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4

Indication details

Control Arm
Placebo
Therapeutic Indication
Treatment of adult patients with unresectable, stage III NSCLC whose disease has not progressed following concurrent platinum-based CRT
Tumour Type
Thoracic Malignancies
Tumour Sub-type
Non-small-cell Lung Cancer
Tumour Stage
Locally advanced
Tumour Sub-Group
PD-L1
Trial Name
PACIFIC
NCT Number
NCT02125461
Trial Phase
Phase III

Approval details

FDA Approval
FDA approval February 2018
EMA Approval
EMA CHMP July 2018 EC decision September 2018
Comment
EMA approval is limited to patients whose tumours express PD-L1 on ≥1% of tumour cells. This approval was based on findings from a post hoc analysis indicating a lack of benefit for patients whose tumours express PD-L1 on <1% of tumour cells.12 Data shown are therefore from the ITT population across all PD-L1 categories

Primary Outcome(s)

Primary Outcome(s)
PFS ITT population across all PD-L1 categories
Evaluated Outcome
OS
Form(s)
Form 2a

Outcome Data

PFS Control
5.6 months
PFS Gain
11.3 months
PFS HR
0.45 (0.44-0.68)
OS Control
29.1 months
OS Gain
18.4 months
OS HR
0.72 (0.59-0.89)

Adjustments

QoL Comment
No QoL benefit

Final Score (after adjustments)

Preliminary non-curative score

4

Final non-curative score

4

Scorecard details

ESMO-MCBS version
ESMO-MCBS v1.1
Scorecard ID
170
Scorecard version
1
Issue date
27.04.2020
Last update
15.11.2023
Durvalumab PACIFIC

PRELIMINARY SCORE

OS

ADJUSTMENTS

No QoL benefit observed
Durvalumab PACIFIC

FINAL 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
Treatment of adult patients with unresectable, stage III NSCLC whose disease has not progressed following concurrent platinum-based CRT
Durvalumab
Placebo

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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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