Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06377735

BAI-BACE for Advanced Lung Squamous Cell Carcinoma

Bronchial arterial infusion plus bronchial arterial chemoembolization (BAI-BACE) has been reported as non-first-line therapy to treat lung cancer in many hospitals in China. BAI, which uses chemotherapeutic drugs directly injected into the tumor and achieved a high concentration in a short time to kill the tumor. Then BACE could seal off the tumor vessels. In this study, we aim to describe the efficacy and safety of BAI-BACE as non-first-line for advanced lung squamous cell carcinoma.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

This study is a multicenter, interventional study to explore the efficacy, safety of BAI-BACE as non-first-line therapy for advanced central squamous cell carcinoma. Lung cancer is the leading cause of cancer-related death worldwide. Owing to the insidious symptom, most patients (about 75 %) are diagnosed at the advanced stage of the disease and, thus, cannot undergo resection. The central squamous cell carcinoma accounts for 25% of all cases of lung cancer. The first-line standard treatment for advanced central squamous cell carcinoma is combined chemoradiotherapy, and chemoradiotherapy is usually as the second-line. However, treatment failure is noted in many patients, and those patients often face the limited therapy choice and poor prognosis. Bronchial arterial infusion plus bronchial arterial chemoembolization (BAI-BACE) has been reported to treat lung cancer in many hospitals in China. BAI, which use chemotherapeutic drugs directly injected into the tumor and achieved a high concentration in a short time to kill the tumor. Then BACE could seal off the tumor vessels. The systemic toxicity of this surgery is low and tolerable. This study will provide clinical evidence that BACE-BAI will provide survival benefit for patients with advanced central squamous cell carcinoma.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Squamous cell carcinoma diagnosed by pathology, and central location by imaging;
  • Age 18-80;
  • Patients failed to the standard first-line or second-line treatment;
  • Tumors limited in the chest;
  • Tumors were fed by bronchial artery through CTA reconstruction;
  • Patents received PD-1 inhibitor or not were also included;
  • Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-2;
  • Images within 2 weeks before inclusion;
  • Life expectancy more than 3 months;
  • Agreed to participated in this clinical trial;
  • Hemameba ≥3.0 x109/L, neutrophil ≥1.5x109/L, hemoglobin≥10.0 g/L, platelet≥100x 109/L, ALT; AST; bilirubin ≤1.5-fold normal, GFR≥60ml/min.

Exclusion criteria

  • Contraindication of BAI or BACE;
  • Under 18 years or over 75 years;
  • extra-chest metastases;
  • Receiving other antitumor treatment;
  • Severe infection or pregnancy;
  • Severe Pulmonary fibrosis and pulmonary artery;
  • liver, kidney or poor physical conditions;
  • Severe pleural effusion or pericardial effusion;
  • Life expectancy less than 3 months.

Treatment and study plan

BAI-BACE

Procedure

Bronchial arterial infusion, bronchial arterial chemoembolization (BACE-BAI) procedure was performed as follows: Bronchial arteriography was performed to find tumor-feeding artery. After the catheter had been inserted into the tumor-feeding artery, paclitaxel (300 mg) was infused slowly at least 30 min. BAI (bronchial arterial infusion) chemotherapy was followed by BACE (Drug-eluting beads bronchial arterial chemoembolization); the CalliSpheres loaded with cis-platinum (30 mg) were infused into the tumor-feeding arteries until stasis or near-stasis of blood flow in the vessel was observed.

Primary outcomes

  1. Progression-Free-Survival (PFS)

    Time frame: 12 months

    Progression was defined as progressive disease by independent radiologic review

Secondary outcomes

  1. Overall survival (OS)

    Time frame: 24 months

    OS is the length of time from the date of inclusion until death from any cause.

  2. Objective response rate (ORR)

    Time frame: 12 months

    ORR, as determined based on tumor response according to RECIST 1.1, is defined as the proportion of all included patients whose best overall response (BOR) is either a complete response or partial response.

  3. Adverse events

    Time frame: 24 months

    Safety will be evaluated according to the NCI CTCAE Version 4.03. All observations

Study contacts

Contact information is provided by the study sponsor or research team.

Feng Duan, MD

CONTACT

[email protected]

86 13910984586

Qunfang Zhou, MD

CONTACT

[email protected]

86 19868000115

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Registry information

Official study title

Bronchial Arterial Infusion Plus Bronchial Arterial Chemoembolization (BAI-BACE) for Advanced Lung Squamous Cell Carcinoma: a Multicenter Single-arm Phase II Study

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Apr 22, 2024
Registry last updated
Aug 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.