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氨苯吖啶治疗难治性食管癌。一项西南肿瘤学组的研究。

Amonafide treatment of refractory esophageal cancer. A Southwest Oncology Group study.

作者信息

Poplin E, Fleming T, MacDonald J S, Eisenberg P, Fisher R I, Conrad M E

机构信息

Wayne State University Medical Center, Detroit, MI.

出版信息

Invest New Drugs. 1993 Feb;11(1):47-51. doi: 10.1007/BF00873910.

DOI:10.1007/BF00873910
PMID:8349435
Abstract

Amonafide, a synthetic benzisoquinolinedione, was evaluated for treatment of squamous esophageal cancer. Eleven men and 5 women were eligible with a median performance status of 1 and median age of 63 years. Six had no prior treatment. All patients had measurable disease. Therapy consisted of amonafide 300 mg/m2d days 1-5 every 21 days. Thirty-five courses of therapy were delivered. The median number of courses received was two. Sixteen patients are evaluable for toxicity. Thirteen are evaluable for response. Toxicity was severe. Seven patients were hospitalized for toxicity. Six patients had grade IV granulocytopenia; two, grade IV thrombocytopenia. Angioedema developed in one patient; severe exfoliative dermatitis in another. A single partial response, with the decrease in size a supraclavicular node, was noted in a previously untreated patient. Amonafide, in this dose and schedule, is associated with occasionally severe toxicity precluding its likely use in squamous cell esophageal carcinoma.

摘要

氨萘非特是一种合成的苯并异喹啉二酮,对其治疗食管鳞状细胞癌的效果进行了评估。11名男性和5名女性符合条件,中位体能状态为1,中位年龄为63岁。6名患者此前未接受过治疗。所有患者均有可测量的病灶。治疗方案为氨萘非特300mg/m²,第1 - 5天给药,每21天为一个疗程。共进行了35个疗程的治疗。接受疗程的中位数为两个。16名患者可评估毒性,13名可评估疗效。毒性严重。7名患者因毒性住院。6名患者出现IV级粒细胞减少;2名患者出现IV级血小板减少。1名患者发生血管性水肿;另1名患者出现严重剥脱性皮炎。在1名此前未接受过治疗的患者中观察到1例部分缓解,表现为锁骨上淋巴结缩小。该剂量和疗程的氨萘非特伴有偶尔出现的严重毒性,使其不太可能用于食管鳞状细胞癌的治疗。

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本文引用的文献

1
Evaluation of amonafide in disseminated malignant melanoma. A Southwest Oncology Group study.氨莫司汀治疗播散性恶性黑色素瘤的评估。一项西南肿瘤协作组的研究。
Invest New Drugs. 1993 May-Aug;11(2-3):223-6. doi: 10.1007/BF00874160.
2
Synthesis and mode(s) of action of a new series of imide derivatives of 3-nitro-1,8 naphthalic acid.一系列新型3-硝基-1,8-萘二甲酸酰亚胺衍生物的合成及其作用方式
Cancer Chemother Pharmacol. 1980;4(1):61-6. doi: 10.1007/BF00255461.
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Phase I clinical investigation of benzisoquinolinedione.苯并异喹啉二酮的I期临床研究。
Cancer Treat Rep. 1987 Dec;71(12):1165-9.
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In vitro toxicity and DNA cleaving capacity of benzisoquinolinedione (nafidimide; NSC 308847) in human leukemia.
Cancer Res. 1987 Feb 15;47(4):1040-4.
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Pharmacokinetics and metabolism of the antitumor drug amonafide (NSC-308847) in humans.抗肿瘤药物氨萘非特(NSC-308847)在人体内的药代动力学与代谢
Drug Metab Dispos. 1987 Nov-Dec;15(6):773-8.
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Phase I clinical investigation of amonafide.氨萘非特的I期临床研究
J Clin Oncol. 1989 Sep;7(9):1351-8. doi: 10.1200/JCO.1989.7.9.1351.
7
Phase II study of amonafide: results of treatment and lessons learned from the study of an investigational agent in previously untreated patients with extensive small-cell lung cancer.氨萘非特的II期研究:在既往未经治疗的广泛期小细胞肺癌患者中使用一种研究性药物的治疗结果及经验教训
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Paradoxical relationship between acetylator phenotype and amonafide toxicity.乙酰化代谢表型与氨萘非特毒性之间的矛盾关系。
Clin Pharmacol Ther. 1991 Nov;50(5 Pt 1):573-9. doi: 10.1038/clpt.1991.183.
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Phase II trial of amonafide in patients with stage III and IV non-small-cell lung cancer.氨萘非特用于III期和IV期非小细胞肺癌患者的II期试验。
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