Newly Diagnosed: FIGO 2 Uterine Cancer: What does this mean?

Hi cmb2022 -

Thank you so much for sharing your story here. It sounds like we had the same diagnosis. My doctor is recommending 4 brachytherapy treatments based on the positive pelvic washing result. They did not recommend external beam therapy for me. Would you mind sharing if you experienced the vaginal "sunburn" I am reading about?

Thank you again - I very much appreciate your information and support.

Hi Helen,

Thank you so much for this information - I really appreciate it. Would you mind sharing the stage of your cancer / if you have a positive pelvic washing and if they did any additional treatments after the surgery? How do you feel two years after the brachytherapy? I'm trying to decide if I should have the treatment now or "save" it.

They would like me to start brachytherapy at the end of April, and as your experience, they did an excellent job of educating me on what to expect.

Thank you again, and all the best to you.

Hi giginorth -

Thank you for sharing your story here. Yes, that is one of my worries - I understand that you only get one chance with the treated brachytherapy area since the radiation "remembers" where the treatment occurred.

Wishing you all the best

Hi Oregonrain7 -

Thank you so much for sharing your story with me. This information is very helpful. Were you notified of any long-term side effects when you went through your brachytherapy? Did you have a positive pelvic washing? They are recommending I have 4 treatments which feels so radical, and I am trying to make my decision with as much information as possible. The treatment is all in the numbers, as they say. Currently, I have a 12% chance or recurrence, and with brachytherapy, it's reduced to 3% so I would do the treatment if I felt confident it wouldn't create more complicated issues down the road.

I also have been working with a genetic counselor to find out if I have Lynch since I also have two of the genetic markers. My family members did not provide their genetic information; we only went through my family history. If I am diagnosed with Lynch, I would need to coordinate all future care through a Lynch specialist/coordinator whom we have here at our local hospital.

I wish you the very best in your journey and will keep you in my thoughts.

I just want to chime in snd wish you luck. I was diagnosed with Stage IVb EC in 2019. Adenocsrcinoma (95%) and papillary serous (5%) grade 2. No radiation but only chemo. Since I was a suboptimal debulking (tumors remained on diaphragm, as well as lymph node that could not be removed due to the ureter and iliac vein basically embedded) radiation is being kept for a likely recurrence.

@gratefulcat
I had Endometriod Adenocarcinoma Stage 1A, Figo grade 2. I initially didn't require any treatments, but had a reoccurance 7 months after surgery and had 28 external beam radiation treatments and 3 high dose brachytherapy ones. For me the external beam ones were very quick and simple. I had plenty of gastrointestinal issues from them and the 3 brachytherapy ones were given after about a 10 day break. They were not painful but awkward and lasted much longer than the external beam ones. I believe mine were about 14 minutes each. Thankfully there were only 3 of them. I finished mine in December and just had my first followup with my Gynocological Oncologist and am currently awaiting the results of my tests. I also had positive pelvic washings but wasn't initially treated with radiation. I wish you well and would be happy to answer any questions you may have.

@gratefulcat That's wonderful that you are three weeks post and you feel well. Also, that's very good news with Stage1a. It could be upsetting but actually helpful that you know you are at high risk for Lynch Syndrome and that you will be carefully monitored.

I had two sessions of brachytherapy when I had a recurrence of endometrial (adenocarcinoma) two years post hysterectomy. The team at Mayo Clinic helped me to feel as a relaxed as one can be in that situation and explained everything before it happened. So, no surprises which I appreciated. I did not have any pain with the procedure and felt comfortable enough to get up and walk away afterwards. I was fatigued overall from the external radiation with the two brachytherapy sessions but that was expected.

Long term side effects? It was explained to me that with external and internal radiation I needed to use a vaginal moisturizer on a regular basis and a vaginal dilator. The scar tissue from radiation can occlude the vagina and it's important to do this for one's long-term comfort and your future vaginal and pelvic exams. Hopefully, your radiation oncologist and/or the education nurse will explain all this to you.

When do you start the radiation and brachytherapy?

There is a discussion on radiation therapy here and you can read what others have shared as well as post your questions or your experiences:

What kind of radiation did you get for your gynecological cancer?

-- https://connect.mayoclinic.org/discussion/types-of-radiation-treatments-for-gynecological-cancers/

Last year I was treated for endometrial cancer - grade 3, clear cell. Fortunately, it was stage 1A. I too was told the there was a possibility of Lynch Syndrome. Because of the clear cell diagnosis, I had chemotherapy which completed in November. In December I had 3 brachytherapy treatments. I had no issues with the treatment. There was almost no pain plus I have had few issues since. My radiologist was very careful about ensuring that my rectum and bladder were not radiated. This treatment was much easier than external radiation.

As for the Lynch Syndrome, I have been working with a geneticist to determine if this is inherited (versus acquired). I have two genes with variants of unknown significance that have been associated with Lynch. This is not enough to prove Lynch. Two of my first cousins have provided their genetic test results. They do not have these variants. I am interested how your medical team is handling the possibility of Lynch.

Hi Everyone - I am almost three weeks post hysterectomy and doing well. My cancer was staged as 1A with a positive pelvic washing which requires follow-up radiation/brachytherapy. During the process, I learned I have a high probability of Lynch Syndrome and will continue with additional cancer screenings over the next few months.

Has anyone experienced brachytherapy for endometrial cancer? How did they feel? Any long-term side effects?

Thanks for your support.

Thank you, and I will keep everyone posted. I very much appreciate all of the support here.