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NCT00866918 · OUTCOME

Hematologic Remission Rate

Combination Chemotherapy in Treating Young Patients With Newly Diagnosed Acute Promyelocytic Leukemia · Source last updated 2022-10-25

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

Measure
NUMBER
Unit
Proportion of participants
Interval / dispersion
Not reported
Time frame
End of consolidation, course 1: up to 5 months

What was measured

Proportion of patients in hematologic remission at end of consolidation, course 1 are reported.

Analysis population: Patients who were ineligible (n=6), inevaluable (n=1), or who electively withdrew during Induction (n=4) were excluded.

Groups in this outcome

Standard Risk

WBC\<10,000/MicroLiter

High Risk

WBC\>=10,000/MicroLiter

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

Analysis denominator · Participants

GroupSource count
Standard Risk63
High Risk34

Reported measurements

Source class 1
Values in Proportion of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Standard Risk1.0000Not reportedNot reportedNot reportedNot reported
High Risk0.8824Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        1.0000
      2. group Id
        OG001
        value
        0.8824
denoms
  1. counts
    1. group Id
      OG000
      value
      63
    2. group Id
      OG001
      value
      34
    units
    Participants
description
Proportion of patients in hematologic remission at end of consolidation, course 1 are reported.
groups
  1. description
    WBC\<10,000/MicroLiter
    id
    OG000
    title
    Standard Risk
  2. description
    WBC\>=10,000/MicroLiter
    id
    OG001
    title
    High Risk
param Type
NUMBER
population Description
Patients who were ineligible (n=6), inevaluable (n=1), or who electively withdrew during Induction (n=4) were excluded.
reporting Status
POSTED
time Frame
End of consolidation, course 1: up to 5 months
title
Hematologic Remission Rate
type
SECONDARY
unit Of Measure
Proportion of participants

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

Preserved source evidence · Not medical advice