Abstract

SBRT demonstrated to increase survival in oligometastatic patients. Nevertheless, little is known regarding the natural history of oligometastatic disease (OMD) and how SBRT may impact the transition to the polymetastatic disease (PMD). 97 liver metastases in 61 oligometastatic patients were treated with SBRT. Twenty patients (33%) had synchronous oligometastases, 41 (67%) presented with metachronous oligometastases. Median number of treated metastases was 2 (range 1-5). Median follow-up was 24months. Median tPMC was 11months (range 4-17months). Median overall survival (OS) was 23months (range 16-29months). Cancer-specific survival predictive factors were having further OMD after SBRT (21months versus 15months; p = 0.00), and local control of treated metastases (27months versus 18months; p = 0.031). Median PFS was 7months (range 4-12months). Patients with 1 metastasis had longer median PFS as compared to those with 2-3 and 4-5 metastases (14.7months versus 5.3months versus 6.5months; p = 0.041). At the last follow-up, 50/61 patients (82%) progressed, 16 of which (26.6%) again as oligometastatic and 34 (56%) as polymetastatic. In the setting of oligometastatic disease, SBRT is able to delay the transition to the PMD. A proportion of patients relapse as oligometastatic and can be eventually evaluated for a further SBRT course. Interestingly, those patients retain a survival benefit as compared to those who had PMD. Further studies are needed to explore the role of SBRT in OMD and to identify treatment strategies able to maintain the oligometastatic state.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call