Abstract

BackgroundCentrally located lung tumors present treatment challenges given their proximity to mediastinal structures including the central airway, esophagus, major vessels, and heart. Therapeutic options can be limited for medically inoperable patients, particularly if they have received previous thoracic radiotherapy. High dose rate (HDR) brachyablation was developed to improve the therapeutic ratio for patients with central lung tumors. The purpose of this study is to report initial safety and efficacy outcomes with this treatment for central lung malignancies.MethodsFrom September 2015 to August 2019, a total of 25 patients with 37 pulmonary tumors were treated with percutaneous HDR brachyablation. Treatment was delivered by a multi-disciplinary team of interventional radiologists, pulmonologists, and radiation oncologists. Twenty-three patients received a median dose of 21.5 Gy (range 15–27.5) in a single fraction, whereas two patients received median dose of 24.75 Gy (range 24–25.5) over 2–3 fractions. Tumor local control (LC) was evaluated by Response Evaluation Criteria in Solid Tumors v1.1. Treatment-related toxicities were graded by Common Terminology Criteria for Adverse Events v5.0, with adverse events less than 90 days defined as acute, and those occurring later were defined as late. LC, progression-free survival (PFS), and overall survival (OS) rates were estimated by the Kaplan–Meier method.ResultsOf 37 treated tumors, 88% were metastatic. Tumor location was central and ultra-central in 24.3% and 54.1%, respectively. Average tumor volume was 11.6 cm3 (SD 12.4, range 0.57–62.8). Median follow-up was 19 months (range 3–48). Two–year LC, PFS, and OS were 96.2%, 29.7%, and 65.5%, respectively. Thirteen of 39 (33.3%) catheter implantation procedures were associated with trace minor pneumothorax requiring no intervention, 1 (2.5%) procedure with minor radiographic pulmonary hemorrhage, and 4 (10.3%) with major pneumothorax requiring chest tube insertions. All procedural complications resolved within 24 h from treatment. Acute grade 1–2 toxicity was identified in 4 patients, whereas none developed late toxicity beyond 90 days of follow-up.ConclusionPercutaneous HDR brachyablation is a safe and promising treatment option for centrally located primary and metastatic lung tumors. Future comparisons with stereotactic body radiotherapy and other ablative techniques are warranted to expand multi-disciplinary management options.

Highlights

  • The uncontrolled growth of central tumors can contribute to significant morbidity, including hemoptysis, lung collapse, vascular obstruction, and dysphagia

  • stereotactic body radiotherapy (SBRT) to centrally located tumors has been associated with severe toxicities [2,3,4,5,6], which has led to the development of alternative strategies such as image-guided thermal ablation (IGTA) that has been associated with variable levels of local control (LC) and complications related to applicator placement and delivery of thermal energy [7,8,9]

  • Patients had been considered for treatment in a multi-disciplinary setting if they had biopsy proven primary non-small cell lung cancer (NSCLC), locally recurrent NSCLC, or metastatic pulmonary tumors confirmed with growth on imaging, who were medically inoperable, not surgical candidates, or refused surgery

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Summary

Introduction

The uncontrolled growth of central tumors can contribute to significant morbidity, including hemoptysis, lung collapse, vascular obstruction, and dysphagia. SBRT to centrally located tumors has been associated with severe toxicities [2,3,4,5,6], which has led to the development of alternative strategies such as image-guided thermal ablation (IGTA) that has been associated with variable levels of LC and complications related to applicator placement and delivery of thermal energy [7,8,9]. Despite such challenges, local control of centrally located tumors is critical for palliation and to improve quality of life. The purpose of this study is to report initial safety and efficacy outcomes with this treatment for central lung malignancies

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