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临床试验/NCT04559308
NCT04559308
Unknown
2 期

The Effect of Metformin on Breast Cancer Patients

Beni-Suef University1 个研究点 分布在 1 个国家目标入组 80 人2019年6月1日

概览

阶段
2 期
干预措施
Metformin
疾病 / 适应症
Breast Cancer
发起方
Beni-Suef University
入组人数
80
试验地点
1
主要终点
Clinical benefit rate (Tumor size)
最后更新
5年前

概览

简要总结

Several clinical trials have addressed the promising anticancer effect of metformin on the survival benefits, clinical response, and pathological response of breast cancer patients.

Therefore, this study will assess the anticancer effect of metformin when added to the neoadjuvant chemotherapy protocol of non-diabetic breast cancer patients. In addition to, the impact of metformin addition to the neoadjuvant chemotherapy on the quality of life of breast cancer patients.

详细描述

This study is conducted to assess the effect of metformin addition to the chemotherapy protocol of non-diabetic breast cancer patients compared to the control group (non-metformin users) in the neoadjuvant setting. Evaluation of the the clinical benefit rate and the rate of pathological complete response will be conducted. In addition, a correlation between the beneficial effect of metformin and the serum concentration of metformin. Also, a comparison in the quality of life between the metformin group and the control group will be evaluated using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ C30) and (EORTC QLQ BR45) questionnaires will be done.

注册库
clinicaltrials.gov
开始日期
2019年6月1日
结束日期
2020年10月
最后更新
5年前
研究类型
Interventional
研究设计
Parallel
性别
Female

研究者

责任方
Principal Investigator
主要研究者

Hadeer Mohamed Ehab

Clinical Pharmacy Researcher

Beni-Suef University

入排标准

入选标准

  • Non-diabetic breast cancer patients, receiving neoadjuvant chemotherapy treatment.
  • Female Age between 18- 65 years.
  • Written informed consent.

排除标准

  • Known hypersensitivity reaction to Metformin.
  • Intolerable Metformin GI complaints.
  • Patients at risk of lactic acidosis.
  • Diabetic breast cancer patients.
  • Body Mass Index \< 18.5 (underweight breast cancer patients).
  • Renal impairment, eGFR \<45 mL/min/1.73 m².

研究组 & 干预措施

metformin arm

4 cycles (Doxorubicin+Cyclophosphamide) followed by 12 cycles Paclitaxel+ Metformin (1000 mg twice daily) followed by surgery.

干预措施: Metformin

metformin arm

4 cycles (Doxorubicin+Cyclophosphamide) followed by 12 cycles Paclitaxel+ Metformin (1000 mg twice daily) followed by surgery.

干预措施: Chemotherapy

control arm

4 cycles (Doxorubicin+Cyclophosphamide) followed by 12 cycles Paclitaxel followed by surgery.

干预措施: Chemotherapy

结局指标

主要结局

Clinical benefit rate (Tumor size)

时间窗: 8 months

Tumor size measured in calipers from baseline till the last cycle of neoadjuvant chemotherapy.

次要结局

  • Pathological complete response(8 months)
  • Number of participants with metformin-related adverse events(8 months)
  • The effect of metformin on the quality of life of breast cancer patients(8 months)

研究点 (1)

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