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首页> 外文期刊>Journal of Bone Oncology >Assessing fracture risk in early stage breast cancer patients treated with aromatase-inhibitors: An enhanced screening approach incorporating trabecular bone score
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Assessing fracture risk in early stage breast cancer patients treated with aromatase-inhibitors: An enhanced screening approach incorporating trabecular bone score

机译:评估使用芳香化酶抑制剂治疗的早期乳腺癌患者的骨折风险:结合小梁骨评分的增强筛查方法

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Introduction: Aromatase-inhibitors (AIs) are commonly used for treatment of patients with hormone-receptor positive breast carcinoma, and are known to induce bone density loss and increase the risk of fractures. The current standard-of-care screening tool for fracture risk is bone mineral density (BMD) by dual-energy X-ray absorptiometry (DXA). The fracture risk assessment tool (FRAX(R)) may be used in conjunction with BMD to identify additional osteopenic patients at risk of fracture who may benefit from a bone-modifying agent (BMA). The trabecular bone score (TBS), a novel method of measuring bone microarchitecture by DXA, has been shown to be an independent indicator of increased fracture risk. We report how the addition of TBS and FRAX(R), respectively, to BMD contribute to identification of elevated fracture risk (EFR) in postmenopausal breast cancer patients treated with AIs. Methods: 100 patients with early stage hormone-positive breast cancer treated with AIs, no prior BMAs, and with serial DXAs were identified. BMD and TBS were measured from DXA images before and following initiation of AIs, and FRAX(R) scores were calculated from review of clinical records. EFR was defined as either: BMD @?-2.5 or BMD between -2.5 and -1 plus either increased risk by FRAX(R) or degraded microstructure by TBS. Results: At baseline, BMD alone identified 4% of patients with EFR. The addition of FRAX(R) increased detection to 13%, whereas the combination of BMD, FRAX(R) and TBS identified 20% of patients with EFR. Following AIs, changes in TBS were independent of changes in BMD. On follow-up DXA, BMD alone detected an additional 1 patient at EFR (1%), whereas BMD+ FRAX(R) identified 3 additional patients (3%), and BMD+FRAX(R)+TBS identified 7 additional patients (7%). Conclusions: The combination of FRAX(R), TBS, and BMD maximized the identification of patients with EFR. TBS is a novel assessment that enhances the detection of patients who may benefit from BMAs.
机译:简介:芳香酶抑制剂(AIs)通常用于治疗荷尔蒙受体阳性的乳腺癌患者,并且已知会导致骨密度降低并增加骨折风险。当前用于骨折风险的护理标准筛查工具是通过双能X线骨密度仪(DXA)进行的骨矿物质密度(BMD)。骨折风险评估工具(FRAX)可以与BMD结合使用,以识别可能受益于骨改良剂(BMA)的其他骨折风险的骨质疏松患者。小梁骨评分(TBS)是一种通过DXA测量骨微结构的新方法,是增加骨折风险的独立指标。我们报告了分别向BMD添加TBS和FRAX(R)如何有助于在经AIs治疗的绝经后乳腺癌患者中鉴定骨折风险(EFR)升高。方法:确定了接受AIs治疗,未接受过BMA治疗和连续DXA治疗的100例早期激素阳性乳腺癌患者。在开始AI之前和之后,从DXA图像中测量BMD和TBS,并根据临床记录来计算FRAX®得分。 EFR被定义为:BMD @-2.5或BMD在-2.5至-1之间,再加上FRAX(R)增加的风险或TBS导致的微结构降低。结果:在基线时,仅BMD可识别4%的EFR患者。 FRAX(R)的添加将检测率提高到13%,而BMD,FRAX(R)和TBS的组合确定了20%的EFR患者。在AI之后,TBS的变化与BMD的变化无关。在随访DXA时,仅BMD便发现另外1例EFR患者(1%),而BMD + FRAX(R)确定了3例患者(3%),BMD + FRAX(R)+ TBS则确定了7例患者(7 %)。结论:FRAX(R),TBS和BMD的组合可最大程度地鉴定EFR患者。 TBS是一种新颖的评估方法,可增强对可能受益于BMA的患者的检测。

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