2
Indication details
- Control Arm
- Single arm
- FDA Therapeutic Indication
- Advanced NSCLC with a BRAF V600 mutation
- Tumour Type
-
Thoracic Malignancies
- Tumour Sub-type
- Non-small-cell Lung Cancer
- Tumour Stage
- Advanced
- Tumour Sub-Group
- BRAF V600E (Treatment-naïve (Cohort C))
- NCT Number
- NCT01336634
- Trial Phase
- Phase II
Approval details
- FDA Approval
- FDA approval June 2017
- EMA Approval
- EMA (CHMP) February 2017 EC decision May 2017
Primary Outcome(s)
- Primary Outcome(s)
- ORR and mPFS
- Evaluated Outcome
- ORR
- Form(s)
- Form 3
Outcome Data
- PFS Control
- 10.2 months
- OS Control
- 18.2 months
- ORR
- 68.40%
Adjustments
- QoL Comment
-
Not qualified for an ESMO-MCBS credit
- Toxicity Comment
-
Serious adverse events: 56%
Score (after adjustments)
- Preliminary non-curative score
-
3
- Toxicity adjustment
- 1-
- Non-curative score
-
2
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 131
- Scorecard version
- 1
- Issue date
- 16.05.2019
- Last update
- 17.08.2023
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: