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Printable Handouts
Navigable Slide Index
- Introduction
- Disclosures
- Enfortumab vedotin phase 1 (EV-101) study in patients with metastatic urothelial cancer
- EV-301: EV vs. chemo post platinum & PD1/L1 inhibitor
- Enfortumab-vedotin + pembrolizumab as first-line therapy for cisplatin-ineligible advanced UC
- EV-302/KEYNOTE-A39 (NCT04223856)
- EV-302 results: Survival
- EV-302 results: Response rates
- EV-302 results: Adverse events
- Updated outcomes in TROPHY-U-01 cohort 1 study
- Phase III trials evaluating salvage sacituzumab govitecan
- Disitamab vedotin + toripalimab (PD1 inhibitor) is active in mUC
- Efficacy and safety of trastuzumab deruxtecan in patients with HER2-expressing solid tumors
- Trastuzumab deruxtecan (T-Dxd) in Her2 IHC 3+ tumors
- FGFR mutations and fusions are important therapeutic targets
- Erdafitinib for mUC following platinum: BLC2001 phase II trial
- Erdafitinib: Most patients with FGFR2/3 mutations/fusions exhibited tumor shrinkage
- Phase 3 THOR study
- Phase 3 THOR study: Overall survival
- Phase 3 THOR study: Response rate
- Urothelial carcinoma therapy, January 2026
- Ongoing first-line phase III trials in advanced UC
- Neoadjuvant MVAC improves survival in resectable MIBC: SWOG-8710
- MRC neoadjuvant CMV trial (N=976): Overall survival
- MRC neoadjuvant trial: Overall survival with radiotherapy and cystectomy
- DD-MVAC x 3-4 cycles as neoadjuvant therapy: Relapse-free survival by pT0 rate
- GETUG/AFU V05 VESPER phase Ill trial
- VESPER peri-op ddMVAC x 6 vs. GC x 4
- S1314: Randomized phase II trial of GC x 4 vs. ddMVAC x 4
- Neoadjuvant cisplatin-based chemotherapy for upper tract urothelial carcinoma (UTUC)
- Pathologic remission with cisplatin-based NAC is associated with survival
- Adjuvant chemotherapy: Randomized trials not definitive
- POUT: A phase Ill randomized trial of peri-operative chemotherapy vs. surveillance in UTUC
- CHECKMATE274: Adjuvant nivolumab for high-risk MIUC will impact firstline therapy for mUC
- A031501 AMBASSADOR: Disease-free survival
- Minimal residual disease using post-op ctDNA to select for adjuvant atezolizumab
- IMvigor010: ctDNA(+) and TMBhigh
- IMvigor011: Post-op atezolizumab (up to 1 year) if MRD by ctDNA turns positive
- IMvigor011: Post-op atezolizumab (up to 1 year) if MRD ctDNA turns positive (1)
- IMvigor011: Post-op atezolizumab (up to 1 year) if MRD ctDNA turns positive (2)
- A032103 (MODERN) schema
- mRNA-4157 (V940): Customizable individualized mRNA immunotherapy
- V940-005 randomized phase II trial
- Neoadjuvant IO therapy trials for MIBC
- Neoadjuvant Chemo-IO combination therapy trials for MIBC
- NIAGARA: Event-free survival by blinded independent central review (ITT)
- NIAGARA: Overall survival (ITT)
- NIAGARA: Pathological complete response
- KEYNOTE-905/EV-303 study
- KEYNOTE-905/EV-303 study: Event free survival (EFS)
- KEYNOTE-905/EV-303 study: Overall survival (OS)
- Key secondary endpoint: pCR
- EV304 (KEYNOTE B-15): EV + Pembrolizumab as perioperative therapy for cisplatin-eligible MIBC
- Neoadjuvant phase III trials in muscle-invasive urothelial carcinoma
- Neoadjuvant ddMVAC +/- durvalumab for UTUC: EA8192
- Chemoradiation for locally advanced bladder cancer: 5-FU + Mitomycin-C
- Bladder-preserving chemoradiation +/- PD1/L1 inhibitor: Ongoing phase III trials
- New agents for BCG-unresponsive or high risk-non-muscle-invasive bladder cancer
- Conclusions
Topics Covered
- Ongoing clinical trials for bladder cancer
- Enfortumab-vedotin & pembrolizumab as first-line therapy
