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首页> 外文期刊>Oncology: International Journal of Cancer Research and Treatment >Evaluation of a standardized protocol of intracavitary recombinant interferon alpha-2b in the palliative treatment of malignant peritoneal effusions. A prospective pilot study.
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Evaluation of a standardized protocol of intracavitary recombinant interferon alpha-2b in the palliative treatment of malignant peritoneal effusions. A prospective pilot study.

机译:评估腔内重组干扰素α-2b在恶性腹膜积液的姑息治疗中的标准化方案。前瞻性试验研究。

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OBJECTIVE: Several schedules with variable doses of intracavitary interferon have been proposed for the management of metastatic peritoneal effusions. This prospective pilot study evaluated the efficacy of a standardized schedule of intraperitoneal interferon alpha(2b). METHODS: In 41 cancer patients with malignant ascites a 9-french intraperitoneal catheter was placed under sonographic guidance, and ascites was drained until abdominal ultrasound showed complete absence of effusion. Interferon alpha(2b), 6 or 9 million units (body weight 50 kg, respectively), was then administered via the tube, which was clamped for 6 h. 6 courses were given at 4-day intervals. In comparison with pretreatment levels, the 30-day response was classified as complete (CR) = no fluid recurrence, partial (PR) = fluid recurrence <50% and no response (NR) = >50%. Responders were monitored until fluid recurrence requiring paracentesis. RESULTS: 12 patients had CR, 15 PR, 14 NR. Global response (GR) was 65.9%. In ovarian cancer, GR was 75% and was not influenced by the quantity of the pretreatment daily fluid production. In the other cancers, a pretreatment fluid production
机译:目的:已提出了几种剂量可变的腔内干扰素方案,用于转移性腹膜积液的管理。这项前瞻性研究评估了腹膜内干扰素α(2b)标准化治疗方案的疗效。方法:在41名恶性腹水癌患者中,在超声引导下放置了一条9法式腹膜内导管,并排空腹水,直到腹部超声显示完全没有积液。然后通过管子将6或900万单位的干扰素α(2b)(分别小于或等于或大于50千克)给药,将其夹紧6小时。每隔4天提供6门课程。与预处理水平相比,30天的反应分为完全(CR)=无液体复发,部分(PR)=液体复发<50%和无反应(NR)=> 50%。监测反应者,直到需要穿刺术的液体复发。结果:12例患者有CR,15 PR,14 NR。全球响应(GR)为65.9%。在卵巢癌中,GR为75%,不受预处理每日液体量的影响。在其他癌症中,预处理液的产生<或= 500 ml /天与显着更高的反应性相关(p <0.05)。在前3个疗程中未显示反应的患者在下一个疗程后没有反应。 60天GR为41.5%,90天GR为26.8%。体液再吸收的平均时间为70.5 +/- 75.3,而治疗前为11.4 +/- 4.4天(p <0.001)。反应者的生存时间为38-394天(平均131天),平均反应时间为101天。结论:该方案可合理地应用于卵巢癌患者和液体分泌量≤500 ml /天的其他癌症患者,如果在3个疗程后未观察到反应,应停止使用该方案。

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