Key result
Cannabinoids pose high drug interaction risks with 25 pediatric antineoplastic agents including cyclophosphamide and doxorubicin.
Why the study?
Growing interest in cannabinoids for pediatric cancer supportive care has raised concerns regarding potential drug-drug interactions with antineoplastic agents.
What are the potential drug-drug interactions between cannabinoids and common antineoplastic agents in pediatric oncology?
What are the potential drug-drug interactions between cannabinoids and common antineoplastic agents in pediatric oncology?
Cannabinoids pose a high risk of drug-drug interactions with several common pediatric antineoplastic agents, highlighting the need for age-appropriate pharmacokinetic and safety studies.
Warrants caution with cannabinoids and antineoplastic agents in pediatric oncology; leaves open clinical impact pending dedicated pharmacokinetic trials.
As interest in the use of cannabinoids for supportive care in pediatric cancers grows, there are emerging concerns about potential interactions with antineoplastic agents. This review provides an overview of potential drug-drug interactions between cannabinoids and 25 antineoplastic agents commonly used in pediatric hematology/oncology. Antineoplastic agents were stratified into low, medium, or high interaction risk based on the potential impact of cannabinoids on metabolic and/or pharmacodynamic pathways. The antineoplastic agents identified as high risk for interactions with cannabinoids included cyclophosphamide, doxorubicin, etoposide, ifosfamide, irinotecan, vinblastine, and vincristine. Key mechanisms of interaction include inhibition of cytochrome P450 enzymes and UDP-glucuronosyltransferases and modulation of drug transporters such as P-glycoprotein and breast cancer resistance protein. There is emerging evidence of a synergistic effect between cannabinoids and antineoplastic agents such as temozolomide, vinblastine, vinorelbine, and irinotecan. Pediatric patients exhibit developmental differences in drug metabolism and transporter expression, yet most pharmacokinetic data on cannabinoids are extrapolated from adult studies. There is a lack of pediatric-specific safety, efficacy, and dosing data that underscores the need for age-appropriate studies to ensure safe and effective integration of cannabinoids in pediatric cancer care.
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Zaman et al. (2026) conducted a review in Pediatric cancers. Cannabinoids was evaluated on Drug-drug interactions. Cannabinoids pose potential drug-drug interactions with 25 common pediatric antineoplastic agents, with high interaction risk identified for drugs like cyclophosphamide, doxorubicin, and etoposide.
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