Low dose of dexamethasone combined with netupitant and palonosetron in preventing nausea and vomiting in breast cancer patients induced by anthracycline drugs.

IF 2.8 3区 医学 Q2 ONCOLOGY Clinical & Translational Oncology Pub Date : 2025-02-01 Epub Date: 2024-07-13 DOI:10.1007/s12094-024-03581-7
Yehuan Liu, Peipei Hu, Yiyan Jiang, Xixiu Chen, Suxia Li
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Abstract

Background: To study the effects of various courses of dexamethasone (DEX) combined with 5-HT3 receptor antagonists (RA) and NK-1 RA in suppressing high-grade nausea and vomiting (CINV) caused by anthracycline and cyclophosphamide chemotherapy regimens (AC or EC) in breast cancer (BC) patients.

Patients and methods: A prospective study was performed with 252 BC patients who received AC between January, 2019 and June, 2022 in our hospital. Patients were randomly separated into control Group (N = 130) who received DEX 12 mg on day 1 and 8 mg per dose on day 2-4 and observation group (N = 122) treated with DEX 5 mg per dose on days 1-4. The response was monitored. Primary study endpoint was complete resolution (CR) of patients nausea or vomiting; secondary study endpoints included acute CR and delayed CR; and complete control (CC), acute CC, delayed CC, and safety.

Results: All patients underwent six rounds of chemotherapy, and no difference was found in the clinical data. CR of acute/delayed phase was (94.3%/88.5%, P > 0.05), (89.3%/90.8%, P > 0.05); total CR was (80.3%/81.5%, P > 0.05); CC was (56.6%/59.2%, P > 0.05), (64.8%/67.7%, P > 0.05); total CR was (48.4%/53.1%, P > 0.05).

Conclusions: The preventive antiemetic effects of NEPA, a fixed-dose combination of netupitant and palonosetron combined with DEX 5 mg per dose on days 1-4, can be similar to DEX 12 mg on day 1 and 8 mg per dose on days 2-4, low-dose hormone with better safety, which is beneficial.

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小剂量地塞米松联合奈吐普坦和帕洛诺司琼预防蒽环类药物引起的乳腺癌患者恶心和呕吐。
研究背景研究不同疗程的地塞米松(DEX)联合5-HT3受体拮抗剂(RA)和NK-1 RA对抑制乳腺癌(BC)患者因蒽环类和环磷酰胺化疗方案(AC或EC)引起的高度恶心和呕吐(CINV)的效果:本院对2019年1月至2022年6月期间接受蒽环类和环磷酰胺化疗的252名乳腺癌患者进行了前瞻性研究。患者被随机分为对照组(N=130)和观察组(N=122),对照组患者在第1天接受12毫克DEX治疗,第2-4天每次接受8毫克DEX治疗,观察组患者在第1-4天每次接受5毫克DEX治疗。对反应进行监测。主要研究终点为患者恶心或呕吐症状完全缓解(CR);次要研究终点包括急性CR和延迟CR;以及完全控制(CC)、急性CC、延迟CC和安全性:所有患者均接受了六次化疗,临床数据无差异。急性期/延迟期CR为(94.3%/88.5%,P>0.05)、(89.3%/90.8%,P>0.05);总CR为(80.3%/81.5%,P>0.05);CC为(56.6%/59.2%,P>0.05)、(64.8%/67.7%,P>0.05);总CR为(48.4%/53.1%,P>0.05):NEPA是一种固定剂量的奈普坦和帕洛诺司琼联合DEX 5 mg/次(第1-4天)的组合药物,其预防性止吐效果与DEX 12 mg/次(第1天)和8 mg/次(第2-4天)相似,低剂量激素具有更好的安全性,是一种有益的药物。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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