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NCT02414139 · OUTCOME

Disease Control Rate (DCR)

Study of Oral cMET Inhibitor INC280 in Patients With EGFR Wild-type (wt), Advanced Non-small Cell Lung Cancer (NSCLC) (Geometry Mono-1) · Source last updated 2024-03-20

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
Up to approximately 5 years

What was measured

Percentage of participants with a best overall response of confirmed CR, PR or stable disease (SD) per RECIST 1.1 by BIRC and investigator assessment. CR: Disappearance of all non-nodal target and non-target lesions. In addition, any pathological lymph nodes assigned as target and non-target lesions must have a reduction in short axis to \< 10 mm. PR: At least a 30% decrease in the sum of diameter of all target lesions, taking as reference the baseline sum of diameters. SD: Neither sufficient shrinkage to qualify for PR or CR nor an increase in lesions which would qualify for progressive disease.

Analysis population: FAS, including all subjects who received at least one dose of capmatinib.

Groups in this outcome

Cohort 1a: Pre-treated Patients With MET GCN ≥ 10 (2/3L)

Pre-treated patients with MET GCN ≥ 10 treated with INC280 at 400mg BID as second or third line (2/3L)

Cohort 1b: Pre-treated Patients With MET GCN ≥ 6 and < 10 (2/3L)

Pre-treated patients with MET GCN ≥ 6 and \< 10 treated with INC280 at 400 mg BID as second or third line (2/3L)

Cohort 2: Pre-treated Patients With MET GCN ≥ 4 and < 6 (2/3L)

Pre-treated patients with MET GCN ≥ 4 and \< 6 treated with INC280 at 400mg BID as second or third line (2/3L)

Cohort 3: Pre-treated Patients With MET GCN < 4 (2/3L)

Pre-treated patients with MET GCN \< 4 treated with INC280 at 400mg BID as second or third line (2/3L)

Cohort 4: Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)

Pre-treated patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as second or third line (2/3L)

Cohort 5a: Treatment-naïve Patients With MET GCN ≥10 (1L)

Treatment-naïve patients with MET GCN ≥10 treated with INC280 at 400mg BID as first-line (1L)

Cohort 5b: Treatment-naïve Patients With MET Mutation Regardless of MET GCN (1L)

Treatment-naïve patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as first line (1L)

Cohort 6.1 (Expansion of Cohort 1a): Pre-treated Patients MET GCN ≥ 10 Without MET Mutation (2L)

Pre-treated patients with MET GCN ≥ 10 without MET mutation treated with INC280 at 400 mg BID as second line (2L) (expansion cohort of Cohort 1a)

Cohort 6.2 (Expansion of Cohort 4): Pre-treated Patients With MET Mutation (2L)

Pre-treated patients with MET mutation regardless of MET GCN treated with INC280 at 400 mg BID as second line (2L)(expansion of Cohort 4)

Cohort 7 (Expansion of Cohort 5b): Treatment-naïve With MET Mutation Regardless of MET GCN (1L)

Treatment-naïve patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as first line (1L) (expansion cohort of Cohort 5b)

Cohort 4 + Cohort 6.2: All Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)

All pre-treated patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as second or third line (2/3L). (Participants from Cohort 4 and Cohort 6.2)

Cohort 5b + Cohort 7: All Treatment-naive With MET Mutation Regardless of MET GCN (1L)

All treatment naive patients with MET mutation regardless of MET GCN treated with INC280 at 400 mg BID as first line (1L) (Participants from Cohort 5b and Cohort 7)

