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Trial · NCT06115681

Real-world Study of Dedifferentiated Liposarcoma Patients in China

NCT06115681, Completed, Boehringer Ingelheim; results first posted 2025-07-10

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Real-world Study of Dedifferentiated Liposarcoma Patients in China. Trials, record NCT06115681. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06115681

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Real-world Study of Dedifferentiated Liposarcoma Patients in China
NCT number
NCT06115681
Status
Completed
Enrollment
1,390 participants, actual
Lead sponsor
Boehringer Ingelheim
Conditions
Dedifferentiated Liposarcoma
First posted
2023-11-03
Last updated
2025-07-10
Results first posted
2025-07-10

Source ClinicalTrials.gov

Registered outcomes9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryCohort 1: Overall SurvivalTime from index date until the earliest record of death or end of the study period, up to 10 years.
Overall survival (OS) as an event for each patient in Cohort 1 was 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 was censored at the last activity date before the end of the study period.
SecondaryCohort 1, Cohort 2: Survival After Initial DiagnosisTime from initial diagnosis until the earliest record of death or end of the study period, up to 10 years.
Survival after initial diagnosis for each patient was defined as the date of death minus the date of initial diagnosis. For patients with no record of death, survival after initial diagnosis was censored at the last activity date before the end of the study period.
SecondaryCohort 1, Cohort 2: Total Number of Treatment LinesAt index date and during follow-up, up to 10 years.
The total number of treatment lines in both cohorts is reported. Lines of therapy (LOT) were defined by the temporal relationship and sequencing of treatment regimens by using the dates of initiation and discontinuation of chemotherapy, targeted therapy, and/or immunotherapy.
SecondaryCohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeAt index date and during follow-up, up to 10 years
Number of patients with first line (1L) therapy by treatment type for both cohorts is reported. Lines of therapy (LOT) were defined by the temporal relationship and sequencing of treatment regimens by using the dates of initiation and discontinuation of chemotherapy, targeted therapy, and/or immunotherapy.
SecondaryCohort 1, Cohort 2: Second Line (2L) of Therapy by Treatment TypeAt index date and during follow-up, up to 10 years
Number of patients with second line (2L) therapy by treatment type for both cohorts is reported. Lines of therapy (LOT) were defined by the temporal relationship and sequencing of treatment regimens by using the dates of initiation and discontinuation of chemotherapy, targeted therapy, and/or immunotherapy.
SecondaryCohort 1, Cohort 2: Third Line (3L) of Therapy by Treatment TypeAt index date and during follow-up, up to 10 years
Number of patients with third line (3L) therapy by treatment type for both cohorts is reported. Lines of therapy (LOT) were defined by the temporal relationship and sequencing of treatment regimens by using the dates of initiation and discontinuation of chemotherapy, targeted therapy, and/or immunotherapy.
SecondaryCohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Steroid TherapyAt index date and during follow-up, up to 10 yearsNumber of patients who received treatments with drugs classified as concurrent steroid therapy for both cohorts is reported.
SecondaryCohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Immunosuppressant TherapyAt index date and during follow-up, up to 10 yearsNumber of patients who received treatments with drugs classified as concurrent immunosuppressant therapy for both cohorts is reported.
SecondaryCohort 1, Cohort 2: Number of Patients With Treatments Classified as Hormone Replacement TherapyAt index date and during follow-up, up to 10 yearsNumber of patients who received treatments with drugs classified as hormone replacement therapy for both cohorts is reported.

Outcomes9

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
SECONDARYCohort 1, Cohort 2: Survival After Initial DiagnosisTime from initial diagnosis until the earliest record of death or end of the study period, up to 10 years.
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and aged ≥18 years at initial diagnosis. Only patients with an existing diagnosis date were included in this analysis.
monthsMEDIAN
SECONDARYCohort 1, Cohort 2: Total Number of Treatment LinesAt index date and during follow-up, up to 10 years.
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and being age ≥18 years at initial diagnosis.
Count of treatment lines per patientMEDIAN
SECONDARYCohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeAt index date and during follow-up, up to 10 years
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and aged ≥18 years at initial diagnosis. Only patients with non-missing data were included in the analysis.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 1, Cohort 2: Second Line (2L) of Therapy by Treatment TypeAt index date and during follow-up, up to 10 years
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and aged ≥18 years at initial diagnosis. Only patients with non-missing data were included in the analysis.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 1, Cohort 2: Third Line (3L) of Therapy by Treatment TypeAt index date and during follow-up, up to 10 years
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and being age ≥18 years at initial diagnosis. Only patients with non-missing data were included in the analysis.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Steroid TherapyAt index date and during follow-up, up to 10 years
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and aged ≥18 years at initial diagnosis.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Immunosuppressant TherapyAt index date and during follow-up, up to 10 years
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and being age ≥18 years at initial diagnosis.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 1, Cohort 2: Number of Patients With Treatments Classified as Hormone Replacement TherapyAt index date and during follow-up, up to 10 years
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and being age ≥18 years at initial diagnosis.
ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYCohort 1: Overall SurvivalTime from index date until the earliest record of death or end of the study period, up to 10 years.
All patients diagnosed with dedifferentiated liposarcoma (DDLPS) who met the inclusion criteria of having at least 2 documented clinical visits in National Anti-Tumor Drug Surveillance System (NATDSS) in China on or after January 1, 2013 and aged ≥18 years at initial diagnosis. Only patients who received at least one line of systemic antineoplastic treatment by the end of cohort identification period were included in this analysis.
monthsMEDIAN

Results by group49

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Cohort 1, Cohort 2: Survival After Initial DiagnosisDDLPS Patients With 1L Treatment at Index Date (Cohort 1)30.395% Confidence Interval 26.8 to 36.7months
Cohort 1, Cohort 2: Survival After Initial DiagnosisDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)38.495% Confidence Interval 35.0 to 42.6months
Cohort 1, Cohort 2: Total Number of Treatment LinesDDLPS Patients With 1L Treatment at Index Date (Cohort 1)1.0Inter-Quartile Range 1.0 to 2.0Count of treatment lines per patient
Cohort 1, Cohort 2: Total Number of Treatment LinesDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)0.0Inter-Quartile Range 0.0 to 0.0Count of treatment lines per patient
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeDDLPS Patients With 1L Treatment at Index Date (Cohort 1)Anthracycline-based regimens119Participants
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)Anthracycline-based regimens12Participants
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeDDLPS Patients With 1L Treatment at Index Date (Cohort 1)Anlotinib-based regimens85Participants
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)Anlotinib-based regimens12Participants
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeDDLPS Patients With 1L Treatment at Index Date (Cohort 1)Apatinib-based regimens15Participants
Cohort 1, Cohort 2: First Line (1L) of Therapy by Treatment TypeDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)Apatinib-based regimens1Participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDDDLPS Patients With 1L Treatment at Index Date (Cohort 1)275
Overall StudySTARTEDDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)1,115
Overall StudyCOMPLETEDDDLPS Patients With 1L Treatment at Index Date (Cohort 1)275
Overall StudyCOMPLETEDDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)1,115
Overall StudyNOT COMPLETEDDDLPS Patients With 1L Treatment at Index Date (Cohort 1)0
Overall StudyNOT COMPLETEDDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)0

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDDLPS Patients With 1L Treatment at Index Date (Cohort 1)175275
Total, all-cause mortalityDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)4231,106
Total, other adverse eventsDDLPS Patients With 1L Treatment at Index Date (Cohort 1)00
Total, other adverse eventsDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)00
Total, serious adverse eventsDDLPS Patients With 1L Treatment at Index Date (Cohort 1)00
Total, serious adverse eventsDDLPS Patients Without 1L Treatment at Index Date (Cohort 2)00

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons4

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
DDLPS Patients With 1L Treatment at Index Date (Cohort 1) vs DDLPS Patients Without 1L Treatment at Index Date (Cohort 2): Cohort 1, Cohort 2: Number of Patients With Treatments Classified as Hormone Replacement Therapy
Trial comparisons
DDLPS Patients With 1L Treatment at Index Date (Cohort 1) vs DDLPS Patients Without 1L Treatment at Index Date (Cohort 2): Cohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Immunosuppressant Therapy
Trial comparisons
DDLPS Patients With 1L Treatment at Index Date (Cohort 1) vs DDLPS Patients Without 1L Treatment at Index Date (Cohort 2): deaths from any causeTrial comparisons
DDLPS Patients With 1L Treatment at Index Date (Cohort 1) vs DDLPS Patients Without 1L Treatment at Index Date (Cohort 2): Cohort 1, Cohort 2: Number of Patients With Treatments Classified as Concurrent Steroid Therapy
Trial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06115681

GET https://conductscience.org/api/trials/v1/NCT06115681/results?page=2