Internal Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Blood. 2013 Jul 4;122(1):68-73. doi: 10.1182/blood-2013-03-487025. Epub 2013 May 22.
POEMS syndrome is a rare plasma cell dyscrasia presenting with polyneuropathy and other systemic findings. Patients with 1 to 3 bone lesions and negative bone marrows are often treated with involved field radiation therapy as the initial and potentially definitive therapy. Long-term outcomes of patients treated with this approach have not been systematically studied. Of the 146 patients with POEMS syndrome seen at the Mayo Clinic between January 1999 and September 2011, 38 (26%) were given targeted radiation as their initial primary therapy and are the ones studied here. The median number of bone lesions was 1 (range: 1-6). The median dose of radiation administered was 45 Gy (range: 35-54 Gy). Complete or partial hematologic, vascular endothelial growth factor, fluorodeoxyglucose-positron emission tomography, and clinical responses were documented in 31%, 14%, 22%, and 47%, respectively. With median follow-up of 43 months, the 4-year overall survival is 97% and event-free survival is 52%. Risk factors for needing salvage therapy included reduced pulmonary diffusing capacity of carbon monoxide and increased urinary total protein. The presence of 3 lesions compared with 1 or 2 did not increase risk for treatment failure. Among selected patients with POEMS syndrome, radiation produces durable, meaningful responses.
POEMS 综合征是一种罕见的浆细胞异常疾病,表现为多发性神经病和其他全身表现。1 至 3 处骨骼病变且骨髓阴性的患者通常采用受累野放射治疗作为初始和潜在的确定性治疗。采用这种方法治疗的患者的长期结果尚未得到系统研究。在 1999 年 1 月至 2011 年 9 月期间,Mayo 诊所共诊治了 146 例 POEMS 综合征患者,其中 38 例(26%)接受了靶向放疗作为初始主要治疗方法,这些患者是本研究的对象。骨病变的中位数为 1 处(范围:1-6 处)。接受的放射治疗中位数剂量为 45 Gy(范围:35-54 Gy)。分别有 31%、14%、22%和 47%的患者完全或部分血液学、血管内皮生长因子、氟脱氧葡萄糖正电子发射断层扫描和临床反应得到了记录。中位随访时间为 43 个月,4 年总生存率为 97%,无事件生存率为 52%。需要挽救性治疗的风险因素包括一氧化碳肺弥散量降低和尿总蛋白增加。与 1 或 2 处病变相比,存在 3 处病变并不会增加治疗失败的风险。在选定的 POEMS 综合征患者中,放射治疗可产生持久、有意义的反应。