- Joined
- Oct 4, 2017
- Messages
- 5,369
- Reaction score
- 10,509
Already implemented at my hospitalSo dumb
Already implemented at my hospitalSo dumb
Aggressive ent and CT surgeons are ruining things for patients as bad as aggressive urologists have been....Already implemented at my hospital
I remain skeptical of the value of surgery in the vast majority of stage III lung CA in the community. My stage III pts are 10 years older than median for Pacific trial. Mediastinal failure remains a problem after surgery and IO helps remarkably with locoregional failure after chemoXRT.And, lo, we are losing steam in Stage III
No one asks my input, but they have operated on 2 stage 3c patients with high pdl1 and tmb. Path was negative in both cases.Aggressive ent and CT surgeons are ruining things for patients as bad as aggressive urologists have been....
I remain skeptical of the value of surgery in the vast majority of stage III lung CA in the community. My stage III pts are 10 years older than median for Pacific trial. Mediastinal failure remains a problem after surgery and IO helps remarkably with locoregional failure after chemoXRT.
Are we really going to push a 74 y/o (or 68 with marginal lungs) with gross mediastinal adenopathy to surgery with the knowledge of outcomes for concurrent chemoXRT and adjuvant IO? Never mind that these folks grow additional cancers with significant frequency.
We could even apply PIVOT prostate data to this type of insane thinking.
For my money, the two most impressive multimodality IO trials in solid tumors I can think of are Pacific and Checkmate 577 for esophagus. Those are some curves worth looking at.
Recent stage 3c pdl1 >50% in young pt. Surgey argued why not neoadjuvant then med and proceed to lobectomy if negrative. Not that unreasonable.I know this is not news and not feasible for all, but tumor boards are helpful for these stage III lungs.
Things I've already seen discussed and had to tell them that this didn't happen in the trial...and I have good med oncs and CT surgeons I work with, but enthusiasm sometimes gets ahead of evidence...:
1. patient's tumor is unresectable, but CT surgeon/med onc want neo to try to convert to resectable. That wasn't a thing on the trial
2. patient has a resectable lung tumor, but a mediastinal node in an area hard to reach/not resectable. It doesn't help us to leave gross disease in there.
3. Keep in mind that reports are now emerging that patient's s/p neoadj chemo/IO that then go on for XRT for whatever reason are showing higher pneumonitis rates. So while I don't think it's crazy to do chemo/IO and then XRT (if surgery is taken off table later)...it's really not ideal.
Recent stage 3c pdl1 >50% in young pt. Surgey argued why not neoadjuvant then med and proceed to lobectomy if negrative. Not that unreasonable.
What more do you need to see? Clearly it's already in full swing.Ralph’s pathological need to be right even in cyberspace. When is the vascular dementia gonna kick in? That’s the Ralph I wanna hear.
Two days to do damage control and spin doctoring is a tall orderJobs analysis is out. Embargoed til 3/8.
PDs apparently have access to the key findings / exec summary.
Jobs analysis is out. Embargoed til 3/8.
PDs apparently have access to the key findings / exec summary.
Gotta wait until the lemmings press submit on their match lists for RO.Jobs analysis is out. Embargoed til 3/8.
PDs apparently have access to the key findings / exec summary.
They didnt ask my opinion. I have no idea if it is better or worse. Wouldn’t surprise me within several years they will be adding and stk11 or some other immune enhancer to the regimen.@RickyScott I wouldn’t support that off trial. We have no data to support doing that… and level 1 data for CRT->IO. There is no reason to think outcomes would be better with surgery, so why do it?
I get the feeling neoadj chemoIO for “unresectable” lung is making thoracic surg “hot” again (their numbers have been pretty stable over last decade… may be getting ready to expand?)They didnt ask my opinion. I have no idea if it is better or worse. Wouldn’t surprise me within several years they will be adding and stk11 or some other immune enhancer to the regimen.
They can run 5-10.+ trials with cr as endpt in the time it takes us to run one. That alone will sink us. Btw-one thought leader in lung (who we all know well)personally told me (after many drinks) he expects to be largely out of the stage 3 game within 10 years.I get the feeling neoadj chemoIO for “unresectable” lung is making thoracic surg “hot” again (their numbers have been pretty stable over last decade… may be getting ready to expand?)
Totally practice dependent.... Honestly don't see this becoming widespread in community practice but who knows. The big difference between CT surgery vs ent/urology is that they don't control the flow of patients from diagnosis in my experience. Pulmonary doesThey can run 5-10.+ trials with cr as endpt in the time it takes us to run one. That alone will sink us. Btw-one thought leader in lung (who we all know well)personally told me (after many drinks) he expects to be largely out of the state 3 game within 10 years.
That’s nonsense, what percentage of IIIa/b patients could even tolerate and or consent to surgical resection, maybe 20% at most 30%?They can run 5-10.+ trials with cr as endpt in the time it takes us to run one. That alone will sink us. Btw-one thought leader in lung (who we all know well)personally told me (after many drinks) he expects to be largely out of the state 3 game within 10 years.
That’s nonsense, what percentage of IIIa/b patients could even tolerate and or constant to surgical resection, maybe 20% at most 30%?
Last time I was checking on this about 75% of Stage III is managed w/ RT now. Assume 100K new Stage III patients per year. Assume stage shift trends lower this by half over next 10 years and the 75% goes to 50% RT utilization. That means 50,000 less Stage III RT patients per year. Perhaps! (NB: I have no data to back this up but the medical operability rate in lung cancer patients in general should be going up, even in stage III, given the significant changes in stage incidences.)That’s nonsense, what percentage of IIIa/b patients could even tolerate and or constant to surgical resection, maybe 20% at most 30%?
