Rischke Nikolaj, Kanbach Josephine, Haug Ulrike
Department of Clinical Epidemiology, Leibniz Institute for Prevention Research and Epidemiology - BIPS, Bremen, Germany.
Faculty of Human and Health Sciences, University of Bremen, Bremen, Germany.
Cancer Rep (Hoboken). 2024 Dec;7(12):e70060. doi: 10.1002/cnr2.70060.
There is a lack of real-world data on the use of targeted cancer drugs requiring molecular tumor diagnostics in the treatment of lung cancer in Germany.
We aimed to characterize the use of such drugs in lung cancer patients based on longitudinal analyses.
Using the GePaRD database (claims data from ~20% of the German population) we identified lung cancer patients diagnosed in 2016 based on a previously developed algorithm and followed them until death, end of continuous insurance, or end of 2019. We determined the proportion of patients treated with at least one of the drugs under study (EGFR, ALK, and BRAF inhibitors). We described these patients regarding demographic characteristics, treatment patterns, and overall survival. We included 7833 incident lung cancer patients. Of these, 392 (5%) were treated with one of the drugs under study, the majority (62%) being female. In 314 out of the 392 patients (80%), the first dispensation was an EGFR inhibitor (afatinib: 54%, erlotinib: 33%), and in 72 patients (18%), it was an ALK inhibitor (crizotinib: 90%). The proportion of patients treated with these drugs was 4.8% in West Germany and 6.2% in East Germany. About half of these patients had chemotherapy before targeted therapy. Median overall survival after the first targeted therapy was 22 months.
One twentieth of lung cancer patients diagnosed in 2016 in Germany received at least one EGFR, ALK, or BRAF inhibitor during follow-up. The proportion was higher in East than in West Germany. As the development and availability of new cancer drugs is a dynamic area, regularly updated utilization studies-ideally as cross-country-comparisons-are required.
在德国,缺乏关于使用需要分子肿瘤诊断的靶向抗癌药物治疗肺癌的真实世界数据。
我们旨在通过纵向分析来描述此类药物在肺癌患者中的使用情况。
利用GePaRD数据库(来自约20%德国人口的索赔数据),我们基于先前开发的算法识别出2016年诊断出的肺癌患者,并对他们进行随访直至死亡、连续保险结束或2019年底。我们确定了接受至少一种研究药物(EGFR、ALK和BRAF抑制剂)治疗的患者比例。我们描述了这些患者的人口统计学特征、治疗模式和总生存期。我们纳入了7833例新发肺癌患者。其中,392例(5%)接受了一种研究药物治疗,大多数(62%)为女性。在392例患者中的314例(80%)中,首次配药为EGFR抑制剂(阿法替尼:54%,厄洛替尼:33%),72例患者(18%)为ALK抑制剂(克唑替尼:90%)。西德接受这些药物治疗的患者比例为4.8%,东德为6.2%。这些患者中约一半在靶向治疗前接受过化疗。首次靶向治疗后的中位总生存期为22个月。
2016年在德国诊断出的肺癌患者中有二十分之一在随访期间接受了至少一种EGFR、ALK或BRAF抑制剂治疗。该比例在东德高于西德。由于新抗癌药物的研发和可及性是一个动态领域,需要定期更新利用研究——理想情况下作为跨国比较。