Bosnjak Snezana M, Zilic Ana, Radhakrishnan Venkatraman, Ostwal Vikas, Aapro Matti, Iihara Hirotoshi, Smit Teresa, Gralla Richard
Department of Supportive Oncology and Palliative Care, Institute for Oncology and Radiology of Serbia, Pasterova 14, Belgrade, Serbia.
Department of Medical Oncology, Cancer Institute (WIA), Adyar, Chennai, India.
Support Care Cancer. 2025 Feb 12;33(3):181. doi: 10.1007/s00520-025-09211-4.
Prevention of chemotherapy-induced nausea and vomiting (CINV) remains an essential supportive care need for patients receiving cancer treatment. Due to inadequate access to antiemetics in many countries, guideline-recommended CINV prophylaxis is not always possible. Our goal was to formulate antiemetic recommendations for resource-limited settings and define alternative antiemetic regimens for the CINV prophylaxis after highly (HEC) and moderately emetic chemotherapy (MEC), when NK-receptor antagonists are not accessible.
The recommendations based on the MASCC/ESMO 2023 Guideline Update were considered as the best option. The stratification based on a meta-analysis published by Filetti et al. (2023) was used in order to select and rank NK-receptor antagonist-free regimens by their probability of achieving complete response. Alternative NK-receptor antagonist-free regimens based on olanzapine are proposed, ranked by their efficacy as "better" and "good" options when "best" regimens recommended by the MASCC/ESMO 2023 Guideline Update were not available or affordable.
For the prevention of acute CINV, in patients receiving HEC (HEC-cisplatin and AC-HEC) with no access to an NK-receptor antagonist, a 3-drug regimen including single doses of a 5-HT-receptor antagonist, dexamethasone, and olanzapine given before chemotherapy is recommended as an alternative option. Olanzapine and dexamethasone are recommended days 2-4 after chemotherapy. The O10PD regimen (10 mg olanzapine, palonosetron, and dexamethasone) is suggested as the alternative regimen in the category "better." Other 5-HT-receptor antagonists (ondansetron, granisetron) may be used if palonosetron is not affordable (category "good"). No guideline is possible for the alternative regimens to prevent acute CINV following MEC because of limited (carboplatin, AUC ≥ 5) or unavailable data (oxaliplatin chemotherapy in women aged < 50 years). Limited data are also available on the management of CINV following trastuzumab-deruxtecan.
The most effective prevention of CINV recommended by the MASCC/ESMO 2023 Guideline Update must be given when available and affordable. These recommendations were developed to facilitate decision on which regimen to use when the best MASCC/ESMO 2023 recommended regimen is not accessible because NK-receptor antagonists are either not available or not affordable.
预防化疗引起的恶心和呕吐(CINV)仍然是癌症治疗患者一项至关重要的支持性护理需求。由于许多国家难以获得止吐药,指南推荐的CINV预防措施并非总是可行。我们的目标是为资源有限的环境制定止吐建议,并确定在无法获得NK受体拮抗剂时,用于高度致吐化疗(HEC)和中度致吐化疗(MEC)后CINV预防的替代止吐方案。
基于MASCC/ESMO 2023指南更新的建议被视为最佳选择。采用Filetti等人(2023年)发表的一项荟萃分析进行分层,以便根据实现完全缓解的概率选择无NK受体拮抗剂的方案并进行排序。提出了基于奥氮平的无NK受体拮抗剂的替代方案,当MASCC/ESMO 2023指南更新推荐的“最佳”方案不可用或无法负担时,根据其疗效将其列为“更好”和“良好”选项。
对于预防急性CINV,在无法获得NK受体拮抗剂的接受HEC(顺铂HEC和蒽环类药物-环磷酰胺HEC)的患者中,建议采用一种三联方案,即在化疗前给予单剂量的5-HT受体拮抗剂、地塞米松和奥氮平作为替代方案。建议在化疗后第2 - 4天使用奥氮平和地塞米松。O10PD方案(10毫克奥氮平、帕洛诺司琼和地塞米松)被建议作为“更好”类别的替代方案。如果帕洛诺司琼无法负担,可以使用其他5-HT受体拮抗剂(昂丹司琼、格拉司琼)(“良好”类别)。由于数据有限(卡铂,AUC≥5)或缺乏数据(年龄<50岁女性的奥沙利铂化疗),无法制定预防MEC后急性CINV的替代方案指南。关于曲妥珠单抗-德曲妥珠单抗治疗后CINV的管理也仅有有限的数据。
MASCC/ESMO 2023指南更新推荐的最有效的CINV预防措施在可行且可负担时必须采用。制定这些建议是为了便于在由于NK受体拮抗剂不可用或无法负担而无法采用MASCC/ESMO 2023推荐的最佳方案时,决定使用哪种方案。