Tungate Robert M, Lara Kristi, Patel Dakshesh, Fedenko Alexander, Hu James
USC Norris Comprehensive Cancer Center and Hospital, Los Angeles, CA, USA.
Rare Tumors. 2022 Jul 4;14:20363613221110836. doi: 10.1177/20363613221110836. eCollection 2022.
Ewing sarcoma is a primitive neuroectodermal tumor which seldom presents with primary disease in people over age 40 and outside of the appendicular or axial skeleton. We examine a case of primary thoracic Ewing Sarcoma diagnosed initially by CT-guided biopsy in a woman at the age of 74 years. The disease progressed after initial combined modality therapy consisting of neoadjuvant chemotherapy, surgical resection, and adjuvant radiation therapy and two additional courses of multiagent chemotherapy. After relapse of her disease, subsequent second- and third-line systemic agents which included chemotherapy and targeted agents were given with disease stabilization achieved now over 30 months from initial diagnosis. To our knowledge, this is the first report of a primary pulmonary Ewing sarcoma diagnosed in a patient greater than 70 years of age in whom multiple remissions have been achieved with tolerable toxicities.
尤因肉瘤是一种原始神经外胚层肿瘤,在40岁以上人群以及四肢或中轴骨骼以外很少以原发性疾病形式出现。我们检查了一例74岁女性原发性胸段尤因肉瘤病例,最初通过CT引导下活检确诊。在初始的综合治疗(包括新辅助化疗、手术切除、辅助放疗以及另外两个疗程的多药化疗)后,疾病仍进展。疾病复发后,给予包括化疗和靶向药物在内的后续二线和三线全身治疗药物,目前从初始诊断起疾病稳定已超过30个月。据我们所知,这是首例在70岁以上患者中诊断出的原发性肺尤因肉瘤,且通过可耐受的毒性实现了多次缓解的报告。