- Joined
- Dec 17, 2007
- Messages
- 3,390
- Reaction score
- 4,403
I am having trouble to understand the rationale.
Because similar trials have been done? Or because 74 gy dose escalation failed
The alternative to this is sib. 60/30 and 66/30 where it's safe. Many of us already do this, and i think standard at mdacc.Because similar trials have been done? Or because 74 gy dose escalation failed
I think the concept of sbrt boost only to primary makes sense as primary disease harder to control than nodal disease.
Would make me nervous if primary is very central or endobronchial
Sounds like authors hypothesized improved oxygenation with up front sbrt
Heard Harvard takes it to 70 if it is safe? Joe Chang has posted on mednet about their 66/30 SIb approachThe alternative to this is sib. 60/30 and 66/30 where it's safe. Many of us already do this, and i think standard at mdacc.
I have thought about this alot and go back and forth between 60 vs 66 Gy, but not sure it makes any difference except to make me feel better b/c I think (with absolutely no proof) that 60 Gy is inadequate. It's funny but I think it really does make us feel better as one of the main reasons. If 74 Gy "hurts" or at best is neutral, what will 70 Gy accomplish? With that said I think if you go to 66 Gy, might as well go to 70 Gy?!?!? Sorry just thinking out loud in my confusion!The alternative to this is sib. 60/30 and 66/30 where it's safe. Many of us already do this, and i think standard at mdacc.
It's fine. On the innovation thread we discussed the peculiarities of dose kinetics and it's an understudied space. This is a low risk trial. Phase III will probably be negative but would anyone really mind accruing to it out in the community?
Do you mind linking some of those studies if you have them? I would love to take a look.Of note RTOG 1308, which had finished accruing BTW, goes to 70/35 with photons and protons. Will be interesting to see results and compare them to RTOG 0617. There has been more recent negative trials of dose escalation in lung with modern isotoxic techniques, however.
There hasnt been any new phase 3 studies that i am aware of recently like 0617. There are multiple smaller studies which are restrostepective, phase 1/2 which have looked at question (search for isotoxic dose escalation NSCLC) . Some have used PETCT. I have not seen a newer ph 3 study clearly showing a benefit to dose escalation which is why i don’t believe we have a positive study to fall back on. Some of the conclusions say it is “promising” or possible without increased toxiticy, worthy of study. I agree with you that it seems like more dose would be better but take a look at the negative oesophageal studies again and again. Higher dose for cervical oesophagus is now completely out of NCCN. I’m simply saying it does not necessarily help as far as I know based on best high level data we have. I do take it to 66 in 33 or 30 from time to time but i wonder if it is something I do for myself lolDo you mind linking some of those studies if you have them? I would love to take a look.
LS sclc should be 70/35 if you treat daily and follow the calgb/nrg intergroup protocol. Less for nsclc. Makes perfect senseI have thought about this alot and go back and forth between 60 vs 66 Gy, but not sure it makes any difference except to make me feel better b/c I think (with absolutely no proof) that 60 Gy is inadequate. It's funny but I think it really does make us feel better as one of the main reasons. If 74 Gy "hurts" or at best is neutral, what will 70 Gy accomplish? With that said I think if you go to 66 Gy, might as well go to 70 Gy?!?!? Sorry just thinking out loud in my confusion!
In a thread about Direct Supervision, Ron is, as always, playing the scare tactic cards.
He had the audacity to post this:
View attachment 383827
Just a reminder, Ron had his therapist licensed revoked by the ASRT:
View attachment 383828
He managed to get this removed from the website list you can easily search (I believe you can...perhaps offer a "donation" if ~10 years have passed) but you can always call the ASRT to verify a revocation.
Now, who can say WHY his license was revoked. I mean, it sure would be weird if it was like, cheating on continuing education credits or something, right? Like that would be super weird for a guy like this, preaching his scary puritanical interpretation of regulations.
Guess it will remain a mystery!
What if it was some sort of...ring? Like a cheating ring?Types of Sanctions - ARRT
R.T.s can face a range of ARRT sanctions and additional actions as a result of ethics violations. Learn more about each type.www.arrt.org
Revocation for cheating on cme seems kind of harsh.
Calling arrt?Where's Limpy?
Haven't read the paper, but wasn't it hypothesized that moderate doses such as 6-8 Gy have the best immunogenic response?
Of course we don’t know if many weeks of traditional fx prior to the large fx kills the possibility of increased immunogenicity from the large fx or not.Haven't read the paper, but wasn't it hypothesized that moderate doses such as 6-8 Gy have the best immunogenic response?
Shrinking tumor/volume with traditional fx and then boosting residual to potentially increase LC and immunogenicity right before IO starts; I kind of like it.
Haven't read the paper, but wasn't it hypothesized that moderate doses such as 6-8 Gy have the best immunogenic response?
Shrinking tumor/volume with traditional fx and then boosting residual to potentially increase LC and immunogenicity right before IO starts; I kind of like it.
Whoops. Yes. You're correct. I like that less.But doesn't this do the opposite? SBRT to bring in all the immune cells. Then conventional fx RT to kill them all.
But doesn't this do the opposite? SBRT to bring in all the immune cells. Then conventional fx RT to kill them all.
If only we could figure out the right sequence of fractions, along with fraction sizes, to reliably usher in this illusive immunogenicity upon command. If you think about it, there’s probably at least a few hundred feasible combos. Maybe more! Are we like Dr. Ehrlich blindly but one day serendipitously happening upon compound 606? Or are we just blind. Time will tell! I predict I’ll be dead before it does.Whoops. Yes. You're correct. I like that less.
