Nobody can reduce the need for a radiation oncologist like a radiation oncologist.
Never ceases to amaze.
Nobody can reduce the need for a radiation oncologist like a radiation oncologist.
I would like to see the breakdown of skeletal events. I am also not going to put too much stock in the survival numbers.Late to this discussion, but receipt of XRT is counted a "skeletal event". Thus, the observation arm is skewed towards having more skeletal events. Bad design
Was kinda tongue in cheek in this case. They proved that giving xrt reduces the need for xrt.Never ceases to amaze.
You could say the same giving surgery prevents the need for surgery (ie prophylactic stabilization)Was kinda tongue in cheek in this case. They proved that giving xrt reduces the need for xrt.
Looking forward to the publication.Was kinda tongue in cheek in this case. They proved that giving xrt reduces the need for xrt.
Looking forward to the publication.
In a tweet Gillespie said even excluding RT for symptoms the results were still significant.
Indeed, but I believe this only has to do with very high BED, especially in the context of single or few fractions (e.g. 1x20 or 2x12 Gy).Prophylactic RT to bone is hit or miss. Sometimes we actually weaken the bone and induce fracture (e.g. vertebral fractures after lung or spine SBRT).
I was under the impression that the post-SBRT fractures are mostly due to the very high BED killing vessels and inducing micro-emboli with avascular necrosis.Sometimes a metastasis is what actually is keeping bone together and prophylactic RT leads to a fracture. A good area to study, though.
I feel like all the situations I've seen where this would be true are not situations that I'd call "prophylactic." There is already a path fracture and pain/mobility limitations and usually need Ortho to intervene first.Prophylactic RT to bone is hit or miss. Sometimes we actually weaken the bone and induce fracture (e.g. vertebral fractures after lung or spine SBRT). Sometimes a metastasis is what actually is keeping bone together and prophylactic RT leads to a fracture. A good area to study, though.
Prophylactic RT to bone is hit or miss. Sometimes we actually weaken the bone and induce fracture (e.g. vertebral fractures after lung or spine SBRT). Sometimes a metastasis is what actually is keeping bone together and prophylactic RT leads to a fracture. A good area to study, though.
there are good data on RT-induced bone fractures, going all the way back to rib fractures in breast Ca, I guessI’ve heard medonc make these comments, but I don’t know that there’s actually any truth to it. It’s kind of like their argument that giving RT to a few vertebrae will cause immunosuppression and prevent them from being able to give chemo.
can’t remember the actual trial, but prophylactic chest RT in metastatic lung Ca does not improve survival (compared to treating pts after they’ve obstructed)if I could count the number of times that told someone “let me know if any other spots seem to become painful” and then hear from them in less than a few weeks. Its definitely a confounded which is almost impossible to control for. But in this case I think the whole of the data is very promising. Let’s not go doing Evicores work for them.
82% including stage 3-4. So I was guesstimating
It means that the patient HAD a neck dissection or some other soft tissue neck surgery, THEN developed cancer. That's when the new lymphatic drainage patterns (due to the patient's history of surgery) can become wonky and spread to contralateral neck because the lymphatics were disturbed (before the patient developed cancer). Is this sarcasm? A joke? Serious question?You guys are confusing me today.
So when does "underwent a neck surgery" become a "HISTORY of neck dissection." One day? One month? One year?
Imagine the rad onc note: "The patient does not have a history of neck dissection but did undergo a neck dissection recently."
Pretty much everyone got CHEMO - if you're saying 90% cure rate for T1N1, they gotta get the chemo!
Not with conventional fractionation? And that is the exact reason I don't like 1 or 2 fraction SBRT given all the compression fractures seen.Prophylactic RT to bone is hit or miss. Sometimes we actually weaken the bone and induce fracture (e.g. vertebral fractures after lung or spine SBRT). Sometimes a metastasis is what actually is keeping bone together and prophylactic RT leads to a fracture. A good area to study, though.
We really need to stop allowing this dogma to define any contemporary rad onc and their role in management of bone mets - RT caused the fracture? For standard palliative doses? C'mon man.I’ve heard medonc make these comments, but I don’t know that there’s actually any truth to it. It’s kind of like their argument that giving RT to a few vertebrae will cause immunosuppression and prevent them from being able to give chemo.
Yes, you are late. Helps with non-RT events as well:Late to this discussion, but receipt of XRT is counted a "skeletal event". Thus, the observation arm is skewed towards having more skeletal events. Bad design
I don’t think they need it.Literally all of these patients received concurrent chemo. You said 90% cure (5-year PFS) with RT alone. I'm not saying 90% isn't doable in T1N1, just saying it's most likely gotta be with chemo.
It means that the patient HAD a neck dissection or some other soft tissue neck surgery, THEN developed cancer. That's when the new lymphatic drainage patterns (due to the patient's history of surgery) can become wonky and spread to contralateral neck because the lymphatics were disturbed (before the patient developed cancer). Is this sarcasm? A joke? Serious question?
Pretty much everyone got CHEMO - if you're saying 90% cure rate for T1N1, they gotta get the chemo!
Otherwise, show me the money!
T1N1 ajcc 7 pretty much excluded from most chemoRT trials (particularly RTOG/NRG until 002/005)... bc cure rate with RT alone so high. 002 PFS at 2 years was ~90% with RT alone (and that was T1-2 N1-2b or T3N0-2b 7th ed).Literally all of these patients received concurrent chemo. You said 90% cure (5-year PFS) with RT alone. I'm not saying 90% isn't doable in T1N1, just saying it's most likely gotta be with chemo.
It means that the patient HAD a neck dissection or some other soft tissue neck surgery, THEN developed cancer. That's when the new lymphatic drainage patterns (due to the patient's history of surgery) can become wonky and spread to contralateral neck because the lymphatics were disturbed (before the patient developed cancer). Is this sarcasm? A joke? Serious question?
Pretty much everyone got CHEMO - if you're saying 90% cure rate for T1N1, they gotta get the chemo!
Otherwise, show me the money!
T1N1 ajcc 7 pretty much excluded from most chemoRT trials (particularly RTOG/NRG until 002/005)... bc cure rate with RT alone so high. 002 PFS at 2 years was ~90% with RT alone (and that was T1-2 N1-2b or T3N0-2b 7th ed).
Up to 3vm Single node t1-t2n0-n1 pfs of 90% using accelerated on rtog 0022
0022 was actually a true "clinical" N1; ie by clinical exam, not radiographic. By CT 10%+ ended up being N2a or N2b.Are we saying that 90% PFS at 2-years (what the original report showed) in 68 patients is the same thing as 90% chance of cure?
46% of 0022 were rN0. 39% were rN1. cN rates are different, but I imagine we're all calling people N1 even if you can't clinically feel the node in the era of high res CT w/ contrast and PET/CT
10-year DFS was 50% on long-term f/u (Final Report of NRG Oncology RTOG 0022: A Phase I/II Study of Conformal and Intensity Modulated Radiation for Oropharyngeal Cancer), 67% OS.
Sure, they report that only 15% of the deaths were due to the index diagnosis, but no information on rates of need for salvage treatment are given. If someone has access to the presentation slides (appears it was presented at ASTRO 2021) please link.
I'm not saying it's wrong to do RT alone for T1N1, but saying cure rate is 90% at 5-years with RT alone.... I just don't think we have data to say that. I think offering RT alone to T1N1 is fine and well supported by NCCN. But, when med onc pushes to give chemo in N+ disease, I don't fight them. T1/T2N0, yes I say RT alone is all I would do, and actively push back against chemo.
0022 was actually a true "clinical" N1; ie by clinical exam, not radiographic. By CT 10%+ ended up being N2a or N2b.
And of the 7 failures, 5 had evaluable plans, 2 of which had major dosimetric deviations (out of 6 total with major deviations).
