Cervix Cancer and HPV Tumor Discussion

This forum made possible through the generous support of SDN members, donors, and sponsors. Thank you.

TheWallnerus

e^(iπ) + 1 = 0
Lifetime Donor
5+ Year Member
Joined
Apr 3, 2019
Messages
4,288
Reaction score
10,018
“Easiest” way would be to increase brachytherapy requirements to the point where graduates would be technically competent in most brachy procedures. This will not happen for obvious reasons.
I wonder how many people would die from cancer in the year after brachytherapy were hypothetically to vanish

Members don't see this ad.
 
  • Like
Reactions: 1 users
I wonder how many people would die from cancer in the year after brachytherapy were hypothetically to vanish
Not insignificant amount and more in years 2-5. There are data for that in cervical Ca literature, too lazy to calculate it for you
 
  • Like
Reactions: 2 users
Not insignificant amount and more in years 2-5. There are data for that in cervical Ca literature, too lazy to calculate it for you
How many cervical cases are treated by xrt per year? 70gy without brachy delivers an overall cure rate of about 60%, but probably much higher for earlier stages when accounting for selection bias.
 
Members don't see this ad :)
How many cervical cases are treated by xrt per year? 70gy without brachy delivers an overall cure rate of about 60%, but probably much higher for earlier stages when accounting for selection bias.
And it’s not like “brachy EBRT” is zero effective (regardless of my doubts that it is totes inferior to the century old standard!)
 
And it’s not like “brachy EBRT” is zero effective (regardless of my doubts that it is totes inferior to the century old standard!)

I'm one of the busier cervical Ca guys and my estimate that durable remission rate is <30% without brachytherapy
 
  • Like
Reactions: 2 users
I'm one of the busier cervical Ca guys and my estimate that durable remission rate is <30% without brachytherapy
Anyone have any idea why anal cancer melts away with 54 Gy almost all of the time and oropharyngeal cancer radiation is being actively deescalated but that doesn't seem to work for cervix?
 
  • Like
Reactions: 5 users
Anyone have any idea why anal cancer melts away with 54 Gy almost all of the time and oropharyngeal cancer radiation is being actively deescalated but that doesn't seem to work for cervix?
Cervical cancers tend to be much larger. Often 6-8 cm. What is the control rate for T3 (over 5 cm anal). I think it’s only a little above 50% that don’t end up needing apr
 
  • Like
Reactions: 4 users
I should have said cervical cancers that we treat with radiation. Gyn onc typically operating on the smaller tumors
 
  • Like
Reactions: 2 users
Anyone have any idea why anal cancer melts away with 54 Gy almost all of the time and oropharyngeal cancer radiation is being actively deescalated but that doesn't seem to work for cervix?

5FU and MMC (or platinum if you're at MDACC for God knows what reason- I mean "internal data") help that 54 Gy punch above its weight, and de-escalation of HPV+ OP RT hasn't been successful just yet.
 
  • Like
  • Haha
Reactions: 2 users
Cervical cancers that evade brachytherapy are usually huge (think > 8 cm actually) and node positive. Thus poor outcomes with EBRT
 
  • Like
Reactions: 1 user
5FU and MMC (or platinum if you're at MDACC for God knows what reason- I mean "internal data") help that 54 Gy punch above its weight, and de-escalation of HPV+ OP RT hasn't been successful just yet.
Maaaan .. the skin reaction is better with cis, I swear.

Act 2 was negative but I think it still showed less tox for Cis
 
Are we on the verge of hypofrac'ing cervix? Like 40/15 or something. If there's a patient population that actually needs a shorter, less complicated treatment course, this is the one.
 
  • Like
Reactions: 2 users
Members don't see this ad :)
  • Like
  • Haha
Reactions: 2 users
I know it's out there, but the one time I discussed doing it with someone, the feeling was that it was quasi-palliative, when in fact it probably would've gotten the patient through with EBRT in 4 weeks instead of 7 (addiction issues...). Wondering when it will become "recommended."
 
