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伊达比星用于广泛期非小细胞肺癌的II期研究。

Phase II study of idarubicin in extensive-disease non-small-cell lung cancer.

作者信息

Umsawasdi T, Holoye P Y, Jeffries D, Carr D T

机构信息

Department of Medical Oncology, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030.

出版信息

Am J Clin Oncol. 1989 Dec;12(6):519-20. doi: 10.1097/00000421-198912000-00012.

Abstract

Fourteen patients with extensive-disease non-small-cell lung cancer (E-NSCLC) were treated with oral 4-demethoxydaunorubicin (idarubicin, 4DMDR) at a dosage of 10 mg/m2/day x 5 days every 3 weeks. The median cumulative dose was 110 mg/m2 (range: 50-1,100). Two patients had stable disease for 12 and 56 weeks, respectively, one patient had failed to respond to a doxorubicin hydrochloride (Adriamycin)-containing regimen, and one had had no prior therapy. Twelve of the 14 patients had prior radiotherapy, chemotherapy, or both. Median survival for this heavily treated group was 16 weeks. Myelosuppression was minimal. Nausea and vomiting occurred in 44% of all courses. No cardiac toxicity and no decrease in cardiac ejection fraction was observed. We conclude that 4DMDR is ineffective in heavily treated E-NSCLC patients. However, the drug's activity in untreated patients is unknown. Further study of 4DMDR is indicated in patients who have had no prior chemotherapy or radiotherapy, with routine administration of antiemetic drugs along with pharmacokinetic studies.

摘要

14例广泛期非小细胞肺癌(E-NSCLC)患者接受口服4-去甲氧柔红霉素(伊达比星,4DMDR)治疗,剂量为10mg/m²/天,连用5天,每3周重复一次。中位累积剂量为110mg/m²(范围:50-1100)。2例患者分别病情稳定12周和56周,1例患者对含盐酸多柔比星(阿霉素)的方案无反应,1例患者未曾接受过治疗。14例患者中有12例曾接受过放疗、化疗或两者皆有。该接受过大量治疗的组的中位生存期为16周。骨髓抑制轻微。44%的疗程出现恶心和呕吐。未观察到心脏毒性,心脏射血分数也未降低。我们得出结论,4DMDR对接受过大量治疗的E-NSCLC患者无效。然而,该药物在未治疗患者中的活性尚不清楚。对于未曾接受过化疗或放疗的患者,应进一步研究4DMDR,并常规给予止吐药物及进行药代动力学研究。

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