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NCT00109928 · FLOW

Participant flow

S0350 Combination Chemotherapy in Treating Patients With Newly Diagnosed Stage II, Stage III, or Stage IV Peripheral T-Cell Non-Hodgkin's Lymphoma · Source last updated 2014-10-01

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

groups
  1. description
    Patients received IV cisplatin 25 mg/m2 days 1-4, etoposide 40 mg/m2 days 1-4, gemcitabine 1000 mg/m2 day 1 and solumedrol 250 mg days 1-4 of a 21 day cycle for 6 cycles.
    id
    FG000
    title
    PEGS
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Progression
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      not protocol specified
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      not eligible
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        34
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        33
      type
      Eligible
    3. achievements
      1. group Id
        FG000
        num Subjects
        33
      type
      Eligible and Began Protocol Therapy
    4. achievements
      1. group Id
        FG000
        num Subjects
        21
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        13
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Patients received IV cisplatin 25 mg/m2 days 1-4, etoposide 40 mg/m2 days 1-4, gemcitabine 1000 mg/m2 day 1 and solumedrol 250 mg days 1-4 of a 21 day cycle for 6 cycles.
    id
    FG000
    title
    PEGS
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Progression
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      not protocol specified
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      not eligible
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        34
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        33
      type
      Eligible
    3. achievements
      1. group Id
        FG000
        num Subjects
        33
      type
      Eligible and Began Protocol Therapy
    4. achievements
      1. group Id
        FG000
        num Subjects
        21
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        13
      type
      NOT COMPLETED
    title
    Overall Study

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Preserved source evidence · Not medical advice