  • Like
Reactions: 1 users
need weekly cisplatin for cervix, so shortening courses is tricky
 
  • Like
Reactions: 2 users
Same reasons we haven't seen it in locally advanced lung and h&n I'm guessing
Also, with high a/b ratio tumors, you lose ground with hypofrac when sensitive stuff is nearby (I know I know… many of you guys think LQM is witchcraft, but it is somewhat true-ish).
 
  • Like
Reactions: 1 users
Head and neck cancers have cell loss factors of about 90%, so you only need to tip the equation so much to see them disappear. I also bet cervical cancer has a high degree of hypoxia.
 
Same reasons we haven't seen it in locally advanced lung and h&n I'm guessing

There is a 5 week H&N regimen in European trials that will catch on, I bet
 
I'm one of the busier cervical Ca guys and my estimate that durable remission rate is <30% without brachytherapy


2-year LC of 70% with SBRT boost, albeit it more toxic. Not good as brachy (and was said as much by the authors) but at least it's a data point.

5FU and MMC (or platinum if you're at MDACC for God knows what reason- I mean "internal data") help that 54 Gy punch above its weight, and de-escalation of HPV+ OP RT hasn't been successful just yet.

Lots of things to come at MDACC for doing things in the weird "MDACC way", won't disagree with you on that.

BUT, ACT-II literally had the exact same oncologic outcomes between 5-FU/MMC and 5-FU/Cis. Really between all 4 of the arms. The reason they probably like Cis more is because the MMC doesn't completely destroy counts the way MMC does.... the reason the UK authors felt MMC "won" is because "holding up a chair to give infusions and fluids rather than just a quick shot of MMC uses up too much resources" despite the increase in G3+ heme toxicity seen with MMC.

1666728874151.png


Full link for those interested: Mitomycin or cisplatin chemoradiation with or without maintenance chemotherapy for treatment of squamous-cell carcinoma of the anus (ACT II): a randomised, phase 3, open-label, 2×2 factorial trial
 
  • Like
Reactions: 1 user
I have moved all the cervix cancer talk into its own thread to facilitate ongoing discussion without taking another thread off-topic.
 
  • Like
Reactions: 1 user

2-year LC of 70% with SBRT boost, albeit it more toxic. Not good as brachy (and was said as much by the authors) but at least it's a data point.



Lots of things to come at MDACC for doing things in the weird "MDACC way", won't disagree with you on that.

BUT, ACT-II literally had the exact same oncologic outcomes between 5-FU/MMC and 5-FU/Cis. Really between all 4 of the arms. The reason they probably like Cis more is because the MMC doesn't completely destroy counts the way MMC does.... the reason the UK authors felt MMC "won" is because "holding up a chair to give infusions and fluids rather than just a quick shot of MMC uses up too much resources" despite the increase in G3+ heme toxicity seen with MMC.

View attachment 361225

Full link for those interested: Mitomycin or cisplatin chemoradiation with or without maintenance chemotherapy for treatment of squamous-cell carcinoma of the anus (ACT II): a randomised, phase 3, open-label, 2×2 factorial trial
Agree
Acting like the act II arms are clinically different from efficacy standpoint has always perplexed me
 
Are we on the verge of hypofrac'ing cervix? Like 40/15 or something. If there's a patient population that actually needs a shorter, less complicated treatment course, this is the one.

You Canadian and UK bastards, stop hypofraccing my LIFE

There's post-op endometrial done in 5 fraction on phase I study from Canada (I think), but not enough late toxicity data to do anything besides wait.

Also, now that this has become a cervix thread, is anyone simming them prone, particularly post-op?
Haven't done prone back since I did a 3D Cervix patient as a PGY-2. I can get IMRT approved without insurance struggles at least at the institutions I've been at.

Also, with high a/b ratio tumors, you lose ground with hypofrac when sensitive stuff is nearby (I know I know… many of you guys think LQM is witchcraft, but it is somewhat true-ish).
The race to the bottom will continue, and there will be continued justification to continue shortening courses, whether it be increased acute or late toxicity.
 
  • Like
Reactions: 1 user
You Canadian and UK bastards, stop hypofraccing my LIFE

There's post-op endometrial done in 5 fraction on phase I study from Canada (I think), but not enough late toxicity data to do anything besides wait.


