Safety and efficacy of netupitant/palonosetron and dexamethasone in classical Hodgkin's lymphoma patients with inadequate chemotherapy-induced nausea and vomiting prophylaxis with palonosetron and dexamethasone: a single-center real-life experience.

Vittorio R Zilioli, Cristina Muzi, Periana Minga, Paolo Codega, Lara Crucitti, Erika Meli, Anna Esposito, Claudia Panico, Chiara Rusconi, Roberto Cairoli
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引用次数: 2

Abstract

We analyzed safety of NEPA (netupitant/palonosetron) and dexamethasone (NEPA+DEX) for the management of chemotherapy-induced nausea and vomiting (CINV) in classical Hodgkin's lymphoma patients that experienced CINV with a prophylaxis with palonosetron (PALO + DEX). In a retrospective, monocentric, noncomparative study, we analyzed adverse events and CINV grading in patients who switched from PALO + DEX to NEPA + DEX. Among 32 patients treated with ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) during the study period, 47% did not properly control CINV with PALO + DEX and were shifted to NEPA + DEX. Among these, 53.3% properly controlled CINV is for all the remaining chemotherapy cycles. We did not observe an increase of adverse events after switching to NEPA. In our study, NEPA did not show drug-drug interaction with ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) chemotherapy agents and NEPA administration was well tolerated with mild and transient adverse events.

Abstract Image

奈吡坦/帕洛诺司琼和地塞米松治疗化疗不充分的经典霍奇金淋巴瘤患者的安全性和有效性:帕洛诺司琼和地塞米松预防化疗引起的恶心和呕吐:单中心现实经验
我们分析了NEPA(尼妥吡坦/帕洛诺司琼)和地塞米松(NEPA+DEX)用于治疗经典霍奇金淋巴瘤患者化疗引起的恶心和呕吐(CINV)的安全性,这些患者在预防使用帕洛诺司琼(PALO +DEX)后出现了CINV。在一项回顾性、单中心、非比较研究中,我们分析了从PALO + DEX切换到NEPA + DEX的患者的不良事件和CINV分级。在研究期间接受ABVD(阿霉素、博来霉素、长春碱、达卡巴嗪)治疗的32例患者中,47%的患者使用PALO + DEX不能很好地控制CINV,转而使用NEPA + DEX。其中53.3%的CINV适用于所有剩余的化疗周期。我们没有观察到改用NEPA后不良事件的增加。在我们的研究中,NEPA未显示出与ABVD(阿霉素、博来霉素、长春碱、达卡巴嗪)化疗药物的药物相互作用,NEPA耐受性良好,有轻微和短暂的不良事件。
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来源期刊
自引率
0.00%
发文量
3
审稿时长
13 weeks
期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
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