Lu Kuo-Cheng, Ho Ching-Liang, Wang Joshua, Zheng Cai-Mei, Tsai Kuo-Wang, Hou Yi-Chou, Lu Chien-Lin
Division of Nephrology, Department of Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan.
Division of Hematology and Oncology, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan.
Cancers (Basel). 2025 Apr 26;17(9):1459. doi: 10.3390/cancers17091459.
Immune checkpoint inhibitors (ICIs) offer a novel approach to cancer treatment by enhancing immune responses against malignant cells. However, ICIs are associated with immune-related adverse events (irAEs), including hyponatremia, a potentially severe electrolyte disturbance. The risk of hyponatremia increases further when ICIs are combined with cisplatin, a nephrotoxic chemotherapy agent widely used in treating respiratory and intrathoracic cancers. This study investigated the incidence, severity, and temporal dynamics of hyponatremia in patients treated with ICIs alone or in combination with cisplatin.
A retrospective cohort study was conducted using data from the TriNetX global health research network. Patients with respiratory or intrathoracic malignancies ( = 14,026) were divided into two groups: ICI-only ( = 7013) and ICI with cisplatin combination ( = 7013), matched using propensity scores. Hyponatremia was categorized into mild (130-134 mmol/L), moderate (125-129 mmol/L), and severe (<125 mmol/L). Temporal trends and cumulative incidence over 90 days were analyzed using Poisson regression.
The combination group exhibited a higher cumulative incidence of hyponatremia across all severity levels, with early-phase risk peaking within 20 days of treatment. Rate ratios for mild, moderate, and severe hyponatremia were significantly elevated in the combination group ( < 0.01).
Hyponatremia is a significant complication in patients receiving ICIs, particularly when combined with cisplatin. Early monitoring and tailored management are essential to mitigate risks and optimize treatment outcomes.
免疫检查点抑制剂(ICIs)通过增强针对恶性细胞的免疫反应,为癌症治疗提供了一种新方法。然而,ICIs与免疫相关不良事件(irAEs)有关,包括低钠血症,这是一种潜在的严重电解质紊乱。当ICIs与顺铂联合使用时,低钠血症的风险会进一步增加,顺铂是一种广泛用于治疗呼吸道和胸内癌症的肾毒性化疗药物。本研究调查了单独使用ICIs或与顺铂联合使用的患者中低钠血症的发生率、严重程度和时间动态。
使用来自TriNetX全球健康研究网络的数据进行了一项回顾性队列研究。患有呼吸道或胸内恶性肿瘤的患者(n = 14,026)被分为两组:仅ICI组(n = 7013)和ICI与顺铂联合组(n = 7013),使用倾向评分进行匹配。低钠血症分为轻度(130 - 134 mmol/L)、中度(125 - 129 mmol/L)和重度(<125 mmol/L)。使用泊松回归分析90天内的时间趋势和累积发病率。
联合组在所有严重程度水平上均表现出较高的低钠血症累积发病率,早期风险在治疗后20天内达到峰值。联合组中轻度、中度和重度低钠血症的率比显著升高(P < 0.01)。
低钠血症是接受ICIs治疗的患者中的一种重要并发症,尤其是与顺铂联合使用时。早期监测和针对性管理对于降低风险和优化治疗结果至关重要。