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Survival of advanced melanoma patients treated with immunotherapy and targeted therapy: A real-world study

机译:接受免疫治疗和靶向治疗的晚期黑色素瘤患者的生存率:一项真实世界研究

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Introduction: We aimed to examine the survival outcomes plus patient and treatment characteristics of advanced melanoma patients treated with first-line immunotherapy (IT), targeted therapy (TT), and chemotherapy (CTH) and compare findings with information from pivotal trials for each therapy.Materials and Methods: We retrospectively reviewed the use of systematic IT, TT and CTH therapies in melanoma patients in four Queensland public hospitals. We estimated median duration of overall survival (OS) and survival rates (6 months, 1, and 2 years) using Kaplan-Meier methods. We compared our findings to those of clinical trials. Results: Five hundred three patients who met the inclusion criteria were divided into three groups based on the first-line treatment: IT 232; TT 157; and CTH 114. OS was 18 months with IT (95 Cl 13, 22); 12 months with TT (95 Cl 8, 15); and 5 months with CTH (95 Cl 5, 6). The demographic characteristics, treatment protocols, and durations for IT and TT were generally consistent with trials but fewer patients in our study had subsequent therapy than in the trials. The OS in our study was slightly lower than the OS reported in trials.Conclusion: The OS of novel cancer therapy in the real world was lower than seen in trials but is expected given these are patients who have a poorer prognosis. A future study could investigate the impact of prognostic factors on survival in the longer term. This study provides evidence that we can use routinely collected real-world data to evaluate the effectiveness of checkpoint and kinase inhibitors in patients with advanced melanoma.
机译:简介: 我们旨在检查接受一线免疫治疗 (IT)、靶向治疗 (TT) 和化疗 (CTH) 的晚期黑色素瘤患者的生存结局以及患者和治疗特征,并将结果与每种治疗的关键试验信息进行比较。材料和方法: 我们回顾性评价了昆士兰州四家公立医院在黑色素瘤患者中使用系统性 IT、TT 和 CTH 疗法的情况。我们使用Kaplan-Meier方法估计了总生存期(OS)的中位持续时间和生存率(6个月、1年和2年)。我们将我们的研究结果与临床试验的结果进行了比较。结果:符合纳入标准的503例患者按一线治疗分为3组:IT 232;TT 157;和 CTH 114。使用 IT 的 OS 为 18 个月 (95% Cl 13, 22);TT 12 个月(95% Cl 8、15);和 CTH 5 个月 (95% Cl 5, 6)。IT和TT的人口统计学特征、治疗方案和持续时间与试验基本一致,但与试验相比,我们研究中接受后续治疗的患者更少。我们研究中的OS略低于试验中报告的OS。结论:在现实世界中,新型癌症治疗的OS低于试验中观察到的,但鉴于这些患者的预后较差,这是预期的。未来的研究可以调查预后因素对长期生存的影响。这项研究提供了证据,表明我们可以使用常规收集的真实世界数据来评估检查点和激酶抑制剂对晚期黑色素瘤患者的有效性。

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