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Clinical efficacy of surgery combined with anlotinib in the treatment of extremity desmoid fibromatosis

Clinical efficacy of surgery combined with anlotinib in the treatment of extremity desmoid fibromatosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064408
Enrollment
Unknown
Registered
2022-10-06
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Desmoid fibromatosis of extremity

Interventions

Control group:Simple operation group
Experimental group:Surgery combined with anlotinib

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 58 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were pathologically diagnosed as fibromatosis in West China Hospital and whose tumors were located in the extremities (including shoulder and hip); 2. Clinical symptoms (swelling pain, nerve damage or functional limitation, etc.) or disease progression (MRI examination indicated that the tumor grew 10% within 3 months).

Exclusion criteria

Exclusion criteria: 1. Patients who have received chemotherapy with other targeted drugs or cytotoxic drugs; 2. Patients who are allergic to anlotinib or have contraindications to the use of anlotinib or cannot tolerate the side effects of anlotinib.

Design outcomes

Primary

MeasureTime frame
Local tumor recurrence rate;

Secondary

MeasureTime frame
Complications of surgery;Side effects of Anlotinib;

Countries

China

Contacts

Public ContactDuan Hong

West China Hospital, Sichuan University

Duanhong1970@126.com+86 18980601402

Outcome results

None listed

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