Tall Allen said...
Of course you can use additional risk factors as an aid to judgment. I'm just saying that research studies are designed with a very specific set of risk factors, and it is inappropriate to reinterpret them. You are also free to go beyond the medical evidence if you want to - that's every patient's prerogative.
Good. Nowhere have I said otherwise. Enough already, end of discussion please.
Tall Allen said...
SBRT can treat any pre-specified margin outside of the prostate. So can HDR brachytherapy. Their precision at doing this is one of their greatest strengths. It sounds like you should be talking to a different specialist if they misinformed you about this.
I do not think I was misinformed. Far from it, actually. The context of the discussion I referenced focused on SBRT treatment for clinically localized prostate cancer in intermediate and high risk patients, including the use of SBRT boost to the prostate after more regional IMRT radiation. Ie., is SBRT a viable alternative RT technique to HDR brachytherapy for boost delivery... in my case... which up to this point may be either fav or unfav intermediate risk depending on who you talk to and why (yeah, yeah, please do your best to let that comment go). As well as reported potential SE's and QOL issues which help me determine whether any particular treatment carries unacceptable risk in the event 'aggressive' treatment actually does become 'over' treatment. The discussion was prompted by a Georgetown study which I quote in part:
https://doi.org/10.3389/fonc.2016.00114 said...
Until recently, there were limited data supporting the safety and efficacy of such SBRT monotherapy in the intermediate-risk population. Current publications by multiple single institutions used SBRT monotherapy regimens of 35–40 Gy, delivered to the prostate in four to five fractions, for intermediate-risk patients. Additionally, a pooled analysis from a multi-institutional consortium has shown a favorable 5-year biochemical disease-free survival of 84% in intermediate-risk patients (33, 34). Following the publication, these papers and the analysis of our own results, it is now our policy to treat intermediate-risk patients with SBRT alone.
For high-risk patients (a category which in newer studies may include unfav int risk patients) there remains a concern that the tight clinical margins required to limit the normal tissue doses to the rectum with SBRT may not be adequate to treat the extent of ECE. While the planned posterior margin for SBRT is 3 mm, the actually treated posterior margin is commonly limited to 2 mm or less to maintain rectal tolerance (1 cc < 36 Gy) (7, 22). In these patients, the risk of ECE beyond 2 mm is approximately 40–70% (35). In many high-risk patients, the SVI extends beyond the proximal seminal vesicles (36) and distal seminal vesicle motion cannot be accounted for by intraprostatic fiducials (37). Thus, we await the mature results of ongoing trials treating high-risk patients with SBRT alone prior to recommending it for all but well selected high-risk patients (38).
Currently, it is our policy to not include pelvic node irradiation in the treatment of high-risk patients. Two randomized trials have been published questioning the benefit of treating pelvic lymph nodes in these patients (39, 40). A prior study with SBRT plus or minus conventional pelvic RT has shown significantly higher bowel toxicity associated with pelvic node treatment (41). Whether the use of pelvic IMRT can reduce bowel toxicity and improve the therapeutic ratio in select patients is an area of current investigation (13).
All of questionable value pending my MRI results and actual face-to-face consults with the top dogs, but I'm trying to get more than a perfunctory education so I can discuss my treatment options in some level of detail or intelligently question a recommendation given at these consults. In any event it's good info to know IMHO, even if SBRT is capable of tighter margins than mentioned in the article.