3
Indication details
- Combined Agent(s)
- IFL (irinotecan, leucovorin, fluorouracil)
- Control Arm
- IFL (irinotecan, leucovorin, fluorouracil) + placebo
- FDA Therapeutic Indication
- Treatment of patients with metastatic carcinoma of the colon or rectum
- Tumour Type
-
Gastrointestinal Cancers
- Tumour Sub-type
- Colon and Rectal Cancer
- Tumour Stage
- Metastatic
- Trial Name
- AVF2107g
- NCT Number
- NCT00109070
- Trial Phase
- Phase III
Approval details
- FDA Approval
- FDA approval February 2004
- EMA Approval
- EMA approval January 2005
Primary Outcome(s)
- Primary Outcome(s)
- OS
- Evaluated Outcome
- OS
- Form(s)
- Form 2a
Outcome Data
- OS Control
- 15.6 months
- OS Gain
- 4.7 months
- OS HR
- 0.66 (0.54-0.81)
Adjustments
- QoL Comment
-
No QoL benefit
Score (after adjustments)
- Preliminary non-curative score
-
3
- Non-curative score
-
3
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 19
- Scorecard version
- 1
- Issue date
- 11.12.2018
- Last update
- 08.02.2024
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: