Department of Medicine, Hematology and Medical Oncology, Mount Sinai School of Medicine, New York, New York 10029-6574, USA.
Oncologist. 2013;18(5):579-83. doi: 10.1634/theoncologist.2012-0349. Epub 2013 Apr 24.
Two cases of adenoid cystic carcinoma (ACC) of the larynx were treated with chemoradiotherapy (CRT) for organ preservation. We reviewed case series and current literature to contrast the potential role of primary CRT as an organ-sparing modality with standard laryngectomy and radiotherapy in patients with laryngeal ACC.
Two treatment-naïve patients with laryngeal ACC treated at Dana-Farber Cancer Institute between 2002 and 2007 were identified. Both patients were offered standard laryngectomy followed by adjuvant radiotherapy or organ-sparing treatment modality.
Both patients were males, aged 57 and 73. The patients completed a course of combined chemoradiotherapy with weekly carboplatin and paclitaxel and 7-8 weeks of radiotherapy to a total dose of 6,600 and 7,000 cGy over 50 and 57 days, respectively. There were no treatment breaks or delays because of toxicity. The major toxicities reported by both patients, as anticipated, were Grade 3 mucositis, desquamative dermatitis, and severe dysphagia, all of which resolved. Both patients are alive with local regional control and functional larynx; one at 112+ months with pulmonary metastases at 54 months, and the other disease free at 60+ months.
Definitive chemoradiation with weekly carboplatin and paclitaxel may be a potential alternative to the current standard of surgery and radiation for patients with locally advanced laryngeal ACC who request an organ-sparing approach. In this group of patients, salvage laryngectomy may be reserved for those who are locally recurrent or chemoradiotherapy resistant. Although CRT provided long-term local regional control in our two patients, there are evident limitations in obtaining evidence for a determination of treatment of rare diseases. This report provides support for following an organ preservation plan in selected patients.
对两例喉腺样囊性癌(ACC)患者采用放化疗(CRT)进行器官保存治疗。我们回顾了病例系列和当前文献,以对比原发 CRT 作为一种保器官治疗模式与标准喉切除术和放疗在喉 ACC 患者中的潜在作用。
在 2002 年至 2007 年期间,我们在达纳-法伯癌症研究所(Dana-Farber Cancer Institute)确定了两名接受 CRT 治疗的初治喉 ACC 患者。两名患者均被提供了标准的喉切除术和辅助放疗,或选择保留器官的治疗方式。
两名患者均为男性,年龄分别为 57 岁和 73 岁。两名患者均完成了联合化疗(每周卡铂和紫杉醇)和放疗,总剂量分别为 6600 和 7000 cGy,共 7-8 周,50 和 57 天。没有因毒性而中断或延迟治疗。两名患者均报告了预期的 3 级黏膜炎、脱屑性皮炎和严重吞咽困难等主要毒性反应,但均已缓解。两名患者均存活且局部区域控制良好,保留了功能喉;其中 1 例在 54 个月时出现肺部转移,存活时间为 112+个月;另 1 例无疾病存活时间为 60+个月。
每周卡铂和紫杉醇的根治性放化疗可能是局部晚期喉 ACC 患者的一种潜在替代治疗方法,这些患者要求保留器官,而不是目前的手术和放疗标准。在这组患者中,挽救性喉切除术可保留给那些局部复发或对放化疗耐药的患者。尽管 CRT 在我们的两名患者中提供了长期的局部区域控制,但在确定罕见疾病的治疗方案方面,仍存在明显的证据获取限制。本报告为在选定患者中实施器官保留计划提供了支持。