跳至主要内容
临床试验/NCT01281137
NCT01281137已完成不适用

SOLE Estrogen Substudy (SOLE-EST) - Investigating Changes in Estrogen Levels and Grip Strength for Patients Participating in the SOLE Trial

ETOP IBCSG Partners Foundation2 个研究点 分布在 2 个国家目标入组 104 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
104
试验地点
2
主要终点
Levels of Estrone (E1), Estradiol (E2), and Estrone Sulphate (E1S) Among Patients in the Longitudinal Analysis Population

研究概览

简要总结

RATIONALE: Studying samples of blood in the laboratory from patients receiving treatment for cancer may help doctors learn more about changes that may occur in DNA and identify biomarkers related to cancer.

PURPOSE: This clinical trial is studying changes in estrogen levels and grip strength in postmenopausal women who have received 4 to 6 years of hormone therapy for breast cancer and are currently receiving letrozole on clinical trial IBCSG-35-07.

详细描述

OBJECTIVES:

Primary

  • To determine the serum level of estrogens (Estradiol [E2], Estrone [E1], and Estrone Sulphate [E1S] and sex hormone binding globulin [SHBG]) in postmenopausal women with prior endocrine-responsive, node-positive, resectable breast cancer completing 4 to 6 years of adjuvant endocrine therapy and enrolled on clinical trial IBCSG-35-07 receiving letrozole.
  • To determine the degree of recovery of E2, E1, and E1S during the 3-month letrozole-off gap.

Secondary

  • To determine the association between estrogen level changes and the clinical outcomes of toxicity and quality of life.
  • To determine the effect of prior adjuvant endocrine therapy, age, body mass index, and type of menopause on estrogen levels.
  • To determine the variability of estrogen level changes and its association with germline single nucleotide polymorphisms.
  • To examine changes in grip-strength score.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Levels of Estrone (E1), Estradiol (E2), and Estrone Sulphate (E1S) Among Patients in the Longitudinal Analysis Population

时间窗: 0 (baseline), 9, 10.5, and 12 months from randomization

In SOLE-EST, levels of E1, E2, and E1S were summarized over time at 0 (baseline), 9, 10.5, and 12 months from randomization among patients in the longitudinal analysis population (N=90 with post-baseline sample).

Percent Change of E1, E2, and E1S Levels at 9, 10.5, and 12 Months From Baseline, by Treatment Group

时间窗: 9, 10.5, and 12 months from baseline

Changes in hormone levels (E1, E2, and E1S levels), as percentage change over time according to treatment assignment (at 9, 10.5 and 12 months from baseline).

次要结局

  • Toxicity Grade Changes for Arthralgia, Hot Flushes, and Insomnia(6 and 12 months)
  • Quality of Life (QoL) Score Changes(6 and 12 months: Change is calculated from 12 months minus 6 months, therefore positive values indicate an improved condition and negative values indicate a declined condition)
  • Change in Grip-strength Score in the Dominant Hand(Changes in grip strength score is calculated at 12 months minus 9 months)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验