A systematic review was undertaken to describe dexamethasone doses studied for chemotherapy-induced vomiting (CIV) prophylaxis in pediatric patients and their effects on achieving complete acute CIV control. No dose-finding studies were identified. However, 16 studies assessing pediatric patients who received dexamethasone were included and classified according to the emetogenicity of chemotherapy administered. Eight different total daily dexamethasone doses were administered to patients on day 1 of highly emetogenic chemotherapy: three in conjunction with aprepitant/fosaprepitant plus a 5HT 3 antagonist and five in conjunction with a 5HT 3 antagonist. Five different total daily dexamethasone doses were administered in conjunction with a 5HT 3 antagonist to patients on day 1 of moderately emetogenic chemotherapy. Due to the heterogeneity of studies identified, meta-analysis was not possible. The optimal dexamethasone dose to control acute CIV and to minimize harms in pediatric patients remains uncertain. This is a key area for future research. K E Y W O R D S chemotherapy-induced nausea and vomiting, dexamethasone, pediatric oncology, supportive care 1 INTRODUCTION Chemotherapy-induced nausea and vomiting (CINV) are two of the most distressing side effects of chemotherapy. 1-3 They have a negative influence on quality of life, have been associated with decreased growth in children, and can lead to patients becoming nonadherent with oral chemotherapy and refusing to continue cancer treatment. 4-6 Dexamethasone has been included in pediatric CINV prophylaxis regimens for over three decades. 7 Current clinical practice guidelines (CPGs) for the prevention of acute CINV strongly recommend that pediatric patients receive dexamethasone in combination with Abbreviations: CINV, chemotherapy-induced nausea and vomiting; CIV, chemotherapy-induced vomiting; CPG, clinical practice guideline; HEC, highly emetogenic chemotherapy; MEC, moderately emetogenic chemotherapy aprepitant and a 5HT 3 antagonist during receipt of highly emetogenic chemotherapy (HEC) or in combination with a 5HT 3 antagonist during receipt of moderately emetogenic chemotherapy (MEC). 8-11 These CPGs acknowledge that there are circumstances when clinicians may wish to avoid the use of dexamethasone as an antiemetic and recommend alternatives. Such circumstances include brain tumors where corticosteroids may prevent chemotherapy distribution into the central nervous system 12 ; acute myelogenous leukemia where corticosteroids may further increase the already high risk of fungal infection 12 ; and use of chemotherapy where efficacy is compromised by concurrent corticosteroid use. 11 Nevertheless, inclusion of dexamethasone in pediatric CINV prophylaxis regimens and its appropriate dose are hotly debated among the pediatric oncology community. For example, two of 36 Children's Oncology Group member institutions responding to a survey in 2015 never administered dexamethasone for CIV