Local therapies have previously had limited utility in the context of metastatic cancer owing to an inability to account for radiologically occult sites of disease. The traditional treatment of patients with metastatic solid tumors involved the use of systemic therapies with the goal of delaying disease progression and extending overall survival (OS).
1,2 In 1995, Hellman and Weichselbaum
3 at the University of Chicago formally defined the oligometastatic paradigm. This paradigm suggests that in certain tumors, anatomic and physiologic factors may limit and concentrate the number of metastases to single or few organs. This concept has been recently expanded in the context of patients with synchronous oligometastatic disease or those with oligoprogressive cancer (defined as patients with the majority of the disease being stable or responding to therapy with a limited number of sites exhibiting progression).
4 Subsequent work building on this hypothesis has found that distinct molecular subgroups exist that, in combination with clinical risk factors, define subpopulations who may preferentially benefit from aggressive local therapy and potentially delay tumor seeding of other sites and the development of more aggressive phenotypes.
5