Department of Pediatric Oncology and Hematology, Medical University of Bialystok, Białystok, Poland.
Department of Pediatrics, Rheumatology, Immunology and Metabolic Bone Diseases, Medical University of Bialystok, University Children's Hospital 'Dr Ludwik Zamenhof', ul. Waszyngtona 17, 15-274, Białystok, Poland.
Arch Osteoporos. 2021 Feb 26;16(1):45. doi: 10.1007/s11657-020-00863-9.
Low bone mineral density (BMD) was diagnosed in 24% of childhood cancer survivors (CCS), whereas very low BMD was relatively uncommon at 8%. We suggest that low BMD in CCS may become alleviated over time. Stem cell transplantation, radiotherapy, and underweight were the strongest independent predictors of decreased BMD.
Childhood cancer survivors (CCS) are at risk of premature bone loss, although published studies are inconsistent. The objective of this study was to evaluate the prevalence and pattern of low bone mineral density (BMD) in short- and long-term CCS, and to determine clinical factors affecting skeleton after anticancer treatment.
This retrospective study was conducted in a cohort of 326 children and young adult CCS (147 females) who completed anticancer treatment. BMD was determined by dual-energy X-ray absorptiometry (DXA). Low BMD was defined as a Z-score ≤ - 1.0, and the very low BMD as a Z-score ≤ - 2.0. Additionally, the changes in BMD over time were studied in 123 CCS who had been re-examined by DXA during follow-up.
Median age at diagnosis was 7.27 years (range, 4.4-10.6); median time between end of treatment and DXA was 6.12 (range, 4.0-22.0). Low BMD was found in 24% of CCS, while very low BMD was relatively uncommon (8%). Based on multivariate analysis, the following were significantly associated with low BMD at the follow-up: hematopoietic stem cell transplantation (OR 3.13, 95% CI 1.02-9.63), head and neck radiotherapy (OR 2.54, 95% CI 1.32-4.90), and body weight below the standard reference (OR 3.57, 95% CI 1.24-10.23). The time-related trajectory showed an improvement (BMD) or stabilization (BMD) in Z-scores values.
These data based on serial DXA measurements, encompassing a long-lasting observation period, show that CCS may not be at risk of premature bone loss in young adulthood. However, it is unknown how the scenario for skeletal mass is until the CCS will achieve older or postmenopausal age.
儿童癌症幸存者(CCS)存在骨密度(BMD)降低的风险,尽管已发表的研究结果并不一致。本研究的目的是评估短期和长期 CCS 中低 BMD 的发生率和模式,并确定抗癌治疗后影响骨骼的临床因素。
本回顾性研究纳入了 326 名完成抗癌治疗的儿童和年轻成人 CCS(147 名女性)。使用双能 X 线吸收法(DXA)测定 BMD。低 BMD 定义为 Z 评分≤-1.0,极低 BMD 定义为 Z 评分≤-2.0。此外,还对 123 名在随访期间接受 DXA 复查的 CCS 进行了 BMD 随时间变化的研究。
诊断时的中位年龄为 7.27 岁(范围,4.4-10.6);治疗结束至 DXA 的中位时间为 6.12 岁(范围,4.0-22.0)。CCS 中低 BMD 发生率为 24%,极低 BMD 发生率相对较低(8%)。基于多变量分析,以下因素与随访时的低 BMD 显著相关:造血干细胞移植(OR 3.13,95%CI 1.02-9.63)、头颈部放疗(OR 2.54,95%CI 1.32-4.90)和体重低于标准参考值(OR 3.57,95%CI 1.24-10.23)。时间相关轨迹显示 Z 评分值有所改善(BMD)或稳定(BMD)。
这些基于 DXA 连续测量的、长期随访的研究数据表明,CCS 在年轻成人期可能不存在骨质丢失的风险。然而,目前尚不清楚 CCS 在达到老年或绝经后年龄时,骨骼质量的情况如何。