Adjuvant treatment of melanoma.

ISRN Dermatology Pub Date : 2013-01-01 Epub Date: 2013-02-17 DOI:10.1155/2013/545631
J A Moreno Nogueira, M Valero Arbizu, R Pérez Temprano
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引用次数: 8

Abstract

Melanomas represent 4% of all malignant tumors of the skin, yet account for 80% of deaths from skin cancer.While in the early stages patients can be successfully treated with surgical resection, metastatic melanoma prognosis is dismal. Several oncogenes have been identified in melanoma as BRAF, NRAS, c-Kit, and GNA11 GNAQ, each capable of activating MAPK pathway that increases cell proliferation and promotes angiogenesis, although NRAS and c-Kit also activate PI3 kinase pathway, including being more commonly BRAF activated oncogene. The treatment of choice for localised primary cutaneous melanoma is surgery plus lymphadenectomy if regional lymph nodes are involved. The justification for treatment in addition to surgery is based on the poor prognosis for high risk melanomas with a relapse index of 50-80%. Patients included in the high risk group should be assessed for adjuvant treatment with high doses of Interferon- α 2b, as it is the only treatment shown to significantly improve disease free and possibly global survival. In the future we will have to analyze all these therapeutic possibilities on specific targets, probably associated with chemotherapy and/or interferon in the adjuvant treatment, if we want to change the natural history of melanomas.

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黑色素瘤的辅助治疗。
黑色素瘤占所有皮肤恶性肿瘤的4%,但却占癌症死亡人数的80%。虽然在早期阶段,患者可以通过手术切除成功治疗,但转移性黑色素瘤的预后却令人沮丧。黑色素瘤中的几种致癌基因已被鉴定为BRAF、NRAS、c-Kit和GNA11-GNAQ,每种都能够激活MAPK途径,从而增加细胞增殖并促进血管生成,尽管NRAS和c-Kit也激活PI3激酶途径,包括更常见的BRAF激活的致癌基因。局部原发性皮肤黑色素瘤的治疗选择是手术加淋巴结切除术(如果涉及区域淋巴结)。除手术外进行治疗的理由是,复发指数为50-80%的高危黑色素瘤预后不佳。应评估高危组患者是否接受高剂量干扰素-α2b的辅助治疗,因为这是唯一一种能显著提高无病生存率和可能的全球生存率的治疗方法。未来,如果我们想改变黑色素瘤的自然史,我们必须分析所有这些针对特定靶点的治疗可能性,可能与辅助治疗中的化疗和/或干扰素有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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