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Chinese Journal of Interventional Radiology(Electronic Edition) ›› 2024, Vol. 12 ›› Issue (04): 303-310. doi: 10.3877/cma.j.issn.2095-5782.2024.04.003

• Monographic Study·Respiratory Intervention • Previous Articles     Next Articles

Clinical efficacy and safety of drug-eluting bead bronchial artery chemoembolization in the treatment of rare non-small cell lung cancer

Wei Cui1, Yi Deng2, Suyi Ye2, Jing Li3, Xiaoming Chen1, Jing Zhang1, Rongde Xu1,()   

  1. 1.Department of Interventional Radiology,Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences),Southern Medical University,Guangdong Guangzhou 510080
    2.Department of Pulmonary and Critical Care Medicine,The First People's Hospital of Yunnan Province,Medical School of Kunming University of Science and Technology,Yunnan Kunming 650093,China
    3.Department of Pulmonary and Critical Care Medicine,Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences),Southern Medical University,Guangdong Guangzhou 510080
  • Received:2024-10-17 Online:2024-11-25 Published:2024-12-19
  • Contact: Rongde Xu

Abstract:

Objective

To explore the clinical efficacy and safety of drug-eluting bead bronchial artery chemoembolization (D-BACE) in the treatment of rare non-small cell lung cancer (NSCLC).

Methods

The clinical data of 8 patients with pathologically confirmed rare NSCLC who underwent D-BACE treatment were analyzed. The types of cancer included adenoid cystic carcinoma (3 cases),lymphoepithelioma-like carcinoma (2 cases), SMACAR4-deficient lung cancer (2 cases), and pulmonary sarcomatoid carcinoma (one case). The clinical efficacy and safety of D-BACE were evaluated by observing objective response rate, disease control rate, progression-free survival (PFS), and overall survival (OS).Adverse reactions during the treatment process were also recorded and assessed.

Results

The average age of the patients was (51.0±3.4) years, with 5 males and 3 females. Among them, 1 patient underwent surgical resection in combination with D-BACE, 4 patients received chemotherapy and immunotherapy in combination with D-BACE, and 3 patients were treated with anlotinib in combination with D-BACE. After the first D-BACE treatment, the objective response rate was 25% (2/8), and the disease control rate was 87.5% (7/8). The median follow-up time was 18 months, with a median PFS of 6 months. The median OS has not yet been reached. Common adverse reactions included mild local pain (2 cases, 25%), nausea and vomiting (2 cases, 25%), fever (1 case, 12.5%), and chest numbness (1 case, 12.5%). All adverse reactions were mild and self-limited or relieved after symptomatic medication treatment. No serious complications were observed.

Conclusion

The combination of D-BACE and systemic treatment for rare non-small cell lung cancer is safe and feasible. However, further studies are needed to evaluate its long-term efficacy as the median overall survival has not yet been reached. The clinical value of D-BACE as a selective local treatment option warrants further exploration.

Key words: Non-small cell lung cancer, Drug-eluting beads, Bronchial arterial chemoembolization

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