Tsang D S, Le L W, Kukreti V, Sun A
Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, and Department of Radiation Oncology, University of Toronto.
Department of Biostatistics, Princess Margaret Cancer Centre, University Health Network; and.
Curr Oncol. 2016 Dec;23(6):e630-e646. doi: 10.3747/co.23.3288. Epub 2016 Dec 21.
Primary cutaneous plasmacytoma (pcp) is a rare disease, with few studies to guide therapy. Our primary study objective was to define treatments used for pcp; a secondary objective was to describe outcomes of patients, including disease recurrence and death.
An institutional cancer registry was used to identify cases for retrospective chart review. In a systematic review, treatments for, and outcomes of, all known cases of pcp were described.
Three eligible cases identified at our institution; each patient had a solitary pcp. The systematic review identified 66 patients. Radiotherapy was the most commonly used primary treatment modality (31% of all patients; 42% for patients with solitary lesions), followed by surgery (28% of all patients; 36% for patients with solitary lesions). Median survival for all patients was 10.4 years [95% ci: 4.3 years to not reached], with a trend toward a decreased risk of death with solitary lesions compared with multiple lesions (hazard ratio: 0.37; 95% ci: 0.13 to 1.08; = 0.059). For patients with solitary lesions, the median and recurrence-free survivals were, respectively, 17.0 years (95% ci: 1.7 years to not reached) and 11.0 years (95% ci: 2 years to not reached); for patients with multiple lesions, they were 4.3 years (95% ci: 1.3 to not reached) and 1.4 years (95% ci: 0.6 years to not reached). Disease recurrence, including progression to multiple myeloma, was the most common cause of death.
Compared with patients having multiple pcp lesions, those presenting with a single pcp lesion might experience longer overall survival. Local therapy (radiation or surgery) is a reasonable curative treatment for a solitary pcp lesion.
原发性皮肤浆细胞瘤(pcp)是一种罕见疾病,指导治疗的研究较少。我们的主要研究目标是确定用于pcp的治疗方法;次要目标是描述患者的预后,包括疾病复发和死亡情况。
利用机构癌症登记处来识别病例以进行回顾性病历审查。在一项系统评价中,描述了所有已知pcp病例的治疗方法和预后。
在我们机构识别出3例符合条件的病例;每位患者均有一个孤立性pcp。系统评价识别出66例患者。放射治疗是最常用的主要治疗方式(占所有患者的31%;孤立性病变患者中占42%),其次是手术(占所有患者的28%;孤立性病变患者中占36%)。所有患者的中位生存期为10.4年[95%置信区间:4.3年至未达到],与多发病变相比,孤立性病变患者的死亡风险有降低趋势(风险比:0.37;95%置信区间:0.13至1.08;P = 0.059)。对于孤立性病变患者,中位生存期和无复发生存期分别为17.0年(95%置信区间:1.7年至未达到)和11.0年(95%置信区间:2年至未达到);对于多发病变患者,分别为4.3年(95%置信区间:1.3至未达到)和1.4年(95%置信区间:0.6年至未达到)。疾病复发,包括进展为多发性骨髓瘤,是最常见的死亡原因。
与有多发性pcp病变的患者相比,患有单个pcp病变的患者可能有更长的总生存期。局部治疗(放疗或手术)是孤立性pcp病变的合理治愈性治疗方法。