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Sequential combined minimally invasive treatment of non small cell lung cancer IIIb-IV

Sequential combined minimally invasive treatment of non small cell lung cancer IIIb-IV

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-15006650
Enrollment
Unknown
Registered
2015-06-26
Start date
2015-07-01
Completion date
Unknown
Last updated
2017-04-18

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 IIIb~?

Interventions

B: Systemic chemotherapy and topical therapy (radioactive particle / RF)
C: Systemic chemotherapy and radiotherapy
D:Systemic chemotherapy plus topical therapy (radioactive particle / RF) +BAE

Sponsors

The First Affiliated Hospital of Zhangzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. aged 18 years old (male or female) 2. histology and cytology confirmed 3. TNM tumor stage IIIb-IV, no operation indications for patients; 4. there is evidence of typical imaging 5. the expected survival time over 12 weeks In blood and liver function examination basically normal, the neutrophil cell >1.5*10^9/L, platelet 60*10^9/L, serum bilirubin efficiency 1.5 times the upper limit of normal value; without liver metastasis. The levels of ALT and AST is less than 2.5 times the upper limit of normal value; liver metastasis AST and alt is less than 5 times the upper limit of normal value; 7. the KPS score of >60; 8. enrolled in the clinical study of patients must sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. the constitution of the patients is too weak, can not be tolerated or unwilling to accept operation; At the same time, 2 with other malignant tumors; 3. serious heart and lung dysfunction, can not tolerate the percutaneous lung puncture operation; 4. serious disease (diabetes and blood coagulation dysfunction) patients; 5. tumor puncture site bleeding, necrosis; 6. pregnant, lactating women and all single and nonparous young patients. 7. contrast agent, local anesthetic allergy.

Design outcomes

Primary

MeasureTime frame
disease control rate;overall survival;

Contacts

Public ContactHan Xinwei
hanxinwei2006@163.com+86 13503842129

Outcome results

None listed

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