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拓扑替康和依托泊苷用于非霍奇金淋巴瘤的评估:拓扑异构酶-DNA复合物形成与临床反应的相关性

Evaluation of topotecan and etoposide for non-Hodgkin lymphoma: correlation of topoisomerase-DNA complex formation with clinical response.

作者信息

Kancherla R R, Nair J S, Ahmed T, Durrani H, Seiter K, Mannancheril A, Tse-Dinh Y C

机构信息

Zalmen A. Arlin Cancer Institute, Division of Oncology/Hematology, Department of Medicine, Rm 250 Munger Pavilion, New York Medical College, Valhalla, NY 10595, USA.

出版信息

Cancer. 2001 Feb 1;91(3):463-71. doi: 10.1002/1097-0142(20010201)91:3<463::aid-cncr1023>3.0.co;2-r.

Abstract

BACKGROUND

Topotecan, a topoisomerase I inhibitor, acts by stabilizing the topoisomerase DNA cleavage complex. Etoposide, a topoisomerase II inhibitor, mediates antitumor activity by stabilizing cleavage complex formed between topoisomerase II and DNA. These two agents have therapeutic activity in non-Hodgkin lymphoma. The authors report Phase I data of topotecan and etoposide combination for patients with recurrent or refractory non-Hodgkin lymphoma and correlation of topoisomerase-DNA complex formation to clinical response.

METHODS

Twenty-two patients with recurrent or refractory aggressive non-Hodgkin lymphoma were treated at four dose levels of topotecan (1 mg/m(2)/day to 2.5 mg/m(2)/day). Topotecan was given at a 30-minute infusion daily with etoposide 150 mg/m(2)/day, both for 5 days. Topoisomerase-DNA covalent complex formation was measured using in vivo link assay, whereas topoisomerase I, IIalpha, and IIbeta in RNA expression levels were determined by reverse transcription-polymerase chain reaction in blood samples. The relation of these levels to clinical response was studied.

RESULTS

The maximum tolerated dose of topotecan was 2.0 mg/m(2)/day for 5 days. Oropharyngeal mucositis was dose-limiting. Of 21 examinable patients, 3 patients achieved complete remission, and 5 patients achieved partial remission. Of six untreated patients who experienced a recurrence, three had complete remission, and the other three had partial remission. Drug-induced topoisomerase-DNA complex formation was observed throughout the treatment in blood samples of all the patients who responded. However, only 4 of 13 patients, who did not respond, formed covalent complex at all time points. This was statistically significant (P = 0.024). In all patients, expression levels of topoisomerase I and IIbeta mRNA remained similar to pretreatment levels, whereas topoisomerase IIalpha mRNA levels decreased dramatically by the third day.

CONCLUSION

The recommended Phase II dose of topotecan with etoposide of 150 mg/m(2)/day for 5 days was 2.0 mg/m(2)/day for 5 days. Topoisomerase-DNA complex formation correlated with response to treatment.

摘要

背景

拓扑替康是一种拓扑异构酶I抑制剂,通过稳定拓扑异构酶-DNA裂解复合物发挥作用。依托泊苷是一种拓扑异构酶II抑制剂,通过稳定拓扑异构酶II与DNA之间形成的裂解复合物介导抗肿瘤活性。这两种药物在非霍奇金淋巴瘤中具有治疗活性。作者报告了拓扑替康与依托泊苷联合治疗复发或难治性非霍奇金淋巴瘤患者的I期数据,以及拓扑异构酶-DNA复合物形成与临床反应的相关性。

方法

22例复发或难治性侵袭性非霍奇金淋巴瘤患者接受了四个剂量水平的拓扑替康治疗(1mg/m²/天至2.5mg/m²/天)。拓扑替康每天静脉输注30分钟,同时给予依托泊苷150mg/m²/天,均持续5天。使用体内连接试验测量拓扑异构酶-DNA共价复合物的形成,而通过逆转录-聚合酶链反应测定血样中拓扑异构酶I、IIα和IIβ的RNA表达水平。研究了这些水平与临床反应的关系。

结果

拓扑替康的最大耐受剂量为2.0mg/m²/天,持续5天。口腔黏膜炎是剂量限制性毒性。在21例可评估患者中,3例患者达到完全缓解,5例患者达到部分缓解。在6例复发后未接受治疗的患者中,3例达到完全缓解,另外3例达到部分缓解。在所有有反应的患者的血样中,在整个治疗过程中均观察到药物诱导的拓扑异构酶-DNA复合物形成。然而,在13例无反应的患者中,只有4例在所有时间点均形成共价复合物。这具有统计学意义(P = 0.024)。在所有患者中,拓扑异构酶I和IIβ mRNA的表达水平与治疗前水平相似,而拓扑异构酶IIα mRNA水平在第三天显著下降。

结论

拓扑替康与150mg/m²/天的依托泊苷联合使用5天的推荐II期剂量为2.0mg/m²/天,持续5天。拓扑异构酶-DNA复合物的形成与治疗反应相关。

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