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在现代治疗环境下,对一组孤立性浆细胞瘤患者的长期临床结果进行评估。

Long-term clinical outcomes in a cohort of patients with solitary plasmacytoma treated in the modern era.

机构信息

Oxford University Hospital NHS Foundation Trust, Oxford, United Kingdom.

Division of Hematology, Hospital das Clinicas of the University of São Paulo, São Paulo, Brazil.

出版信息

PLoS One. 2019 Jul 23;14(7):e0219857. doi: 10.1371/journal.pone.0219857. eCollection 2019.

Abstract

BACKGROUND

The risk of recurrence of solitary plasmacytoma (SP)/progression to MM is well established, but patient, imaging and treatment factors influencing risk of progression require further evaluation.

METHODS

This is a retrospective analysis of 66 SP patients (23 UK, 43 Brazil) diagnosed 1989-2016. Patient baseline characteristics were recorded. The incidence of progression to MM was calculated, including biochemical and imaging findings and the treatment modality received. Survival estimates were determined by Kaplan-Meier analyses.

RESULTS

With a median follow-up of 53.6 months the 5 year overall survival (OS) was 90.7% (95%CI 79-96%). The median progression free survival (PFS) from diagnosis was 61 months. Cumulative incidence of progression to MM was 49.9% at 5 years (95% CI 35.6-62.6%) and was significantly higher with bone plasmacytoma (47.2%, 95%CI 31.9-61.1%), than an extramedullary location (8.3%, 95%CI 0.4-32.3%, Gray test p = 0.0095)). The majority of patients with solitary bony plasmacytoma (SBP) received radiotherapy (RT) (51/53, 96.2%) whereas most extramedullary cases were treated with surgical resection (7/13, 53.8%). A small proportion of SBP patients received additional upfront chemotherapy, with 5/6 in remission after a median follow-up (FU) of 10 years. The diagnostic yield of surveillance functional FU imaging without other indications of relapse/progression was low. The positive predictive value of functional FU imaging was high but with a low negative predictive value, especially in cases of suspected relapse/progression.

CONCLUSION

Our data suggests functional imaging should be used if clinical suspicion of relapse/progression, rather than a routine surveillance tool, and upfront adjuvant chemotherapy is worthy of prospective evaluation.

摘要

背景

孤立性浆细胞瘤(SP)/进展为多发性骨髓瘤(MM)的复发风险已得到充分证实,但影响进展风险的患者、影像学和治疗因素仍需进一步评估。

方法

这是一项对 1989 年至 2016 年间诊断的 66 例 SP 患者(英国 23 例,巴西 43 例)的回顾性分析。记录患者的基线特征。计算进展为 MM 的发生率,包括生化和影像学发现以及所接受的治疗方式。通过 Kaplan-Meier 分析确定生存估计值。

结果

中位随访 53.6 个月时,5 年总生存率(OS)为 90.7%(95%CI 79-96%)。从诊断到无进展生存期(PFS)的中位时间为 61 个月。5 年内进展为 MM 的累积发生率为 49.9%(95%CI 35.6-62.6%),且骨浆细胞瘤(47.2%,95%CI 31.9-61.1%)明显高于骨髓外位置(8.3%,95%CI 0.4-32.3%,Gray 检验 p = 0.0095)。大多数孤立性骨浆细胞瘤(SBP)患者接受了放射治疗(RT)(51/53,96.2%),而大多数骨髓外病例则接受了手术切除(7/13,53.8%)。一小部分 SBP 患者接受了额外的初始化疗,其中 6 例中有 5 例在中位随访 10 年后缓解。在没有其他复发/进展迹象的情况下,进行常规监测功能影像学检查的诊断效果较差。功能影像学检查的阳性预测值较高,但阴性预测值较低,尤其是在怀疑复发/进展的情况下。

结论

我们的数据表明,如果怀疑复发/进展,应使用功能影像学检查,而不是常规监测工具,并且初始辅助化疗值得前瞻性评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2eb4/6650037/57f417a407a1/pone.0219857.g001.jpg

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