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

Analysis denominator · Participants

GroupSource count
Cohort 1a: Pre-treated Patients With MET GCN ≥ 10 (2/3L)69
Cohort 1b: Pre-treated Patients With MET GCN ≥ 6 and < 10 (2/3L)42
Cohort 2: Pre-treated Patients With MET GCN ≥ 4 and < 6 (2/3L)54
Cohort 3: Pre-treated Patients With MET GCN < 4 (2/3L)30
Cohort 4: Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)69
Cohort 5a: Treatment-naïve Patients With MET GCN ≥10 (1L)15
Cohort 5b: Treatment-naïve Patients With MET Mutation Regardless of MET GCN (1L)28
Cohort 6.1 (Expansion of Cohort 1a): Pre-treated Patients MET GCN ≥ 10 Without MET Mutation (2L)3
Cohort 6.2 (Expansion of Cohort 4): Pre-treated Patients With MET Mutation (2L)31
Cohort 7 (Expansion of Cohort 5b): Treatment-naïve With MET Mutation Regardless of MET GCN (1L)32
Cohort 4 + Cohort 6.2: All Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)100
Cohort 5b + Cohort 7: All Treatment-naive With MET Mutation Regardless of MET GCN (1L)60

Reported measurements

By BIRC assessment
Values in Percentage of participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Cohort 1a: Pre-treated Patients With MET GCN ≥ 10 (2/3L)71.0Not reported58.881.3Not reported
Cohort 1b: Pre-treated Patients With MET GCN ≥ 6 and < 10 (2/3L)54.8Not reported38.770.2Not reported
Cohort 2: Pre-treated Patients With MET GCN ≥ 4 and < 6 (2/3L)46.3Not reported32.660.4Not reported
Cohort 3: Pre-treated Patients With MET GCN < 4 (2/3L)53.3Not reported34.371.7Not reported
Cohort 4: Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)78.3Not reported66.787.3Not reported
Cohort 5a: Treatment-naïve Patients With MET GCN ≥10 (1L)66.7Not reported38.488.2Not reported
Cohort 5b: Treatment-naïve Patients With MET Mutation Regardless of MET GCN (1L)96.4Not reported81.799.9Not reported
Cohort 6.1 (Expansion of Cohort 1a): Pre-treated Patients MET GCN ≥ 10 Without MET Mutation (2L)100.0Not reported29.2100.0Not reported
Cohort 6.2 (Expansion of Cohort 4): Pre-treated Patients With MET Mutation (2L)90.3Not reported74.298.0Not reported
Cohort 7 (Expansion of Cohort 5b): Treatment-naïve With MET Mutation Regardless of MET GCN (1L)100.0Not reported89.1100.0Not reported
Cohort 4 + Cohort 6.2: All Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)82.0Not reported73.189.0Not reported
Cohort 5b + Cohort 7: All Treatment-naive With MET Mutation Regardless of MET GCN (1L)98.3Not reported91.1100.0Not reported
By investigator assessment
Values in Percentage of participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Cohort 1a: Pre-treated Patients With MET GCN ≥ 10 (2/3L)60.9Not reported48.472.4Not reported
Cohort 1b: Pre-treated Patients With MET GCN ≥ 6 and < 10 (2/3L)45.2Not reported29.861.3Not reported
Cohort 2: Pre-treated Patients With MET GCN ≥ 4 and < 6 (2/3L)44.4Not reported30.958.6Not reported
Cohort 3: Pre-treated Patients With MET GCN < 4 (2/3L)46.7Not reported28.365.7Not reported
Cohort 4: Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)76.8Not reported65.186.1Not reported
Cohort 5a: Treatment-naïve Patients With MET GCN ≥10 (1L)73.3Not reported44.992.2Not reported
Cohort 5b: Treatment-naïve Patients With MET Mutation Regardless of MET GCN (1L)96.4Not reported81.799.9Not reported
Cohort 6.1 (Expansion of Cohort 1a): Pre-treated Patients MET GCN ≥ 10 Without MET Mutation (2L)100.0Not reported29.2100.0Not reported
Cohort 6.2 (Expansion of Cohort 4): Pre-treated Patients With MET Mutation (2L)90.3Not reported74.298.0Not reported
Cohort 7 (Expansion of Cohort 5b): Treatment-naïve With MET Mutation Regardless of MET GCN (1L)96.9Not reported83.899.9Not reported
Cohort 4 + Cohort 6.2: All Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)81.0Not reported71.988.2Not reported
Cohort 5b + Cohort 7: All Treatment-naive With MET Mutation Regardless of MET GCN (1L)96.7Not reported88.599.6Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        58.8
