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A Multi-center collaborative Clinical Study of Treatment Guided by patient-derived tumor xenograft in Patients with Bone and soft tissue sarcoma

A Multi-center collaborative Clinical Study of Treatment Guided by patient-derived tumor xenograft in Patients with Bone and soft tissue sarcoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17013617
Enrollment
Unknown
Registered
2017-11-30
Start date
2017-03-15
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

bone and soft tissue sarcoma

Interventions

Sponsors

Beijing Jishuitan Hospital; 81th Hospital of PLA; Dongfang Hospital Affiliated to Shanghai Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 8 to 75 years old, male and female; (2) bone and soft tissue sarcoma diagnosed by histopathological examination, and patients with advanced stage of sarcoma treated with systemic treatment and failure of first-line treatment; (3) capable of obtaining sufficient amounts of fresh tumor tissue (surgical resection or biopsy to obtain primary or metastatic foci); (4) all patients should have measurable lesions, and the efficacy evaluation should be evaluated by RECIST 1.1 standard; (5) ECOG score 02, expected survival should be more than 3 months; (6) anticancer drugs (previous chemotherapy and / or targeted therapy) were enrolled in the study from the last time should be over 2 weeks; (7) the participants volunteered to sign the informed consent and had good compliance. They were able to actively treat and cooperate with the follow-up.

Exclusion criteria

Exclusion criteria: (1) participate in clinical study of other drugs; (2) liver and renal function and hematopoietic function of bone marrow do not meet the requirements of chemotherapy; (3) reluctant to undergo subsequent chemotherapy after the failure of the previous treatment using the anticancer drugs or protocols recommended by the researchers in conjunction with the test results; (4) those suffering from severe uncontrolled acute infection or major organ disease.

Design outcomes

Primary

MeasureTime frame
ORR;PFS;OS;

Countries

China

Contacts

Public ContactNiu Xiaohui

Beijing Jishuitan Hospital

moonlight003@163.com+86 138011325222

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 17, 2026