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Novel Approaches to Treatment of Advanced Melanoma: A Review on Targeted Therapy and Immunotherapy

机译:治疗晚期黑色素瘤的新方法:靶向治疗和免疫疗法的综述。

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The incidence of malignant melanoma is increasing. The majority of patients are diagnosed in early stages when the disease is highly curable. However, the more advanced or metastatic cases have always been a challenge for clinicians. The poor prognosis for patients with melanoma is now changing as numerous of promising approaches have appeared recently. The discovery of aberrations of pathways responsible for intracellular signal transduction allowed us to introduce agents specifically targeting the mutated cascades. Numerous clinical studies have been conducted to improve effectiveness of melanoma treatment. From 2011 until now, the U.S. FDA has approved seven novel agents, such as BRAF-inhibitors (vemurafenib 2011, dabrafenib 2013), MEK-inhibitors (trametinib 2013), anti-PD1 antibodies (nivolumab 2014, pembrolizumab 2014), anti-CTLA-4 antibody (ipilimumab 2011), or peginterferon-alfa-2b (2011) intended to be used in most advanced cases of melanoma. Nevertheless, clinicians continue working on new possible methods of treatment as resistance to the novel drugs is a commonly observed problem. This paper is based on latest data published until the end of January 2015.
机译:恶性黑色素瘤的发病率正在增加。大多数患者被诊断为可高度治愈的早期阶段。然而,对于临床医生而言,更晚期或转移性病例一直是挑战。由于最近出现了许多有希望的方法,因此黑色素瘤患者的不良预后正在改变。细胞内信号转导通路异常的发现使我们能够引入特异性针对突变级联的药物。已经进行了许多临床研究以改善黑色素瘤治疗的有效性。从2011年到现在,美国FDA已批准了7种新型药物,例如BRAF抑制剂(vemurafenib 2011,dabrafenib 2013),MEK抑制剂(trametinib 2013),抗PD1抗体(nivolumab 2014,pembrolizumab 2014),抗CTLA -4抗体(ipilimumab 2011)或peginterferon-alfa-2b(2011)用于黑色素瘤的大多数晚期病例。然而,由于对新药的耐药性是普遍观察到的问题,临床医生仍在继续研究新的可能的治疗方法。本文基于截至2015年1月底发布的最新数据。

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