Radiotherapy for Solitary Bony or Extramedullary Plasmacytoma.

Cancer diagnosis & prognosis Pub Date : 2024-07-03 eCollection Date: 2024-07-01 DOI:10.21873/cdp.10350
Atsuto Katano, Subaru Sawayanagi, Masanari Minamitani, Shingo Ohira, Hideomi Yamashita
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Abstract

Background/aim: This study aimed to determine the oncological outcomes associated with curative radiotherapy for solitary bony or extramedullary plasmacytomas by drawing on clinical data from a single tertiary center. This study aimed to provide a comprehensive understanding of the efficacy of radiotherapeutic interventions and delineate the patterns of disease recurrence.

Patients and methods: Eleven consecutive patients diagnosed with solitary bony or extramedullary plasmacytomas and treated between May 2007 and November 2023 were retrospectively screened. Different radiotherapy doses and fractionations were employed, and statistical analyses were performed to assess overall survival (OS) and disease-free survival (DFS).

Results: Among the 11 patients (9 males and 2 females), primary tumors were located within the bone in seven patients, whereas extramedullary tumors were observed in four patients. The median prescribed radiation dose was 46 Gy. The 5-year OS and DFS were 83.3% and 28.9%, respectively. Progression to multiple myeloma occurred in four patients with primary bony plasmacytoma. Local control rate was 88.9%, and one patient experienced distant metastasis after 32 months. Bony plasmacytoma has a high tendency of leading to multiple myeloma rather than extramedullary plasmacytoma (5-year progression to multiple myeloma-free survival rate, 20.8% vs. 100%, p=0.08).

Conclusion: Radiotherapy is effective for solitary plasmacytomas with favorable local control and high objective response rates. A comparison with the existing literature supports the role of radiotherapy in the management of these conditions. The differences in outcomes between bony and extramedullary plasmacytomas emphasize the need for personalized treatment approaches.

单发骨性或髓外性浆细胞瘤的放射治疗。
背景/目的:本研究旨在利用一家三级医疗中心的临床数据,确定与单发骨性或髓外浆细胞瘤根治性放疗相关的肿瘤治疗效果。这项研究旨在全面了解放射治疗干预的疗效,并描述疾病复发的模式:回顾性筛选了2007年5月至2023年11月期间诊断为单发骨性或髓外浆细胞瘤并接受治疗的11例连续患者。采用了不同的放疗剂量和分次,并对总生存期(OS)和无病生存期(DFS)进行了统计分析:11名患者(9男2女)中,7名患者的原发肿瘤位于骨内,4名患者的肿瘤位于髓外。中位放射剂量为46 Gy。5年的OS和DFS分别为83.3%和28.9%。4名原发性骨浆细胞瘤患者进展为多发性骨髓瘤。局部控制率为88.9%,一名患者在32个月后出现远处转移。骨浆细胞瘤比髓外浆细胞瘤更容易发展为多发性骨髓瘤(5年无多发性骨髓瘤生存率为20.8%对100%,P=0.08):放疗对单发浆细胞瘤有效,局部控制良好,客观反应率高。结论:放疗对单发浆细胞瘤有效,具有良好的局部控制效果和较高的客观反应率,与现有文献的比较支持放疗在此类疾病治疗中的作用。骨性浆细胞瘤和髓外浆细胞瘤的疗效差异强调了个性化治疗方法的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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