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NCT03762018 · FLOW

Participant flow

BEAT-meso: Bevacizumab and Atezolizumab in Malignant Pleural Mesothelioma · Source last updated 2026-07-22

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

groups
  1. description
    Atezolizumab 1200mg intravenously on day 1 every 3 weeks plus bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
    id
    FG000
    title
    Atezolizumab Plus Bevacizumab Plus Chemotherapy
  2. description
    Bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
    id
    FG001
    title
    Bevacizumab Plus Chemotherapy
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        145
      2. group Id
        FG001
        num Subjects
        150
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        4
      2. group Id
        FG001
        num Subjects
        2
      type
      Withdrawal/Lost to follow-up
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        200
      2. group Id
        FG001
        num Subjects
        200
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        198
      2. comment
        There is one patient assigned in the BC arm who actually received ABC treatment. This patient is evaluated in the treatment arm to which he/she was randomly assigned (BC) for all the efficacy (Intention-to-Treat (ITT)) analyses. For the safety analysis the patient is evaluated according to the treatment he/she received (ABC treatment), irrespective of the allocated treatment at randomization.
        group Id
        FG001
        num Subjects
        200
      type
      Received at least one dose of trial treatment
    3. achievements
      1. group Id
        FG000
        num Subjects
        8
      2. group Id
        FG001
        num Subjects
        4
      comment
      Patients who were on treatment at database cut-off for final efficacy analysis: September 01, 2023
      type
      On treatment
    4. achievements
      1. group Id
        FG000
        num Subjects
        192
      2. group Id
        FG001
        num Subjects
        196
      comment
      Atezolizumab plus bevacizumab plus chemotherapy: 109 progressions, 62 toxicities, 9 deaths, 7 investigator decisions, 1 patient decision, 2 other; Bevacizumab plus chemotherapy: 141 progressions, 35 toxicities, 9 deaths, 1 investigator decision, 2 patient decisions, 8 other
      type
      Treatment failures
    5. achievements
      1. group Id
        FG000
        num Subjects
        2
      2. group Id
        FG001
        num Subjects
        0
      type
      Never started treatment
    6. achievements
      1. group Id
        FG000
        num Subjects
        51
      2. group Id
        FG001
        num Subjects
        48
      comment
      Patients who were on follow-up at database cut-off for final efficacy analysis: September 01, 2023
      type
      COMPLETED
    7. achievements
      1. group Id
        FG000
        num Subjects
        149
      2. group Id
        FG001
        num Subjects
        152
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Atezolizumab 1200mg intravenously on day 1 every 3 weeks plus bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
    id
    FG000
    title
    Atezolizumab Plus Bevacizumab Plus Chemotherapy
  2. description
    Bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
    id
    FG001
    title
    Bevacizumab Plus Chemotherapy
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        145
      2. group Id
        FG001
        num Subjects
        150
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        4
      2. group Id
        FG001
        num Subjects
        2
      type
      Withdrawal/Lost to follow-up
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        200
      2. group Id
        FG001
        num Subjects
        200
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        198
      2. comment
        There is one patient assigned in the BC arm who actually received ABC treatment. This patient is evaluated in the treatment arm to which he/she was randomly assigned (BC) for all the efficacy (Intention-to-Treat (ITT)) analyses. For the safety analysis the patient is evaluated according to the treatment he/she received (ABC treatment), irrespective of the allocated treatment at randomization.
        group Id
        FG001
        num Subjects
        200
      type
      Received at least one dose of trial treatment
    3. achievements
      1. group Id
        FG000
        num Subjects
        8
      2. group Id
        FG001
        num Subjects
        4
      comment
      Patients who were on treatment at database cut-off for final efficacy analysis: September 01, 2023
      type
      On treatment
    4. achievements
      1. group Id
        FG000
        num Subjects
        192
      2. group Id
        FG001
        num Subjects
        196
      comment
      Atezolizumab plus bevacizumab plus chemotherapy: 109 progressions, 62 toxicities, 9 deaths, 7 investigator decisions, 1 patient decision, 2 other; Bevacizumab plus chemotherapy: 141 progressions, 35 toxicities, 9 deaths, 1 investigator decision, 2 patient decisions, 8 other
      type
      Treatment failures
    5. achievements
      1. group Id
        FG000
        num Subjects
        2
      2. group Id
        FG001
        num Subjects
        0
      type
      Never started treatment
    6. achievements
      1. group Id
        FG000
        num Subjects
        51
      2. group Id
        FG001
        num Subjects
        48
      comment
      Patients who were on follow-up at database cut-off for final efficacy analysis: September 01, 2023
      type
      COMPLETED
    7. achievements
      1. group Id
        FG000
        num Subjects
        149
      2. group Id
        FG001
        num Subjects
        152
      type
      NOT COMPLETED
    title
    Overall Study

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

Preserved source evidence · Not medical advice