Haven't done prone back since I did a 3D Cervix patient as a PGY-2. I can get IMRT approved without insurance struggles at least at the institutions I've been at.


The race to the bottom will continue, and there will be continued justification to continue shortening courses, whether it be increased acute or late toxicity.
Closest uk to me is still my most despised NCAA bb team. I only want to hypofrac cervix given the frequently concurrent meth addiction in the patient population and the fact that 15 is less than 25, though we may need a trial to prove that.
 
  • Love
Reactions: 1 user
Closest uk to me is still my most despised NCAA bb team. I only want to hypofrac cervix given the frequently concurrent meth addiction in the patient population and the fact that 15 is less than 25, though we may need a trial to prove that.
Not 'you' specifically, more so the general 'you' as in those folks running those trials
 
if we can give 80+ to a prostate with IMRT why can’t we give the same to cervical cancer patients. By the time we get to Brachy, the tumor should be <4cm unless we’re using needles. No reason to think we couldn’t resim and finish with external. I have a very busy general practice and am only guy in town who does brachy. I have around 10 patients a year with advanced cervical cancer. A couple a year are undocumented or have some other reason they can’t get to OR for smit sleeve so I just sbrt boost the remaining mri disease and document the hell out of why I’m deviated from soc. Probably 15 cases over my tenure here, some with 8 years of f/u. Everybody disease free and no significant side effects. I don’t buy into needing 100+ Gy to kill this cancer. I always think we will look back at this 50 years from now and think gyn brachy is barbaric.
 
  • Like
  • Hmm
  • Dislike
Reactions: 5 users
if we can give 80+ to a prostate with IMRT why can’t we give the same to cervical cancer patients. By the time we get to Brachy, the tumor should be <4cm unless we’re using needles. No reason to think we couldn’t resim and finish with external. I have a very busy general practice and am only guy in town who does brachy. I have around 10 patients a year with advanced cervical cancer. A couple a year are undocumented or have some other reason they can’t get to OR for smit sleeve so I just sbrt boost the remaining mri disease and document the hell out of why I’m deviated from soc. Probably 15 cases over my tenure here, some with 8 years of f/u. Everybody disease free and no significant side effects. I don’t buy into needing 100+ Gy to kill this cancer. I always think we will look back at this 50 years from now and think gyn brachy is barbaric.
PREACH

I look back on every gyn brachy case 50...milliseconds from reading your post and think it's barbaric.

It defies logic that we can treat EVERY OTHER TYPE OF CANCER with modern EBRT except for JUST THIS.
 
  • Like
Reactions: 1 user
if we can give 80+ to a prostate with IMRT why can’t we give the same to cervical cancer patients. By the time we get to Brachy, the tumor should be <4cm unless we’re using needles. No reason to think we couldn’t resim and finish with external. I have a very busy general practice and am only guy in town who does brachy. I have around 10 patients a year with advanced cervical cancer. A couple a year are undocumented or have some other reason they can’t get to OR for smit sleeve so I just sbrt boost the remaining mri disease and document the hell out of why I’m deviated from soc. Probably 15 cases over my tenure here, some with 8 years of f/u. Everybody disease free and no significant side effects. I don’t buy into needing 100+ Gy to kill this cancer. I always think we will look back at this 50 years from now and think gyn brachy is barbaric.
It literally was evaluated prospectively by UTSW (Timmerman senior author!) and found to have poor outcomes and increased toxicity to brachy. To do it the rare times when a patient is not a candidate for brachy either medically or socially, then OK. But it is not as conformal as brachy is. And even if it looks similar on the computer, the results in a patient are worse than brachy.

If you can't do T&O and you don't offer Hybrid/interstitial you should make a timely referral to a center that does. Not saying that's you specifically, but more of a general 'you' for those folks who are seeing cervical cancer patients but don't offer brachy beyond T&O.

If anyone reading this is struggling to get in touch with somebody to do interstitial on their patient, feel free to PM me and I am happy to help identify folks that could at least try to help in your region.
 
