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Establishment of the screening method and evaluation system of Individualized Precision Medical Drugs for Non-small Cell Lung Cancer

Establishment of the screening method and evaluation system of Individualized Precision Medical Drugs for Non-small Cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016954
Enrollment
Unknown
Registered
2018-07-04
Start date
2018-08-15
Completion date
Unknown
Last updated
2018-07-09

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

Conditions

Non - small Cell Lung Cancer

Interventions

Case series:Establishment of PDX models and mini-PDX susceptibility testing using tumor tissue and puncture samples

Sponsors

The First Affiliated Hospital of Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Histopathological examination confirmed the diagnosis of NSCLC, and needs systematic anticancer therapy; 2. Clinical examination with no other tumor; 3. Can obtain fresh tumor tissues or pleural effusion or ascites samples by surgical resection or biopsy; 4. With tumor foci meeting the RECIST 1.1 standard; can evaluate the efficacy by CT/MRI; 5. KPS scores=60; expected survival = 3 months; 6. Voluntary to participate and sign informed consent document; Compliance is good, can actively treat and cooperate with follow-ups.

Exclusion criteria

Exclusion criteria: 1. Unplanned reoperation after surgery; 2. During the course of treatment, the patient was found to have other tumors, or a second tumor was found, which interfered with this experimental study; 3. KPS score = 60 points or blood biochemical tests suggest that patients are not suitable for continuing chemotherapy or chemotherapy has been delayed; 4. Cannot or refuse to collect tumor samples, including tumor tissue blocks, or malignant pleural effusion and ascites; 5. Refused to receive treatment plans or follow-up plans.

Design outcomes

Primary

MeasureTime frame
Overall survival;Progressive Free survival;Objective response rate;

Countries

China

Contacts

Public ContactXiuyi Yu

he First Affiliated Hospital of Xiamen University

xiuyiyu@126.com+86 15959279001

Outcome results

None listed

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