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Recent developments in oral chemotherapy options for gastric carcinoma.

机译:胃癌口服化疗方案的最新进展。

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摘要

The incidence of carcinoma of the stomach is low in the United States, Canada, and Australia but is a significant health problem in Asia, South America, Eastern Europe, and countries of the previous Soviet Union. For patients with advanced disease, chemotherapy remains palliative. With the increasing emphasis on patients' quality of life, convenience, and cost containment, oral chemotherapy has come into increasing focus. We review oral chemotherapy agents for use in patients with advanced gastric carcinoma. Etoposide, given intravenously, has modest activity in gastric carcinoma. We studied oral etoposide, which was administered to 28 patients at the starting dose of 50 mg/m2/day for 21 days followed by a 7-day rest period. Five patients achieved a partial response and 4 patients achieved a minor response. The drug was well tolerated. Common toxicities included myelosuppression, alopecia, and nausea. Oral etoposide thus shows evidence of modest activity against gastric carcinoma. In Japan, considerable advances have been made in the oral chemotherapy of gastric carcinoma. The second generation fluorouracil prodrug tegafur/uracil (UFT) has been extensively evaluated in Japan, Korea, and Spain. Data predominantly from Japan indicate that tegafur/uracil has a response rate of approximately 20% in treatment naive patients with advanced gastric carcinoma. When combined with other active agents, tegafur/uracil has a response rate of more than 30% in these patients. The available data also suggest that tegafur/uracil is well tolerated and that patient acceptance is high. In conclusion, future clinical research is likely to focus on the development of convenient outpatient regimens with efficacy equal to that of intravenous regimens.
机译:在美国,加拿大和澳大利亚,胃癌的发病率较低,但在亚洲,南美,东欧和前苏联国家中,这是一个重大的健康问题。对于晚期疾病患者,化学疗法仍然是姑息治疗。随着对患者生活质量,便利性和成本控制的日益重视,口服化疗已成为越来越多的关注焦点。我们审查了用于晚期胃癌患者的口服化疗药物。静脉给予的依托泊苷在胃癌中具有中等活性。我们研究了口服依托泊苷,它以50毫克/平方米/天的起始剂量给予28例患者,共21天,然后休息7天。 5名患者获得了部分缓解,4名患者获得了轻微缓解。该药耐受性良好。常见的毒性包括骨髓抑制,脱发和恶心。因此,口服依托泊苷显示出适度的抗胃癌活性的证据。在日本,胃癌的口服化学疗法已经取得了相当大的进步。第二代氟尿嘧啶前药替加氟/尿嘧啶(UFT)已在日本,韩国和西班牙进行了广泛的评估。来自日本的主要数据表明,替加氟/尿嘧啶对未接受治疗的晚期胃癌患者的缓解率约为20%。与其他活性剂合用时,替加福/尿嘧啶对这些患者的缓解率超过30%。现有数据还表明,替加福/尿嘧啶耐受性良好,患者的接受程度很高。总而言之,未来的临床研究可能会集中在开发与静脉注射疗法疗效相当的便捷门诊疗法上。

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