3
Indication details
- Control Arm
- Single arm (Phase II)
- Therapeutic Indication
- Efficacy in Patients With Advanced Malignant Perivascular Epithelioid Cell Tumors (PEComa)
- Tumour Type
-
Sarcoma
- Tumour Sub-type
- Perivascular epithelioid
- Tumour Stage
- Locally advanced unresectable or metastatic
- Trial Name
- AMPECT
- NCT Number
- NCT02494570
- Trial Phase
- Phase II
Approval details
- FDA Approval
- FDA approval November 2021
Primary Outcome(s)
- Primary Outcome(s)
- ORR, DoR
- Evaluated Outcome
- ORR, DoR
- Form(s)
- Form 3
Outcome Data
- PFS Control
- 10.6 months
- ORR
- 39% (21.8-57.8%)
- EFS control
- 9+ months
- DoR
- 9+ months
Adjustments
- QoL Comment
-
Not qualified for an ESMO-MCBS credit
Score (after adjustments)
- Preliminary non-curative score
-
3
- Non-curative score
-
3
- Comment
-
FDA approval November 2021
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 312
- Scorecard version
- 1
- Issue date
- 20.01.2022
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: