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临床试验/JPRN-UMIN000018178
JPRN-UMIN000018178已完成未知

Prospective observational Study to explore the efficacy of Eribulin as 1st-line or 2nd-line chemotherapy in patients with HER2-negative hormone-resistant inoperable or recurrent metastatic breast cancer - E-SPEC

Kyoto Breast Cancer Research Network (KBCRN)0 个研究点目标入组 180 人开始时间: 2015年7月6日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
180

研究概览

简要总结

Among 201 patients enrolled, 180 were included in the final analysis. Eribulin was administered as first- and second-line chemotherapy to 46 (26.6%) and 70 (47.9%) patients, respectively. Median OS1 and OS2 were 2.25 (95% CI 1.07-2.68) and 1.75 (95% CI, 1.28-2.45) years for first- and second-line eribulin, respectively. Oral 5-FU followed by eribulin had a numerically longer OS1 (2.84 years) than the other sequences.

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 75years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1) Patients with symptomatic metastasis in the central nervous system. 2) Patients with a previous history of hypersensitivity to any component of drugs administered in the treatment. 3) Patients considered inappropriate for the study participation judged by the primary physician.

研究者

发起方
Kyoto Breast Cancer Research Network (KBCRN)

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