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NCT01771107 · OUTCOME

CD8 Counts

Brentuximab Vedotin and Combination Chemotherapy in Treating Patients With Stage II-IV HIV-Associated Hodgkin Lymphoma · Source last updated 2025-08-15

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

Measure
MEDIAN
Unit
cells/µL
Interval / dispersion
Inter-Quartile Range
Time frame
5 months

What was measured

Absolute CD8 counts at cycle 5

Analysis population: Participants with absolute CD8 counts at cycle 5

Groups in this outcome

Phase I - Brentuximab 1.2 mg/kg

Patients receive doxorubicin hydrochloride IV, vinblastine sulfate IV, and dacarbazine IV on days 1 and 15. Patients also receive brentuximab vedotin IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. Brentuximab Vedotin: Given IV Dacarbazine: Given IV Doxorubicin Hydrochloride: Given IV Pharmacological Study: Correlative studies Vinblastine: Given IV

Phase II - Brentuximab 1.2 mg/kg

Patients receive doxorubicin hydrochloride IV, vinblastine sulfate IV, and dacarbazine IV on days 1 and 15. Patients also receive brentuximab vedotin IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. Brentuximab Vedotin: Given IV Dacarbazine: Given IV Doxorubicin Hydrochloride: Given IV Pharmacological Study: Correlative studies Vinblastine: Given IV

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

Analysis denominator · Participants

GroupSource count
Phase I - Brentuximab 1.2 mg/kg6
Phase II - Brentuximab 1.2 mg/kg26

Reported measurements

Source class 1
Values in cells/µL · Interval/dispersion: Inter-Quartile Range
GroupValueSpreadLowerUpperComment
Phase I - Brentuximab 1.2 mg/kg719.5Not reported596883Not reported
Phase II - Brentuximab 1.2 mg/kg666.5Not reported470954Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        596
        upper Limit
        883
        value
        719.5
      2. group Id
        OG001
        lower Limit
        470
        upper Limit
        954
        value
        666.5
denoms
  1. counts
    1. group Id
      OG000
      value
      6
    2. group Id
      OG001
      value
      26
    units
    Participants
description
Absolute CD8 counts at cycle 5
dispersion Type
Inter-Quartile Range
groups
  1. description
    Patients receive doxorubicin hydrochloride IV, vinblastine sulfate IV, and dacarbazine IV on days 1 and 15. Patients also receive brentuximab vedotin IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. Brentuximab Vedotin: Given IV Dacarbazine: Given IV Doxorubicin Hydrochloride: Given IV Pharmacological Study: Correlative studies Vinblastine: Given IV
    id
    OG000
    title
    Phase I - Brentuximab 1.2 mg/kg
  2. description
    Patients receive doxorubicin hydrochloride IV, vinblastine sulfate IV, and dacarbazine IV on days 1 and 15. Patients also receive brentuximab vedotin IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. Brentuximab Vedotin: Given IV Dacarbazine: Given IV Doxorubicin Hydrochloride: Given IV Pharmacological Study: Correlative studies Vinblastine: Given IV
    id
    OG001
    title
    Phase II - Brentuximab 1.2 mg/kg
param Type
MEDIAN
population Description
Participants with absolute CD8 counts at cycle 5
reporting Status
POSTED
time Frame
5 months
title
CD8 Counts
type
SECONDARY
unit Of Measure
cells/µL

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

Preserved source evidence · Not medical advice