A
Indication details
- Control Arm
- Placebo
- FDA Therapeutic Indication
- Adjuvant treatment of patients with urothelial carcinoma who are at high risk of recurrence after undergoing radical resection
- Tumour Type
-
Genitourinary Cancers
- Tumour Sub-type
- Urothelial Carcinoma
- Tumour Stage
- Adjuvant
- Trial Name
- CheckMate 274
- NCT Number
- NCT02632409
- Trial Phase
- Phase III
Approval details
- FDA Approval
- FDA approval August 2021
Primary Outcome(s)
- Primary Outcome(s)
- DFS in ITT and PDL1>1% (coprimary)
- Evaluated Outcome
- DFS
- Form(s)
- Form 1
Outcome Data
- OS HR
- OS immature
- DFS Control
- 6 months DFS 60.3%, median 10.8 months
- DFS Gain
- 6 months DFS 14.6%, median gain 10 months
- DFS HR
- 6 months DFS 14.6%, median gain 10 months
Adjustments
- QoL Comment
-
QoL was an exploratory endpoint
- Toxicity Comment
-
Discontinuation due to adverse effects 12.8% vs 2.0%
Score (after adjustments)
- Curative score
-
A
- Comment
-
EMA (CHMP) February 2022 EC decision April 2022 in the PD-L1 expression ≥1% population
FDA approval August 2021 in the ITT population
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 325
- Scorecard version
- 1
- Issue date
- 31.03.2021
- Last update
- 11.11.2022
Legend
Information about symbols, abbrevations and color codes
- DFS
- Disease-Free Survival
- DoR
- Duration of Response
- EFS
- Event-Free Survival
- HR
- Hazard Ratio
- NEB
- No evaluable benefit
- NI
- Non-inferiority Study
- ORR
- Overall Response Rate
- OS
- Overall Surival
- pCR
- Pathological Complete Response/Remission
- PFS
- Progression-Free Survival
- QoL
- Quality of Life
- RFS
- Relapse-Free Survival
- RR
- Response Rate
QoL adjustments
Other adjustments*
Serious and disabling adverse effects
Red = negative / deterioration
Green = positive / improvement
Red = negative / deterioration
Green = positive / improvement
Red = negative / deterioration
Green = positive / improvement
Red = negative / deterioration
Green = positive / improvement
* Other adjustments include: