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2

Indication details

Control Arm
Single arm (Phase II)
Therapeutic Indication
Cholangiocarcinoma with a FGFR2 fusion or rearrangement that has progressed after at least one prior line of systemic therapy
Tumour Type
Gastrointestinal Cancers
Tumour Sub-type
Cholangiocarcinoma
Tumour Stage
Locally advanced or metastatic
Tumour Sub-Group
FGFR2 gene fusion or rearrangement
Trial Name
FIGHT-202
NCT Number
NCT02924376
Trial Phase
Phase II

Approval details

FDA Approval
FDA approval April 2020
EMA Approval
EMA (CHMP) approved February 2021. EC decision May 2021

Primary Outcome(s)

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

Outcome Data

PFS Control
7.0 months
ORR
37.0 %
DoR
9.1 months

Adjustments

QoL Comment
Not qualified for an ESMO-MCBS credit
Toxicity Comment
>30% Grade 3+ adverse effects impacting daily living

Score (after adjustments)

Preliminary non-curative score

3

Toxicity adjustment
-1
Non-curative score

2

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
231
Scorecard version
1
Issue date
5.11.2020
Last update
13.06.2024
Pemigatinib FIGHT-202

PRELIMINARY SCORE

ORR

ADJUSTMENTS

Not qualified for an ESMO-MCBS credit
>30% Grade 3+ adverse effects impacting daily living
Pemigatinib FIGHT-202

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
2
Overall Response Rate / Duration of Response
Gastrointestinal Cancers
Cholangiocarcinoma with a FGFR2 fusion or rearrangement that has progressed after at least one prior line of systemic therapy
Pemigatinib
Single arm (Phase II)

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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