Regidor P A, Nelken B, Regidor M, Bier U, Oberhoff C, Schindler A E
Abteilung für Gynäkologie, Universität-Essen.
Zentralbl Gynakol. 1996;118(3):148-53.
Efficacy and safety of the antiemetic agent Navoban (5HT3-receptor-antagonist Tropisetron) on cytostatic-induced emesis of breast cancers and gynecological cancers was tested in 28 female patients receiving a total of 127 chemotherapy courses containing high (cisplatin), moderate high (cyclophosphamid) or moderate (for example 5 FU) emetogenic cytostatic drugs. We studied antiemetic response rates of Navoban (5 mg/d) during the first 24 hours after administration of the chemotherapy as well as response rates of the "delayed nausea and emesis" (days 2-9 after chemotherapy). A complete response was observed in 103 chemotherapy courses (= 81.1%) during the first 24 hours after chemotherapy and in 93 courses (= 73.2%) for the "delayed emesis". Treatment failures (more than 5 vomiting episodes) during the first 24 hours were present in four courses and for the "delayed emesis" in 11 courses. The side effects of Navoban such as constipation, headache or tiredness were minimum. Therefore no patient refused to receive the necessary chemotherapy. Navoban is, with its single dose application, an effective therapeutic drug for the prevention of nausea and emesis in patients receiving a chemotherapy.
在28名接受了总共127个化疗疗程的女性患者中,测试了止吐药奈妥吡坦(5-羟色胺3受体拮抗剂托烷司琼)对乳腺癌和妇科癌症细胞抑制剂诱发呕吐的疗效和安全性。这些化疗疗程包含高致吐性(顺铂)、中度高致吐性(环磷酰胺)或中度致吐性(如5-氟尿嘧啶)的细胞毒性药物。我们研究了化疗给药后最初24小时内奈妥吡坦(5毫克/天)的止吐反应率以及“延迟性恶心和呕吐”(化疗后第2至9天)的反应率。化疗后最初24小时内,103个化疗疗程(=81.1%)观察到完全缓解,“延迟性呕吐”为93个疗程(=73.2%)。最初24小时内有4个疗程出现治疗失败(呕吐发作超过5次),“延迟性呕吐”有11个疗程出现治疗失败。奈妥吡坦的副作用如便秘、头痛或疲劳最小。因此,没有患者拒绝接受必要的化疗。奈妥吡坦单剂量应用,是预防接受化疗患者恶心和呕吐的有效治疗药物。