4
Indication details
- Combined Agent(s)
- Cisplatin and 5-FU ChT
- Control Arm
- Placebo + cisplatin and 5-FU ChT
- FDA Therapeutic Indication
- First-line treatment
- Tumour Type
-
Gastrointestinal Cancers
- Tumour Sub-type
- Oesophageal squamous cell carcinoma
- Tumour Stage
- Locally advanced unresectable or metastatic
- Tumour Sub-Group
- HER2- GEJ PD-L1 (squamous cell) CPS ≥10
- Trial Name
- KEYNOTE-590
- NCT Number
- NCT03189719
- Trial Phase
- Phase III
Approval details
- FDA Approval
- FDA approval March 2021 Scoring of sub-group analysis
- EMA Approval
- EMA (CHMP) May 2021 EC decision July 2021
Primary Outcome(s)
- Primary Outcome(s)
- OS
- Evaluated Outcome
- OS
- Form(s)
- Form 2a
Outcome Data
- OS Control
- 8.8 months
- OS Gain
- 5.1 months
- OS HR
- 0.57 (0.43-0.75)
Adjustments
- QoL Comment
-
QoL data pending
Score (after adjustments)
- Preliminary non-curative score
-
4
- Non-curative score
-
4
- Comment
-
Scoring of sub-group analysis
EMA (CHMP) May 2021
EC decision July 2021
FDA approval March 2021
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 311
- Scorecard version
- 1
- Issue date
- 20.12.2021
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: