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1

Indication details

Combined Agent(s)
Fluoropyrimidine and platinum ChT (FOLFOX or CAPOX)
Control Arm
ChT (FOLFOX or CAPOX)
FDA Therapeutic Indication
First-line treatment for patients with advanced or metastatic gastric cancer, gastroesophageal junction cancer and oesophageal adenocarcinoma
Tumour Type
Gastrointestinal Cancers
Tumour Sub-type
Gastric or gastroesophageal junction cancer and oesophageal adenocarcinoma
Tumour Stage
Advanced or metastatic
Trial Name
CheckMate 649
NCT Number
NCT02872116
Trial Phase
Phase III

Approval details

FDA Approval
FDA approval April 2021
Comment
FDA approval is irrespective of tumour PD-L1 status and so data shown are for all randomised patients.

Primary Outcome(s)

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

Outcome Data

OS Control
11.6 months
OS Gain
2.2 months
OS HR
0.79 (0.71-0.88)

Adjustments

QoL Comment
QoL was an exploratory endpoint

Score (after adjustments)

Preliminary non-curative score

1

Non-curative score

1

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
289
Scorecard version
1
Issue date
17.09.2021
Last update
28.11.2023
Nivolumab CheckMate 649

PRELIMINARY SCORE

OS

ADJUSTMENTS

Nivolumab CheckMate 649

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
1
Overall Survival
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Gastrointestinal Cancers
First-line treatment for patients with advanced or metastatic gastric cancer, gastroesophageal junction cancer and oesophageal adenocarcinoma
Nivolumab + Fluoropyrimidine and platinum ChT (FOLFOX or CAPOX)
ChT (FOLFOX or CAPOX)

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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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