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乳腺癌和骨质疏松症 - 乳腺癌绝经后妇女癌症治疗相关骨丢失的管理。

Breast cancer and osteoporosis - management of cancer treatment-induced bone loss in postmenopausal women with breast cancer.

机构信息

Department of Obstetrics and Gynecology, Philipps University of Marburg, Germany.

Department of Bone Oncology, Endocrinology and Reproductive Medicine, Hospital Nordwest, Frankfurt/M., Germany.

出版信息

Breast Care (Basel). 2014 Oct;9(5):312-7. doi: 10.1159/000368843.

Abstract

The incidence of breast cancer (BC) in postmenopausal women is continuously rising. Due to early diagnosis and various treatment designs, the long-term clinical outcome has improved. Frequent settings are chemotherapy as well as endocrine treatment. Both have proven to interfere with bone health resulting in cancer treatment-induced bone loss (CTIBL). Whereas chemotherapy is associated with increased bone resorption, aromatase inhibitor (AI) therapy reduces residual estrogen and is associated with decreased bone mineral density. Independent of the AI administered, the loss of bone mineral density is twice as high compared to healthy postmenopausal women. As a consequence of CTIBL, both chemotherapy and AI treatment can lead to a significantly increased fracture risk. Therefore, several guidelines have emerged for the management of CTIBL in women with BC, including strategies to identify and treat those at high risk for fractures. Further research on tracking guideline adherence examining the feasibility and practicability of guideline implementation to bridge the gap between determined scientific best evidence and applied best practice is needed to adjust these guidelines in the future.

摘要

绝经后妇女的乳腺癌(BC)发病率持续上升。由于早期诊断和各种治疗设计,长期的临床结果得到了改善。常见的治疗方法包括化疗和内分泌治疗。这两种方法都已被证明会干扰骨骼健康,导致癌症治疗引起的骨丢失(CTIBL)。虽然化疗会增加骨吸收,但芳香化酶抑制剂(AI)治疗会降低残留雌激素,从而导致骨密度降低。无论使用哪种 AI,与健康绝经后妇女相比,骨密度的丢失要高出两倍。由于 CTIBL,化疗和 AI 治疗都会导致骨折风险显著增加。因此,已经出现了一些针对 BC 妇女 CTIBL 管理的指南,包括识别和治疗骨折高风险患者的策略。需要进一步研究跟踪指南的遵守情况,检查指南实施的可行性和实用性,以缩小确定的最佳科学证据和应用的最佳实践之间的差距,从而在未来调整这些指南。

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