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4

Indication details

Combined Agent(s)
Carboplatin + Etoposide
Control Arm
Placebo + Carboplatin + Etoposide
FDA Therapeutic Indication
Serplulimab in combination with carboplatin and etoposide is indicated for the first‑line treatment of adult patients with extensive‑stage small cell lung cancer (ES‑SCLC).
Tumour Type
Thoracic Malignancies
Tumour Sub-type
Small-cell Lung Cancer
Trial Name
ASTRUM-005
NCT Number
NCT04063163
Trial Phase
Phase III

Approval details

EMA Approval
EMA (CHMP) approved September 2024. Pending EC decision

Primary Outcome(s)

Primary Outcome(s)
OS
Evaluated Outcome
OS
Form(s)
Form 2a

Outcome Data

PFS Control
4.3 months
PFS Gain
1.4 months
PFS HR
0.48 (0.38-0.59)
OS Control
10.9 months
OS Gain
4.5 months
OS HR
0.63 (0.49-0.82). P < 0.001 (boundary at interim was 0.012)

Adjustments

QoL Comment
QoL data pending

Score (after adjustments)

Preliminary non-curative score

4

Non-curative score

4

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
470
Scorecard version
1
Issue date
08.11.2024
Serplulimab ASTRUM-005

PRELIMINARY SCORE

OS

ADJUSTMENTS

?
QoL data pending
Serplulimab ASTRUM-005

SCORE

Overall Survival / Disease-Free Survival / Pathological Complete Response
4
Overall Survival
Progression-Free Survival
Non-inferiority (Improved Quality of Life or Reduced Adverse Events) / Response Rate
Overall Response Rate / Duration of Response
Thoracic Malignancies
Serplulimab in combination with carboplatin and etoposide is indicated for the first‑line treatment of adult patients with extensive‑stage small cell lung cancer (ES‑SCLC).
Serplulimab + Carboplatin + Etoposide
Placebo + Carboplatin + Etoposide

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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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