Antonelli Giovanna, Ferraù Francesco
Oncologia Medica, Ospedale San Vincenzo, Taormina.
Recenti Prog Med. 2020 Nov;111(11):33e-37e. doi: 10.1701/3474.34581.
The management of advanced lung cancer has changed in recent years, young and long-surviving patients with chronic diseases and good clinical conditions are frequently observed. These patients need complex, integrated and personalized treatments. The possibility of obtaining more information about the genomic profile would allow the identification of patients who could benefit from chemotherapy rather than immunotherapy or molecular target therapies. Below is the case of a 44-year-old man, ECOG PS 0, with stage IV lung cancer. This clinical history confirms the importance of a personalized approach. The patient, with non-oncogene addicted lung adenocarcinoma, achieves a good clinical-instrumental response after a first line of treatment, followed by a long maintenance phase for a total of 52 weeks. Upon progression, the patient maintains excellent clinical conditions over time, and three additional lines of therapy are carried out. At the end of this sequence, we have proposed a genomic profiling test on a tissue sample of the disease (next generation sequencing - NGS). The study, which also included the state of microsatellites and tumour mutational burden, identified the genetic alteration ATM - Q2762fs*6 (ataxia telangiectasia mutated, ATM) and for this reason we have administered niraparib for off-label use. Although this is not a standard clinical practice context, the case presented can be considered an example of a future strategy in which the ab initio identification of the rare genetic alteration, driver for tumour disease, could represent the first step in the diagnostic-therapeutic process. By improving knowledge on genetic alterations and identifying the most influential alterations for each single solid tumour, it will be possible to identify the most effective therapy, probably with even lower costs in terms of overall patient management.
近年来,晚期肺癌的治疗方式发生了变化,经常能看到患有慢性病且临床状况良好的年轻且长期存活的患者。这些患者需要复杂、综合且个性化的治疗。获取更多关于基因组图谱信息的可能性,将有助于识别那些可能从化疗而非免疫疗法或分子靶向疗法中获益的患者。以下是一名44岁男性患者的病例,其东部肿瘤协作组(ECOG)体能状态评分为0,患有IV期肺癌。该临床病例证实了个性化治疗方法的重要性。这名患有非癌基因成瘾性肺腺癌的患者,在一线治疗后取得了良好的临床影像学反应,随后进入了长达52周的长期维持治疗阶段。病情进展后,该患者长期保持着良好的临床状况,并接受了另外三线治疗。在这一系列治疗结束时,我们建议对疾病的组织样本进行基因组图谱检测(二代测序 - NGS)。该研究还包括微卫星状态和肿瘤突变负荷,结果发现了基因改变ATM - Q2762fs*6(共济失调毛细血管扩张症突变基因,ATM),因此我们给予了尼拉帕利进行非标签用药。尽管这并非标准的临床实践情况,但所呈现的病例可被视为未来一种策略的示例,即从一开始就识别出罕见的基因改变,也就是肿瘤疾病的驱动因素,这可能代表着诊断 - 治疗过程的第一步。通过增进对基因改变的了解,并识别出每种实体肿瘤中最具影响力的改变,将有可能确定最有效的治疗方法,从总体患者管理的角度来看,甚至可能降低成本。