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NCT02102490 · OUTCOME

Overall Survival (OS)

A Study of Abemaciclib (LY2835219) In Participants With Previously Treated Breast Cancer That Has Spread · Source last updated 2020-01-21

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
From Date of First Dose until Death Due to Any Cause (Up To 27 Months)

What was measured

OS defined as the time from first dose date to the date of death due to any cause. For each participant who is not known to have died as of the data-inclusion cutoff date for overall survival analysis, OS time was censored on the last date the participant is known to be alive.

Analysis population: All enrolled participants who received at least one dose of study drug. Censored participants: Abemaciclib=70.

Groups in this outcome

Abemaciclib

200 mg abemaciclib given orally once every 12 hours for 28 days (1 cycle). Participants may continue to receive treatment until discontinuation criteria are met.

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

Analysis denominator · Participants

GroupSource count
Abemaciclib132

Reported measurements

Source class 1
Values in Months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Abemaciclib22.32Not reported17.72NAThe upper limit of the 95% confidence interval (CI) was not calculated due to the high censoring rate.
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        The upper limit of the 95% confidence interval (CI) was not calculated due to the high censoring rate.
        group Id
        OG000
        lower Limit
        17.72
        upper Limit
        NA
        value
        22.32
denoms
  1. counts
    1. group Id
      OG000
      value
      132
    units
    Participants
description
OS defined as the time from first dose date to the date of death due to any cause. For each participant who is not known to have died as of the data-inclusion cutoff date for overall survival analysis, OS time was censored on the last date the participant is known to be alive.
dispersion Type
95% Confidence Interval
groups
  1. description
    200 mg abemaciclib given orally once every 12 hours for 28 days (1 cycle). Participants may continue to receive treatment until discontinuation criteria are met.
    id
    OG000
    title
    Abemaciclib
param Type
MEDIAN
population Description
All enrolled participants who received at least one dose of study drug. Censored participants: Abemaciclib=70.
reporting Status
POSTED
time Frame
From Date of First Dose until Death Due to Any Cause (Up To 27 Months)
title
Overall Survival (OS)
type
SECONDARY
unit Of Measure
Months

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

Preserved source evidence · Not medical advice