So with modern staging and appropriate targeting/treatment planning 90% is a reasonable estimate for these patients.
From MD Anderson's HPVish experience:
"When the analysis was limited to 324 patients treated with intact primary disease and without systemic therapy, the 5-year PFS rates for T1,T2, and T3 disease were 90%, 83%..."
"The 2- and 5-year actuarial locoregional control rates were 96% and 94%, respectively". This is the overall cohort ie T1-3 N0-2b. "Five percent of patients treated with radiation had locoregional recurrences, whereas 8%of patients treated with radiation and systemic therapy did."
Is this regimen it better than PACIFIC?Meanwhile, why isn't anyone talking about this: Keynote 799 -phase II for Pem/chemo -> Pem CRT -> Pem maintenance for unresectable stage III NSCLC. PFS competes very favorably with the EFS data from Checkmate 816... for resectable stage II/III
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If it is replicated in a phase III, it could become the new SOC for unresectable… then someone may ask, is it ever worth resecting LN+ NSCLC if you can get the same results with NOM?Is this regimen it better than PACIFIC?
Or is it going to enable RT to replace surgery in stage III disease?
If equivocal, then operate is typically the paradigm in surgical oncology- prostate, bladder etcIf it is replicated in a phase III, it could become the new SOC for unresectable… then someone may ask, is it ever worth resecting LN+ NSCLC if you can get the same results with NOM?
Lung isn't like those.... Different issues when lung vs prostate tissue removed. @Lamount is correct, unlike gu, CT surgeons aren't gatekeepersIf equivocal, then operate is typically the paradigm in surgical oncology- prostate, bladder etc
RT has more of a foothold in LA-NSCLC and the surgeons aren’t the gatekeepers…If equivocal, then operate is typically the paradigm in surgical oncology- prostate, bladder etc
How many of you don’t bother referring to thoracic surgery if the pulmonologist has referred directly to you because they unilaterally made the decision the patient isn’t medically operable? I feel compelled to get a surgery opinion on the record based on NCCNRT has more of a foothold in LA-NSCLC and the surgeons aren’t the gatekeepers…
Also willl be interesting to see if it truly is equivocal. right now we are comparing operable stage II/ III patients to inoperable stage III. Wonder what the outcomes would be comparing apples to apples.
All that aside, 0617 had an OS ~30 months… now that may be the new PFS. Would be a huge advance in tx of LA-NSCLC
I refer to surgery or at least curbside, assuming pt hasn't already been discussed at our multi-D conference.How many of you don’t bother referring to thoracic surgery if the pulmonologist has referred directly to you because they unilaterally made the decision the patient isn’t medically operable? I feel compelled to get a surgery opinion on the record based on NCCN
For any <N2 disease who doesn’t have home O2 and happens to come to me first, I will refer to surgery (or curbside). For N2+, I am usually not sending them to see surgery. Most of these patients will get CRT and only the young fit ones with single station N2 are even considered for surgery (vast minority of N2+ in our population)… and these elite folks have likely already been presented at TB. Our group works together well so we usually all end up agreeing.How many of you don’t bother referring to thoracic surgery if the pulmonologist has referred directly to you because they unilaterally made the decision the patient isn’t medically operable? I feel compelled to get a surgery opinion on the record based on NCCN
Very community place where I'm at but pretty much same deal. We do have a thoracic board. Outside of when left upper lobectomy with dissection of an isolated level 6 node is going to get gross disease, I'm pushing chemorads and IO for all N2+.only the young fit ones with single station N2 are even considered for surgery
I ask that even now in PACIFIC era for cN2 patients...If it is replicated in a phase III, it could become the new SOC for unresectable… then someone may ask, is it ever worth resecting LN+ NSCLC if you can get the same results with NOM?
How many of you don’t bother referring to thoracic surgery if the pulmonologist has referred directly to you because they unilaterally made the decision the patient isn’t medically operable? I feel compelled to get a surgery opinion on the record based on NCCN