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Guidance for the assessment and management of prostate cancer treatment-induced bone loss. A consensus position statement from an expert group

机译:前列腺癌治疗诱导的骨质损失评估和管理的指导。专家组的共识位置声明

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Context and objective Incidence of prostate cancer (PC) is increasing, but androgen deprivation therapy (ADT) and other therapies are substantially improving survival. In this context, careful consideration of skeletal health is required to reduce the risk of treatment-related fragility fractures and their associated morbidity and mortality. This risk is currently not well-managed. ADT causes significant loss of bone mineral density (BMD). In the metastatic setting, systemic treatments (e.g. chemotherapy, abiraterone, enzalutamide) are used alongside ADT and may require concomitant glucocorticoids. Both ADT and glucocorticoids pose significant challenges to skeletal health in a population of patients already likely to have ongoing age-related bone loss and/or comorbid conditions. Current PC guidelines lack specific recommendations for optimising bone health. This guidance presents evidence for assessment and management of bone health in this population, with specific recommendations for clinical practitioners in day-to-day PC management. Methods Structured meetings of key opinion leaders were integrated with a systematic literature review. Input and endorsement was sought from patients, nursing representatives and specialist societies. Summary of guidance All men starting or continuing long-term ADT should receive lifestyle advice regarding bone health. Calcium/vitamin D supplementation should be offered if required. Fracture risk should be calculated (using the FRAX? tool), with BMD assessment included where feasible. BMD should always be assessed where fracture risk calculated using FRAX? alone is close to the intervention threshold. Intervention should be provided if indicated by local or national guidelines e.g. UK National Osteoporosis Guideline Group (NOGG) thresholds. Men requiring bone protection therapy should be further assessed (e.g. renal function), with referral to specialist centres if available and offered appropriate treatment to reduce fracture risk. Those near to, but below an intervention threshold, and patients going on to additional systemic therapies (particularly those requiring glucocorticoids), should have FRAX? (including BMD) repeated after 12–18?months. Patient summary Modern treatments for prostate cancer have led to significant improvements in survival and quality of life. However, some of these treatments may lead to weakening of patient’s bones with risk of fracture and it is therefore important to monitor patients’ bone health and provide bone protection where needed. This paper provides specific guidance to clinical teams, based on the most recent research evidence, to ensure optimal bone health in their patients.
机译:前列腺癌(PC)的上下文和客观发病率正在增加,但雄激素剥夺治疗(ADT)和其他疗法显着改善存活率。在这种情况下,需要仔细考虑骨骼健康,以降低治疗相关脆弱性骨折及其相关的发病率和死亡率的风险。目前不受管理的风险。 ADT导致骨矿物密度(BMD)的显着损失。在转移性环境中,与ADT一起使用全身治疗(例如化学疗法,ABIRATERONE,烯甲醛酰胺),并且可能需要伴随的糖皮质激素。 ADT和糖皮质激素均对已经有可能具有持续年龄相关的骨质损失和共用病症的患者患者骨骼健康产生重大挑战。目前的PC指南缺乏优化骨骼健康的具体建议。本指南呈现了本人骨骼健康评估和管理的证据,并在日常PC管理中对临床从业者的特定建议。方法与系统文献综述相结合了关键意见领导人的结构性会议。从患者,护理代表和专家社团寻求投入和认可。指导摘要所有男子开始或继续长期ADT应该接受有关骨骼健康的生活方式建议。如果需要,应提供钙/维生素D补充剂。应计算裂缝风险(使用Fraxα工具),包括BMD评估,包括可行的地方。应始终评估BMD,其中使用Frax计算的裂缝风险?单独接近干预阈值。如果由当地或国家指南表示,则应提供干预。英国国家骨质疏松症准则组(NOGG)阈值。应进一步评估需要骨保护疗法的人(例如肾功能),如果可用,并提供适当的治疗,以降低骨折风险的适当治疗。那些靠近但低于干预阈值的人和患者进入额外的全身疗法(特别是那些需要糖皮质激素的患者)应该具有frax? (包括BMD)在12-18岁之后重复?月份。患者概述前列腺癌的现代治疗导致了生存和生活质量的显着改善。然而,这些治疗中的一些可能导致患者的骨骼具有骨折风险的弱化,因此重要的是监测患者的骨骼健康,并在需要时提供骨保护。本文为临床团队提供了基于最近的研究证据的具体指导,以确保其患者的最佳骨骼健康。

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