Mackiewicz Jacek
Department of Cancer Immunology, Chair of Medical Biotechnology, Poznan University of Medical Sciences, Greater Poland Cancer Centre, Poznan, Poland.
Contemp Oncol (Pozn). 2012;16(5):363-70. doi: 10.5114/wo.2012.31763. Epub 2012 Nov 20.
The incidence of melanoma is increasing steadily both in Poland and worldwide. Until 2010 three drugs were approved for the treatment of metastatic melanoma - dacarbazine (DTIC) in Europe and USA, fotemustine in Europe and interleukin-2 (IL-2) in USA. Approval of ipilimumab and vemurafenib in Europe and USA has changed the standard of care, while the next candidates such as dabrafenib and trametinib have improved survival in phase III studies in metastatic melanoma patients. An encouraging treatment strategy is the combination of dabrafenib and trametinib, evaluated in a phase I/II study with an ongoing phase III trial. Another promising new immune modulating monoclonal antibody (mAb) is anti-PD1 (BMS-936558), tested in an early phase trial in monotherapy or in combination with a multipeptide vaccine in metastatic melanoma patients. Ipilimumab or BRAF inhibitors (vemurafenib, dabrafenib) seem to be active in patients with brain metastases. Intensive research of melanoma vaccines is currently being carried out in a number of countries worldwide. However, no vaccine in the treatment of melanoma has been approved by regulatory authorities so far. Lack of effective therapy in patients with high-risk resected melanoma led to a number of clinical studies of adjuvant treatment. Interferon-α (INF-α) therapy in this setting is still controversial. A dendritic cell-based vaccine in a randomized phase II trial showed a survival benefit over the control group in patients with high-risk resected melanoma. Promising results of long-term survival of advanced resected melanoma patients in a phase II study evaluating the genetically modified tumour vaccine (GMTV) AGI-101 were reported. This review provides an update on clinical strategies used or tested in patients with metastatic melanoma.
在波兰乃至全球,黑色素瘤的发病率都在稳步上升。直到2010年,有三种药物被批准用于治疗转移性黑色素瘤——欧洲和美国的达卡巴嗪(DTIC)、欧洲的福莫司汀以及美国的白细胞介素-2(IL-2)。欧洲和美国批准使用伊匹单抗和维罗非尼改变了治疗标准,而接下来的候选药物如达拉非尼和曲美替尼在转移性黑色素瘤患者的III期研究中提高了生存率。一种令人鼓舞的治疗策略是达拉非尼和曲美替尼联合使用,该联合用药在一项I/II期研究中进行了评估,一项III期试验正在进行。另一种有前景的新型免疫调节单克隆抗体(mAb)是抗PD1(BMS-936558),在转移性黑色素瘤患者的早期试验中进行了单药治疗或与多种肽疫苗联合治疗的测试。伊匹单抗或BRAF抑制剂(维罗非尼、达拉非尼)似乎对脑转移患者有效。目前全球多个国家都在对黑色素瘤疫苗进行深入研究。然而,迄今为止,尚无治疗黑色素瘤的疫苗获得监管机构的批准。高危切除性黑色素瘤患者缺乏有效的治疗方法,导致了多项辅助治疗的临床研究。在这种情况下,干扰素-α(INF-α)治疗仍存在争议。一项基于树突状细胞的疫苗在随机II期试验中显示,高危切除性黑色素瘤患者的生存率优于对照组。在一项评估基因改造肿瘤疫苗(GMTV)AGI-101的II期研究中,报告了晚期切除性黑色素瘤患者长期生存的有前景结果。本综述提供了转移性黑色素瘤患者使用或测试的临床策略的最新情况。