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NCT00261846 · OUTCOME

Percentage of Participants With Change From Baseline in Physical Examinations and Vital Signs

Study Evaluating SKI-606 (Bosutinib) In Philadelphia Chromosome Positive Leukemias · Source last updated 2017-07-27

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
Not reported
Time frame
Screening, Baseline, and end of treatment

What was measured

Percentage of participants with PCI physical examinations and vital signs is reported during therapy and at post therapy. Criteria for PCI change in vital signs: heart rate value of \<40 beats per min and value \>150 beats per min, systolic blood pressure (SBP) of \<80 or \>210 millimeter of mercury (mmHg), diastolic blood pressure (DBP) of \<40 or \>130 mmHg, temperature \<32 or \>40 degree centigrade, respiratory rate (Resp) of \<10 or \>50 breaths/min and criteria for PCI change in physical examination: \>=10% increase or decrease of body weight in kilogram (kg).

Analysis population: Safety population included all participants who receive at least one dose of study medication. 'N' (number of participants analyzed) signifies number of participants who were evaluable for this measure.

Groups in this outcome

Bosutinib 500 mg, CP2L-CML IM-R (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with CP2L IM-R CML; who had no prior proto-oncogene tyrosine-protein kinase Src, Abl, or Src-Abl inhibitor exposure other than IM.

Bosutinib 500 mg, CP2L-CML IM-I (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with CP2L IM-I CML; who had no prior proto-oncogene tyrosine-protein kinase Src, Abl, or Src-Abl inhibitor exposure other than IM.

Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I, D and NI R/I or IM R/I and NI-I CML.

Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I and D-R CML.

Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I and D-I CML.

Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I and NI-R CML.

AP-CML Total (Part 2)

All participants who received bosutinib 500 mg orally once daily in AP CML who were IM R/I or multiple tyrosine kinase inhibitor (Multi-TKI): IM, D and/or NI R/I.

BP-CML Total (Part 2)

All participants who received bosutinib 500 mg orally once daily in blast phase (BP) CML who were IM R/I or Multi-TKI: IM, D and/or NI R/I.

Bosutinib 500 mg, Ph+ ALL (Part 2)

Bosutinib 500 mg was administered orally once-daily in participants with Ph+ ALL

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

Analysis denominator · Participants

GroupSource count
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)188
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)81
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)5
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)35
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)46
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)25
AP-CML Total (Part 2)75
BP-CML Total (Part 2)56
Bosutinib 500 mg, Ph+ ALL (Part 2)20

