3
Indication details
- Combined Agent(s)
- Bevacizumab, paclitaxel and carboplatin
- Control Arm
- Bevacizumab, paclitaxel and carboplatin
- Therapeutic Indication
- In patients with EGFR mutant or ALK-positive NSCLC, atezolizumab, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies
- Tumour Type
-
Thoracic Malignancies
- Tumour Sub-type
- Non-small-cell Lung Cancer
- Tumour Stage
- Advanced
- Tumour Sub-Group
- EGFR+ or ALK-positive
- Trial Name
- IMpower150
- NCT Number
- NCT02366143
- Trial Phase
- Phase III
Approval details
- FDA Approval
- FDA approval December 2018
- EMA Approval
- EMA (CHMP) January 2019 EC decision March 2019
Primary Outcome(s)
- Primary Outcome(s)
- PFS
- Evaluated Outcome
- PFS
- Form(s)
- Form 2b
Outcome Data
- PFS Control
- 6.1 months
- PFS Gain
- 3.1 months
- PFS HR
- 0.59 (0.37–0.94)
Adjustments
- QoL Comment
-
QoL data pending
- Toxicity Comment
-
Similar toxicity
Score (after adjustments)
- Preliminary non-curative score
-
3
- Non-curative score
-
3
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 156
- Scorecard version
- 1
- Issue date
- 16.03.2020
- 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: