Abstract

Bronchogenicadenoid cystic carcinoma (ACC) is a rare malignancy particularly challenging to irradiate, largely owing to anatomic location and associated toxicities. Proton beam therapy (PBT) can reduce doses to nearby organs at risk, but only one case report has been published detailing PBT for this neoplasm. This study was an institutional review board-approved retrospective chart review of all patients at one institution with bronchogenic ACC treated with PBT. Toxicities were assessed per Common Toxicity Criteria for Adverse Events, version 4.0. Five patients, median age 67 years (range = 40-97 years), were all symptomatic before PBT. Two patients were debulked before PBT, which was delivered at a median 66.6 Gy (RBE) (range, 57.5-80 Gy (RBE)). Two patients received concurrent platinum-based chemotherapy. Symptoms improved in all patients. Acute toxicities included the following: grade 1 fatigue (n = 3), grade 1 dermatitis (n = 2), grade 1 esophagitis (n = 1), grade 2 fatigue (n = 1), grade 2 dermatitis (n = 1), grade 2 esophagitis (n = 2). There was one case of late radiation fibrosis causing bronchial stenosis and requiring a stent, and another of late grade 1 dysphagia. All grade 2 toxicities occurred in patients receiving concurrent chemoradiotherapy. At median follow-up of 10 months (range = 5-47 months), no patient experienced tumor recurrence and none had symptoms impairing daily functioning or quality of life. Although statistically nonsignificant owing to low sample sizes, dosimetric data revealed that PBT numerically reduced doses, most notably to the heart and to low-dose volumes of the lung. This is the largest series to date evaluating PBT for bronchogenic ACC. PBT is associated with low rates of acute and late toxicities and excellent early local control.

Highlights

  • Most commonly occurring in the salivary glands, adenoid cystic carcinoma (ACC) rarely arises in the thorax and accounts for approximately 0.2% of primary respiratory system neoplasms [1]

  • ACCs most commonly develop in the proximal portion of the tracheobronchial tree and histologically arise from submucosal

  • Glandular tissue is most commonly observed on pathological evaluation, more aggressive ACCs may contain larger components of solid cells [6]

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Summary

Introduction

Most commonly occurring in the salivary glands, adenoid cystic carcinoma (ACC) rarely arises in the thorax and accounts for approximately 0.2% of primary respiratory system neoplasms [1]. These tumors are often tracheal or bronchial in origin. ACC and squamous cell carcinoma are the most common primary bronchial cancers [2]. ACCs most commonly develop in the proximal portion of the tracheobronchial tree and histologically arise from submucosal. PBT for bronchogenic adenoid cystic carcinoma glands, ductal/myoepithelial origins have been posited [3,4,5]. The most recognized first-line treatment for bronchogenic ACC is definitive surgical resection with a goal of complete tumor resection as well as relief of any potential obstruction and restoration of ventilation. Complete resection is often not feasible, especially in cases with large tumor bulk, anatomically central disease, and/or extensive submucosal spread, or in patients who are medically inoperable due to advanced age or comorbidities [8]

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