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Cetuximab

Study of cetuximab as a single agent in patients with recurrent and/or metastatic SCCHN who failed to respond to platinum-based therapy
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NEB

Indication details

Control Arm
Single arm
Therapeutic Indication
Recurrent or metastatic SCCHN progressing after platinum-based therapy
Tumour Type
Head and neck cancer
Tumour Sub-type
Squamous cell
Tumour Stage
Recurrent or metastatic second line
Trial Name
Study of cetuximab as a single agent in patients with recurrent and/or metastatic SCCHN who failed to respond to platinum-based therapy
Trial Phase
Phase II

Approval details

FDA Approval
FDA approval April 2006
EMA Approval
Not EMA approved

Primary Outcome(s)

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

Outcome Data

ORR
13%
DoR
126 days (4.1 months)

Adjustments

QoL Comment
QoL was not a prespecified endpoint

Score (after adjustments)

Preliminary non-curative score

NEB

Non-curative score

NEB

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
393
Scorecard version
1
Issue date
10.08.2023
Cetuximab Study of cetuximab as a single agent in patients with recurrent and/or metastatic SCCHN who failed to respond to platinum-based therapy

PRELIMINARY SCORE

NEB

ADJUSTMENTS

Cetuximab Study of cetuximab as a single agent in patients with recurrent and/or metastatic SCCHN who failed to respond to platinum-based therapy

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
NEB
Overall Response Rate / Duration of Response
Head and neck cancer
Recurrent or metastatic SCCHN progressing after platinum-based therapy
Cetuximab
Single arm

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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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