Papillary renal cell carcinoma
Prepared with OnCo (onco.cc/prep/papillary-rcc/). 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
13 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 MET mutation, amplification or chromosome 7 gain, Fumarate hydratase losswith germline FH testing, CDKN2A loss, Germline MET testing in young or multifocal disease), 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 (localised), which of the standard options do you recommend and why?
- 6.For my situation (metastatic), which of the standard options do you recommend and why?
- 7.Am I a candidate for Cabozantinib, Savolitinib, Sunitinib or related drugs, and what side effects should I expect?
- 8.For my situation (hereditary syndromes), which of the standard options do you recommend and why?
- 9.Are there clinical trials I could join, for example of Savolitinib, Cabozantinib?
- 10.Would a second opinion at a high-volume centre change anything, and can you help arrange it?
- 11.What supportive care (symptom control, nutrition, exercise, mental health, financial help) is available from the start?
- 12.I read that “Small trials; most evidence is extrapolated from clear cell disease”. How does that affect my plan?
- 13.I read that “No approved therapy specific to FH-deficient cancer”. How does that affect my plan?
Tests and results to bring
Biomarker results to ask for: MET mutation, amplification or chromosome 7 gain, Fumarate hydratase loss (2SC immunohistochemistry) with germline FH testing, CDKN2A loss (poor outlook), Germline MET testing in young or multifocal disease.
Scans and tests linked to this cancer: Active surveillance.
Bring copies of scan reports, pathology and blood results, and a list of every medicine and supplement.
The treatments I may be offered
- Localised: Partial or radical nephrectomy, ablation or surveillance as for other kidney cancers; adjuvant therapy evidence is thin. (Thermal ablation (RFA, microwave, cryo), Active surveillance)
- Metastatic: Cabozantinib first line (PAPMET); savolitinib for MET-driven tumours; immunotherapy combinations on single-arm data; clinical trials preferred. (Cabozantinib, Savolitinib, MET, Sunitinib, Pembrolizumab)
- Hereditary syndromes: Early surgery for FH-deficient tumours because they spread early; surveillance in MET carriers; genetic counselling of relatives. (MET)
From the standard of care recorded for this cancer; which apply depends on your stage and biomarkers. Ask which the team recommends and why.