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黑色素瘤的辅助治疗。

Adjuvant treatment of melanoma.

作者信息

Moreno Nogueira J A, Valero Arbizu M, Pérez Temprano R

机构信息

Department of Oncology, Virgen del Rocio University Hospital, Royal Academy of Medicine, 41001 Seville, Spain.

出版信息

ISRN Dermatol. 2013;2013:545631. doi: 10.1155/2013/545631. Epub 2013 Feb 17.

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.

摘要

黑色素瘤占所有皮肤恶性肿瘤的4%,却导致了80%的皮肤癌死亡。虽然早期患者可通过手术切除成功治疗,但转移性黑色素瘤的预后很差。在黑色素瘤中已鉴定出几种致癌基因,如BRAF、NRAS、c-Kit以及GNA11、GNAQ,它们均能激活丝裂原活化蛋白激酶(MAPK)通路,该通路可增加细胞增殖并促进血管生成,不过NRAS和c-Kit也会激活磷脂酰肌醇-3激酶(PI3)通路,其中BRAF是更常见的被激活的致癌基因。对于局限性原发性皮肤黑色素瘤,若累及区域淋巴结,治疗选择是手术加淋巴结清扫术。除手术外进行治疗的依据是高危黑色素瘤预后较差,复发指数为50%-80%。高危组患者应评估是否采用高剂量干扰素-α 2b进行辅助治疗,因为这是唯一显示能显著改善无病生存期并可能提高总生存期的治疗方法。未来,如果我们想改变黑色素瘤的自然病程,就必须分析针对特定靶点的所有这些治疗可能性,可能在辅助治疗中联合化疗和/或干扰素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff3/3588212/400dc3ff9444/ISRN.DERMATOLOGY2013-545631.001.jpg

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