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1

Indication details

Combined Agent(s)
Capecitabine
Control Arm
Lapatinib plus capecitabine
FDA Therapeutic Indication
Treatment of HER2-positive breast cancer patients who have received two or more prior anti-HER2 based regimens in the metastatic setting
Tumour Sub-type
Breast Cancer
Tumour Stage
Metastatic
Tumour Sub-Group
HER2+
Trial Name
NALA
NCT Number
NCT01808573
Trial Phase
Phase III

Approval details

FDA Approval
FDA approval February 2020
EMA Approval
Not EMA approved

Primary Outcome(s)

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

Outcome Data

PFS Control
6.6 months
PFS Gain
0.1 months
PFS HR
0.76 (0.63-0.93)
OS Control
18.7 months
OS Gain
2.3 months
OS HR
0.88 (0.72-1.07) Not significant (mature)

Adjustments

QoL Comment
No QoL benefit
Toxicity Comment
Increased toxicity (>10% increment in grade >3 diarrhoea)

Score (after adjustments)

Preliminary non-curative score

2

Toxicity adjustment
1-
Non-curative score

1

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
225
Scorecard version
1
Issue date
4.11.2020
Last update
25.04.2024
Neratinib NALA

PRELIMINARY SCORE

PFS

ADJUSTMENTS

No QoL benefit
Increased toxicity
Neratinib NALA

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
Overall Survival
1
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Treatment of HER2-positive breast cancer patients who have received two or more prior anti-HER2 based regimens in the metastatic setting
Neratinib + Capecitabine
Lapatinib plus capecitabine

My watchlist

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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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