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NCT05140382 · OUTCOME

Duration of Response (DoR)

AZD4573 as Monotherapy or in Combinations With Anti-cancer Agents in Patients With r/r PTCL or r/r cHL · Source last updated 2024-08-28

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 Screening (Day -30 to Day-1) until disease progression or survival until death (26 months).

What was measured

Duration of response is defined as the time from the first objective response to the time of documented disease progression or death due to any cause, whichever occurs first.

Analysis population: Response evaluable set included all dosed participants who have measurable disease at baseline and had objective response.

Groups in this outcome

Cohort 1 Non-NK PTCL

Participants with non-NK PTCL received 12 mg dose of AZD4573 once weekly until disease progression.

Cohort 2 NK PTCL

Participants with NK PTCL received 12 mg dose of AZD4573 once weekly until disease progression.

Cohort 3 cHL

Participants with cHL received 12 mg dose of AZD4573 once weekly until disease progression.

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

Analysis denominator · Participants

GroupSource count
Cohort 1 Non-NK PTCL7
Cohort 2 NK PTCL0
Cohort 3 cHL4

Reported measurements

Source class 1
Values in Months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Cohort 1 Non-NK PTCLNANot reported1.8NAThe median and 95% CI were calculated with the Kaplan Meier process (a process in medical research to measure the proportion of participants surviving for a certain time after receiving treatment) and were non estimable as there was insufficient number of participants with the event of interest (less than 50%) occurred in the study.
Cohort 3 cHL5.2Not reported1.9NAThe 95% CI was calculated with the Kaplan Meier process (a process in medical research to measure the proportion of participants surviving for a certain time after receiving treatment) and was non estimable as there was insufficient number of participants with the event of interest (less than 50%) occurred in the study.
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        The median and 95% CI were calculated with the Kaplan Meier process (a process in medical research to measure the proportion of participants surviving for a certain time after receiving treatment) and were non estimable as there was insufficient number of participants with the event of interest (less than 50%) occurred in the study.
        group Id
        OG000
        lower Limit
        1.8
        upper Limit
        NA
        value
        NA
      2. comment
        The 95% CI was calculated with the Kaplan Meier process (a process in medical research to measure the proportion of participants surviving for a certain time after receiving treatment) and was non estimable as there was insufficient number of participants with the event of interest (less than 50%) occurred in the study.
        group Id
        OG002
        lower Limit
        1.9
        upper Limit
        NA
        value
        5.2
denoms
  1. counts
    1. group Id
      OG000
      value
      7
    2. group Id
      OG001
      value
      0
    3. group Id
      OG002
      value
      4
    units
    Participants
description
Duration of response is defined as the time from the first objective response to the time of documented disease progression or death due to any cause, whichever occurs first.
dispersion Type
95% Confidence Interval
groups
  1. description
    Participants with non-NK PTCL received 12 mg dose of AZD4573 once weekly until disease progression.
    id
    OG000
    title
    Cohort 1 Non-NK PTCL
  2. description
    Participants with NK PTCL received 12 mg dose of AZD4573 once weekly until disease progression.
    id
    OG001
    title
    Cohort 2 NK PTCL
  3. description
    Participants with cHL received 12 mg dose of AZD4573 once weekly until disease progression.
    id
    OG002
    title
    Cohort 3 cHL
param Type
MEDIAN
population Description
Response evaluable set included all dosed participants who have measurable disease at baseline and had objective response.
reporting Status
POSTED
time Frame
From Screening (Day -30 to Day-1) until disease progression or survival until death (26 months).
title
Duration of Response (DoR)
type
SECONDARY
unit Of Measure
Months

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice