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C

Indication details

Control Arm
Ipilimumab 10mg/kg
Therapeutic Indication
Adjuvant treatment of adults and adolescents 12 years of age and older with Stage IIB or IIC melanoma, or melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection
Tumour Type
Skin Cancers
Tumour Sub-type
Cutaneous Melanoma
Tumour Stage
Adjuvant
Trial Name
CheckMate 238
NCT Number
NCT02388906
Trial Phase
Phase III

Approval details

EMA Approval
EMA (June 2018) EC decision October 2018
Comment
EMA treatment setting updated in July 2023

Primary Outcome(s)

Primary Outcome(s)
RFS
Evaluated Outcome
RFS
Form(s)
Form 1

Outcome Data

OS Control
4-years 76.6%
OS Gain
4-years 1.3%
OS HR
0.87 (0.66-1.14) Not significant
RFS Control
24.1 months 4-year 41.2%
RFS Gain
28.3 months 4-year 10.5%
RFS HR
0.71 (0.60-0.86)

Adjustments

QoL Comment
QoL data pending
Toxicity Comment
Fewer treatment-related grade 3 or 4 AEs: 14.4% versus 45.9%
Fewer treatment discontinuation due to treatment-related AEs: 7.7% versus 41.7%

Final Score (after adjustments)

Final curative score

C

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
174
Scorecard version
1
Issue date
09.06.2020
Last update
24.07.2023
Nivolumab CheckMate 238

PRELIMINARY SCORE

RFS

ADJUSTMENTS

?
QoL data pending
Nivolumab CheckMate 238

FINAL SCORE

C

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
Skin Cancers
Adjuvant treatment of adults and adolescents 12 years of age and older with Stage IIB or IIC melanoma, or melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection
Nivolumab
Ipilimumab 10mg/kg

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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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