Department of Surgery and Orthopaedics, University of Rochester Medical Center (URMC), 265 Crittenden Blvd, CU 420658, Rochester, NY, 14642, USA.
Department of Radiation Oncology, URMC, Rochester, NY, USA.
Support Care Cancer. 2018 Aug;26(8):2675-2683. doi: 10.1007/s00520-018-4094-4. Epub 2018 Feb 22.
Cancer treatment-induced bone loss (CTIBL) is a long-term side effect of breast cancer therapy. Both calcitriol and weight-bearing exercise improve bone metabolism for osteoporotic patients, but are unproven in a breast cancer population. We used a novel high-dose calcitriol regimen with an individualized exercise intervention to improve bone metabolism in breast cancer survivors.
We accrued 41 subjects to this open label, 2 × 2 factorial, randomized feasibility trial. Breast cancer survivors were randomized to receive the following: (1) calcitriol (45 micrograms/week), (2) individualized exercise with progressive walking and resistance training, (3) both, or (4) a daily multivitamin (control condition) for 12 weeks. Primary outcomes included changes in biomarkers of bone formation, bone resorption, and the bone remodeling index, a composite measure of bone formation and resorption. Safety measures included clinical and biochemical adverse events. A main effect analysis was used for these endpoints.
Hypercalcemia was limited to three grade I cases with no grade ≥ 2 cases. Among exercisers, 100% engaged in the prescribed aerobic training and 44.4% engaged in the prescribed resistance training. Calcitriol significantly improved bone formation (Cohen's d = 0.64; p < 0.01), resulting in a non-significant increase in the bone remodeling index (Cohen's d = 0.21; p = 31). Exercise failed to improve any of the bone biomarkers.
Both calcitriol and exercise were shown to be feasible and well tolerated. Calcitriol significantly improved bone formation, resulting in a net increase of bone metabolism. Compliance with the exercise intervention was sub-optimal, which may have led to a lack of effect of exercise on bone metabolism.
癌症治疗相关的骨丢失(CTIBL)是乳腺癌治疗的一个长期副作用。骨化三醇和负重运动都能改善骨质疏松患者的骨代谢,但在乳腺癌患者中尚未得到证实。我们使用了一种新的高剂量骨化三醇方案,并结合个体化运动干预,以改善乳腺癌幸存者的骨代谢。
我们进行了这项开放性标签、2×2 析因随机可行性试验,共纳入了 41 名受试者。乳腺癌幸存者被随机分为以下四组:(1)骨化三醇(每周 45 微克),(2)个体化运动,包括渐进性步行和抗阻训练,(3)两者都用,或(4)每日服用复合维生素(对照组),为期 12 周。主要结局指标包括骨形成标志物、骨吸收标志物和骨重塑指数的变化,骨重塑指数是骨形成和骨吸收的综合指标。安全性措施包括临床和生化不良事件。这些终点采用主效应分析。
高钙血症仅限于 3 例 1 级病例,无 2 级以上病例。在运动者中,100%完成了规定的有氧运动,44.4%完成了规定的抗阻运动。骨化三醇显著改善了骨形成(Cohen's d=0.64;p<0.01),导致骨重塑指数的非显著增加(Cohen's d=0.21;p=0.31)。运动未能改善任何骨生物标志物。
骨化三醇和运动都被证明是可行且耐受良好的。骨化三醇显著改善了骨形成,导致骨代谢的净增加。运动干预的依从性不理想,这可能导致运动对骨代谢没有效果。