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Eribulin

Study 305 & Study 301 (Pooled analysis)
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1

Indication details

Control Arm
Treatment of physician's choice
FDA Therapeutic Indication
Treatment of patients with locally advanced or metastatic breast cancer who have progressed after at least one chemotherapeutic regimens for advanced disease. Prior therapy should have included an anthracycline and a taxane unless patients were not suitable for these treatments
Tumour Sub-type
Breast Cancer
Tumour Stage
Metastatic
Tumour Sub-Group
HER2-
Trial Name
Study 305 & Study 301 (Pooled analysis)
NCT Number
NCT00388726│NCT00337103
Trial Phase
Phase III

Approval details

EMA Approval
EMA approved

Primary Outcome(s)

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

Outcome Data

OS Control
12 months
OS Gain
3.1 months
OS HR
0.84 (0.74-0.96)

Adjustments

QoL Comment
Not qualified for an ESMO-MCBS credit

Score (after adjustments)

Preliminary non-curative score

1

Non-curative score

1

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
14
Scorecard version
1
Issue date
11.12.2018
Last update
14.08.2023
Eribulin Study 305 & Study 301 (Pooled analysis)

PRELIMINARY SCORE

OS

ADJUSTMENTS

Not qualified for an ESMO-MCBS credit
Eribulin Study 305 & Study 301 (Pooled analysis)

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
Treatment of patients with locally advanced or metastatic breast cancer who have progressed after at least one chemotherapeutic regimens for advanced disease. Prior therapy should have included an anthracycline and a taxane unless patients were not suitable for these treatments
Eribulin
Treatment of physician's choice

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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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