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Clinical Study for Gemcitabine Drug-Eluting Beads Transarterial Chemoembolization by Callispheres Beads in Patients with Central Non-Small Cell Lung Cancer

Clinical Study for Gemcitabine Drug-Eluting Beads Transarterial Chemoembolization by Callispheres Beads in Patients with Central Non-Small Cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900020620
Enrollment
Unknown
Registered
2019-01-10
Start date
2019-02-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Central non-small cell lung cancer

Interventions

Case series:Gemcitabine Drug-Eluting Beads Transarterial Chemoembolization by Callispheres Beads

Sponsors

Minimally Invasive Tumor Therapies Center, Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18-75 years male and female; 2) Non-small cell lung cancer was diagnosed by histopathology, and central lung cancer was classified by CT and other imaging examination; 3) Reject or intolerance of radiotherapy or chemotherapy due to the severe heart failure, emphysema, interstitial lung fibrosis, etc., or have a recurrence after surgery or a local progression after radiotherapy or chemotherapy; 4) No extrapulmonary metastases, or metastases were controlled and stable after treatment; 5) ECOG PS = 2; 6) Life expectancy > 6 months.

Exclusion criteria

Exclusion criteria: 1) With extensive, uncontrolled extrapulmonary metastases; 2) Past or present history of other malignant tumors (except cured basal cell carcinoma or squamous cell carcinoma of skin, or cervical carcinoma in situ); 3) WBC 2 mg/L, AST and/or ALT > 2 times of the upper limit); 5) Coagulation disorders (INR >1.5) or hemorrhagic diseases, or anticoagulant therapy; 6) Patients with active infection requiring antibiotic treatment; 7) Allergic to contrast agent; 8) During pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Response rate;

Secondary

MeasureTime frame
Progression-free survival;Overall survival;Quality of life;

Countries

China

Contacts

Public ContactBie Zhixin

Beijing Hospital

zhxbiejn@qq.com+86 13651151077

Outcome results

None listed

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