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E5501 研究:拓扑替康序贯依托泊苷/顺铂,伊立替康序贯依托泊苷/顺铂治疗广泛期小细胞肺癌的 II 期研究。

E5501: phase II study of topotecan sequenced with etoposide/cisplatin, and irinotecan/cisplatin sequenced with etoposide for extensive-stage small-cell lung cancer.

机构信息

Emory University, Atlanta, GA, USA.

出版信息

Cancer Chemother Pharmacol. 2014 Jan;73(1):171-80. doi: 10.1007/s00280-013-2338-z. Epub 2013 Nov 28.

Abstract

PURPOSE

Sequence-dependent improved efficacy of topoisomerase I followed by topoisomerase 2 inhibitors was assessed in a randomized phase II study in extensive-stage small-cell lung cancer (SCLC).

METHODS

Patients with previously untreated extensive-stage SCLC with measurable disease, ECOG performance status of 0-3 and stable brain metastases were eligible. Arm A consisted of topotecan (0.75 mg/m(2)) on days 1, 2 and 3, etoposide (70 mg/m(2)) and cisplatin (20 mg/m(2)) (PET) on days 8, 9 and 10 in a 3-week cycle. Arm B consisted of irinotecan (50 mg/m(2)) and cisplatin (20 mg/m(2)) on days 1 and 8 followed by etoposide (85 mg/m(2) PO bid) on days 3 and 10 (PIE) in a 3-week cycle.

RESULTS

We enrolled 140 patients and randomized 66 eligible patients to each arm. Only 54.5 % of all patients completed the planned maximum 6 cycles. There were grade ≥3 treatment-related adverse events in approximately 70 % of the patients on both arms including 6 treatment-related grade 5 events. The overall response rates (CR + PR) were 69.7 % (90 % CI 59.1-78.9, 95 % CI 57.1-80.4 %) for arm A and 57.6 % (90 % CI 46.7-67.9, 95 % CI 44.8-69.7 %) for arm B. The median progression-free survival and overall survival were 6.4 months (95 % CI 5.4-7.5 months) and 11.9 months (95 % CI 9.6-13.7 months) for arm A and 6.0 months (95 % CI 5.4-7.0 months) and 11.0 months (95 % CI 8.6-13.1 months) for arm B.

CONCLUSION

Sequential administration of topoisomerase inhibitors did not improve on the historical efficacy of standard platinum-doublet chemotherapy for extensive-stage SCLC.

摘要

目的

在一项广泛期小细胞肺癌(SCLC)的随机 II 期研究中,评估拓扑异构酶 I 与拓扑异构酶 2 抑制剂的序列依赖性疗效改善。

方法

符合条件的患者为未经治疗的广泛期 SCLC,有可测量的疾病,ECOG 表现状态为 0-3 级,且稳定的脑转移。A 组包括拓扑替康(0.75mg/m2),第 1、2 和 3 天;依托泊苷(70mg/m2)和顺铂(20mg/m2)(PET),第 8、9 和 10 天,每 3 周一个周期。B 组包括伊立替康(50mg/m2)和顺铂(20mg/m2),第 1 和 8 天;依托泊苷(85mg/m2 PO bid),第 3 和 10 天(PIE),每 3 周一个周期。

结果

我们共纳入 140 例患者,随机分为两组,每组 66 例。仅有 54.5%的所有患者完成了计划的最大 6 个周期。两组患者均有约 70%出现≥3 级与治疗相关的不良事件,包括 6 例与治疗相关的 5 级事件。A 组的总缓解率(CR+PR)为 69.7%(90%CI 59.1-78.9,95%CI 57.1-80.4%),B 组为 57.6%(90%CI 46.7-67.9,95%CI 44.8-69.7%)。A 组的中位无进展生存期和总生存期分别为 6.4 个月(95%CI 5.4-7.5 个月)和 11.9 个月(95%CI 9.6-13.7 个月),B 组分别为 6.0 个月(95%CI 5.4-7.0 个月)和 11.0 个月(95%CI 8.6-13.1 个月)。

结论

与标准铂类双药化疗相比,拓扑异构酶抑制剂的序贯给药并不能提高广泛期 SCLC 的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/467d/4705842/fa777217c21f/nihms545348f1.jpg

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