Skip to content
← Full study record

NCT00557193 · OUTCOME

Percent Probability of Event Free Survival (EFS) by MRD Status and Treatment Arm

Combination Chemotherapy With or Without Lestaurtinib in Treating Younger Patients With Newly Diagnosed Acute Lymphoblastic Leukemia · Source last updated 2024-07-15

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

Measure
NUMBER
Unit
percent probability
Interval / dispersion
90% Confidence Interval
Time frame
3 Years from end of Induction)

What was measured

Three-year EFS estimates and 90% CI will be reported by treatment arm and end-induction MRD status.

Analysis population: Patients who had data collected

Groups in this outcome

Arm A (MRD Negative)

Arm A, standard risk MLL-G

Arm A (MRD Positive)

Arm A, standard risk MLL-G

Arm B (MRD Negative)

Arm B, IR/HR MLL-R chemotherapy

Arm B (MRD Positive)

Arm B, IR/HR MLL-R chemotherapy

Arm C (MRD Negative)

Arm C, IR/HR MLL-R chemotherapy and lestaurtinib

Arm C (MRD Positive)

Arm C, IR/HR MLL-R chemotherapy and lestaurtinib

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

Analysis denominator · Participants

GroupSource count
Arm A (MRD Negative)43
Arm A (MRD Positive)8
Arm B (MRD Negative)19
Arm B (MRD Positive)22
Arm C (MRD Negative)27
Arm C (MRD Positive)37

Reported measurements

Source class 1
Values in percent probability · Interval/dispersion: 90% Confidence Interval
GroupValueSpreadLowerUpperComment
Arm A (MRD Negative)86.05Not reported77.3694.74Not reported
Arm A (MRD Positive)87.5Not reported68.27100Not reported
Arm B (MRD Negative)47.37Not reported28.5366.21Not reported
Arm B (MRD Positive)22.73Not reported8.0437.42Not reported
Arm C (MRD Negative)51.85Not reported36.0367.67Not reported
Arm C (MRD Positive)27.03Not reported13.6140.45Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        77.36
        upper Limit
        94.74
        value
        86.05
      2. group Id
        OG001
        lower Limit
        68.27
        upper Limit
        100
        value
        87.5
      3. group Id
        OG002
        lower Limit
        28.53
        upper Limit
        66.21
        value
        47.37
      4. group Id
        OG003
        lower Limit
        8.04
        upper Limit
        37.42
        value
        22.73
      5. group Id
        OG004
        lower Limit
        36.03
        upper Limit
        67.67
        value
        51.85
      6. group Id
        OG005
        lower Limit
        13.61
        upper Limit
        40.45
        value
        27.03
denoms
  1. counts
    1. group Id
      OG000
      value
      43
    2. group Id
      OG001
      value
      8
    3. group Id
      OG002
      value
      19
    4. group Id
      OG003
      value
      22
    5. group Id
      OG004
      value
      27
    6. group Id
      OG005
      value
      37
    units
    Participants
description
Three-year EFS estimates and 90% CI will be reported by treatment arm and end-induction MRD status.
dispersion Type
90% Confidence Interval
groups
  1. description
    Arm A, standard risk MLL-G
    id
    OG000
    title
    Arm A (MRD Negative)
  2. description
    Arm A, standard risk MLL-G
    id
    OG001
    title
    Arm A (MRD Positive)
  3. description
    Arm B, IR/HR MLL-R chemotherapy
    id
    OG002
    title
    Arm B (MRD Negative)
  4. description
    Arm B, IR/HR MLL-R chemotherapy
    id
    OG003
    title
    Arm B (MRD Positive)
  5. description
    Arm C, IR/HR MLL-R chemotherapy and lestaurtinib
    id
    OG004
    title
    Arm C (MRD Negative)
  6. description
    Arm C, IR/HR MLL-R chemotherapy and lestaurtinib
    id
    OG005
    title
    Arm C (MRD Positive)
param Type
NUMBER
population Description
Patients who had data collected
reporting Status
POSTED
time Frame
3 Years from end of Induction)
title
Percent Probability of Event Free Survival (EFS) by MRD Status and Treatment Arm
type
SECONDARY
unit Of Measure
percent probability

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

Preserved source evidence · Not medical advice