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Predicting postoperative recurrence and optimizing adjuvant therapy strategies of leiomyosarcoma based on molecular residual disease

Predicting postoperative recurrence and optimizing adjuvant therapy strategies of leiomyosarcoma based on molecular residual disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100782
Enrollment
Unknown
Registered
2025-04-15
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leiomyosarcoma

Interventions

Observation group:None

Sponsors

Zhongshan Hospital affiliated Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1 sign an informed consent form before the start of the study 2 aged 18-70; 3 pathologically diagnosed with LMS; 4 eligible for radical surgery.

Exclusion criteria

Exclusion criteria: Patients meeting any of the following exclusion criteria will not be enrolled in the study: 1 Concurrent active malignant neoplasms other than leiomyosarcoma; 2 Evidence of any severe or uncontrolled systemic disease, including uncontrolled hypertension or active bleeding factors (assessed by the investigator for their 3 potential to reduce the patient’s willingness to participate or compliance with the study treatment regimen), or active infectious diseases such as hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) infection; 4 Patients deemed ineligible by the investigator, such as those likely to be non-compliant with the study protocol, restrictions, or requirements, or other situations at the investigator’s discretion.

Design outcomes

Primary

MeasureTime frame
Recurrence free survival;

Countries

China

Contacts

Public ContactChenlu Zhang

Zhongshan Hospital affiliated Fudan University

zhang.chenlu@zs-hospital.sh.cn+86 188 1693 3564

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026