3
Indication details
- Control Arm
- Single arm
- Therapeutic Indication
- Advanced NSCLC with activating EGFR exon 20 insertion mutations, after failure of platinum-based therapy
- Tumour Type
-
Thoracic Malignancies
- Tumour Sub-type
- Non-small-cell Lung Cancer
- Tumour Stage
- Advanced
- Tumour Sub-Group
- EGFR+ exon 20 insertion mutations
- Trial Name
- CHRYSALIS
- NCT Number
- NCT02609776
- Trial Phase
- Phase I
Approval details
- FDA Approval
- FDA accelerated approval May 2021. FDA approval March 2024
- EMA Approval
- EMA (CHMP) October 2021 EC decision February 2022
Primary Outcome(s)
- Primary Outcome(s)
- ORR/DoR
- Evaluated Outcome
- PFS
- Form(s)
- Form 3
Outcome Data
- PFS Control
- 8.3 months
- ORR
- 40%
- DoR
- 11.1 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
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 317
- Scorecard version
- 1
- Issue date
- 16.03.2022
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: