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NCT03849651 · OUTCOME

The Cumulative Incidence of Any Grade Acute Graft-Versus-Host Disease (GVHD)

TCRαβ-depleted Progenitor Cell Graft With Additional Memory T-cell DLI, Plus Selected Use of Blinatumomab, in Naive T-cell Depleted Haploidentical Donor Hematopoietc Cell Transplantation for Hematologic Malignancies · Source last updated 2026-07-22

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

Measure
NUMBER
Unit
percentage of participants
Interval / dispersion
95% Confidence Interval
Time frame
One year after receiving transplant

What was measured

Kalbfleisch and Prentice estimate of the percentage of experiencing any grade acute GVHD one year after the date of transplant. (Events=acute GVHD, competing events=death) Groups with insufficient events for confidence interval estimation have confidence intervals written as "NA to NA."

Analysis population: Patients who met eligibility criteria and received transplant.

Groups in this outcome

All Transplant Participants

Patients who met eligibility criteria and received transplant.

Dose 1

Patients who met eligibility criteria, received transplant, and received 1x10\^5 cells/kg

Dose 2

Patients who met eligibility criteria, received transplant, and received 1x10\^6 cells/kg

Dose 3

Patients who met eligibility criteria, received transplant, and received 1x10\^7 cells/kg

Phase 2

Patients who met eligibility criteria, received transplant, and were assigned the MED dose of 1x10\^7 cells/kg

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

Analysis denominator · Participants

GroupSource count
All Transplant Participants69
Dose 19
Dose 210
Dose 310
Phase 240

Reported measurements

Source class 1
Values in percentage of participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
All Transplant Participants27.5Not reported17.638.4Not reported
Dose 10Not reportedNANANo patients experienced outcome, so confidence interval is not applicable"?
Dose 250.0Not reported16.376.8Not reported
Dose 330.0Not reported6.259.3Not reported
Phase 227.5Not reported14.741.9Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        17.6
        upper Limit
        38.4
        value
        27.5
      2. comment
        No patients experienced outcome, so confidence interval is not applicable"?
        group Id
        OG001
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      3. group Id
        OG002
        lower Limit
        16.3
        upper Limit
        76.8
        value
        50.0
      4. group Id
        OG003
        lower Limit
        6.2
        upper Limit
        59.3
        value
        30.0
      5. group Id
        OG004
        lower Limit
        14.7
        upper Limit
        41.9
        value
        27.5
denoms
  1. counts
    1. group Id
      OG000
      value
      69
    2. group Id
      OG001
      value
      9
    3. group Id
      OG002
      value
      10
    4. group Id
      OG003
      value
      10
    5. group Id
      OG004
      value
      40
    units
    Participants
description
Kalbfleisch and Prentice estimate of the percentage of experiencing any grade acute GVHD one year after the date of transplant. (Events=acute GVHD, competing events=death) Groups with insufficient events for confidence interval estimation have confidence intervals written as "NA to NA."
dispersion Type
95% Confidence Interval
groups
  1. description
    Patients who met eligibility criteria and received transplant.
    id
    OG000
    title
    All Transplant Participants
  2. description
    Patients who met eligibility criteria, received transplant, and received 1x10\^5 cells/kg
    id
    OG001
    title
    Dose 1
  3. description
    Patients who met eligibility criteria, received transplant, and received 1x10\^6 cells/kg
    id
    OG002
    title
    Dose 2
  4. description
    Patients who met eligibility criteria, received transplant, and received 1x10\^7 cells/kg
    id
    OG003
    title
    Dose 3
  5. description
    Patients who met eligibility criteria, received transplant, and were assigned the MED dose of 1x10\^7 cells/kg
    id
    OG004
    title
    Phase 2
param Type
NUMBER
population Description
Patients who met eligibility criteria and received transplant.
reporting Status
POSTED
time Frame
One year after receiving transplant
title
The Cumulative Incidence of Any Grade Acute Graft-Versus-Host Disease (GVHD)
type
SECONDARY
unit Of Measure
percentage of participants

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Preserved source evidence · Not medical advice