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The efficacy and safety of drug loaded microsphere bronchial artery chemoembolization (DEB-BACE) combined with anlotinib and adebelimumab in the third line treatment of advanced NSCLC: a prospective, single arm, single center, exploratory clinical study

The efficacy and safety of drug loaded microsphere bronchial artery chemoembolization (DEB-BACE) combined with anlotinib and adebelimumab in the third line treatment of advanced NSCLC: a prospective, single arm, single center, exploratory clinical study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083717
Enrollment
Unknown
Registered
2024-04-30
Start date
2024-01-19
Completion date
Unknown
Last updated
2024-05-06

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:DEB-BACE+Anlotinib+Adebelimumab

Sponsors

Ningbo Medical Center Li Huili Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age>18 years old, gender unlimited,According to the Diagnosis and Treatment Guidelines for Primary Lung Cancer (2018 Edition), the pathological diagnosis of NSCLC was made by histological examination,TNM staging is III - IV,Failure of second-line treatment according to CSCO guidelines,ECOG PS score = 2 points,Expected survival time>3 months,Sign informed consent form

Exclusion criteria

Exclusion criteria: Individuals who have previously received interventional therapy (iodine particle implantation, ablation, BACE treatment), or have received PD-L1 inhibitor immunotherapy during the first or second line standard treatment period of the patient,Patients with other malignant tumors that have not been cured,White blood cells176.8) µ Mol/L, Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT)>twice the normal upper limit),Central squamous cell carcinoma with cavity features,Uncorrectable coagulation dysfunction or concomitant active massive hemoptysis,Patients with concurrent active infections who require antibiotic treatment,Uncontrollable hypertension, diabetes, cardiovascular disease with obvious symptoms,Contrast agent allergy,Women with concurrent pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Objective relief rate;

Secondary

MeasureTime frame
Overall survival;Progression free survival;Disease control rate;Duration of relief;safety;

Countries

China

Contacts

Public ContactKaitai Liu

Ningbo Medical Center Li Huili Hospital

liukaitai@nbu.edu.cn+86 137 3211 2205

Outcome results

None listed

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