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Therapeutic effect of drug-loaded embolization microsphere embolization chemotherapy and bronchial arterial infusion chemotherapy for middle and advanced lung cancer patients----open, control, observational study

Therapeutic effect of drug-loaded embolization microsphere embolization chemotherapy and bronchial arterial infusion chemotherapy for middle and advanced lung cancer patients----open, control, observational study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025586
Enrollment
Unknown
Registered
2019-09-02
Start date
2019-09-01
Completion date
Unknown
Last updated
2019-09-02

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

Conditions

Lung cancer

Interventions

Experimental group :Drug-loaded microsphere embolization chemotherapy
control group :Guànzhù huàliáo 4/5000 Infusion chemotherapy

Sponsors

Shandong Institute of Medical Imaging
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old, male or female; 2. Diagnosis of lung cancer by gastroscopy or biopsy of histology; 3. Patients with intermediate or advanced stage who have lost their chance of surgery or who cannot tolerate surgery; 4. The patient's survival is expected to exceed 3 months; 5. ECOG =3.0x10^9/L, NE>=1.5x10^9/L, Hgb>=10.0g/L, PLT>=100x10^9/L, ALT, AST and bilirubin levels <=1.5 times the upper limit of normal, coagulation function is normal, blood CREA <=1.5 times the upper limit of normal, BUN is normal; 7. Cardiopulmonary function is basically normal; 8. Subjects volunteered to join the study, signed informed consent, and were well-adhered to follow-up.

Exclusion criteria

Exclusion criteria: 1. There are contraindications for general endovascular treatment and contrast agent application; 2. Patients with cachexia or heart, lung, liver and kidney failure; 3. Patients with severe infections and chemotherapy contraindications with severe reduction of white blood cells and platelets; 4. Patients with severe bleeding tendency and iodine allergy and other angiographic contraindications; 5. The bronchial artery and the spinal cord artery coexist or coincide with the traffic is a relative contraindication. 6. Patients with other malignancies within 5 years; 7. Patients with a history of psychotropic substance abuse who are unable to quit or have a mental disorder; 8. Patients who have participated in other drug clinical trials within 4 weeks; 9. According to the investigator's judgment, there are serious patients who are at risk to the patient's safety or affect the patient's accompanying disease to complete the study; 10. The investigator believes that it is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
PFS;

Countries

China

Contacts

Public ContactJianqiang Shang

Shandong Institute of Medical Imaging

yysljj@sina.com13969019186

Outcome results

None listed

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