个体化剂量后大剂量甲氨蝶呤致口腔黏膜炎的临床危险因素。
Clinical Risk Factors for High-Dose Methotrexate-Induced Oral Mucositis Following Individualized Dosing.
机构信息
Hospitalist Medicine Program, Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Pediatric Oncology Education Program 2023, School of Medicine, Ponce Health Sciences University, Ponce, Puerto Rico.
出版信息
Cancer Med. 2024 Nov;13(21):e70351. doi: 10.1002/cam4.70351.
BACKGROUND
Oral mucositis affects about 20% of children undergoing high-dose methotrexate (HDMTX) for acute lymphoblastic leukemia (ALL), despite existing management strategies. Personalized HDMTX dosing, adjusted by pharmacokinetics and leukemia risk, has reduced mucositis incidence, but variations still occur with similar 24-h methotrexate levels.
METHODS
This retrospective study investigated risk factors for oral mucositis under individualized methotrexate protocols. Data from patients with ≥ Grade 2 oral mucositis (CTCAE v4.0) were analyzed from the St. Jude Children's Research Hospital total 16 trial. A 1:1 case-control matching method considered age, sex, risk classification, immunophenotype, and methotrexate course. McNemar's, Bowker's symmetry, and Wilcoxon signed-rank tests were used for statistical analyses. Risk factors for recurrent mucositis were identified in a case-only analysis.
RESULTS
The study found significant associations between methotrexate-induced mucositis and new-onset skin rashes (p = 0.0027), fever (p = 0.0016), neutropenic fever (p = 0.0008), lower absolute neutrophil count (p < 0.0001), acute kidney injury (AKI) (p = 0.0164), delayed methotrexate clearance (p = 0.0133), and higher 42-h methotrexate levels (p = 0.0179). In the standard/high-risk group, mercaptopurine dose was also linked to mucositis (p = 0.0495). Multivariable analysis showed that skin rashes (OR 6.5, p = 0.0016), fever (OR 2.8, p = 0.009), and neutropenia (OR 2.3, p = 0.0106) were independent risk factors for mucositis. Female sex (OR 7.12, p = 0.015) and AKI (OR 3.819, p = 0.037) were associated with recurrent mucositis.
CONCLUSIONS
Fever, skin rashes, AKI, delayed methotrexate clearance, and higher 42-h methotrexate levels were key risk factors for HDMTX-induced oral mucositis. Skin rashes, fever, and neutropenia were independent predictors, while female sex and AKI were linked to recurrent mucositis.
背景
尽管存在现有管理策略,但仍有约 20%接受高剂量甲氨蝶呤(HDMTX)治疗急性淋巴细胞白血病(ALL)的儿童发生口腔黏膜炎。通过药代动力学和白血病风险调整的个性化 HDMTX 剂量已降低了黏膜炎的发生率,但在类似的 24 小时甲氨蝶呤水平下,仍存在变异。
方法
本回顾性研究调查了个性化甲氨蝶呤方案下口腔黏膜炎的危险因素。来自圣裘德儿童研究医院总 16 试验的≥2 级口腔黏膜炎(CTCAE v4.0)患者的数据进行了分析。1:1 病例对照匹配方法考虑了年龄、性别、风险分类、免疫表型和甲氨蝶呤疗程。McNemar 检验、Bowker 对称检验和 Wilcoxon 符号秩检验用于统计分析。在仅病例分析中确定了复发性黏膜炎的危险因素。
结果
研究发现,甲氨蝶呤引起的黏膜炎与新发皮疹(p=0.0027)、发热(p=0.0016)、中性粒细胞减少性发热(p=0.0008)、绝对中性粒细胞计数较低(p<0.0001)、急性肾损伤(AKI)(p=0.0164)、甲氨蝶呤清除延迟(p=0.0133)和 42 小时甲氨蝶呤水平较高(p=0.0179)之间存在显著关联。在标准/高危组中,巯基嘌呤剂量也与黏膜炎有关(p=0.0495)。多变量分析显示皮疹(OR 6.5,p=0.0016)、发热(OR 2.8,p=0.009)和中性粒细胞减少症(OR 2.3,p=0.0106)是黏膜炎的独立危险因素。女性(OR 7.12,p=0.015)和 AKI(OR 3.819,p=0.037)与复发性黏膜炎相关。
结论
发热、皮疹、AKI、甲氨蝶呤清除延迟和 42 小时甲氨蝶呤水平是 HDMTX 引起的口腔黏膜炎的关键危险因素。皮疹、发热和中性粒细胞减少症是独立预测因素,而女性和 AKI 与复发性黏膜炎有关。
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