IRCCS Policlinico San Martino, Genoa, Italy.
Section of Geriatrics, Department of Internal Medicine and Medical Specialties (DIMI), University of Genoa, Genoa, Italy.
Intern Emerg Med. 2024 Nov;19(8):2193-2199. doi: 10.1007/s11739-024-03725-1. Epub 2024 Aug 2.
The raising number of older patients who are diagnosed with breast cancer represents a significant medical and societal challenge. Aromatase inhibitors (AI), which are commonly utilized to treat this condition in these patients have significant adverse events on bone and muscle health. Falling estrogen production leads to an increase in RANKL secretion by osteoblasts with accelerated bone remodeling due to osteoclast activity. Furthermore, estrogen deficiency reduces skeletal muscle strength and mass. The humanized monoclonal antibody, denosumab, neutralizes RANKL, thereby inhibiting osteoclast formation, function and survival and ultimately exerting powerful anti-resorptive effects.. In this study, we report on the efficacy of denosumab in mitigating aromatase inhibitor-induced bone loss (AIBL) and sarcopenia in older women with breast cancer. From January 2022 to January 2023, we enrolled 30 patients (female sex, ≥ 65 years) diagnosed with non-metastatic breast cancer undergoing adjuvant endocrine therapy; patients received, as per clinical practice, primary bone prophylaxis with denosumab (60 mg via subcutaneous injection every 6 months) according to oncologic guidelines. This group was matched with 30 patients with non-metastatic breast cancer, who were treated with biphosphonates (BF) therapy (oral alendronate 70 mg/week). For each patient bone mineral density (BMD) and bone quality in terms of trabecular bone score (TBS) in addition to body composition and Relative Skeletal Muscle Index (RSMI) was assessed by bone densitometry at baseline and after one year of treatment. Significant improvements in TBS at the lumbar spine, RSMI and whole-body composition (arms, legs, and trunk) were observed in the denosumab group compared with the BF group. These findings underscore the role of denosumab as an effective strategy in managing AIBL and osteosarcopenia in older women with breast cancer and undergoing adjuvant endocrine therapy, which is crucial for improving quality of life, preventing functional decline, and optimizing treatment outcomes.
越来越多的老年乳腺癌患者是一个重大的医学和社会挑战。芳香化酶抑制剂(AIs)常用于治疗这些患者的乳腺癌,但会对骨骼和肌肉健康产生严重的不良反应。雌激素产生减少导致成骨细胞中 RANKL 分泌增加,破骨细胞活性导致骨重塑加速。此外,雌激素缺乏会降低骨骼肌强度和质量。人源化单克隆抗体地舒单抗可中和 RANKL,从而抑制破骨细胞的形成、功能和存活,最终发挥强大的抗吸收作用。在这项研究中,我们报告了地舒单抗在缓解老年乳腺癌患者因芳香化酶抑制剂引起的骨丢失(AIBL)和肌肉减少症方面的疗效。2022 年 1 月至 2023 年 1 月,我们纳入了 30 名(女性,≥65 岁)诊断为非转移性乳腺癌且正在接受辅助内分泌治疗的患者;根据肿瘤学指南,患者按照临床实践接受地舒单抗(每 6 个月皮下注射 60mg)作为初级骨预防治疗。该组与 30 名接受双膦酸盐(BF)治疗(每周口服阿仑膦酸钠 70mg)的非转移性乳腺癌患者相匹配。对每位患者进行骨密度(BMD)和骨质量(骨小梁评分[TBS])评估,以及身体成分和相对骨骼肌指数(RSMI),在基线和治疗 1 年后进行骨密度测量。与 BF 组相比,地舒单抗组的腰椎 TBS、RSMI 和全身成分(手臂、腿部和躯干)显著改善。这些发现强调了地舒单抗在管理接受辅助内分泌治疗的老年乳腺癌患者的 AIBL 和骨肌减少症中的作用,这对于提高生活质量、预防功能下降和优化治疗结果至关重要。