Martoni A, Piana E, Strocchi E, Angelelli B, Guaraldi M, Zamagni C, Camaggi C M, Pannuti F
Division of Medical Oncology, S. Orsola-Malpighi Hospital, Bologna, Italy.
Anticancer Res. 1998 Jul-Aug;18(4B):2799-803.
The 5HT3 receptor antagonist Granisetron (GRA) is available on the market as a 1 mg vial in USA and as a 3 mg vial in Europe. This study aimed to compare the two i.v. doses of GRA (3 mg vs 1 mg), both of which combined with Dexamethasone (DEX) (20 mg) in the prevention of acute Cisplatinum (CP)-induced emesis.
One hundred and ninety-eight consecutive chemotherapy-naive cancer patients, mainly suffering from lung and bladder cancer, were randomized at their first cycle to receive either GRA 1 mg + DEX or GRA 3 mg + DEX as i.v. bolus prior to chemotherapy and crossed-over to another GRA dose at the second cycle. The cytotoxic treatment included different multi-drug regimens containing CP (median dose 60 mg/m2, range 50-70) administered on day 1 and repeated every 21-28 days.
Of the 192 evaluable patients complete protection from acute emesis with GRA 1 and GRA 3, was observed after the 1st + 2nd cycles as follows: nausea 70% and 74%, vomiting 90% and 94%, nausea and vomiting 67% and 74% respectively (no statistically significant difference). No carry-over effect was observed on the complete protection from emesis. The crossover analysis comprising 156 patients confirmed there were no differences between the two antiemetic treatments. Twenty-seven per cent of patients preferred GRA 1, 31% preferred GRA 3, while 42% expressed no preference (P = 0.75). Nor was any difference observed for tolerability, the only reported side-effects being mild headache (16% vs 17%) and constipation (18% vs 25%).
This study shows that, under the above conditions, the 1 mg and 3 mg i.v. GRA doses are comparably effective when combined with DEX 20 mg in the prevention of acute CP-induced emesis.
5-羟色胺3(5HT3)受体拮抗剂格拉司琼(GRA)在美国市场上以1毫克小瓶形式供应,在欧洲则以3毫克小瓶形式供应。本研究旨在比较两种静脉注射剂量的GRA(3毫克与1毫克),二者均与地塞米松(DEX)(20毫克)联合使用,以预防顺铂(CP)急性诱导的呕吐。
198例初治癌症患者连续入组,主要为肺癌和膀胱癌患者,在其第一个化疗周期被随机分组,在化疗前静脉推注接受GRA 1毫克+DEX或GRA 3毫克+DEX,并在第二个周期交叉接受另一种GRA剂量。细胞毒性治疗包括不同的多药方案,其中CP(中位剂量60毫克/平方米,范围50 - 70)于第1天给药,每21 - 28天重复一次。
在192例可评估患者中,在第1 + 2个周期后观察到GRA 1毫克和GRA 3毫克对急性呕吐的完全保护情况如下:恶心分别为70%和74%,呕吐分别为90%和94%,恶心和呕吐分别为67%和74%(无统计学显著差异)。在呕吐的完全保护方面未观察到延续效应。包含156例患者的交叉分析证实两种止吐治疗之间无差异。27%的患者更喜欢GRA 1毫克,31%更喜欢GRA 3毫克,而42%表示无偏好(P = 0.75)。在耐受性方面也未观察到差异,唯一报告的副作用是轻度头痛(分别为16%和17%)和便秘(分别为18%和25%)。
本研究表明,在上述条件下,1毫克和3毫克静脉注射GRA剂量与20毫克DEX联合使用时,在预防CP急性诱导的呕吐方面效果相当。