- Disitamab vedotin & toripalimab (PD1 inhibitor) for the treatment of metastatic UC
- Erdafitinib for the treatment of metastatic UC with FGFR2/3 mutations/fusions
- Remission with cisplatin-based NAC
- mRNA-4157 (V940): customizable individualized mRNA immunotherapy
- Adjuvant chemotherapy
- Neoadjuvant Chemo-IO combination therapy
Links
Categories:
Therapeutic Areas:
Talk Citation
Sonpavde, G.P. (2026, September 30). Bladder cancer: types, risk factors, diagnosis, treatment and prevention: further clinical trials [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved October 1, 2026, from https://doi.org/10.69645/NTSU9220.Export Citation (RIS)
Publication History
- Published on September 30, 2026
Financial Disclosures
- Conflicts and Disclosures in the past 24 months are as follows: Advisory Board: EMD Serono, BMS, Merck, Seattle Genetics, Astellas, Janssen, Bicycle Therapeutics, Pfizer, Gilead, Scholar Rock, Eli Lilly, Loxo Oncology, Vial, Aktis, Daiichi-Sankyo, GSK • Consultant/Scientific Advisory Board (SAB)/trial steering committee: Syapse, Merck, Servier, Ellipses, Biosite Research • Research Support to institution: EMD Serono, Jazz Therapeutics, Bayer, Sumitomo Pharma, Blue Earth Diagnostics, Exelixis • Speaker: Seagen, Gilead, Natera, Exelixis, Janssen, Astellas, Bayer, Aveo, Pfizer, Merck, Astrazeneca • Data safety monitoring committee (honorarium): None • Employment: Spouse employed by Myriad, Exact Sciences • Travel: BMS, Astellas • CME-certified speaking: Research to Practice, PeerView Institute, Ideology Health, IBCU/Grand Rounds in Urology, Targeted Oncology, Total health Conference (THC) • Writing/Educational fees: Uptodate, Practice Update, Onviv, DAVA Oncology, PrecisCa
Bladder cancer: types, risk factors, diagnosis, treatment and prevention: further clinical trials
Published on September 30, 2026
37 min
A selection of talks on Clinical Practice
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. I'm Dr. Guru Sonpavde.
I'm the GU oncology and phase
one director at
the Advent Health Cancer
Istitute in Orlando, Florida.
So I'm here to discuss
bladder cancer, types,
risk factors, diagnosis,
treatment, and prevention.
Welcome to Part 2 of my talk.
0:23
These are my disclosures.
0:27
Next we move on to the era of
antibody-drug conjugates
in the next slide.
This shows you a drug
called enfortumab vedotin.
This is an antibody
drug conjugate.
This is an antibody backbone
which targets nectin-4.
It binds to nectin-4,
which is a surface
membrane protein
overexpressed in
urothelial carcinoma.
This [inaudible]
monoclonal antibody is
conjugated to a toxin called
monomethyl auristatin E,
so MMAE.This is a tubulin toxin,
very potent tubulin-disrupting
chemotherapy essentially.
So this agent was
looked at early
on in patients who
are progressing
post-chemotherapy and PD-L1
immune checkpoint inhibition
and demonstrated a
high response rate of
approximately 40-45%
as shown here.
1:21
So these data led to,
on the next slide,
the EV-301 trial where
EV the enfortumab vedotin
antibody drug conjugate,
was compared versus
historical chemotherapy,
which was taxane or vinflunine,
in patients in the
third-line setting which is
post-platinum and PD-1/L1
inhibitor-treated patients.
As shown here, there was an
improvement in survival,
the survival median was
12.9 months for
enfortumab vedotin
versus 8.9 months for
chemotherapy and these data
with a hazard ratio of 0.7.
These led to approval of
enfortumab vedotin as therapy
for post-platinum and PD-1/L1
inhibitor-treated patients.