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NCT02454972 · OUTCOME

Overall Response Rate (ORR)

Clinical Trial of Lurbinectedin (PM01183) in Selected Advanced Solid Tumors · Source last updated 2023-03-02

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
From the start of treatment to the date of progression or the start of a subsequent therapy or end of patient's follow-up, until Cycle 6 (21-day cycle)

What was measured

Overall Response Rate was defined as the percentage of patients with a confirmed response, either CR or PR, according to the RECIST v.1.1. Complete Response (CR): Disappearance of all target lesions; Partial Response (PR): ≥30% decrease in the sum of the longest diameters of target lesions compared with baseline; Progressive disease: ≥20% increase in the sum of the longest diameter of target lesions compared with the smallest-sum longest; diameter recorded or the appearance of one or more new lesions; Stable Disease: Neither PR or PD

Analysis population: Treated patients and with disease measurement

Groups in this outcome

Biliary Tract Carcinoma Cohort

Patients with Pathologically proven diagnosis of biliary tract carcinoma

Carcinoma of Unknown Primary Site Cohort

Patients with pathologically proven diagnosis of carcinoma of unknown primary site

Endometrial Carcinoma Cohort

Patients with pathologically proven diagnosis of endometrial carcinoma

Ewing's Family of Tumors Cohort

Patients with pathologically proven diagnosis of Ewing's Family of Tumors

Germ Cell Tumors Cohort

Patients with pathologically proven diagnosis of Germ Cell Tumors, excluding immature teratoma, or teratoma with malignant transformation.

Head and Neck Carcinoma Cohort

Patients with Pathologically proven diagnosis of Head and Neck Carcinoma. Salivary glands tumors were excluded.

BRCA1/2-associated Metastatic Breast Carcinoma Cohort

Patients with pathologically proven diagnosis of BRCA1/2-associated metastatic breast carcinoma

Neuroendocrine Tumors Cohort

Patients with Pathologically proven diagnosis of Neuroendocrine Tumors, grade 2 and 3 according to World Health Organization (WHO) classification.

Small Cell Lung Cancer Cohort

Patients with pathologically proven diagnosis of small cell lung cancer

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

Analysis denominator · Participants

GroupSource count
Biliary Tract Carcinoma Cohort18
Carcinoma of Unknown Primary Site Cohort19
Endometrial Carcinoma Cohort71
Ewing's Family of Tumors Cohort28
Germ Cell Tumors Cohort23
Head and Neck Carcinoma Cohort13
BRCA1/2-associated Metastatic Breast Carcinoma Cohort21
Neuroendocrine Tumors Cohort31
Small Cell Lung Cancer Cohort105

Reported measurements

Source class 1
Values in percentage of participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Biliary Tract Carcinoma Cohort5.6Not reported0.127.3Not reported
Carcinoma of Unknown Primary Site Cohort0.0Not reported0.017.6Not reported
Endometrial Carcinoma Cohort11.3Not reported5.021.0Not reported
Ewing's Family of Tumors Cohort14.3Not reported4.032.7Not reported
Germ Cell Tumors Cohort4.3Not reported0.121.9Not reported
Head and Neck Carcinoma Cohort0.0Not reported0.024.7Not reported
BRCA1/2-associated Metastatic Breast Carcinoma Cohort28.6Not reported11.355.2Not reported
Neuroendocrine Tumors Cohort6.5Not reported0.821.4Not reported
Small Cell Lung Cancer Cohort36.2Not reported27.046.1Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        0.1
        upper Limit
        27.3
        value
        5.6
      2. group Id
        OG001
        lower Limit
        0.0
        upper Limit
        17.6
        value
        0.0
      3. group Id
        OG002
        lower Limit
        5.0
        upper Limit
        21.0
        value
        11.3
      4. group Id
        OG003
        lower Limit
        4.0
        upper Limit
        32.7
        value
        14.3
      5. group Id
        OG004
        lower Limit
        0.1
        upper Limit
        21.9
        value
        4.3
      6. group Id
        OG005
        lower Limit
        0.0
        upper Limit
        24.7
        value
        0.0
      7. group Id
        OG006
        lower Limit
        11.3
        upper Limit
        55.2
        value
        28.6
      8. group Id
        OG007
        lower Limit
        0.8
        upper Limit
        21.4
        value
        6.5
      9. group Id
        OG008
        lower Limit
        27.0
        upper Limit
        46.1
        value
        36.2
denoms
  1. counts
    1. group Id
      OG000
      value
      18
    2. group Id
      OG001
      value
      19
    3. group Id
      OG002
      value
      71
    4. group Id
      OG003
      value
      28
    5. group Id
      OG004
      value
      23
    6. group Id
      OG005
      value
      13
    7. group Id
      OG006
      value
      21
    8. group Id
      OG007
      value
      31
    9. group Id
      OG008
      value
      105
    units
    Participants
description
Overall Response Rate was defined as the percentage of patients with a confirmed response, either CR or PR, according to the RECIST v.1.1. Complete Response (CR): Disappearance of all target lesions; Partial Response (PR): ≥30% decrease in the sum of the longest diameters of target lesions compared with baseline; Progressive disease: ≥20% increase in the sum of the longest diameter of target lesions compared with the smallest-sum longest; diameter recorded or the appearance of one or more new lesions; Stable Disease: Neither PR or PD
dispersion Type
95% Confidence Interval
groups
  1. description
    Patients with Pathologically proven diagnosis of biliary tract carcinoma
    id
    OG000
    title
    Biliary Tract Carcinoma Cohort
  2. description
    Patients with pathologically proven diagnosis of carcinoma of unknown primary site
    id
    OG001
    title
    Carcinoma of Unknown Primary Site Cohort
  3. description
    Patients with pathologically proven diagnosis of endometrial carcinoma
    id
    OG002
    title
    Endometrial Carcinoma Cohort
  4. description
    Patients with pathologically proven diagnosis of Ewing's Family of Tumors
    id
    OG003
    title
    Ewing's Family of Tumors Cohort
  5. description
    Patients with pathologically proven diagnosis of Germ Cell Tumors, excluding immature teratoma, or teratoma with malignant transformation.
    id
    OG004
    title
    Germ Cell Tumors Cohort
  6. description
    Patients with Pathologically proven diagnosis of Head and Neck Carcinoma. Salivary glands tumors were excluded.
    id
    OG005
    title
    Head and Neck Carcinoma Cohort
  7. description
    Patients with pathologically proven diagnosis of BRCA1/2-associated metastatic breast carcinoma
    id
    OG006
    title
    BRCA1/2-associated Metastatic Breast Carcinoma Cohort
  8. description
    Patients with Pathologically proven diagnosis of Neuroendocrine Tumors, grade 2 and 3 according to World Health Organization (WHO) classification.
    id
    OG007
    title
    Neuroendocrine Tumors Cohort
  9. description
    Patients with pathologically proven diagnosis of small cell lung cancer
    id
    OG008
    title
    Small Cell Lung Cancer Cohort
param Type
NUMBER
population Description
Treated patients and with disease measurement
reporting Status
POSTED
time Frame
From the start of treatment to the date of progression or the start of a subsequent therapy or end of patient's follow-up, until Cycle 6 (21-day cycle)
title
Overall Response Rate (ORR)
type
PRIMARY
unit Of Measure
percentage of participants

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Preserved source evidence · Not medical advice