Itchins Malinda, Pavlakis Nick
Department of Medical Oncology, Northern Sydney Cancer Centre, Royal North Shore Hospital, St Leonards, NSW, Australia.
Northern Clinical School, University of Sydney, Kolling Institute, St Leonards, NSW, Australia.
Front Oncol. 2022 Aug 8;12:959637. doi: 10.3389/fonc.2022.959637. eCollection 2022.
Since the discovery 15 years ago, we have seen a quantum leap in the treatment and survival for individuals diagnosed with ALK+ lung cancers. Unfortunately however, for most, the diagnosis is made in an incurable circumstance given the late presentation of symptoms. Through a revolutionary wave of therapeutics, individuals may remarkably live over a decade, however many fall short of this milestone, as the molecular profile of this disease is very heterogeneous, reflected in variable survival outcomes. Despite a significant improval in survival and quality of life with ALK-inhibitor monotherapies, now available across multiple-generations, drug resistance and disease relapse remains inevitable, and treatment is offered in an empiric, stepwise, non personalised biomarker informed fashion. A proposed future focus to treating ALK to improve the chronicity of this disease and even promote cure, is to deliver a personalised dynamic approach to care, with rational combinations of drugs in conjunction with local ablative therapies to prevent and constantly proactively alter clonal selection. Such an approach would be informed by precision imaging with MRI-brain and FDG-PETs sequentially, and by regular plasma sampling including for circulating tumour DNA sequencing with personalised therapeutic switches occurring prior to the emergence of radiological and clinical relapse. Such an approach to care will require a complete paradigm shift in the way we approach the treatment of advanced cancer, however evidence to date in ALK+ lung cancers, support this new frontier of investigation.
自15年前发现以来,我们目睹了ALK阳性肺癌患者在治疗和生存方面的巨大飞跃。然而不幸的是,由于症状出现较晚,大多数患者在确诊时已处于无法治愈的阶段。通过一波革命性的治疗手段,患者可能显著存活超过十年,但仍有许多人未能达到这一里程碑,因为这种疾病的分子特征非常异质,体现在不同的生存结果上。尽管多代ALK抑制剂单药治疗在生存和生活质量方面有了显著改善,但耐药性和疾病复发仍然不可避免,治疗是以经验性、逐步、非个性化的生物标志物指导方式进行的。未来治疗ALK以改善这种疾病的慢性病程甚至促进治愈的一个重点是采用个性化的动态护理方法,合理联合药物并结合局部消融治疗,以预防并不断主动改变克隆选择。这种方法将通过依次使用MRI脑成像和FDG-PET进行精准成像,以及定期进行血浆采样(包括用于循环肿瘤DNA测序)来指导,在影像学和临床复发出现之前进行个性化的治疗转换。这种护理方法将需要我们在治疗晚期癌症的方式上进行彻底的范式转变,然而迄今为止ALK阳性肺癌的证据支持了这一新的研究前沿。