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Efficacy and safety of eribulin monotherapy or combination therapy in Chinese adults with soft tissue sarcoma

Efficacy and safety of eribulin monotherapy or combination therapy in Chinese adults with soft tissue sarcoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053594
Enrollment
Unknown
Registered
2021-11-24
Start date
2021-11-26
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

soft tissue sarcoma (STS)

Interventions

Group 1:Anthracycline-based drugs
Group 2:Ifosfamide-based
Group 3:Other chemotherapy options
Group 4:Combined molecular targeted therapy
Group 5:Combination immune checkpoint inhibitor therapy

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 years and above; 2. After anthracycline therapy progresses or is not suitable for anthracyclines, choose eribulin or eribulin combination therapy; 3. At least one target lesion according to RECIST1.1; 4. The included pathological subtypes include but are not limited to: undifferentiated sarcoma, liposarcoma, leiomyosarcoma, synovial sarcoma, fibrosarcoma, angiosarcoma, etc.

Exclusion criteria

Exclusion criteria: 1. History of other malignant tumors, excluding basal cell carcinoma of the skin and carcinoma in situ of the cervix; 2. Participate in other clinical research cases; 3. According to CTCAE 5.0, there were adverse reactions greater than grade 2 before the use of eribulin, which was not suitable for intravenous chemotherapy, and had central nervous system metastasis.

Design outcomes

Primary

MeasureTime frame
Objective response rate (ORR);Time to progression (TTP);Overall survival time (OS);Safey;Disease control rate (DCR);

Countries

China

Contacts

Public ContactZhou Yuhong

Zhongshan Hospital, Fudan University

zhou.yuhong@zs-hospital.sh.cn+86 13918286810

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026