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3

Indication details

Combined Agent(s)
Enzalutamide
Control Arm
Placebo plus enzalutamide
Therapeutic Indication
Talazoparib is indicated in combination with enzalutamide for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) in whom chemotherapy is not clinically indicated.
Tumour Type
Genitourinary Cancers
Tumour Sub-type
Prostate cancer
Tumour Stage
Metastatic castration-resistant
Trial Name
TALAPRO-2
NCT Number
NCT03395197
Trial Phase
Phase III

Approval details

EMA Approval
EMA (CHMP) November 2023. EC decision January 2024
Comment
The presented score is for the all-comers cohort (ITT)

Primary Outcome(s)

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

Outcome Data

PFS Control
21.9 months
PFS Gain
12.9 months
PFS HR
0.63 (0.57-0.78)

Adjustments

QoL Comment
QoL data pending

Score (after adjustments)

Preliminary non-curative score

3

Non-curative score

3

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
383
Scorecard version
1
Issue date
19.07.2023
Talazoparib TALAPRO-2

PRELIMINARY SCORE

PFS (ITT)

ADJUSTMENTS

?
QoL data pending
Talazoparib TALAPRO-2

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
Overall Survival
3
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Genitourinary Cancers
Talazoparib is indicated in combination with enzalutamide for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) in whom chemotherapy is not clinically indicated.
Talazoparib + Enzalutamide
Placebo plus enzalutamide

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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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