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

NCT ID: NCT06188650

Last Updated: 2024-01-03

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-12-09
• Study Completion Date: 2026-09-30

Brief Summary

The goal of this clinical trial is to learn about Drug loaded microspheres for bronchial artery chemoembolization (DEB-BACE) combined with anlotinib and adebelimumab in patients with advanced NSCLC after second-line treatment.

The main question it aims to answer is:

The efficacy and safety of Drug Loading Beads Bronchial Arterial Chemoembolization (DEB-BACE) combined with Anlotinib and Adebelimumab in the third line treatment of advanced NSCLC.

Participants will receive DEB-BACE treatment, rest for 1 week and then undergo 1 cycle of treatment with combination of Anlotinib and Adebelimumab. With a maximum of 4 DEB-BACE treatments depending on the therapeutic effect, followed by continued treatment with Anlotinib and Adebelimumab.

Conditions

Non-Small Cell Lung Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

experimental group

Group Type: EXPERIMENTAL

Anlotinib

Intervention Type: DRUG

After receiving DEB-BACE treatment, the enrolled patients will rest for one week and then undergo one cycle of treatment with the combination of Anlotinib and Adebelimumab. After one course of treatment, the efficacy will be re evaluated, such as CR, and the treatment with Anlotinib and Adebelimumab will continue; For PR, SD, or PD, continue to receive DEB-BACE combined with anlotinib and adebelimumab as needed, with a maximum of 4 DEB-BACE treatments, followed by continued treatment with anlotinib and adebelimumab

Interventions

Anlotinib

After receiving DEB-BACE treatment, the enrolled patients will rest for one week and then undergo one cycle of treatment with the combination of Anlotinib and Adebelimumab. After one course of treatment, the efficacy will be re evaluated, such as CR, and the treatment with Anlotinib and Adebelimumab will continue; For PR, SD, or PD, continue to receive DEB-BACE combined with anlotinib and adebelimumab as needed, with a maximum of 4 DEB-BACE treatments, followed by continued treatment with anlotinib and adebelimumab

Intervention Type: DRUG

Other Intervention Names

Adebrelimab; Drug-eluting Beads Bronchial Arterial Chemoembolization，DEB-BACE

Eligibility Criteria

Inclusion Criteria

1. Age>18 years old, gender unlimited;

2. According to the Diagnosis and Treatment Guidelines for Primary Lung Cancer (2018 Edition), NSCLC was diagnosed by pathological histology;

3. TNM staging is III - IV;

4. Failure of second-line treatment according to the CSCO guidelines;

5. ECOG PS score ≤ 2 points;

6. Estimated survival time>3 months;

7. Sign informed consent form

Exclusion Criteria

1. 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;

2. Patients with other malignant tumors that have not been cured;

3. White blood cells<3 × 109/L, absolute value of neutrophils<1.5 × 109/L, neutrophil/lymphocyte ratio ≥ 3, platelet count<50 × 109/L, hemoglobin concentration<90 g/L;

4. Liver and kidney dysfunction (creatinine>176.8) μ Mol/L; Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT)>twice the normal upper limit;

5. Central squamous cell carcinoma with cavity features;

6. Incorrectable coagulation dysfunction or concomitant active massive hemoptysis;

7. Patients with concurrent active infections who require antibiotic treatment;

8. Uncontrollable hypertension, diabetes, and cardiovascular diseases with obvious symptoms;

9. Contrast agent allergy;

10. Women with concurrent pregnancy or lactation

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ningbo Medical Center Lihuili Hospital

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Kaitai Liu

Ningbo, Zhejiang, China

Site Status: RECRUITING

Countries

China

Central Contacts

kaitai liu, doctor

Role: CONTACT

liukaitai@nbu.edu.cn

+8613732112205

jingtao tong, master

Role: CONTACT

vanssi@163.com

+8615088440328

Facility Contacts

jingtao tong, master

Role: primary

vanssi@163.com

+8615088440328

Other Identifiers

KY2023PJ261

Identifier Type: -

Identifier Source: org_study_id