Department of Orthopaedics, Chengdu Jinniu District People's Hospital, China.
Department of Pathology, China-Japan Friendship Hospital, Beijing, China.
Adv Clin Exp Med. 2022 Mar;31(3):223-230. doi: 10.17219/acem/142332.
Chemotherapy-induced nausea and vomiting (CINV) is a troublesome side-effect of chemotherapy in pediatric patients undergoing osteosarcoma treatment. In this context, the role of 5-hydroxytryptamine-3 (5-HT3) receptor antagonists needs to be explored.
To evaluate the superiority of single-dose palonosetron over granisetron in pediatric patients undergoing highly emetogenic chemotherapy (HEC) for osteosarcoma.
In this double-blind, randomized study, pediatric patients were assessed in terms of acute nausea and vomiting following HEC for osteosarcoma. These children were assigned to group 1 (palonosetron) and group 2 (granisetron) without any other antiemetic prophylaxis. The primary outcome variable was the children's segment with a complete response (CR) during the acute phase of the 1st on-study chemotherapy cycle. The risk factors associated with the emesis were analyzed. The patients were followed up for the first 24 h after chemotherapy.
A total number of 200 children were evaluated in terms of the response, and other factors that might alter the response were assessed in the 2 groups. These 200 children underwent 604 blocks of chemotherapy. Complete responses were documented in 83% and 72% of children receiving palonosetron and granisetron, respectively, during the acute phase. Only dexamethasone, used as a rescue medication, was found to be a significant risk factor that predisposed to the response (p < 0.05).
Single-dose palonosetron is an effective alternative to granisetron for preventing CINV in children receiving HEC for osteosarcoma.
化疗引起的恶心和呕吐(CINV)是骨肉瘤患儿接受化疗的一种麻烦的副作用。在这种情况下,需要探索 5-羟色胺 3(5-HT3)受体拮抗剂的作用。
评估单剂量帕洛诺司琼优于格拉司琼在接受骨肉瘤高致吐性化疗(HEC)的儿科患者中的优势。
在这项双盲、随机研究中,评估了接受骨肉瘤 HEC 的儿科患者的急性恶心和呕吐情况。这些患儿被分配到第 1 组(帕洛诺司琼)和第 2 组(格拉司琼),没有任何其他止吐预防措施。主要结局变量是第 1 个研究化疗周期急性期儿童的完全缓解(CR)段。分析了与呕吐相关的危险因素。对患者进行了化疗后 24 小时内的随访。
在 200 名接受反应评估的患儿中,评估了其他可能改变反应的因素。这 200 名患儿共接受了 604 个化疗周期。在急性期,接受帕洛诺司琼和格拉司琼的患儿分别有 83%和 72%的患儿获得完全缓解。只有地塞米松作为解救药物,被发现是导致反应的显著危险因素(p < 0.05)。
单剂量帕洛诺司琼是预防骨肉瘤接受 HEC 的儿童 CINV 的格拉司琼的有效替代药物。