The high lesional control rates seen with SABR, in conjunction with its modest side effect profile, have since resulted in an increasing trend to treat oligometastatic lesions in an attempt to improve overall survival (OS) and progression free survival (PFS), delay initiation of systemic therapies with unfavorable toxicity profiles, and offer treatment breaks for individuals amassing toxicity from systemic therapy [ 7 ].
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A phase II randomized trial of RAdium-223 dichloride and SABR Versus SABR for oligomEtastatic prostate caNcerS (RAVENS).
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