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A Multi-center collaborative Clinical Study of Treatment Guided by patient-derived tumor xenograft in Patients with Advanced digestive system tumors

A Multi-center collaborative Clinical Study of Treatment Guided by patient-derived tumor xenograft in Patients with Advanced digestive system tumors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17012731
Enrollment
Unknown
Registered
2017-09-19
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

Advanced digestive system tumors

Interventions

Sponsors

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 18 to 75 years old, male or female; 2. Pathological examination of the diagnosis of advanced digestive system malignancy, the need for anti-cancer drug chemotherapy; 3. able to take surgical resection or biopsy to obtain fresh tumor tissue; 4. Objective objective tumor in line with RECIST 1.1, CT / MRI can be used to evaluate efficacy; 5. ECOG score 0 ~ 2, the expected survival time to be = 3 months; 6. For previous postoperative subjects, previous anti-cancer drug therapy (chemotherapy and / or targeted therapy) failure from the group of study time to be = 4 weeks, and adverse reactions have been basically restored; 7. Participants volunteered to sign informed consent, good compliance, active treatment and follow-up.

Exclusion criteria

Exclusion criteria: 1. Participate in other drug clinical studies at the same time; 2. liver, kidney function and bone marrow hematopoietic function does not meet the requirements of chemotherapy; 3. Do not want to use the researchers after the failure of the previous treatment with the results of the recommended anti-cancer drugs or programs for follow-up chemotherapy; 4. suffering from severe uncontrolled acute infection or major organ disease; 5. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
ORR;DCR;Serum tumor markers;

Countries

China

Contacts

Public ContactQin shukui

81th Hospital of PLA

qinsk@csco.org.cn+86 025-80864029

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 19, 2026