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3

Indication details

Combined Agent(s)
Carboplatin and Pemetrexed
Control Arm
Carboplatin and Pemetrexed
FDA Therapeutic Indication
FDA: Amivantamab with carboplatin and pemetrexed for the first-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations. EMA: Amivantamab in combination with carboplatin and pemetrexed for the first line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) with activating EGFR Exon 20 insertion mutations
Tumour Type
Thoracic Malignancies
Tumour Sub-type
Non-small-cell Lung Cancer
Tumour Stage
Locally advanced or metastatic
Tumour Sub-Group
EGFR+ exon 20 insertion mutations
Trial Name
PAPILLON
NCT Number
NCT04538664
Trial Phase
Phase III

Approval details

FDA Approval
FDA approval March 2024
EMA Approval
EMA (CHMP) April 2024. EC decision September 2024.

Primary Outcome(s)

Primary Outcome(s)
PFS (BICR) as primary endpoint. OS as secondary endpoint
Evaluated Outcome
PFS
Form(s)
Form 2b

Outcome Data

PFS Control
6.7 months
PFS Gain
4.7 months
PFS HR
0.40 (0.30-0.53)
OS HR
Immature: Interim overall survival analysis. 0.67 (0.42-1.09)

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
436
Scorecard version
1
Issue date
06.05.2024
Last update
18.09.2024
Amivantamab PAPILLON

PRELIMINARY SCORE

PFS

ADJUSTMENTS

?
QoL data pending
Amivantamab PAPILLON

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
Thoracic Malignancies
FDA: Amivantamab with carboplatin and pemetrexed for the first-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations. EMA: Amivantamab in combination with carboplatin and pemetrexed for the first line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) with activating EGFR Exon 20 insertion mutations
Amivantamab + Carboplatin and Pemetrexed
Carboplatin and Pemetrexed

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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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