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镭-223(Xofigo)对转移性去势抵抗性前列腺癌患者全血细胞减少症影响的单中心回顾性分析

A Single-center Retrospective Analysis of the Effect of Radium-223 (Xofigo) on Pancytopenia in Patients with Metastatic Castration-resistant Prostate Cancer.

作者信息

Skelton William P, Dibenedetto Samantha W, Pang Shiyi S, Pan Kelsey, Barish Jacob L, Nwosu-Iheme Adaeze, Dang Long

机构信息

Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, USA.

Internal Medicine, University of Florida, Gainesville, USA.

出版信息

Cureus. 2020 Jan 28;12(1):e6806. doi: 10.7759/cureus.6806.

Abstract

Introduction Radium-223 (Xofigo, Bayer Pharmaceuticals Inc., Whippany, NJ) has been shown to increase overall survival in patients with metastatic castration-resistant prostate cancer (mCRPC), via the phase 3 ALpharadin in SYMPtomatic Prostate CAncer (ASLYMPCA) study. Hematologic side effects of radium-223 included all-grade anemia in 31% of the patients, thrombocytopenia in 12%, and neutropenia in 5%, and persistent pancytopenia noted in 2%. However, the incidence seen in our institutional clinical practice is higher than that reported in the literature. Methods A retrospective analysis was performed by analyzing patients with mCRPC who received Xofigo at the University of Florida Health Shands Hospital (UF Health Shands) in a three-year span. Data collected included complete blood count (CBC), ECOG (Eastern Cooperative Oncology Group) functional status, kidney and liver function, evidence of bony disease on imaging, prior chemotherapy regimens, total radiation dose, and prostate-specific antigen (PSA).  Results Twenty-three patients received Xofigo at UF Health, and one was lost to follow-up. Sixteen patients (73%) completed the full course (six doses) of Xofigo, while six did not. Ten patients (45%) developed pancytopenia, with two recovering counts within eight months while the other eight had persistent cytopenias (six of which were transfusion-dependent). Older age and higher ECOG score correlated with increased risk of pancytopenia. In addition, a higher percentage of patients who received prior radiation therapy were more likely to develop pancytopenia (90% vs 75%). Conclusions  We found a higher rate of Xofigo-induced pancytopenia in our patient population than the 2% reported in the literature, albeit with a limited sample size, This may influence clinical decision making in the treatment of mCRPC, as pancytopenia may preclude patients from other survival-prolonging therapies. Factors such as age, functional status, and prior radiation therapy have to be considered prior to Xofigo treatment.

摘要

引言 镭-223(Xofigo,拜耳制药公司,新泽西州惠普尼)已通过3期转移性去势抵抗性前列腺癌(mCRPC)的有症状前列腺癌中的α镭(ASLYMPCA)研究显示可提高患者的总生存期。镭-223的血液学副作用包括31%的患者出现所有级别的贫血、12%的患者出现血小板减少症、5%的患者出现中性粒细胞减少症,以及2%的患者出现持续性全血细胞减少症。然而,我们机构临床实践中观察到的发生率高于文献报道。方法 通过分析在三年时间内在佛罗里达大学健康珊兹医院(UF Health Shands)接受Xofigo治疗的mCRPC患者进行回顾性分析。收集的数据包括全血细胞计数(CBC)、东部肿瘤协作组(ECOG)功能状态、肾和肝功能、影像学上的骨病证据、先前的化疗方案、总辐射剂量以及前列腺特异性抗原(PSA)。结果 23名患者在UF Health接受了Xofigo治疗,1名患者失访。16名患者(73%)完成了Xofigo的全疗程(六剂),而6名患者未完成。10名患者(45%)出现全血细胞减少症,其中2名患者在八个月内血细胞计数恢复,而其他8名患者出现持续性血细胞减少症(其中6名依赖输血)。年龄较大和ECOG评分较高与全血细胞减少症风险增加相关。此外,接受过先前放疗的患者中出现全血细胞减少症的比例更高(90%对75%)。结论 尽管样本量有限,但我们发现我们的患者群体中Xofigo诱导的全血细胞减少症发生率高于文献报道的2%。这可能会影响mCRPC治疗中的临床决策,因为全血细胞减少症可能使患者无法接受其他延长生存期的治疗。在进行Xofigo治疗之前,必须考虑年龄、功能状态和先前放疗等因素。

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