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4

Indication details

Combined Agent(s)
Fulvestrant
Control Arm
Fulvestrant + placebo
FDA Therapeutic Indication
Patients with hormone receptor-positive, HER2-negative locally advanced or MBC who have received prior endocrine therapy (ET)
Tumour Sub-type
Breast Cancer
Tumour Stage
Locally advanced or metastatic
Tumour Sub-Group
HR+ HER2-
Trial Name
PALOMA-3
NCT Number
NCT01942135
Trial Phase
Phase III

Approval details

EMA Approval
EMA (CHMP) September 2016 EC decision November 2016
Comment
FDA approval February 2026

Primary Outcome(s)

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

Outcome Data

PFS Control
4.6 months
PFS Gain
4.9 months
PFS HR
0.46 (0.36-0.59)
OS Control
28.0 months
OS Gain
6.9 months
OS HR
0.81 (0.64-1.03) Not significant (mature)

Adjustments

QoL Comment
Delayed deterioration of global QoL

Score (after adjustments)

Preliminary non-curative score

3

QoL adjustment
1+
Non-curative score

4

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
6
Scorecard version
1
Issue date
11.12.2018
Last update
25.04.2024
Palbociclib PALOMA-3

PRELIMINARY SCORE

PFS

ADJUSTMENTS

Delayed deterioration in global QoL
Palbociclib PALOMA-3

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
Overall Survival
4
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Patients with hormone receptor-positive, HER2-negative locally advanced or MBC who have received prior endocrine therapy (ET)
Palbociclib + Fulvestrant
Fulvestrant + placebo

My watchlist

    pdf
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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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