3
Indication details
- Combined Agent(s)
- Binimetinib
- Control Arm
- Single arm
- FDA Therapeutic Indication
- Encorafenib plus binimetinib for adult patients with metastatic non-small cell lung cancer (NSCLC) with a BRAF V600E mutation - previously treated
- Tumour Type
-
Thoracic Malignancies
- Tumour Sub-type
- Non-small-cell Lung Cancer
- Tumour Stage
- Metastatic
- Tumour Sub-Group
- BRAF V600E mutation
- Trial Name
- PHAROS
- NCT Number
- NCT03915951
- Trial Phase
- Phase II
Approval details
- FDA Approval
- FDA approval October 2023
- EMA Approval
- EMA (CHMP) Positive recommendations on new therapeutic indications July 2024
Primary Outcome(s)
- Primary Outcome(s)
- ORR DoR- previously treated
- Evaluated Outcome
- ORR
- Form(s)
- Form 3
Outcome Data
- PFS Control
- 9.3 months
- ORR
- 46%
- DoR
- 16.7 months
Adjustments
- QoL Comment
-
Not qualified for an ESMO-MCBS credit
Score (after adjustments)
- Preliminary non-curative score
-
3
- Non-curative score
-
3
Scorecard details
- Scorecard ID
- 404
- Scorecard version
- 1
- Issue date
- 20.11.2023
- Last update
- 29.07.2024
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: