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N/A N=1,390

Real-world Study of Dedifferentiated Liposarcoma Patients in China

Dedifferentiated Liposarcoma

Enrolled (actual)
1,390
Serious AEs
Results posted
Jul 2025
Primary outcome: Primary: Cohort 1: Overall Survival — 13.4; 11.9; 8.1 months

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Boehringer Ingelheim
Primary completion
May 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Cohort 1: Overall Survival
13.4; 11.9; 8.1
SECONDARY
Cohort 1, Cohort 2: Survival After Initial Diagnosis
30.3; 38.4
SECONDARY
Cohort 1, Cohort 2: Total Number of Treatment Lines
1.0; 0.0
SECONDARY
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment Type
119; 12; 85; 12; 15; 1
SECONDARY
Cohort 1, Cohort 2: Second Line (2L) of Therapy by Treatment Type
37; 4; 22; 2; 13; 1
SECONDARY
Cohort 1, Cohort 2: Third Line (3L) of Therapy by Treatment Type
16; 1; 11; 1; 5; 0
SECONDARY
Cohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Steroid Therapy
1; 1
SECONDARY
Cohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Immunosuppressant Therapy
32; 2
SECONDARY
Cohort 1, Cohort 2: Number of Patients With Treatments Classified as Hormone Replacement Therapy
10; 0

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.

Eligibility Criteria

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.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06115681). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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