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A Population-based Study of Survival Impact of New Targeted and Immune-based Therapies for Metastatic or Unresectable Melanoma

机译:一种基于人群的转移或不可切长的黑色素瘤的新靶向和免疫疗法的生存影响研究

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AimsNew targeted drugs and immune therapies reported since 2010 for metastatic or unresectable melanoma (MM) have shown improved survival in randomised trials. We studied the uptake of these new drugs and their impact on population-based survival. Materials and methodsThis was a retrospective, population-based cohort study of all patients treated for MM in Ontario 2007–2015. Provincial administrative sources covering the whole population identified palliative systemic therapy, radiotherapy and metastasis surgery. Temporal trends in utilisation and survival were investigated, as was survival of treatments predefined as ‘new drugs’ (BRAF or MEK inhibitors, anti-CTLA4 and anti-PD-1 antibodies). ResultsWe identified 2793 treated MM patients. First treatment was systemic therapy (46%), radiotherapy (41%) and metastasis surgery (14%). Systemic treatment increased from 53% of patients (2007) to 75% (2015). New drug treatments increased from <6% of known first-line regimens in 2007 to 82% in 2015. One and 2 year overall survival was 28% and 15%, respectively, for all MM 2007–2009, rising to 46% and 35% for 2014–2015 (adjusted hazard ratio 0.56, 95% confidence interval 0.49–0.63,P?
机译:旨在自2010年以来报告的旨在的靶向药物和免疫疗法,用于转移或不可选择的黑素瘤(MM)显示出改善随机试验中的存活。我们研究了这些新药的吸收及其对基于人群的生存的影响。材料和方法是一种回顾性,基于人群的群组,对2007 - 2015年安大略省治疗的所有患者的群体研究。省级行政来源涵盖全人口鉴定了姑息性的全身治疗,放疗和转移手术。研究了利用和存活的时间趋势,作为预定义为“新药”(BRAF或MEK抑制剂,抗CTLA4和抗PD-1抗体)的治疗的存活。结果我们确定了2793名治疗mm患者。第一次治疗是全身治疗(46%),放射疗法(41%)和转移手术(14%)。全身治疗从53%的患者(2007)增加到75%(2015年)。新药物治疗从2007年的6%的6%的6%增加到2015年的82%,总生存率分别为28%和15%,适用于所有MM 2007-2009,上升至46%和35 2014 - 2015年的%(调整后危险比0.56,95%置信区间0.49-0.63,P?<0.0001)。始建生存增益主要观察到最初用全身治疗疗法治疗的病例,该病例是在研究期间使用新药的主导(2年整体生存16%2007-2009与44%-2015;调整后危险比0.46,95 %置信区间0.38-0.56,p?<?0.0001)。在2007 - 2015年的常规实践中,结论新的靶向药物和免疫疗法的免疫疗法在2007 - 2015年的常规实践中得到了显着增加。与临床试验的结果一致,采用与一般人群患者存活的大幅增加有关。

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