Advanced or recurrent endometrial cancer
Prepared with OnCo (onco.cc/prep/advanced-recurrent-endometrial-cancer/). Orientation, not medical advice; your team knows your case.
My details
What I know, what is unclear, changes to discuss
Saved in this browserMy questions
21 on the sheet- 1.What is my exact diagnosis, stage, and grade, and which tests established them?
- 2.Which biomarkers have been tested on my tumour (for example MMR and MSI status, p53 and POLE, HER2 immunohistochemistry, Oestrogen and progesterone receptors, PD-L1), and what were the results?
- 3.Which subtype is my cancer, and does that change the recommended treatment?
- 4.Is germline (inherited) genetic testing recommended for me or my family?
- 5.For my situation (first line, dmmr), which of the standard options do you recommend and why?
- 6.Am I a candidate for Dostarlimab, Pembrolizumab, Carboplatin or related drugs, and what side effects should I expect?
- 7.How do the results of RUBY / ENGOT-EN6 / GOG-3031 and NRG-GY018 / KEYNOTE-868 apply to someone like me?
- 8.For my situation (first line, pmmr), which of the standard options do you recommend and why?
- 9.Am I a candidate for Pembrolizumab, Dostarlimab, Durvalumab or related drugs, and what side effects should I expect?
- 10.How do the results of DUO-E / GOG-3041 / ENGOT-EN10 apply to someone like me?
- 11.For my situation (after platinum, pmmr), which of the standard options do you recommend and why?
- 12.Am I a candidate for Lenvatinib, Pembrolizumab, Trastuzumab deruxtecan or related drugs, and what side effects should I expect?
- 13.How do the results of KEYNOTE-775 / Study 309 and DESTINY-PanTumor02 apply to someone like me?
- 14.For my situation (after platinum, dmmr without prior immunotherapy), which of the standard options do you recommend and why?
- 15.Am I a candidate for Dostarlimab, Pembrolizumab, and what side effects should I expect?
- 16.For my situation (isolated pelvic recurrence), which of the standard options do you recommend and why?
- 17.Are there clinical trials I could join, for example of Sacituzumab tirumotecan, Rinatabart sesutecan, RAINFOL-01 (Rina-S), Trastuzumab deruxtecan?
- 18.Would a second opinion at a high-volume centre change anything, and can you help arrange it?
- 19.What supportive care (symptom control, nutrition, exercise, mental health, financial help) is available from the start?
- 20.I read that “What to give after progression on first-line immunotherapy”. How does that affect my plan?
- 21.I read that “The small benefit and real toxicity of immunotherapy in proficient tumours”. How does that affect my plan?
The words I may hear
- POLE ultramutation (POLEmut): A pathogenic mutation in the proofreading part of the POLE gene gives an endometrial tumour hundreds of mutations per megabase and, paradoxically, one of the best outlooks of any womb cancer, so finding it can spare a woman chemotherapy or radiotherapy.
- Microsatellite-stable (MSS) / mismatch-repair proficient (pMMR): The 'normal' result on the mismatch-repair test: the tumour has intact DNA spell-checking and few mutations.
- Radiotherapy: Using high-energy X-rays or particles to damage the DNA of cancer cells in a precisely aimed volume of the body.
- Microsatellite instability (MSI-H) / mismatch repair deficiency (dMMR): Microsatellite instability is the mark of a broken DNA spell-checker (loss of MLH1, MSH2, MSH6 or PMS2) that leaves thousands of mutations, so the tumour displays abnormal proteins that T cells can recognise.
Tests and results to bring
Biomarker results to ask for: MMR and MSI status (drives the size of immunotherapy benefit), p53 and POLE (molecular class), HER2 immunohistochemistry (trastuzumab deruxtecan), Oestrogen and progesterone receptors (endocrine therapy), PD-L1 (not required), TROP2 and folate receptor alpha (antibody-drug conjugate trials), CA-125 for monitoring.
Bring copies of scan reports, pathology and blood results, and a list of every medicine and supplement.
The treatments I may be offered
- First line, dMMR: Carboplatin-paclitaxel with dostarlimab (RUBY) or pembrolizumab (NRG-GY018), then maintenance immunotherapy for up to three years or two years respectively. (Dostarlimab, Pembrolizumab, Carboplatin, Paclitaxel / nab-paclitaxel, RUBY / ENGOT-EN6 / GOG-3031, NRG-GY018 / KEYNOTE-868, Chemotherapy + PD-1/PD-L1 blockade, first-line advanced endometrial cancer, Microsatellite instability (MSI-H) / mismatch repair deficiency (dMMR))
- First line, pMMR: Carboplatin-paclitaxel with pembrolizumab or dostarlimab, or durvalumab followed by durvalumab-olaparib maintenance (DUO-E); trastuzumab added for HER2-positive serous carcinoma. (Pembrolizumab, Dostarlimab, Durvalumab, Olaparib, DUO-E / GOG-3041 / ENGOT-EN10, Trastuzumab, Microsatellite-stable (MSS) / mismatch-repair proficient (pMMR))
- Isolated pelvic recurrence: Radiotherapy with brachytherapy for vaginal recurrence after surgery alone; exenteration in selected central recurrences after radiotherapy. (IMRT / IGRT (modern external beam), Brachytherapy, Radiotherapy)
- After platinum, pMMR: Lenvatinib with pembrolizumab (KEYNOTE-775); trastuzumab deruxtecan for HER2-expressing tumours; aromatase inhibitors or progestins for low-grade receptor-positive disease. (Lenvatinib, Pembrolizumab, KEYNOTE-775 / Study 309, Trastuzumab deruxtecan, DESTINY-PanTumor02, Letrozole (and other aromatase inhibitors), Progestins (megestrol acetate, medroxyprogesterone, levonorgestrel IUD))
- After platinum, dMMR without prior immunotherapy: Single-agent dostarlimab or pembrolizumab. (Dostarlimab, Pembrolizumab, Immune checkpoint inhibitors)
From the standard of care recorded for this cancer; which apply depends on your stage and biomarkers. Ask which the team recommends and why.