        upper Limit
        81.3
        value
        71.0
      2. group Id
        OG001
        lower Limit
        38.7
        upper Limit
        70.2
        value
        54.8
      3. group Id
        OG002
        lower Limit
        32.6
        upper Limit
        60.4
        value
        46.3
      4. group Id
        OG003
        lower Limit
        34.3
        upper Limit
        71.7
        value
        53.3
      5. group Id
        OG004
        lower Limit
        66.7
        upper Limit
        87.3
        value
        78.3
      6. group Id
        OG005
        lower Limit
        38.4
        upper Limit
        88.2
        value
        66.7
      7. group Id
        OG006
        lower Limit
        81.7
        upper Limit
        99.9
        value
        96.4
      8. group Id
        OG007
        lower Limit
        29.2
        upper Limit
        100.0
        value
        100.0
      9. group Id
        OG008
        lower Limit
        74.2
        upper Limit
        98.0
        value
        90.3
      10. group Id
        OG009
        lower Limit
        89.1
        upper Limit
        100.0
        value
        100.0
      11. group Id
        OG010
        lower Limit
        73.1
        upper Limit
        89.0
        value
        82.0
      12. group Id
        OG011
        lower Limit
        91.1
        upper Limit
        100.0
        value
        98.3
    title
    By BIRC assessment
  2. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        48.4
        upper Limit
        72.4
        value
        60.9
      2. group Id
        OG001
        lower Limit
        29.8
        upper Limit
        61.3
        value
        45.2
      3. group Id
        OG002
        lower Limit
        30.9
        upper Limit
        58.6
        value
        44.4
      4. group Id
        OG003
        lower Limit
        28.3
        upper Limit
        65.7
        value
        46.7
      5. group Id
        OG004
        lower Limit
        65.1
        upper Limit
        86.1
        value
        76.8
      6. group Id
        OG005
        lower Limit
        44.9
        upper Limit
        92.2
        value
        73.3
      7. group Id
        OG006
        lower Limit
        81.7
        upper Limit
        99.9
        value
        96.4
      8. group Id
        OG007
        lower Limit
        29.2
        upper Limit
        100.0
        value
        100.0
      9. group Id
        OG008
        lower Limit
        74.2
        upper Limit
        98.0
        value
        90.3
      10. group Id
        OG009
        lower Limit
        83.8
        upper Limit
        99.9
        value
        96.9
      11. group Id
        OG010
        lower Limit
        71.9
        upper Limit
        88.2
        value
        81.0
      12. group Id
        OG011
        lower Limit
        88.5
        upper Limit
        99.6
        value
        96.7
    title
    By investigator assessment
denoms
  1. counts
    1. group Id
      OG000
      value
      69
    2. group Id
      OG001
      value
      42
    3. group Id
      OG002
      value
      54
    4. group Id
      OG003
      value
      30
    5. group Id
      OG004
      value
      69
    6. group Id
      OG005
      value
      15
    7. group Id
      OG006
      value
      28
    8. group Id
      OG007
      value
      3
    9. group Id
      OG008
      value
      31
    10. group Id
      OG009
      value
      32
    11. group Id
      OG010
      value
      100
    12. group Id
      OG011
      value
      60
    units
    Participants
description
