- Joined
- Dec 15, 2014
- Messages
- 306
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- 580
Are you really trying to imply that the decreases in radiation indications/schedule for breast and prostate are made up for a recent phase II abstract presented at ASTRO this past year for SBRTing oligomets?
I think what the other poster was trying to get at is where was RO leadership when med onc tried to make AI the preferred adjuvant tx in early stage breast in older patients? For the record, I've treated a handful of patients where they refused or didn't tolerate AI therapy.
Why does the NCCN talk about omitting rt but not AI therapy in that population?
Again, moving the goalposts.
First point he made (and others have parroted) -- "only rad onc does de-escalation!". Totally false.
Next point he made -- "no research has been done to expand the indication for rad onc" Again, totally false. There's not just the SABR-COMET trial (which btw is coming out in Lancet...so yes just a phase II abstract at ASTRo *eyeroll*), but STAMPEDE which IS in the new NCCN guidelines to allow RT to prostate primary in metastatic disease. There's also the MDACC trial of local therapy for metastatic disease that responds to treatment (which is being published soon) and the STOMP trial for oligometastatic prostate cancer (already published in JCO) and the ORIOLES oligometastatic prostate cancer trial (accrued). Just because your particular groups apparently don't refer these patients doesn't mean it doesn't happen elsewhere, let alone that the research has not been done.
Not to mention the false idea that reduced # of fractions = reduced # of patients. The problem is residency expansion, not research designed to make our treatments more appropriate and convenient.