Ogawa Aoi, Kishimoto Kenji, Horikawa Shogo, Uemura Suguru, Hyodo Sayaka, Kozaki Aiko, Saito Atsuro, Ishida Toshiaki, Mori Takeshi, Hasegawa Daiichiro, Kosaka Yoshiyuki
Department of Hematology & Oncology, Children's Cancer Center, Kobe Children's Hospital, Minatojima-Minamimachi 1-6-7, Chuo-Ku, Kobe, 650-0047, Japan.
Eur J Pediatr. 2025 Feb 1;184(2):170. doi: 10.1007/s00431-025-06002-1.
The aim of this study was to determine the incidence of hypophosphatemia and identify factors associated with high-risk hypophosphatemia in children and adolescents with cancer. Patients aged 0-18 years who developed hypophosphatemia during treatment for cancer in our hospital between January 2021 and March 2023 were enrolled. Hypophosphatemia was defined as a serum phosphorus level < 2.5 mg/dL. The high-risk group for symptomatic hypophosphatemia was defined as patients with a serum phosphorus level of 1.5-1.9 mg/dL lasting for 2 weeks or more and patients with a serum phosphorus level < 1.5 mg/dL. During the study period, 48 of 253 (19%) patients developed a total of 108 episodes of hypophosphatemia. Symptomatic episodes were more frequent in the high-risk group (n = 31; 84% vs. 39%). Elevated total bilirubin level (> 0.50 mg/dL) (adjusted odds ratio (OR), 3.60; 95% confidence interval (CI), 1.37-9.48) and stem cell transplantation (adjusted OR, 4.83; 95% CI, 1.69-13.81) were found to be potential baseline predictors of high-risk hypophosphatemia in the logistic regression model. Fasting, diarrhea, and vomiting after initiation of treatment were also associated with the development of high-risk hypophosphatemia.
The incidence of hypophosphatemia was relatively high in children and adolescents receiving treatment for cancer. The results suggest that baseline characteristics and therapy-related toxicities may be associated with the development of high-risk hypophosphatemia.
• Patients with cancer are at increased risk of hypophosphatemia in adults. • Hypophosphatemia may be a factor associated with a poor prognosis in hospitalized patients.
• The incidence of hypophosphatemia was relatively high in children and adolescents receiving treatment for cancer. • Both baseline characteristics and therapy-related factors may be associated with the development of high-risk hypophosphatemia.
本研究的目的是确定癌症患儿和青少年低磷血症的发生率,并识别与高危低磷血症相关的因素。纳入了2021年1月至2023年3月期间在我院接受癌症治疗期间发生低磷血症的0至18岁患者。低磷血症定义为血清磷水平<2.5mg/dL。有症状低磷血症的高危组定义为血清磷水平为1.5 - 1.9mg/dL持续2周或更长时间的患者以及血清磷水平<1.5mg/dL的患者。在研究期间,253例患者中有48例(19%)共发生108次低磷血症发作。有症状发作在高危组中更频繁(n = 31;84%对39%)。在逻辑回归模型中,总胆红素水平升高(>0.50mg/dL)(调整优势比(OR),3.60;95%置信区间(CI),1.37 - 9.48)和干细胞移植(调整OR,4.83;95%CI,1.69 - 13.81)被发现是高危低磷血症的潜在基线预测因素。治疗开始后的禁食、腹泻和呕吐也与高危低磷血症的发生有关。
接受癌症治疗的儿童和青少年中低磷血症的发生率相对较高。结果表明基线特征和治疗相关毒性可能与高危低磷血症的发生有关。
• 癌症患者成人发生低磷血症的风险增加。• 低磷血症可能是住院患者预后不良的一个因素。
• 接受癌症治疗的儿童和青少年中低磷血症的发生率相对较高。• 基线特征和治疗相关因素都可能与高危低磷血症的发生有关。