Percentage of participants with a best overall response of confirmed CR, PR or stable disease (SD) per RECIST 1.1 by BIRC and investigator assessment. CR: Disappearance of all non-nodal target and non-target lesions. In addition, any pathological lymph nodes assigned as target and non-target lesions must have a reduction in short axis to \< 10 mm. PR: At least a 30% decrease in the sum of diameter of all target lesions, taking as reference the baseline sum of diameters. SD: Neither sufficient shrinkage to qualify for PR or CR nor an increase in lesions which would qualify for progressive disease.
dispersion Type
95% Confidence Interval
groups
  1. description
    Pre-treated patients with MET GCN ≥ 10 treated with INC280 at 400mg BID as second or third line (2/3L)
    id
    OG000
    title
    Cohort 1a: Pre-treated Patients With MET GCN ≥ 10 (2/3L)
  2. description
    Pre-treated patients with MET GCN ≥ 6 and \< 10 treated with INC280 at 400 mg BID as second or third line (2/3L)
    id
    OG001
    title
    Cohort 1b: Pre-treated Patients With MET GCN ≥ 6 and < 10 (2/3L)
  3. description
    Pre-treated patients with MET GCN ≥ 4 and \< 6 treated with INC280 at 400mg BID as second or third line (2/3L)
    id
    OG002
    title
    Cohort 2: Pre-treated Patients With MET GCN ≥ 4 and < 6 (2/3L)
  4. description
    Pre-treated patients with MET GCN \< 4 treated with INC280 at 400mg BID as second or third line (2/3L)
    id
    OG003
    title
    Cohort 3: Pre-treated Patients With MET GCN < 4 (2/3L)
  5. description
    Pre-treated patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as second or third line (2/3L)
    id
    OG004
    title
    Cohort 4: Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)
  6. description
    Treatment-naïve patients with MET GCN ≥10 treated with INC280 at 400mg BID as first-line (1L)
    id
    OG005
    title
    Cohort 5a: Treatment-naïve Patients With MET GCN ≥10 (1L)
  7. description
    Treatment-naïve patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as first line (1L)
    id
    OG006
    title
    Cohort 5b: Treatment-naïve Patients With MET Mutation Regardless of MET GCN (1L)
  8. description
    Pre-treated patients with MET GCN ≥ 10 without MET mutation treated with INC280 at 400 mg BID as second line (2L) (expansion cohort of Cohort 1a)
    id
    OG007
    title
    Cohort 6.1 (Expansion of Cohort 1a): Pre-treated Patients MET GCN ≥ 10 Without MET Mutation (2L)
  9. description
    Pre-treated patients with MET mutation regardless of MET GCN treated with INC280 at 400 mg BID as second line (2L)(expansion of Cohort 4)
    id
    OG008
    title
    Cohort 6.2 (Expansion of Cohort 4): Pre-treated Patients With MET Mutation (2L)
  10. description
    Treatment-naïve patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as first line (1L) (expansion cohort of Cohort 5b)
    id
    OG009
    title
    Cohort 7 (Expansion of Cohort 5b): Treatment-naïve With MET Mutation Regardless of MET GCN (1L)
  11. description
    All pre-treated patients with MET mutation regardless of MET GCN treated with INC280 at 400mg BID as second or third line (2/3L). (Participants from Cohort 4 and Cohort 6.2)
    id
    OG010
    title
    Cohort 4 + Cohort 6.2: All Pre-treated Patients With MET Mutation Regardless of MET GCN (2/3L)
  12. description
    All treatment naive patients with MET mutation regardless of MET GCN treated with INC280 at 400 mg BID as first line (1L) (Participants from Cohort 5b and Cohort 7)
    id
    OG011
    title
    Cohort 5b + Cohort 7: All Treatment-naive With MET Mutation Regardless of MET GCN (1L)
param Type
NUMBER
population Description
FAS, including all subjects who received at least one dose of capmatinib.
reporting Status
POSTED
time Frame
Up to approximately 5 years
title
Disease Control Rate (DCR)
type
SECONDARY
unit Of Measure
Percentage of participants

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Preserved source evidence · Not medical advice