For this trial, the rationale is more than immunogenicity of course, although it would be nice if some magic happened. The more prosaic motivation is to see if one can safely improve local control and thus maybe pFS and OS by judiciously dose escalating with a highly conformal and upfront boost.If only we could figure out the right sequence of fractions, along with fraction sizes, to reliably usher in this illusive immunogenicity upon command. If you think about it, there’s probably at least a few hundred feasible combos. Maybe more! Are we like Dr. Ehrlich blindly but one day serendipitously happening upon compound 606? Or are we just blind. Time will tell! I predict I’ll be dead before it does.
Agreed completely.For this trial, the rationale is more than immunogenicity of course, although it would be nice if some magic happened. The more prosaic motivation is to see if one can safely improve local control and thus maybe pFS and OS by judiciously dose escalating with a highly conformal and upfront boost.
This is a lot different than escalating all disease from 60-74 Gy...not exciting, but different.
Agree about the sequencing question though, and all these arguments come out with every negative concurrent XRT/IO trial.
I'm convinced that radiation induced immunogenicity is a high variance problem in people. (Much less so in nude mice...why we have baller pre-clinical data.) In fact, I'm convinced that prior to the advent of targeted IO to conserved proteins like PD-L1, the high variance problem was why IO had been such a flop over 30 years of clinical research, despite clear evidence of periodic complete responses in patients.
$500 for a benign minor case? sounds about right, can be compared to brachyReminder: Hospitals always win. You are nothing.
Further proof that for employed docs, prof fees don’t set our salary. Increasing proportion of money goes to technical, and hospitals hire/pay docs based on supply and demand.Reminder: Hospitals always win. You are nothing.
Inside joke?Where's Limpy?
Inside joke?
Neo IS the chosen one!
I'm assuming they are referencing the Ribociclib trial?
[Edit] Wow if you read this physican's Twitter feed (she is a Med Onc), you can tell that she has some pent up issues. Maybe she ought to take up MMA or kickboxing to vent. Also, she REALLY likes N95 masks.
Everyone else is crazy but me...
“You mean to tell me doc this albendazole aint going to cure my stage 3 cancer? Lies!”I still wear a mask, mainly because I can hide my facial reactions whenever patients say dumb 💩
Wonder when her midnight hour finally occurred.
no that’s real!“You mean to tell me doc this albendazole aint going to cure my stage 3 cancer? Lies!”
Uh I take it this concept is going viral right now? Pun...somewhat intended...When the Canadian naturopathic clinics are telling you it's quackery, you know you are in another level. Kind of like that time Kanye made Alex Jones look normal.
Fenbendazole - Is It Safe in Those with Cancer? (Joe Tippens Protocol)
The fenbendazole controversy was an incident in which inaccurate claims about the efficacy of fenbendazole, an anthelmintic primarily used to treat various parasitic infections in dogs, in curing terminal lung cancer gained widespread attention among patients.[1] This situation originated with...www.simcoenaturopathic.ca
Unless NEJM is putting pronouns, race/ethnicity, and age in the author byline these days - this is not a Tweet you can make without intentionally doing detective work on each author's pronouns, race/ethnicity, and age...
Uh I take it this concept is going viral right now? Pun...somewhat intended...
I encountered this for the first time in my clinic two days ago.
"Is it OK to keep doing my holistic treatments during radiation?"
"What kind of holistic treatments?"
I think I confused the heck out of the patient when I told them using an actual, honest-to-God drug was NOT something you can call "holistic"...
NEW GRAY ZONE CASEGet a CMP on any patient coming in on any sort of dewormer.
The transaminase elevations will garner honorary membership at the local college fraternity.
Unless NEJM is putting pronouns, race/ethnicity, and age in the author byline these days - this is not a Tweet you can make without intentionally doing detective work on each author's pronouns, race/ethnicity, and age...
Karen is upset!As an aside, I find it so interesting that for a while it was basically a cardinal sin to assume gender or ethnicity in these kinds of DEI papers.
Yet, the ones most vocal about it seem to do it all the time when it is really the only way to complete the "study".
The fact that this medical oncologist pointed out THAT aspect of THAT study as what she is mad about... man, oncology is so far gone
As an aside, I find it so interesting that for a while it was basically a cardinal sin to assume gender or ethnicity in these kinds of DEI papers.
Yet, the ones most vocal about it seem to do it all the time when it is really the only way to complete the "study".
The fact that this medical oncologist pointed out THAT aspect of THAT study as what she is mad about... man, oncology is so far gone
"No worries, we have better drugs for stage 4"“You mean to tell me doc this albendazole aint going to cure my stage 3 cancer? Lies!”
i just don't get it.As an aside, I find it so interesting that for a while it was basically a cardinal sin to assume gender or ethnicity in these kinds of DEI papers.
Yet, the ones most vocal about it seem to do it all the time when it is really the only way to complete the "study".
The fact that this medical oncologist pointed out THAT aspect of THAT study as what she is mad about... man, oncology is so far gone
The "DEI/Woke" pendulum swung too far.i just don't get it.
i am all about equity, but DEI being applied to everything is just ridiculous.
Applying her logic - you can always find something to be upset about. If there were women on the paper, then the next logical step is...well are they diverse?
I mean should we start applying DEI to athletics? I guess there is some work in the NFL for head coaches.