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NCT01283516 · OUTCOME

Progression-free Survival Based on Investigator Assessment

A Dose Escalation/Expansion Study of LDK378 in Patients With Tumors Characterized by Genetic Abnormalities in Anaplastic Lymphoma Kinase · Source last updated 2019-03-15

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEDIAN
Unit
months
Interval / dispersion
95% Confidence Interval
Time frame
275 weeks

What was measured

Progression-free survival (PFS) was defined as the time from the start date of study drug to the date of the first radiologically documented progressive disease (PD) per RECIST 1.0. or death due to any cause.

Analysis population: Full analysis set (FAS) - NSCLC: Subset of Full Analysis Set including ALK-positive NSCLC patients who received at least one dose of LDK378 in the 750 mg dose group.

Groups in this outcome

NSCLC With Prior ALKi (Arms 1A + 1B)

Patients with ALK-translocated NSCLC who were previously treated with an ALK inhibitor.

NSCLC ALKi Naive (Arm 2)

Patients with ALK-translocated NSCLC not previously treated with an ALK inhibitor.

All NSCLC

all NSCLC patients

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
NSCLC With Prior ALKi (Arms 1A + 1B)163
NSCLC ALKi Naive (Arm 2)83
All NSCLC246

Reported measurements

Source class 1
Values in months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
NSCLC With Prior ALKi (Arms 1A + 1B)6.93Not reported5.558.48Not reported
NSCLC ALKi Naive (Arm 2)15.21Not reported12.1219.48Not reported
All NSCLC8.74Not reported6.9310.97Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        5.55
        upper Limit
        8.48
        value
        6.93
      2. group Id
        OG001
        lower Limit
        12.12
        upper Limit
        19.48
        value
        15.21
      3. group Id
        OG002
        lower Limit
        6.93
        upper Limit
        10.97
        value
        8.74
denoms
  1. counts
    1. group Id
      OG000
      value
      163
    2. group Id
      OG001
      value
      83
    3. group Id
      OG002
      value
      246
    units
    Participants
description
Progression-free survival (PFS) was defined as the time from the start date of study drug to the date of the first radiologically documented progressive disease (PD) per RECIST 1.0. or death due to any cause.
dispersion Type
95% Confidence Interval
groups
  1. description
    Patients with ALK-translocated NSCLC who were previously treated with an ALK inhibitor.
    id
    OG000
    title
    NSCLC With Prior ALKi (Arms 1A + 1B)
  2. description
    Patients with ALK-translocated NSCLC not previously treated with an ALK inhibitor.
    id
    OG001
    title
    NSCLC ALKi Naive (Arm 2)
  3. description
    all NSCLC patients
    id
    OG002
    title
    All NSCLC
param Type
MEDIAN
population Description
Full analysis set (FAS) - NSCLC: Subset of Full Analysis Set including ALK-positive NSCLC patients who received at least one dose of LDK378 in the 750 mg dose group.
reporting Status
POSTED
time Frame
275 weeks
title
Progression-free Survival Based on Investigator Assessment
type
SECONDARY
unit Of Measure
months

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice