Jankovic Radmila, J Goncalves Helena, Cavic Milena, Clemente Carla, Lind Michael, Murillo Carrasco Alexis, Nadifi Selama, Khyatti Meriem, Adebambo Tumininu, Egamberdiev Dilshod
Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
J BUON. 2019 Jan-Feb;24(1):11-19.
The management of advanced lung cancer has evolved tremendously over the past two decades. Increasing understanding of the molecular changes that drive tumor progression has transformed the treatment of this disease. Nevertheless, various countries differ in the degree of implementation of genetic tests and the availability of innovative drugs. The LungCARD consortium created a questionnaire to collect information about the local research and clinical practices related to lung cancer diagnosis and therapy.
A survey composed of 37 questions related to specific lung cancer pharmacogenomics and therapy, was distributed among 18 countries.
All together 36 responses were gathered, answered mainly by clinicians. The majority attends 50-200 cancer cases per month, 20-50% of all cancer cases are lung cancer patients, and more than 80% are with non-small-cell lung cancer (NSCLC). Targeted therapy is applied to 50% on average of all NSCLC patients. Forty five percent of participating medical oncologists are treating their patients with immunotherapy. More than 90% of the respondents are guided by results of genetic tests in introducing targeted treatment. As expected, the majority orders EGFR gene testing (85%), followed by ALK (58%) and KRAS testing (32%). Almost all (96%) agreed that more biomarkers should be included in routine genetic testing (ROS1, anti-PDL1, KRAS, MET, HER2, BRAF...), and that blood test is useful in pharmacogenomic testing.
There is a great variation between countries with respect to all discussed topics. However, the majority recognized a necessity of introducing next generation sequencing (NGS)-based diagnostics and potential of testing from blood. The biggest problem in the treatment of NSCLC is still an access to innovative drugs.
在过去二十年中,晚期肺癌的管理发生了巨大变化。对驱动肿瘤进展的分子变化的深入了解改变了这种疾病的治疗方式。然而,各国在基因检测的实施程度和创新药物的可及性方面存在差异。LungCARD联盟创建了一份问卷,以收集有关肺癌诊断和治疗的当地研究及临床实践的信息。
一项由37个与特定肺癌药物基因组学和治疗相关问题组成的调查在18个国家进行了分发。
共收集到36份回复,主要由临床医生回答。大多数人每月诊治50 - 200例癌症病例,所有癌症病例中有20 - 50%是肺癌患者,超过80%是非小细胞肺癌(NSCLC)患者。平均而言,所有NSCLC患者中有50%接受了靶向治疗。45%的参与肿瘤内科医生正在用免疫疗法治疗他们的患者。超过90%的受访者在引入靶向治疗时以基因检测结果为指导。不出所料,大多数人进行EGFR基因检测(85%),其次是ALK检测(58%)和KRAS检测(32%)。几乎所有(96%)人都同意应将更多生物标志物纳入常规基因检测(ROS1、抗PDL1、KRAS、MET、HER2、BRAF……),并且血液检测在药物基因组学检测中很有用。
在所讨论的所有主题方面,各国之间存在很大差异。然而,大多数人认识到引入基于下一代测序(NGS)的诊断方法的必要性以及血液检测的潜力。NSCLC治疗中最大的问题仍然是获得创新药物。