  • Like
Reactions: 4 users
It literally was evaluated prospectively by UTSW (Timmerman senior author!) and found to have poor outcomes and increased toxicity to brachy. To do it the rare times when a patient is not a candidate for brachy either medically or socially, then OK. But it is not as conformal as brachy is. And even if it looks similar on the computer, the results in a patient are worse than brachy.

If you can't do T&O and you don't offer Hybrid/interstitial you should make a timely referral to a center that does. Not saying that's you specifically, but more of a general 'you' for those folks who are seeing cervical cancer patients but don't offer brachy beyond T&O.

If anyone reading this is struggling to get in touch with somebody to do interstitial on their patient, feel free to PM me and I am happy to help identify folks that could at least try to help in your region.
Those tumor volumes were huge. There are a few retrospective publications with similar number of patients that show good outcomes with sbrt in “non-brachy” candidates. I’m not advocating for people to not treat with SOC Brachy. I just feel it’s barbaric and very 1970’s of us. In this era of de-escalation and non-inferiority studies, I think there should be a non-inferiority study of appropriate cervical tumor sizes randomized to brachy Vsexternal boost technique. If people give 75 Gy in 25 fractions (BED 97.5) for pancreas with a loop of small bowel as dose limiting structure, isn’t it reasonable to hypothesize that one could safely give similar BED with bladder and rectum as rate limiting structure?
 
Last edited:
  • Like
Reactions: 1 user
Those tumor volumes were huge. There are a few retrospective publications with similar number of patients that show good outcomes with sbrt in “non-brachy” candidates. I’m not advocating for people to not treat with SOC Brachy. I just feel it’s barbaric and very 1970’s of us. In this era of de-escalation and non-inferiority studies, I think there should be a non-inferiority study of appropriate cervical tumor sizes randomized to brachy Vsexternal boost technique. If people give 75 Gy in 25 fractions (BED 97.5) for pancreas with a loop of small bowel as dose limiting structure, isn’t it reasonable to hypothesize that one could safely give similar BED with bladder and rectum as rate limiting structure?
Links to those retrospective pubs, please.

I think there's too much non-inferiority study already in Rad Onc, and it does a disservice.

Cervix patients who receive chemoRT do well in regards to LR but frequently don't do well in other schema. It's not like HPV+ OPhx where we are curing SO many of them with such high toxicity (given improvements in CT and MRI based planning for cervix patients) that we're really ready to start figuring out safety of de-escalation and non-inferiority at this time, IMO.

A T&O done under at least moderate sedation is not really barbaric. Doing it in an awake woman just medicated with orals (see recent thread in private forum), sure yes, not ideal. Sure, Syed interstitial cases are a different beast, won't argue regarding the barbarity of that either.
 
Links to those retrospective pubs, please.

I think there's too much non-inferiority study already in Rad Onc, and it does a disservice.

Cervix patients who receive chemoRT do well in regards to LR but frequently don't do well in other schema. It's not like HPV+ OPhx where we are curing SO many of them with such high toxicity (given improvements in CT and MRI based planning for cervix patients) that we're really ready to start figuring out safety of de-escalation and non-inferiority at this time, IMO.

A T&O done under at least moderate sedation is not really barbaric. Doing it in an awake woman just medicated with orals (see recent thread in private forum), sure yes, not ideal. Sure, Syed interstitial cases are a different beast, won't argue regarding the barbarity of that either.





 
Last edited:
Take well-trained staff + Smit sleeves + outpatient suite, and your GYN brachytherapy is entirely tolerable experience
 
  • Like
Reactions: 2 users
Take well-trained staff + Smit sleeves + outpatient suite, and your GYN brachytherapy is entirely tolerable experience
I have a Brachy-suite, smit sleeve, conscience sedation team and a well-trained staff. It’s definitely “tolerable”, but is it all necessary?
 
I have a Brachy-suite, smit sleeve, conscience sedation team and a well-trained staff. It’s definitely “tolerable”, but is it all necessary?
Yes. I have a personal experience similar to what you've described, and EBRT does not approach brachytherapy in efficacy.
 
  • Like
Reactions: 1 users
Top