Raynov J, Danon S, Valerianova Z
Department of Haematology & Oncology, Military Medical Academy, Sofia, Bulgaria.
J BUON. 2002 Jan-Mar;7(1):57-60.
Cyclophosphamide (CY)-containing chemotherapy is usually characterized as moderately emetogenic. The aim of this study was to evaluate the efficacy of different antiemetics in the control of acute emesis in repeated cycles of moderately emetogenic chemotherapy.
A total of 101 patients with breast cancer (41, 40.6%), Hodgkin's disease (46, 45.5%) and non-Hodgkin's lymphoma (14, 13.9%) were studied. These patients received standard protocols of CY-based (>/=750 mg/m(2)) moderately emetogenic chemotherapy. Intravenous (i.v.) bolus metoclopramide (MCL), ondansetron (OND) and their combinations with corticosteroids (CS) were administered to the patients. The MCL-alone group of patients was used as control group. Emesis was evaluated during the first 3 courses of chemotherapy according to the internationally accepted criteria. All calculations were performed using the SPSS-5.0 statistical computing package.
During the first course of chemotherapy no differences in the efficacy between the control group and the other groups were noted (p >0.05). On the contrary, during the next 2 courses the efficacy of MCL progressively decreased and OND, OND plus CS and MCL plus CS showed significantly higher efficacy compared with MCL alone (p <0.05). Excluding MCL alone, the other antiemetics showed similar efficacy in the 2nd and 3rd course of chemotherapy (p >0.05). Patients aged over 35 years had more severe emesis.
The combination of MCL plus CS showed similar efficacy compared with OND and OND plus CS, and is cost-effective. The control of acute emesis in the first course and the patients' age are significant factors, influencing the efficacy of the antiemetic therapy in repeated courses of moderately emetogenic chemotherapy.
含环磷酰胺(CY)的化疗通常被认为具有中度致吐性。本研究旨在评估不同止吐药在控制中度致吐性化疗重复周期中急性呕吐的疗效。
共研究了101例乳腺癌患者(41例,40.6%)、霍奇金病患者(46例,45.5%)和非霍奇金淋巴瘤患者(14例,13.9%)。这些患者接受了基于CY(≥750 mg/m²)的中度致吐性化疗标准方案。对患者静脉推注甲氧氯普胺(MCL)、昂丹司琼(OND)及其与皮质类固醇(CS)的联合用药。仅使用MCL的患者组作为对照组。根据国际公认标准在化疗的前3个疗程中评估呕吐情况。所有计算均使用SPSS - 5.0统计计算软件包进行。
在化疗的第一个疗程中,对照组与其他组之间的疗效无差异(p>0.05)。相反,在接下来的2个疗程中,MCL的疗效逐渐降低,与单独使用MCL相比,OND、OND加CS以及MCL加CS显示出显著更高的疗效(p<0.05)。除单独使用MCL外,其他止吐药在化疗的第2和第3疗程中显示出相似的疗效(p>0.05)。年龄超过35岁的患者呕吐更严重。
MCL加CS的联合用药与OND和OND加CS显示出相似的疗效,且具有成本效益。第一个疗程中急性呕吐的控制以及患者年龄是影响中度致吐性化疗重复疗程中止吐治疗疗效的重要因素。