Reported measurements

SBP >210 mmHg
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)1.1Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
Weight increase 10%
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)16.0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)6.3Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)20.0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)12.1Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)6.5Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)16.0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)11.0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)7.5Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)6.3Not reportedNot reportedNot reportedNot reported
Weight decrease 10%
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)21.9Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)16.3Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)6.1Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)15.2Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)23.3Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)9.4Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
SBP <80 mmHg
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)4.0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
Temperature <32C
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)4.0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
Pulse <40bpm
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)1.4Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
Resp >50 breaths/min
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)5.0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
Resp <10 breaths/min
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bosutinib 500 mg, CP2L-CML IM-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP2L-CML IM-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)2.4Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)0Not reportedNot reportedNot reportedNot reported
AP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
BP-CML Total (Part 2)0Not reportedNot reportedNot reportedNot reported
Bosutinib 500 mg, Ph+ ALL (Part 2)0Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        1.1
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
    title
    SBP >210 mmHg
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        16.0
      2. group Id
        OG001
        value
        6.3
      3. group Id
        OG002
        value
        20.0
      4. group Id
        OG003
        value
        12.1
      5. group Id
        OG004
        value
        6.5
      6. group Id
        OG005
        value
        16.0
      7. group Id
        OG006
        value
        11.0
      8. group Id
        OG007
        value
        7.5
      9. group Id
        OG008
        value
        6.3
    title
    Weight increase 10%
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        21.9
      2. group Id
        OG001
        value
        16.3
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        6.1
      5. group Id
        OG004
        value
        15.2
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        23.3
      8. group Id
        OG007
        value
        9.4
      9. group Id
        OG008
        value
        0
    title
    Weight decrease 10%
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        4.0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
    title
    SBP <80 mmHg
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        4.0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
    title
    Temperature <32C
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        1.4
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
    title
    Pulse <40bpm
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        5.0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
    title
    Resp >50 breaths/min
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        2.4
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
    title
    Resp <10 breaths/min
denoms
  1. counts
    1. group Id
      OG000
      value
      188
    2. group Id
      OG001
      value
      81
    3. group Id
      OG002
      value
      5
    4. group Id
      OG003
      value
      35
    5. group Id
      OG004
      value
      46
    6. group Id
      OG005
      value
      25
    7. group Id
      OG006
      value
      75
    8. group Id
      OG007
      value
      56
    9. group Id
      OG008
      value
      20
    units
    Participants
description
Percentage of participants with PCI physical examinations and vital signs is reported during therapy and at post therapy. Criteria for PCI change in vital signs: heart rate value of \<40 beats per min and value \>150 beats per min, systolic blood pressure (SBP) of \<80 or \>210 millimeter of mercury (mmHg), diastolic blood pressure (DBP) of \<40 or \>130 mmHg, temperature \<32 or \>40 degree centigrade, respiratory rate (Resp) of \<10 or \>50 breaths/min and criteria for PCI change in physical examination: \>=10% increase or decrease of body weight in kilogram (kg).
groups
  1. description
    Bosutinib 500 mg was administered orally once-daily in participants with CP2L IM-R CML; who had no prior proto-oncogene tyrosine-protein kinase Src, Abl, or Src-Abl inhibitor exposure other than IM.
    id
    OG000
    title
    Bosutinib 500 mg, CP2L-CML IM-R (Part 2)
  2. description
    Bosutinib 500 mg was administered orally once-daily in participants with CP2L IM-I CML; who had no prior proto-oncogene tyrosine-protein kinase Src, Abl, or Src-Abl inhibitor exposure other than IM.
    id
    OG001
    title
    Bosutinib 500 mg, CP2L-CML IM-I (Part 2)
  3. description
    Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I, D and NI R/I or IM R/I and NI-I CML.
    id
    OG002
    title
    Bosutinib 500 mg, CP3L-CML IM R/I, (D+NI) R/I or NI-I (Part 2)
  4. description
    Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I and D-R CML.
    id
    OG003
    title
    Bosutinib 500 mg, CP3L-CML IM R/I + D-R (Part 2)
  5. description
    Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I and D-I CML.
    id
    OG004
    title
    Bosutinib 500 mg, CP3L-CML IM R/I + D-I (Part 2)
  6. description
    Bosutinib 500 mg was administered orally once-daily in participants with CP3L IM R/I and NI-R CML.
    id
    OG005
    title
    Bosutinib 500 mg, CP3L-CML IM R/I + NI-R (Part 2)
  7. description
    All participants who received bosutinib 500 mg orally once daily in AP CML who were IM R/I or multiple tyrosine kinase inhibitor (Multi-TKI): IM, D and/or NI R/I.
    id
    OG006
    title
    AP-CML Total (Part 2)
  8. description
    All participants who received bosutinib 500 mg orally once daily in blast phase (BP) CML who were IM R/I or Multi-TKI: IM, D and/or NI R/I.
    id
    OG007
    title
    BP-CML Total (Part 2)
  9. description
    Bosutinib 500 mg was administered orally once-daily in participants with Ph+ ALL
    id
    OG008
    title
    Bosutinib 500 mg, Ph+ ALL (Part 2)
param Type
NUMBER
population Description
Safety population included all participants who receive at least one dose of study medication. 'N' (number of participants analyzed) signifies number of participants who were evaluable for this measure.
reporting Status
POSTED
time Frame
Screening, Baseline, and end of treatment
title
Percentage of Participants With Change From Baseline in Physical Examinations and Vital Signs
type
SECONDARY
unit Of Measure
percentage of participants

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Preserved source evidence · Not medical advice