4.7 Article

Clinical pharmacology of cytotoxic drugs in neonates and infants: Providing evidence-based dosing guidance

期刊

EUROPEAN JOURNAL OF CANCER
卷 164, 期 -, 页码 137-154

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ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2021.11.001

关键词

Paediatrics; Pharmacokinetics; Pharmacology; Therapeutic drug monitoring; Antineoplastic agents; Child; Clinical protocols; Infant; Medical oncology

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资金

  1. National Institute for Health Research (NIHR) Research for Patient Benefit programme [PB-PG-1216-20032]
  2. Cancer Research UK [C9380/A25138]
  3. Experimental Cancer Medicine Centre Network [C9380/A25169]
  4. Sir Bobby Robson Foundation
  5. National Institutes of Health Research (NIHR) [PB-PG-1216-20032] Funding Source: National Institutes of Health Research (NIHR)

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Cancer treatment in neonates and infants is complex, and dose optimization plays a crucial role in improving outcomes. This review provides clinically relevant pharmacological evidence-based dosing guidance for a wide range of cytotoxic drugs in this population.
Cancer in neonates and infants is a rare but challenging entity. Treatment is complicated by marked physiological changes during the first year of life, excess rates of toxicity, mortality, and late effects. Dose optimisation of chemotherapeutics may be an important step to improving outcomes. Body size-based dosing is used for most anticancer drugs used in infants. However, dose regimens are generally not evidence based, and dosing strategies are frequently inconsistent between tumour types and treatment protocols. In this review, we collate available pharmacological evidence supporting dosing regimens in infants for a wide range of cytotoxic drugs. A systematic review was conducted, and available data ranked by a level of evidence (1-5) and a grade of recommendation (A-D) provided on a consensus basis, with recommended dosing approaches indicated as appropriate. For 9 of 29 drugs (busulfan, carboplatin, cyclophosphamide, daunorubicin, etoposide, fludarabine, isotretinoin, melphalan and vincristine), grade A was scored, indicating sufficient pharmacological evidence to recommend a dosing algorithm for infants. For busulfan and carboplatin, sufficient data were available to recommend therapeutic drug monitoring in infants. For eight drugs (actinomycin D, blinatumomab, dinutuximab, doxorubicin, mercaptopurine, pegaspargase, thioguanine and topotecan), some pharmacological evidence was available to guide dosing (graded as B). For the remaining drugs, including commonly used agents such as cisplatin, cytarabine, ifosfamide, and methotrexate, pharmacological evidence for dosing in infants was limited or non-existent: grades C and D were scored for 10 and 2 drugs, respectively. The review provides clinically relevant evidence-based dosing guidance for cytotoxic drugs in neonates and infants. 2021 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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