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2

Indication details

Control Arm
Placebo
FDA Therapeutic Indication
Treatment of aggressive and symptomatic MTC in patients with unresectable locally acvanced or metastatic disease in adults, children and adolescents aged 5 years and older. For patients in whom re-arranged-during-transfection(RET) mutation is not known or is negative, a possible lower benefit should be taken into account before individual treatment decision
Tumour Type
Endocrine Tumours
Tumour Sub-type
Thyroid Cancer - medullary
Tumour Stage
Unresectable locally advanced or metastatic
Tumour Sub-Group
MKI targeting RET, VEGFR2 and EGFR
Trial Name
ZETA
NCT Number
NCT00410761
Trial Phase
Phase III

Approval details

FDA Approval
FDA approval April 2011
EMA Approval
EMA (CHMP) November 2011 EC decision January 2012

Primary Outcome(s)

Primary Outcome(s)
mPFS
Evaluated Outcome
PFS
Form(s)
Form 2b

Outcome Data

PFS Control
19.3 months
PFS Gain
11.2 months (reported estimate)
PFS HR
0.46 (0.31-0.69)
OS HR
OS immature, not significant

Adjustments

QoL Comment
Not qualified for an ESMO-MCBS credit
Time to worsening of pain was assessed as a secondary endpoint; this does not constitute a QoL evaluation.
Toxicity Comment
Increased toxicity (11% Grade ≥3 diarrhoea vs 2%)

Score (after adjustments)

Preliminary non-curative score

3

Toxicity adjustment
-1
Non-curative score

2

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
137
Scorecard version
1
Issue date
06.11.2019
Last update
21.07.2023
Vandetanib ZETA

PRELIMINARY SCORE

PFS

ADJUSTMENTS

Not qualified for an ESMO-MCBS credit
More serious and disabling adverse events observed
Vandetanib ZETA

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
Overall Survival
2
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Endocrine Tumours
Treatment of aggressive and symptomatic MTC in patients with unresectable locally acvanced or metastatic disease in adults, children and adolescents aged 5 years and older. For patients in whom re-arranged-during-transfection(RET) mutation is not known or is negative, a possible lower benefit should be taken into account before individual treatment decision
Vandetanib
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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