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Translational medical research for personlized therapy of advanced or relapsed gastric cancer based on MINIPDX

Translational medical research for personlized therapy of advanced or relapsed gastric cancer based on MINIPDX

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019568
Enrollment
Unknown
Registered
2018-11-18
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Gastric cancer

Interventions

Case series:MINIPDX susceptibility testing for personalized therapy

Sponsors

Wuxi Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Histopathological examination of patients with advanced or recurrent gastric cancer; 2. The time post-chemotherapy is = 4 weeks; 3. The damage caused by other treatment has been restored; 4. No other neoplastic diseases based on clinical diagnosis; the main organs (liver, kidney, heart) are healthy; 5. The patients could provide biopsy or fresh tumor tissue samples; 6. Objective tumors that meet RECIST 1.1 criteria and can be evaluated by CT/MRI; 7. KPS score = 60, expected survival time = 3 months; Comprehensive assessment of patients who can tolerate chemotherapy and targeted therapy; 8. Subjects volunteered to participate, signed informed consent, good compliance, active treatment and follow-up;

Exclusion criteria

Exclusion criteria: 1. The patients were in poor condition without tolerance of surgery or post-surgery chemtherapy; 2. Combined metastasis; unstable angina, symptomatic congestive heart failure, severe arrhythmia, myocardial infarction in the past 6 months, prolonged QT interval (>450ms); 3. Other malignant tumor occurred within the past 5 years; 4. The patient cannot be followed up or is participating in other clinical trials; 5. There is drug abuse; or any medical, psychological or social condition that may affect the study, patient compliance, or even compromise the safety of the patient; 6. Perform other experimental drug treatments other than this test within 4 weeks before the start of the study; or participate in another clinical study that has an impact on the results of this study; 7. Mental or medical instability makes the patient unable or unwilling to sign an informed consent form; 8. The patients were considered unsuitable for participating in the study by the investigators based on comprehensive assessments.

Design outcomes

Primary

MeasureTime frame
Objective response rate;Progress-free survival;

Secondary

MeasureTime frame
Overall survival;Five-year survival rate;Quality of life score;

Countries

China

Contacts

Public ContactChunhui Jin

Wuxi Hospital of Traditional Chinese Medicine

jickim@163.com+86 13861868628

Outcome results

None listed

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