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NCT00943319 · OUTCOME

Overall Survival

Busulfan-fludarabine Conditioning and T-cell Depleted Allogeneic Stem Cell Transplantation for Patients With Advanced Hematologic Malignancies · Source last updated 2019-02-04

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

Measure
MEDIAN
Unit
days
Interval / dispersion
95% Confidence Interval
Time frame
5 years

What was measured

Overall Survival measured as median survival in days

Groups in this outcome

Busulfan and Fludarabine

Intravenous busulfan (Busulfan®) in combination with fludarabine Busulfan: Daily intravenous dosing to target AVC Fludarabine: Fludarabine dosing will be based on actual body weight. Fludarabine will be infused over 30 minutes before busulfan treatment dose. Campath: All patients will receive premedication for Campath (daily doses of 20 mg are repeated for up to five times). Stem Cell Transplant: Infusion of bone marrow and donors(related/ unrelated).

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

Analysis denominator · Participants

GroupSource count
Busulfan and Fludarabine50

Reported measurements

Source class 1
Values in days · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Busulfan and Fludarabine161Not reported121305Not reported

Source statistical analyses

Group order, estimate direction, methods and comments are retained. No treatment ranking is inferred.

  1. ci Lower Limit
    121
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    95
    ci Upper Limit
    305
    group Ids
    1. OG000
    non Inferiority Type
    OTHER
    param Type
    Median Survival time
    param Value
    161
    statistical Method
    Product limit survival estimate
Complete source fields
analyses
  1. ci Lower Limit
    121
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    95
    ci Upper Limit
    305
    group Ids
    1. OG000
    non Inferiority Type
    OTHER
    param Type
    Median Survival time
    param Value
    161
    statistical Method
    Product limit survival estimate
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        121
        upper Limit
        305
        value
        161
denoms
  1. counts
    1. group Id
      OG000
      value
      50
    units
    Participants
description
Overall Survival measured as median survival in days
dispersion Type
95% Confidence Interval
groups
  1. description
    Intravenous busulfan (Busulfan®) in combination with fludarabine Busulfan: Daily intravenous dosing to target AVC Fludarabine: Fludarabine dosing will be based on actual body weight. Fludarabine will be infused over 30 minutes before busulfan treatment dose. Campath: All patients will receive premedication for Campath (daily doses of 20 mg are repeated for up to five times). Stem Cell Transplant: Infusion of bone marrow and donors(related/ unrelated).
    id
    OG000
    title
    Busulfan and Fludarabine
param Type
MEDIAN
reporting Status
POSTED
time Frame
5 years
title
Overall Survival
type
SECONDARY
unit Of Measure
days

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

Preserved source evidence · Not medical advice