Mariotti Veronica, Page David B, Davydov Oksana, Hans Didier, Hudis Clifford A, Patil Sujata, Kunte Siddharth, Girotra Monica, Farooki Azeez, Fornier Monica N
Rutgers New Jersey Medical School, Department of Internal Medicine, Newark, NJ, United States.
Providence Portland Medical Center/Robert W. Franz Cancer Research Center, Portland, OR, United States.
J Bone Oncol. 2016 Oct 18;7:32-37. doi: 10.1016/j.jbo.2016.10.004. eCollection 2017 Jun.
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®) 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®, respectively, to BMD contribute to identification of elevated fracture risk (EFR) in postmenopausal breast cancer patients treated with AIs.
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® 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® or degraded microstructure by TBS.
At baseline, BMD alone identified 4% of patients with EFR. The addition of FRAX® increased detection to 13%, whereas the combination of BMD, FRAX® 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® identified 3 additional patients (3%), and BMD+FRAX®+TBS identified 7 additional patients (7%).
The combination of FRAX®, 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.
芳香化酶抑制剂(AIs)常用于治疗激素受体阳性乳腺癌患者,已知其会导致骨密度降低并增加骨折风险。目前用于骨折风险筛查的标准护理工具是通过双能X线吸收法(DXA)测量骨矿物质密度(BMD)。骨折风险评估工具(FRAX®)可与BMD联合使用,以识别更多有骨折风险的骨质减少患者,这些患者可能从骨改良剂(BMA)中获益。小梁骨评分(TBS)是一种通过DXA测量骨微结构的新方法,已被证明是骨折风险增加的独立指标。我们报告了分别将TBS和FRAX®添加到BMD中如何有助于识别接受AIs治疗的绝经后乳腺癌患者中骨折风险升高(EFR)的情况。
确定了100例接受AIs治疗、未使用过BMA且进行了系列DXA检查的早期激素阳性乳腺癌患者。在开始使用AIs之前和之后,从DXA图像中测量BMD和TBS,并根据临床记录回顾计算FRAX®评分。EFR定义为以下两种情况之一:BMD≤-2.5或BMD在-2.5至-1之间,且FRAX®显示风险增加或TBS显示骨微结构退化。
在基线时,仅BMD识别出4%的EFR患者。添加FRAX®后,检测率提高到13%,而BMD、FRAX®和TBS联合使用识别出20%的EFR患者。使用AIs后,TBS的变化与BMD的变化无关。在随访DXA时,仅BMD又检测出1例EFR患者(1%),而BMD+FRAX®识别出另外3例患者(3%),BMD+FRAX®+TBS识别出另外7例患者(7%)。
FRAX®、TBS和BMD联合使用可最大限度地识别EFR患者。TBS是一种新的评估方法,可增强对可能从BMA中获益的患者的检测。