性黑色素瘤已成为最重要的任务。恶性黑色素瘤的分期是根据浸润水平(克拉克分级)和垂直厚度( Breslow 量表)来确定的。除了手术治疗(这是恶性黑色素瘤唯一有效的治疗方法)外,术后辅助化疗、免疫治疗、放疗和生物治疗也非常重要。近年来,人们尝试了包括肿瘤疫苗和干扰素 -α 辅助治疗在内的免疫策略,以提高晚期恶性黑色素瘤患者的生存率。最近的黑色素瘤研究集中在免疫治疗(疫苗、单克隆抗体、树突状细胞)和基因治疗等靶向治疗上。基因免疫已成为开发黑色素瘤疫苗的一种有吸引力的策略,因为在分子水平上已经鉴定出许多被免疫系统细胞成分识别的抗原。许多化疗药物已显示出对转移性恶性黑色素瘤的治疗活性,如达卡巴嗪(二甲基三氮烯咪唑甲酰胺);然而,其他药物的使用效果较差。不过,在晚期恶性黑色素瘤中记录到的效果非常有限。有许多针对恶性黑色素瘤的联合治疗的实验性试验,包括化疗(二甲基三氮烯咪唑甲酰胺)和生物治疗(白细胞介素 (IL)-2、干扰素 (IFN)-γ、IFN-α)。所获得的结果为恶性黑色素瘤领域开辟了特别有趣的前景,这与其发展和进展高度相关。分子治疗和疫苗开发可能会成为未来黑色素瘤治疗的一个重要重点。