跳至主要内容
临床试验/NCT00424203
NCT00424203已完成2 期

Multicenter Pilot Clinical Study of Adjuvant Chemotherapy for Subjects Over 70 Years: Impact on the Independence and Quality of Life of the Administration of Anthracycline-Based Chemotherapy in Adjuvant Setting for Patients Presenting With Immediately Operable Breast Cancer, Hormone Receptor Negative (RH-), and Lymph Node Positive (pN+) or pN0 But of Scarff-Bloom-Richardson* Grade III and ≥ 2cm [GERICO]

UNICANCER17 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2006年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
UNICANCER
入组人数
40
试验地点
17
主要终点
Percentage of patients maintaining their independence as assessed by Activities of Daily Living (ADL) score on 6 items after the fourth course of chemotherapy

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as doxorubicin and cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving combination chemotherapy after surgery may kill any tumor cells that remain after surgery.

PURPOSE: This phase II trial is studying how well giving doxorubicin together with cyclophosphamide works in treating older women with stage I , stage II, or stage III breast cancer that has been removed by surgery.

详细描述

OBJECTIVES:

Primary

  • Determine the independence of older women with resected stage I, II, or III breast cancer treated with adjuvant doxorubicin hydrochloride and cyclophosphamide.

Secondary

  • Determine the impact of this regimen on other aspects of the patient's life, utilizing the Comprehensive Geriatric Assessment, the Mini-Nutritional Assessment, the Folstein Mini-Mental State Exam, the Geriatric Depression Scale, and the Cumulative Illness Rating Scale-Geriatrics.
  • Determine the quality of life of patients treated with this regimen.
  • Determine the acceptability of this regimen in these patients.
  • Determine the toxicity of this regimen, in terms of cardiac issues and anemia, in these patients.
  • Determine recurrence-free survival, event-free survival, and overall survival of patients treated with this regimen.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
70 Years 至 —(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

研究组 & 干预措施

Myocet, Endoxan

Experimental

干预措施: cyclophosphamide (Drug)

Myocet, Endoxan

Experimental

干预措施: doxorubicin hydrochloride (Drug)

Myocet, Endoxan

Experimental

干预措施: AC regimen (Drug)

Myocet, Endoxan

Experimental

干预措施: adjuvant therapy (Procedure)

Myocet, Endoxan

Experimental

干预措施: cognitive assessment (Procedure)

Myocet, Endoxan

Experimental

干预措施: management of therapy complications (Procedure)

Myocet, Endoxan

Experimental

干预措施: psychosocial assessment and care (Procedure)

Myocet, Endoxan

Experimental

干预措施: quality-of-life assessment (Procedure)

结局指标

主要结局

Percentage of patients maintaining their independence as assessed by Activities of Daily Living (ADL) score on 6 items after the fourth course of chemotherapy

时间窗: 12 weeks

次要结局

  • Impact of adjuvant chemotherapy on ADL score, quality of life, treatment acceptability, toxicity, and survival (recurrence-free, progression-free, and overall survival)(3 years)

研究者

发起方
UNICANCER
申办方类型
Other
责任方
Sponsor

研究点 (17)

Loading locations...

相似试验

Doxorubicin and Cyclophosphamide in Treating Older... | 临床试验