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Embrace BFE. It's the last bastion of hope for this generation of young physicians. After that, we are all cooked...
If you don't have a specific job ad to offer to be helpful, please just stop posting about how there are opportunities out there. Maybe you like your job that you've had. Good for you. Please hire me. Oh, I already know that you're not hiring. Any good practice is already full since the market isn't expanding and everyone is too concerned about the future of our specialty.
The job market died and needs a eulogy, not a posthumous attempt at Weekend at Bernie's.
1) At some point BFE will be saturated. Good read- how some may make statements like "supply does not affect demand, or ignore that pre hypofractionation 100,000 population supported around 15-20 pts on beam)Embrace BFE. It's the last bastion of hope for this generation of young physicians. After that, we are all cooked...
It's heartening you brought this up. Radiation oncology is in need of a Bayesian revolution. If I had the time, will, money, and biostatistical colleagues, I would re-analyse some of the recent practice-changing trials in radiation oncology from a Bayesian vs frequentist (frequentism: what all tests/trials in radiation oncology have used for the past five decades, and you didn't even know you were a frequentist!) interpretation. This would be a rather large undertaking. I have a hunch that many hypofractionation results would not have been accepted as new standards of care were the oncology world Bayesian instead of frequentist. I'm a wannabe philosopher, and this thought process gets into pretty deep subjects (what is one's viewpoint of the world) which might be best alluded to in the fiction piece "The Story of Your Life" by Ted Chiang.
I think so. Because in regards to long-term accepted standards of care, it's hypofractionation vs. standard which has in my opinion most supplanted previously accepted standards of care in radiation oncology. I can think of other situations where other trials produced disruption in the standard of care (Smalley's trial, Calais' trial leap to mind) in rad onc. Still, seems like there has been a bit more disruption in the fractionation arena, and that disruption has been against previous very robust data. My opinion only. It's at best a wild guess on my part. I have pointed out previously that there is a crisis in reproducibility and that there's a p-value war: taken together, previous trials which have changed the standard of care wouldn't have done so if the standards for significance were different (and/or we were all more skeptical I suppose). Feel free to ignore me 'bout all that. Although when I read this thing recently, I thought "pretty Bayesian."You state "I have a hunch that many hypofractionation results would not have been accepted as new standards of care were the oncology world Bayesian instead of frequentist".
Do you think this applies to hypofractionation studies more than other studies? If so, why?
Hi all,
I appreciate everyone's time as I am trying to figure out what to do with my life. We are now getting to the end of M3 and I haven't really liked much and am starting to panic because I don't know what to do. My priorities are lifestyle, enjoying the work, and pay in that order.
I am a third year, going to be starting M4 around April/May and have been set on Rad Onc since the beginning of medical school and have made myself somewhat competitive for it (i.e. step 1 >260; ~8ish publications). However, given the posts I see around here and what I hear about the job market I am very reluctant to apply to this field. From what I have seen shadowing and doing research I like the work but I don't think I would enjoy living in the middle of nowhere working a high volume job for declining compensation (considering i have ~300k in loans).
Would you advise someone like me to apply to this field? Why or why not?
For those who regret entering this field, what would you have applied to instead?
Thank you so much,
Cremaster Reflex
This being an Internet forum, there is plenty of venting and arguing, and the more positive comments are diluted out. But in the real world, the vast majority of radiation oncologists I know are collegial, highly professional, and a pleasure to work with, are excellent doctors, and love what they do.
We're still seeing survival advances from RT trials. The COMET results were huge- RT for oligomets led to a doubling (!) of overall survival at 5 years.Our med onc colleagues are routinely publishing trials that shows improved overall survival while our rad onc leaders are pushing protons that have never shown an overall survival benefit. If you enjoy being a snake oil salesman, choose rad onc. Rad oncs emphasizes "perceived" quality when we choose our residents or who to dole out jobs to while the med oncs are focusing on NIH funding and pushing out clinical trials that show real improvements in survival. My med onc friends are getting offers of $350-450K in major metro areas like Atlanta and Chicago while I am not even getting a single interview.
If you are a med student, the very least you can do at this moment is to rank prelim medicine over transition year because you might just want that additional year of medicine training when you decide to bail on rad onc in the near future. Hell, I would not have chosen rad onc if I can get my 5 years of life back, but I am too old and lazy to retrain now. Our leaders are money hungry and disgusting. They are liars who will enslave you.
Just wait until this July when the ABR fails another 40% of the graduating PGY5 class on our clinical boards, and you'll understand why not to choose rad onc.
Choosing rad onc has been the biggest mistake of my life.
While those trials are promising, most positive randomized phase II trials in oncology do not translate into the phase III setting! This was mentioned in one of the lung sessions at ASTRO. (For investors, you can loose big money in biotech stock by betting on a randomized phase II) I wouldnt advise a medstudent to bank on this kind of thing, when historitcal odds are that it will not hold up. Anyway, increasing hypofractionation will more than offset oligomets, so much so, that I am advising our hospital to go down to one machine, when our second one enters "end of life" in several years.We're still seeing survival advances from RT trials. The COMET results were huge- RT for oligomets led to a doubling (!) of overall survival at 5 years.
Parachute use to prevent death and major trauma when jumping from aircraft: randomized controlled trial finally, a phase II update to the famous article.While those trials are promising, most positive randomized phase II trials in oncology do not translate into the phase III setting! This was mentioned in one of the lung sessions at ASTRO. (For investors, you can loose big money in biotech stock by betting on a randomized phase II) I wouldnt advise a medstudent to bank on this kind of thing, when historitcal odds are that it will not hold up. Anyway, increasing hypofractionation will more than offset oligomets, so much so, that I am advising our hospital to go down to one machine, when our second one enters "end of life" in several years.
The hazards of randomized phase II trials
"This is somewhat borne out of historical experience: the likelihood of a positive phase II combination chemotherapy trial resulting in a subsequently positive phase III trial within 5 years was reported to be just 0.038 [3]. The randomized phase II design was supposed to rescue us from this rather dismal yield. Unfortunately, for all its promises and advantages, we must recognize its many limitations and pitfalls"
Not to mention the trial showing a survival benefit to palliative dose consolidative thoracic xrt in extensive stage sclc that was published a few years ago.We're still seeing survival advances from RT trials. The COMET results were huge- RT for oligomets led to a doubling (!) of overall survival at 5 years.
Hi all,
I appreciate everyone's time as I am trying to figure out what to do with my life. We are now getting to the end of M3 and I haven't really liked much and am starting to panic because I don't know what to do. My priorities are lifestyle, enjoying the work, and pay in that order.
I am a third year, going to be starting M4 around April/May and have been set on Rad Onc since the beginning of medical school and have made myself somewhat competitive for it (i.e. step 1 >260; ~8ish publications). However, given the posts I see around here and what I hear about the job market I am very reluctant to apply to this field. From what I have seen shadowing and doing research I like the work but I don't think I would enjoy living in the middle of nowhere working a high volume job for declining compensation (considering i have ~300k in loans).
Would you advise someone like me to apply to this field? Why or why not?
For those who regret entering this field, what would you have applied to instead?
Thank you so much,
Cremaster Reflex