Mugnier Bénédicte, Goncalves Anthony, Daumas Aurélie, Couderc Anne-Laure, Mezni Essia, Viret Frédéric, de Nonneville Alexandre, Villani Patrick
APHM, Hôpital Sainte Marguerite, Service de Médecine Interne Gériatrie Et Thérapeutique, Marseille, France.
Département d'Oncologie Médicale, Centre de Recherche en Cancérologie de Marseille INSERM, Institut Paoli-Calmettes, CNRS, Université d'Aix-Marseille, Marseille, France.
Osteoporos Int. 2023 Apr;34(4):703-711. doi: 10.1007/s00198-023-06683-0. Epub 2023 Jan 30.
We assessed if antiresorptive treatment can prevent aromatase inhibitor-induced bone loss in patients with early breast cancer. We observed that patients who did not receive antiresorptive treatment had a 20.8-fold increase in risk of bone loss after 24 months of aromatase inhibitors therapy.
This study aimed to describe changes in femoral and lumbar bone mineral density (BMD) after 24 months of aromatase inhibitors (AIs) and antiresorptive treatment in postmenopausal women with estrogen receptor-positive breast cancer.
Prospective, longitudinal study in a real-life setting with a 2-year follow-up. Patients underwent a complete baseline bone assessment including clinical assessment, biological evaluation, BMD measurement, and spine X-ray. Antiresorptive treatment was prescribed to patients with a T-score < - 2 or a T-score < - 1.5 SD with additional osteoporosis risk factors. A follow-up bone assessment was carried out after 24 months.
Among 328 patients referred to our center, 168 patients (67.7 ± 10.6 years) were included in our study, and 144 were eligible for antiresorptive treatment. After 24 months, patients receiving antiresorptive treatment experienced a significant increase of + 6.28% in femoral-BMD (F-BMD) and + 7.79% in lumbar-BMD (L-BMD). This increase was not significantly different between osteoporotic and osteopenic patients. Conversely, patients not receiving antiresorptive treatment presented significant F-BMD and L-BMD loss regardless of the baseline BMD. In the multivariate logistic model, the lack of antiresorptive treatment was the only predictive factor for major femoral bone loss with a 20.83 odds ratio (CI95%:4.2-100, p < 0.001).
This real-life study confirmed that antiresorptive treatment significantly increases femoral and lumbar BMD regardless of the baseline BMD in postmenopausal patients receiving AIs for early breast cancer. Patients who did not receive antiresorptive treatment had a 20.8-fold increased risk of major bone loss. Nevertheless, the best threshold to adopt for starting antiresorptive agents remains undetermined.
我们评估了抗吸收治疗能否预防早期乳腺癌患者芳香化酶抑制剂所致的骨质流失。我们观察到,未接受抗吸收治疗的患者在接受芳香化酶抑制剂治疗24个月后骨质流失风险增加了20.8倍。
本研究旨在描述绝经后雌激素受体阳性乳腺癌患者在接受24个月芳香化酶抑制剂(AIs)及抗吸收治疗后股骨和腰椎骨密度(BMD)的变化。
在实际临床环境中进行的前瞻性纵向研究,随访2年。患者接受了全面的基线骨评估,包括临床评估、生物学评估、骨密度测量和脊柱X线检查。T值< -2或T值< -1.5标准差且伴有其他骨质疏松风险因素的患者接受抗吸收治疗。24个月后进行随访骨评估。
在转诊至我们中心的328例患者中,168例患者(67.7±10.6岁)纳入本研究,其中144例符合抗吸收治疗条件。24个月后,接受抗吸收治疗的患者股骨骨密度(F-BMD)显著增加了+6.28%,腰椎骨密度(L-BMD)显著增加了+7.79%。骨质疏松患者和骨量减少患者之间的这种增加无显著差异。相反,无论基线骨密度如何,未接受抗吸收治疗的患者均出现了显著的F-BMD和L-BMD丢失。在多变量逻辑模型中,未接受抗吸收治疗是股骨主要骨质流失的唯一预测因素,比值比为20.83(95%CI:4.2 - 100,p<0.001)。
这项实际临床研究证实,在接受AIs治疗早期乳腺癌的绝经后患者中,无论基线骨密度如何,抗吸收治疗均能显著增加股骨和腰椎骨密度。未接受抗吸收治疗的患者主要骨质流失风险增加了20.8倍。然而,启动抗吸收药物治疗的最佳阈值仍未确定。