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Nivo/Ipi (nivolumab and ipilimumab)

CheckMate 040
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3

Indication details

Control Arm
Single arm (Phase II)
FDA Therapeutic Indication
Patients with HCC who have been previously treated with sorafenib
Tumour Type
Gastrointestinal Cancers
Tumour Sub-type
Hepatobiliary Cancers - Hepatocellular Carcinoma
Tumour Stage
Unresectable or metastatic
Trial Name
CheckMate 040
NCT Number
NCT01658878
Trial Phase
Phase I/II

Approval details

FDA Approval
FDA approval March 2020
EMA Approval
Not approved by the EMA

Primary Outcome(s)

Primary Outcome(s)
ORR/DoR
Evaluated Outcome
ORR
Form(s)
Form 3

Outcome Data

ORR
32%
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
Approval was based on Arm A (4 doses nivolumab 1 mg/kg plus ipilimumab 3 mg/kg Q3W then nivolumab 240 mg Q2W)



Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
251
Scorecard version
1
Issue date
23.03.2021
Last update
15.06.2023
Nivo/Ipi (nivolumab and ipilimumab) CheckMate 040

PRELIMINARY SCORE

ORR

ADJUSTMENTS

Not qualified for an ESMO-MCBS credit
Nivo/Ipi (nivolumab and ipilimumab) CheckMate 040

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
Overall Survival
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
3
Overall Response Rate / Duration of Response
Gastrointestinal Cancers
Patients with HCC who have been previously treated with sorafenib
Nivo/Ipi (nivolumab and ipilimumab)
Single arm (Phase II)

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    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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