Liu Yehuan, Hu Peipei, Jiang Yiyan, Chen Xixiu, Li Suxia
Department of General Medicine, The 1st Affiliated Hospital of Wenzhou Medical University, No.2, Fuxue Lane, Lucheng, Wenzhou, 325000, China.
Department of Medical Oncology, The 1st Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Clin Transl Oncol. 2025 Feb;27(2):785-789. doi: 10.1007/s12094-024-03581-7. Epub 2024 Jul 13.
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.
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.
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).
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.
研究不同疗程的地塞米松(DEX)联合5-羟色胺3受体拮抗剂(RA)和神经激肽-1受体拮抗剂(NK-1 RA)对抑制乳腺癌(BC)患者蒽环类和环磷酰胺化疗方案(AC或EC)所致重度恶心和呕吐(CINV)的效果。
对2019年1月至2022年6月在我院接受AC治疗的252例BC患者进行前瞻性研究。患者被随机分为对照组(N = 130),于第1天接受12 mg DEX,第2 - 4天每剂接受8 mg DEX;以及观察组(N = 122),于第1 - 4天每剂接受5 mg DEX治疗。监测反应情况。主要研究终点是患者恶心或呕吐的完全缓解(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轮化疗,临床数据无差异。急性/延迟期CR分别为(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)。
奈妥匹坦和帕洛诺司琼的固定剂量组合NEPA联合第1 - 4天每剂5 mg DEX的预防性止吐效果可能与第1天12 mg DEX和第2 - 4天每剂8 mg DEX相似,低剂量激素安全性更好,这是有益的。