Bladder & urothelial cancer: guideline history
4 dated versions from 2020 to 2025 listing 8 changes. Pick two versions to see what changed between them; the timeline below shows every version with the event it is anchored to.
- RecategorisedMetastatic, first lineEnfortumab vedotin plus pembrolizumab becomes the preferred first-line regimen for all patients; platinum chemotherapy moves to other recommended regimens.cisplatin-based chemotherapy preferred EV plus pembrolizumab preferred (category 1)
- AddedMetastatic, cisplatin-eligible, first lineNivolumab with gemcitabine-cisplatin as an alternative first-line regimen.
- AddedMuscle-invasive, cisplatin-eligible, perioperativeDurvalumab with neoadjuvant gemcitabine-cisplatin, continued after cystectomy.
- AddedNon-muscle-invasive, BCG-unresponsiveTAR-200 intravesical gemcitabine system as a bladder-sparing option.
Timeline
Anchored to: FDA accelerated approval of enfortumab vedotin (December 2019) and approval of avelumab maintenance (June 2020, JAVELIN Bladder 100)
- addedMetastatic, after platinum and PD-(L)1: Enfortumab vedotin as a category 1 option after platinum chemotherapy and a checkpoint inhibitor.
- addedMetastatic, maintenance after platinum: Avelumab maintenance for patients without progression on first-line platinum chemotherapy.
Anchored to: Annals of Oncology publication, 2022
- addedMetastatic, maintenance after platinum: Avelumab maintenance recommended after platinum-based chemotherapy [I, A; ESMO-MCBS 4].
- addedMuscle-invasive, adjuvant: Adjuvant nivolumab for high-risk disease after cystectomy [I, B].
Anchored to: FDA approvals of enfortumab vedotin with pembrolizumab (December 2023, EV-302) and nivolumab with gemcitabine-cisplatin (March 2024, CheckMate 901)
- recategorisedMetastatic, first line: Enfortumab vedotin plus pembrolizumab becomes the preferred first-line regimen for all patients; platinum chemotherapy moves to other recommended regimens.cisplatin-based chemotherapy preferred → EV plus pembrolizumab preferred (category 1)
- addedMetastatic, cisplatin-eligible, first line: Nivolumab with gemcitabine-cisplatin as an alternative first-line regimen.
Anchored to: FDA approvals of perioperative durvalumab with gemcitabine-cisplatin (March 2025, NIAGARA) and the TAR-200 intravesical gemcitabine system for BCG-unresponsive disease (September 2025, SunRISe-1)
- addedMuscle-invasive, cisplatin-eligible, perioperative: Durvalumab with neoadjuvant gemcitabine-cisplatin, continued after cystectomy.
- addedNon-muscle-invasive, BCG-unresponsive: TAR-200 intravesical gemcitabine system as a bladder-sparing option.
Where the bodies stand today
| Setting and intervention | NCCN | ESMO | NICE | ASCO | Verdict |
|---|---|---|---|---|---|
Bladder & urothelial cancer · Metastatic, first line Enfortumab vedotin plus pembrolizumab (EV-302) | Preferred Category 1, preferred 2024-03 | Recommended I, A; ESMO-MCBS 4 2024 | Recommended 2024 | · | Bodies agree |
Other cancers
Each entry is anchored to a dated public event and links to the guideline body’s page for the disease; NCCN “Summary of changes” pages sit behind a free login and are not reproduced. Version labels say “update” where the NCCN version number has not been verified. Corrections are welcome via the repository.