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5

Indication details

Control Arm
Docetaxel
Therapeutic Indication
Locally advanced or metastatic squamous NSCLC after prior ChT
Tumour Type
Thoracic Malignancies
Tumour Sub-type
Non-small-cell Lung Cancer - Squamous cell
Tumour Stage
Locally advanced or metastatic
Trial Name
CheckMate 017
NCT Number
NCT01642004
Trial Phase
Phase III

Approval details

FDA Approval
FDA approved
EMA Approval
EMA approved

Primary Outcome(s)

Primary Outcome(s)
OS
Evaluated Outcome
OS
Form(s)
Form 2a

Outcome Data

PFS Control
2.8 months
PFS Gain
0.7 months
PFS HR
0.62 (0.47-0.81)
OS Control
6 months
OS Gain
3.2 months, 5-year survival gain: 8.7%
OS HR
0.62 (0.48-0.79)

Adjustments

Toxicity Comment
Reduced grade 3/4 AE 7% vs 55%

Final Score (after adjustments)

Preliminary non-curative score

4

Toxicity adjustment
1+
Final non-curative score

5

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
55
Scorecard version
1
Issue date
11.12.2018
Last update
17.08.2023
Nivolumab CheckMate 017

PRELIMINARY SCORE

OS

ADJUSTMENTS

Less serious adverse events observed
Nivolumab CheckMate 017

FINAL SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
5
Overall Survival
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Thoracic Malignancies
Locally advanced or metastatic squamous NSCLC after prior ChT
Nivolumab
Docetaxel

My watchlist

    pdf
    pptx

    Legend

    Information about symbols, abbrevations and color codes

    Red = negative
    Green = positive
    Grey = neutral
    ? Grey + ? = neutral with pending data
    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

    QoL adjustments

    Red = negative / deterioration

    Green = positive / improvement

    Other adjustments*

    Red = negative / deterioration

    Green = positive / improvement

    Serious and disabling adverse effects

    Red = negative / deterioration

    Green = positive / improvement

    * Other adjustments include:

    - Long-term plateau in the survival curve
    - Long-term plateau in the PFS curve
    - Early stopping or crossover
    - Only improved PFS mature data shows no OS advantage and no improved Qol.

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