Real-world Study of Dedifferentiated Liposarcoma Patients in China

Sponsor
Boehringer Ingelheim (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT06115681
Collaborator
(none)
1,400
1
3.1
458.2

Study Details

Study Description

Brief Summary

This study will characterize patients with dedifferentiated liposarcoma (DDLPS) in China, including an understanding of demographic, and clinical characteristics as well as treatment patterns and clinical outcomes associated with the current real-world treatment.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1400 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Demographic, Clinical Characteristics, and Treatment Outcomes Associated With Dedifferentiated Liposarcoma Patients in China
    Anticipated Study Start Date :
    Dec 29, 2023
    Anticipated Primary Completion Date :
    Mar 31, 2024
    Anticipated Study Completion Date :
    Mar 31, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    Cohort 1

    Patients with unresectable locally advanced or metastatic differentiated liposarcoma (DDLPS) who received at least one line of systemic antineoplastic treatment by the end of cohort identification period (index date = start date of first line (1L) treatment).

    Cohort 2

    Patients with DDLPS who have not initiated 1L systemic antineoplastic treatment by the end of cohort identification period (index date = date of initial DDLPS diagnosis during cohort identification period). Patients initiated 1L treatment afterwards or patients received adjuvant and/or neoadjuvant therapy only through follow-up will be included in Cohort 2.

    Outcome Measures

    Primary Outcome Measures

    1. Cohort 1: Overall survival [Up to 10 years]

      Overall survival (OS) as an event for each patient in Cohort 1 will be defined as the date of death minus the index date or the start day of each line of therapy (LOT). For patients with no record of death, OS will be censored at the last activity date before the end of the study period.

    Secondary Outcome Measures

    1. Cohort 1, Cohort 2: Survival after initial diagnosis [Up to 10 years]

      Survival after initial diagnosis for each patient will be defined as the date of death minus the date of initial diagnosis. For patients with no record of death, survival after initial diagnosis will be censored at the last activity date before the end of the study period.

    2. Cohort 1, Cohort 2: First line (1L) of therapy by treatment type [Up to 10 years]

    3. Cohort 1, Cohort 2: Second line (2L) of therapy by treatment type [Up to 10 years]

    4. Cohort 1, Cohort 2: Third line (3L) of therapy by treatment type [Up to 10 years]

    5. Cohort 1, Cohort 2: Total number of treatment lines [Up to 10 years]

    6. Cohort 1, Cohort 2: Number of treatments with drugs classified as steroid therapy [Up to 10 years]

    7. Cohort 1, Cohort 2: Number of treatments with drugs classified as concurrent immunosuppressant therapy [Up to 10 years]

    8. Cohort 1, Cohort 2: Number of treatments with drugs classified as hormone replacement therapy [Up to 10 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion criteria:
    • Patient has two or more documented clinical visits in the National Anti-Tumor Drug Surveillance System (NATDSS) network on or after January 1, 2013.

    • Patient has a confirmed diagnosis of dedifferentiated liposarcoma (DDLPS) during his/her lifetime.

    • At least 18 years old at the date of initial diagnosis.

    No exclusion criteria are applied.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Jishuitan hospital Beijing China 102208

    Sponsors and Collaborators

    • Boehringer Ingelheim

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Boehringer Ingelheim
    ClinicalTrials.gov Identifier:
    NCT06115681
    Other Study ID Numbers:
    • 1403-0024
    First Posted:
    Nov 3, 2023
    Last Update Posted:
    Nov 3, 2023
    Last Verified:
    Oct 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 3, 2023