医学
背景(考古学)
靶向治疗
间变性淋巴瘤激酶
疾病
克里唑蒂尼
肿瘤科
重症监护医学
精密医学
内科学
癌症
肺癌
病理
生物
古生物学
恶性胸腔积液
作者
Chiara Pisano,Marco De Filippis,Francesca Jacobs,Silvia Novello,Maria Lucia Reale
出处
期刊:Cancers
[MDPI AG]
日期:2022-01-30
卷期号:14 (3): 718-718
被引量:10
标识
DOI:10.3390/cancers14030718
摘要
Personalized treatment based on driver molecular alterations, such as ALK rearrangement, has revolutionized the therapeutic management of advanced oncogene-addicted NSCLC patients. Multiple effective ALK tyrosine kinase inhibitors (TKIs), with the amelioration of the activity at central nervous system level, are now available, leading to substantial prognosis improvement. The exposure to TKIs triggers resistance mechanisms and the sequential administration of other TKIs and chemotherapy is, for the most part, not targeted. In this context, extending the benefit deriving from precision medicine is paramount, above all, when disease progression occurs in a limited number of sites. Retrospective data indicate that, in oligoprogressive disease, targeted therapy beyond progression combined with definitive local treatment of the progressing site(s) is an effective alternative. In these cases, a multidisciplinary approach becomes essential for an integrated treatment strategy, depending on the site of disease progression, in order to improve not only survival, but also quality of life. In this review we provide an updated and comprehensive overview of the main treatment strategies in cases of ALK rearranged oligoprogression, including systemic treatment as well as local therapy, and report a real-world clinical story, with the final aim of identifying the most promising management for this subset of patients.
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