| Literature DB >> 31719806 |
Brandon T Mullins1, Gaorav Gupta1,2.
Abstract
BACKGROUND: While patients with ataxia telangiectasia are known to have increased radiation sensitivity, patients with germline heterozygous ataxia telangiectasia mutated (ATM) mutations can have widely varying functional and clinical effects, which can make management decisions difficult. With an increased prevalence of gene panel-based testing for breast cancer patients, radiation oncologists are increasingly confronted with patients who carry germline ATM variants of uncertain clinical significance. This study describes the clinical courses and outcomes of 5 breast cancer patients with varying germline heterozygous ATM mutations undergoing radiation therapy at our institution in order to provide additional knowledge of the varying clinical effects to aid future decision making. CASE SERIES: We identified 5 patients with breast cancer and varying germline heterozygous ATM mutations treated at the University of North Carolina Hospitals between 2015 and 2017. The median age at breast cancer diagnosis for the patient series was 46. Clinical effects of radiation treatment varied amongst the 5 patients. The one patient with a pathogenic ATM mutation had no increased radiation related toxicity. Of the 4 patients with ATM variants of uncertain significance, one patient had increased radiation sensitivity with Grade 3 dermatitis. All patients have remained recurrence free with a median duration of 18 months.Entities:
Keywords: ALND, Axillary Lymph Node Dissection; ATM; ATM, Ataxia Telangiectasia Mutated; Ataxia telangiectasia; Breast cancer; DCIS, Ductal Carcinoma In-situ; ER, Estrogen Receptor; Her2, Human Epidermal Growth Factor Receptor 2; IDC, Invasive Ductal Carcinoma; IMN, Internal Mammary Lymph Node; PR, Progesterone Receptor; Radiation therapy; SLNB, Sentinel Lymph Node Biopsy; TC, Taxol & Cyclophosphamide; TCH, Taxol, Cyclophosphamide, Herceptin; Toxicity; VUS; VUS, Variant of Uncertain Significance; ddAC, Dose Dense Adriamycin & Cyclophosphamide
Year: 2019 PMID: 31719806 PMCID: PMC6839001 DOI: 10.1016/j.rpor.2019.09.008
Source DB: PubMed Journal: Rep Pract Oncol Radiother ISSN: 1507-1367