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骨转移嗜铬细胞瘤/副神经节瘤患者的骨骼相关不良事件。

Adverse skeletal related events in patients with bone-metastatic pheochromocytoma/paraganglioma.

机构信息

Medical Oncology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, ASST Spedali Civili, Brescia, Italy.

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Eur J Cancer. 2024 Sep;208:114122. doi: 10.1016/j.ejca.2024.114122. Epub 2024 Jul 3.

DOI:10.1016/j.ejca.2024.114122
PMID:39047533
Abstract

Metastatic pheochromocytomas and paragangliomas (PPGLs) are frequently associated with skeletal complications. Primary objective: to describe the frequency of adverse skeletal related events (SREs) in PPGL patients with bone metastases (BMs). Secondary objectives: to 1) identify predictive and prognostic factors for SREs and 2) obtain information on the effectiveness of bone resorption inhibitors in reducing SRE risk and improving outcomes in term of survival and SREs time onset. In this retrospective multicenter, multinational study, 294 PPGL patients were enrolled. SREs occurred in 90 patients (31 %). Fifty-five patients (19 %) had bone fractures, 47 (16 %) had spinal cord compression, and 11 (4 %) had hypercalcemia. Twenty-two patients (7 %) had more than one SRE. Sixty-four patients (22 %) underwent surgery, and 136 (46 %) underwent radiotherapy. SREs occurred a median of 4.4 months after diagnosis of BM (range, 0-246.6 months). Independent factors associated with reduced risk of SREs in multivariable analysis were I-131-MIBG radionuclide therapy (hazard ratio [HR], 0.536 [95 % CI, 0.309-0.932]; P = .027) and absence of liver metastases (HR, 0.638 [95 % CI, 0.410-0.992]; P = .046). The median overall survival duration was 5.3 year. In multivariable analysis, age younger than 48 years at PPGL diagnosis (HR, 0.558 [95 % CI, 0.3877-0.806]; P = .002), absence of liver metastases (HR, 0.618 [95 % CI, 0.396-0.965]; P = .034), treatment with bisphosphonates or denosumab (HR, 0.598 [95 % CI, 0.405-0.884]; P = .010), and MIBG radionuclide therapy (HR, 0.444 [95 % CI, 0.274-0.718]; P = .001) were associated with a reduced risk of death. SREs occur frequently and early in bone-metastatic PPGL patients but do not negatively impact survival. MIBG radionuclide therapy and treatment with bone resorption inhibitors are associated with favorable outcome.

摘要

转移性嗜铬细胞瘤和副神经节瘤(PPGLs)常与骨骼并发症相关。主要目的:描述伴有骨转移(BMs)的 PPGL 患者不良骨骼相关事件(SREs)的频率。次要目标:1)确定 SREs 的预测和预后因素,2)了解骨吸收抑制剂在降低 SRE 风险和改善生存和 SRE 发病时间方面的有效性方面的信息。在这项回顾性多中心、多国研究中,纳入了 294 名 PPGL 患者。90 名患者(31%)发生了 SREs。55 名患者(19%)发生了骨骨折,47 名患者(16%)发生了脊髓压迫,11 名患者(4%)发生了高钙血症。22 名患者(7%)发生了不止一次 SRE。64 名患者(22%)接受了手术,136 名患者(46%)接受了放疗。SREs 在 BM 诊断后中位数为 4.4 个月(范围,0-246.6 个月)发生。多变量分析中与 SRE 风险降低相关的独立因素是 I-131-MIBG 放射性核素治疗(风险比[HR],0.536[95%CI,0.309-0.932];P=0.027)和无肝转移(HR,0.638[95%CI,0.410-0.992];P=0.046)。中位总生存时间为 5.3 年。多变量分析中,PPGL 诊断时年龄小于 48 岁(HR,0.558[95%CI,0.3877-0.806];P=0.002)、无肝转移(HR,0.618[95%CI,0.396-0.965];P=0.034)、使用双膦酸盐或地舒单抗(HR,0.598[95%CI,0.405-0.884];P=0.010)和 MIBG 放射性核素治疗(HR,0.444[95%CI,0.274-0.718];P=0.001)与降低死亡风险相关。骨转移的 PPGL 患者中 SREs 发生频繁且较早,但不会对生存产生负面影响。MIBG 放射性核素治疗和骨吸收抑制剂治疗与良好的预后相关。

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