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A

Indication details

Control Arm
Placebo
FDA Therapeutic Indication
Adjuvant treatment of patients with urothelial carcinoma who are at high risk of recurrence after undergoing radical resection
Tumour Type
Genitourinary Cancers
Tumour Sub-type
Urothelial Carcinoma
Tumour Stage
Adjuvant
Trial Name
CheckMate 274
NCT Number
NCT02632409
Trial Phase
Phase III

Approval details

FDA Approval
FDA approval August 2021

Primary Outcome(s)

Primary Outcome(s)
DFS in ITT and PDL1>1% (coprimary)
Evaluated Outcome
DFS
Form(s)
Form 1

Outcome Data

OS HR
OS immature
DFS Control
6 months DFS 60.3%, median 10.8 months
DFS Gain
6 months DFS 14.6%, median gain 10 months
DFS HR
6 months DFS 14.6%, median gain 10 months

Adjustments

QoL Comment
QoL was an exploratory endpoint
Toxicity Comment
Discontinuation due to adverse effects 12.8% vs 2.0%

Score (after adjustments)

Curative score

A

Comment
EMA (CHMP) February 2022 EC decision April 2022 in the PD-L1 expression ≥1% population

FDA approval August 2021 in the ITT population

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
325
Scorecard version
1
Issue date
31.03.2021
Last update
11.11.2022
Nivolumab CheckMate 274

PRELIMINARY SCORE

DFS

ADJUSTMENTS

Nivolumab CheckMate 274

SCORE

A

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
Overall Response Rate / Duration of Response
Genitourinary Cancers
Adjuvant treatment of patients with urothelial carcinoma who are at high risk of recurrence after undergoing radical resection
Nivolumab
Placebo

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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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