Jennifer A. Belsky, Ashley Chavana, Ankona Banerjee, Mark Zobeck, Eric S. Schafer, Karen R. Rabin, Monica Gramatges, Alex Sim, Audrey Leisinger, Trisha Reddy, Megan J. Parod, Philip Lupo, Michael Scheurer, Austin L. Brown, M. Brooke Bernhardt
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Delayed excretion was defined as a serum MTX concentration greater than 0.4 µM at Hour 48. We identified use of laxative medications after each HD-MTX infusion, with receipt of two or more doses considered a proxy for constipation. Multilevel logistic regression models evaluated associations between clinical factors and delayed HD-MTX excretion to account for multiple MTX cycles per individual.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 533 eligible patients received 1875 HD-MTX infusions. Patients were mostly male (59.8%), Hispanic (56.7%), with a median age of 9.5 years. Delayed excretion was observed following 42.7% of HD-MTX infusions, and patients received two or more laxative doses during 19.9% of infusions. Independent of other factors, individuals who received two or more laxative doses were nearly 60% (odds ratio 1.58; 95% confidence interval: 1.19–2.09; <i>p</i> = .002) more likely to experience delayed excretion compared to those receiving fewer than two laxative doses.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Receipt of at least two laxative doses was independently associated with delayed methotrexate excretion in pediatric patients with ALL. Future prospective studies are needed to confirm the secondary effects of constipation and confirm the association with constipation and identify clinical benefits that optimize drug excretion.</p>\n </section>\n </div>","PeriodicalId":19822,"journal":{"name":"Pediatric Blood & Cancer","volume":"72 1","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/pbc.31377","citationCount":"0","resultStr":"{\"title\":\"Delayed excretion of high-dose methotrexate in pediatric acute leukemia correlates with laxative and constipation management\",\"authors\":\"Jennifer A. Belsky, Ashley Chavana, Ankona Banerjee, Mark Zobeck, Eric S. Schafer, Karen R. Rabin, Monica Gramatges, Alex Sim, Audrey Leisinger, Trisha Reddy, Megan J. Parod, Philip Lupo, Michael Scheurer, Austin L. Brown, M. Brooke Bernhardt\",\"doi\":\"10.1002/pbc.31377\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Delayed excretion of high-dose methotrexate (HD-MTX) in pediatric acute lymphoblastic leukemia (ALL) can result in significant morbidity. While methotrexate is primarily renally excreted, HD-MTX may overwhelm renal excretion and increase reliance on fecal elimination. This study evaluated the association between laxative use for constipation and delayed excretion of HD-MTX.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>This multisite chart review included pediatric patients with ALL (2010–2020) who received HD-MTX (5 g/m<sup>2</sup>). Delayed excretion was defined as a serum MTX concentration greater than 0.4 µM at Hour 48. We identified use of laxative medications after each HD-MTX infusion, with receipt of two or more doses considered a proxy for constipation. 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引用次数: 0
摘要
背景:小儿急性淋巴细胞白血病(ALL)患者延迟排泄大剂量甲氨蝶呤(HD-MTX)会导致严重的发病率。虽然甲氨蝶呤主要通过肾脏排泄,但HD-MTX可能会抑制肾脏排泄并增加对粪便排泄的依赖。本研究评估了因便秘而使用泻药与 HD-MTX 排泄延迟之间的关联:这项多站点病历回顾纳入了接受 HD-MTX(5 克/平方米)治疗的儿童 ALL 患者(2010-2020 年)。第48小时时血清MTX浓度大于0.4 µM即为排泄延迟。我们确定了每次输注 HD-MTX 后通便药物的使用情况,使用两次或两次以上药物被视为便秘的代表。多层次逻辑回归模型评估了临床因素与HD-MTX排泄延迟之间的关系,以考虑每个人的多个MTX周期:共有533名符合条件的患者接受了1875次HD-MTX输注。患者大多为男性(59.8%)和西班牙裔(56.7%),中位年龄为 9.5 岁。42.7%的患者在输注 HD-MTX 后出现排泄延迟,19.9%的患者在输注期间服用了两次或两次以上的泻药。与其他因素无关,与接受少于两次泻药治疗的患者相比,接受两次或两次以上泻药治疗的患者出现排泄延迟的几率高出近60%(几率比1.58;95%置信区间:1.19-2.09;p = .002):结论:至少服用两次泻药与儿童 ALL 患者甲氨蝶呤排泄延迟有独立关联。未来需要进行前瞻性研究,以确认便秘的继发性影响,确认与便秘的关联,并确定优化药物排泄的临床益处。
Delayed excretion of high-dose methotrexate in pediatric acute leukemia correlates with laxative and constipation management
Background
Delayed excretion of high-dose methotrexate (HD-MTX) in pediatric acute lymphoblastic leukemia (ALL) can result in significant morbidity. While methotrexate is primarily renally excreted, HD-MTX may overwhelm renal excretion and increase reliance on fecal elimination. This study evaluated the association between laxative use for constipation and delayed excretion of HD-MTX.
Methods
This multisite chart review included pediatric patients with ALL (2010–2020) who received HD-MTX (5 g/m2). Delayed excretion was defined as a serum MTX concentration greater than 0.4 µM at Hour 48. We identified use of laxative medications after each HD-MTX infusion, with receipt of two or more doses considered a proxy for constipation. Multilevel logistic regression models evaluated associations between clinical factors and delayed HD-MTX excretion to account for multiple MTX cycles per individual.
Results
A total of 533 eligible patients received 1875 HD-MTX infusions. Patients were mostly male (59.8%), Hispanic (56.7%), with a median age of 9.5 years. Delayed excretion was observed following 42.7% of HD-MTX infusions, and patients received two or more laxative doses during 19.9% of infusions. Independent of other factors, individuals who received two or more laxative doses were nearly 60% (odds ratio 1.58; 95% confidence interval: 1.19–2.09; p = .002) more likely to experience delayed excretion compared to those receiving fewer than two laxative doses.
Conclusion
Receipt of at least two laxative doses was independently associated with delayed methotrexate excretion in pediatric patients with ALL. Future prospective studies are needed to confirm the secondary effects of constipation and confirm the association with constipation and identify clinical benefits that optimize drug excretion.
期刊介绍:
Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.