They can run 5-10.+ trials with cr as endpt in the time it takes us to run one. That alone will sink us. Btw-one thought leader in lung (who we all know well)personally told me (after many drinks) he expects to be largely out of the stage 3 game within 10 years.
by the time it would come out, it would already be outdated by 5 other neoadjuvant pharma trials.If only that thought leader would think of doing a Phase III RCT to actually answer the question
Hmmm... I hear the concern, but I don't think this is the case.They can run 5-10.+ trials with cr as endpt in the time it takes us to run one. That alone will sink us. Btw-one thought leader in lung (who we all know well)personally told me (after many drinks) he expects to be largely out of the stage 3 game within 10 years.
Are you aware of any Pharma trials trying to convert unresectable to resectable? I am not. Nor is there much of an appetite for this in the cooperative groups.by the time it would come out, it would already be outdated by 5 other neoadjuvant pharma trials.
If only that thought leader would think of doing a Phase III RCT to actually answer the question
It depends what you mean by unresectable. 3c due to nodal involvement, but a small primary is very “resectavle” but traditionally surgey was avoided because the prognosis was poor. When the prognosis changes (pdl1>50 has high cr rate), the role of surgery will change as well.Are you aware of any Pharma trials trying to convert unresectable to resectable? I am not. Nor is there much of an appetite for this in the cooperative groups.
The pace of trial accrual in the US is pretty stunning in comparison to the European/Asian groups. I don't see it changing.Seems like a no-brainer to re-run Albain with the modern regimens, but sadly I don't think we could accrue it in the US. Our biases are pretty embarrassing.
Trial data to your average RadOnc is like garlic to a vampire.I think radoncs get too focused on the studies. We can opine all we want on the flaws in a hodgkins study ommitting radiation, but at the end of the day xrt will still go bye-bye in that disease.
May have something to do with where you reside in the referral chain.Trial data to your average RadOnc is like garlic to a vampire.
To everyone else in medicine, it's a flavor you can choose to use in a meal, based on the pairing and your personal tastes.
To us...well, you get the idea.
Are you aware of any Pharma trials trying to convert unresectable to resectable? I am not. Nor is there much of an appetite for this in the cooperative groups.
My question to any surgeon convinced that you can turn unressectable to ressectable…
Why does this strike me as an “If a tree falls in the forest and no one is around, does it make a sound” question. You can’t really know it’s a CR until you do the surgery, I hear them saying. “Nuke it/operate on it from orbit… it’s the only way to be sure.”My question to any surgeon convinced that you can turn unressectable to ressectable…
If a CR is really a CR, can’t we just omit surgery? *Ruh Roh*
You really can’t know it’s ressectable than either 🤔Why does this strike me as an “If a tree falls in the forest and no one is around, does it make a sound” question. You can’t really know it’s a CR until you do the surgery, I hear them saying. “Nuke it/operate on it from orbit… it’s the only way to be sure.”
All bleeding stops."Almost all tumors are technically resectable" is like a Glaucomflecken line.
I think I can argue signals for surgery adding to survival in lung and esophagus. Perhaps even prostate. We shouldn’t underestimate how much new targeted immunotherapies are going to change all our “old rules” though.Median age at diagnosis of stage III lung cancer from trials is 65-79 years old.
What is the life expectancy of this group independent of their NSCLCA diagnosis?
At what time point is it likely that OS curves are going to deviate between chemorads then IO vs whatever plus surgery?
We know that the initial survival curves are going to favor the non-surgical approach. They always do.
Surgery in the elderly should be limited to:
1. Procedures that are addressing an imminent threat to life (as in days to weeks): aortic dissection, active CAD, GB on the verge of sepsis
2. Procedure that will immediately improve quality of life: (ortho, TURP).
3. Oncologic procedures where reasonable alternatives are not available (see below).
How sh*%ty is even a chest tube in an elderly patient?
When I think of solid tumors where the evidence for the addition of surgery in terms of OS benefit is nil relative to alternative therapies, I think H&N (exempting OC and salivary), esophagus, cervical and anal CA, prostate and lung cancer.
Surgical disease? Melanoma (XRT helps almost none), colorectal, upper GI exempting gus, sarcoma and endometrial CA.
There are signals, and the young should be considered for surgery for early stage lung and intermediate (some high risk) prostate cancer, as well as triple modality therapy for esophageal CA.I can argue signals for surgery adding to survival in lung and esophagus. Perhaps even prostate
There are signals, and the young should be considered for surgery for early stage lung and intermediate (some high risk) prostate cancer, as well as triple modality therapy for esophageal CA.
Competing risks are competing risks however, and 85% of our lung patients are one big competing risk.
Also, what are the targeted therapies and IO doing? What does effective systemic therapy do?
In prostate (I know I keep mentioning this), the best data for local therapy improving survival is in low burden metastatic disease with 55 Gy.
Do we need to surgerize these same patients?
But you and @RickyScott are right about clinical trials and the synergy of surgery and improved systemics in trialists minds.
I'm already seeing my future role in lung CA as treating oligoprogressive stage IV disease.
But, on a population based level, I think this is wrong in the present day. Lots of OR time spent, unnecessary treatment related M&M and rare benefit as we push for more oncologic surgery in the 75+ yo crowd.
Yes, yes, a million of these trials coming down the pipe. But what does the trial say about the value of surgery?
It says the slope of the line plotting the incidence of using the words “resectable” and “stage III lung cancer” together in the same sentence versus time in oncology is positive.Yes, yes, a million of these trials coming down the pipe. But what does the trial say about the value of surgery?