Alrasheedi Hanan M, Malaeb Farah, Awwad Sameh, Alnakhli Ali, Alrashidi Nourah, Alharbi Rawand, Almolaiki Dema, Alahmari Zainab S, Alyousif Ghadah M, Alshakhs Hasan, ALfouzan Renad A, Alajlan Abdulrahman K, Alhaddad Fatima, Alqussair Nora, Daama Saad, Al Ali Nasseem, Al Amer Abeer, Alsultan Murtada H
Pediatric Hematology and Oncology, King Fahad Medical City, Riyadh, SAU.
Clinical Pharmacy, King Fahad Medical City, Riyadh, SAU.
Cureus. 2025 Aug 1;17(8):e89198. doi: 10.7759/cureus.89198. eCollection 2025 Aug.
Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer globally. PEG-asparaginase (PEG-ASPA), a cornerstone of ALL treatment, significantly improves outcomes but is associated with serious toxicities, including acute pancreatitis (AP). This study evaluates the incidence and associated risk factors of PEG-ASPA-induced AP among pediatric ALL patients in Saudi Arabia.
This multicenter retrospective cohort study included pediatric ALL patients treated with PEG-ASPA between January 2019 and October 2023 at three tertiary Saudi centers. Data included demographics, risk stratification, PEG-ASPA doses, and toxicity. AP was defined per CTCAE v5.0 criteria. A multivariate logistic regression model was used to evaluate risk factors.
Of 322 pediatric patients, 5% (n=16) developed AP. Events were more frequent in children >10 years old (44%) and during consolidation (38%) and interim maintenance 2 (38%) phases. Multivariate analysis showed that age >10 years (OR=3.65), high-risk protocols (OR=2.07), and >5 PEG-ASPA doses (OR=1.58) were associated with increased AP risk. Most cases were grade 2 or 3 and resolved with supportive care.
The incidence of PEG-ASPA-induced AP among pediatric ALL patients in Saudi Arabia is consistent with international data. Higher age, intensive protocols, and cumulative dosing may increase risk. Routine monitoring of pancreatic enzymes and triglycerides prior to PEG-ASPA administration is recommended to enhance early detection and reduce the risk of severe toxicity.
急性淋巴细胞白血病(ALL)是全球最常见的儿童癌症。聚乙二醇天冬酰胺酶(PEG-ASPA)是ALL治疗的基石,可显著改善治疗结果,但会引发包括急性胰腺炎(AP)在内的严重毒性反应。本研究评估了沙特阿拉伯儿科ALL患者中PEG-ASPA诱导的AP的发生率及相关危险因素。
这项多中心回顾性队列研究纳入了2019年1月至2023年10月在沙特三个三级中心接受PEG-ASPA治疗的儿科ALL患者。数据包括人口统计学信息、风险分层、PEG-ASPA剂量和毒性反应。AP根据CTCAE v5.0标准定义。采用多变量逻辑回归模型评估危险因素。
在322例儿科患者中,5%(n = 16)发生了AP。事件在10岁以上儿童中更常见(44%),在巩固期(38%)和强化维持2期(38%)更为频繁。多变量分析显示,年龄大于10岁(OR = 3.65)、高危方案(OR = 2.07)和PEG-ASPA剂量大于5次(OR = 1.58)与AP风险增加相关。大多数病例为2级或3级,通过支持性治疗得以缓解。
沙特阿拉伯儿科ALL患者中PEG-ASPA诱导的AP的发生率与国际数据一致。年龄较大、强化方案和累积给药可能会增加风险。建议在给予PEG-ASPA之前常规监测胰腺酶和甘油三酯,以加强早期检测并降低严重毒性反应的风险。