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3

Indication details

Control Arm
Single arm (Phase I)
FDA Therapeutic Indication
Treatment of adult patients with dMMR/MSI-H recurrent or advanced endometrial cancer that have progressed on or following prior treatment with a platinum-containing regimen
Tumour Type
Gynaecological Malignancies
Tumour Sub-type
Endometrial Cancer
Tumour Stage
Recurrent or advanced
Tumour Sub-Group
dMMR or MSI-H
Trial Name
GARNET
NCT Number
NCT02715284
Trial Phase
Phase I

Approval details

FDA Approval
FDA accelerated approval April 2021 FDA regular approval February 2023
EMA Approval
EMA (CHMP) February 2021 EC decision May 2021

Primary Outcome(s)

Primary Outcome(s)
ORR
Evaluated Outcome
ORR
Form(s)
Form 3

Outcome Data

PFS Control
12.2 months
ORR
43.5%
DoR
>9 months (Not reached)

Adjustments

QoL Comment
Not qualified for an ESMO-MCBS credit

Score (after adjustments)

Preliminary non-curative score

3

Non-curative score

3

Comment
EMA (CHMP) February 2021 EC decision May 2021
FDA accelerated approval April 2021
FDA regular approval February 2023

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
256
Scorecard version
1
Issue date
29.03.2020
Last update
11.02.2023
Dostarlimab GARNET

PRELIMINARY SCORE

ORR

ADJUSTMENTS

Not qualified for an ESMO-MCBS credit
Dostarlimab GARNET

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
Overall Survival
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
3
Overall Response Rate / Duration of Response
Gynaecological Malignancies
Treatment of adult patients with dMMR/MSI-H recurrent or advanced endometrial cancer that have progressed on or following prior treatment with a platinum-containing regimen
Dostarlimab
Single arm (Phase I)

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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