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临床试验/NCT03833466
NCT03833466Unknown2 期

Metformin in Combined With Cisplatin Plus Paclitaxel as Neoadjuvant Therapy With Advanced Esophageal Squamous Cell Carcinoma (ESCC)

Peking University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2019年2月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
15
试验地点
1
主要终点
Tumor metabolic pathway

研究概览

简要总结

This is an open-label phase II trial investigating the effect of metformin in combined with cisplatin plus paclitaxel as neoadjuvant therapy with advanced esophageal squamous cell carcinoma.

详细描述

In this prospective phase II study, eligible patients are received cisplatin plus paclitaxel for 2-4 cycles combined with metformin orally. The investigators aim to compare the tumor metabolic pathway and tumor microenvironment of pre-chemotherapy endoscopic biopsy samples and post-chemotherapy surgical resection samples.

研究设计

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

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Having signed informed consent.
  • Age 18 to 70 years old
  • Histologically confirmed esophageal squamous carcinoma
  • Computed tomography (CT) or magnetic resonance imaging (MRI) confirmed advanced ESCC which need neoadjuvant chemotherapy before surgical resection.
  • Measurable disease according to the Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 criteria(diameter of the lesion should be more than 10mm by spiral CT or MRI, more than 20mm by common CT, the date of image should be less than 21 days before enrollment)
  • Life expectancy of ≥3 month
  • Eastern Cooperative Oncology Group (ECOG) 0-1
  • Body Mass Index (BMI) ≥18.5kg/m2
  • WBC>3,000/mm3, absolute neutrophil count ≥1500/mm3, platelet>100,000/mm3, Hb>9g/dl,Bilirubin level < 1.5 times ULN,Serum creatinine <1.5 times ULN,ALT and AST<2.5 times ULN ,AKP < 2.5 times ULN ,(≤5 times ULN in patients with liver metastases)(within 7 days before enrollment)
  • No sever complication, such as active gastrointestinal bleeding, perforation, jaundice, obstruction, non-cancerous fever>38℃.
  • Good compliance

排除标准

  • Have used metformin or biguanide in the past
  • Contraindications of metformin
  • Unable to take metformin orally because of esophageal stenosis
  • Currently receiving other effective regimens
  • Previous anticipate other clinical trial within 4 weeks before entering this study
  • No measurable lesions, eg. pleural fluid and ascites\
  • Only with other previous malignancy within 5 year, except non-melanoma skin cancer and cervical carcinoma in situ
  • Heart failure or other sever organ dysfunction, eg. coronary artery disease, myocardial infarction within the last 6 months only Brain or bone metastasis
  • Mentally abnormal or disable cognition,including central nervous system (CNS) metastasis
  • HIV infection, active hepatitis B or hepatitis C
  • Unstable systemic diseases such as poorly controlled diabetes
  • Interstitial lung disease, such as interstitial pneumonia, pulmonary fibrosis, or evidence of interstitial lung disease showed in X-ray/CT
  • Known hypersensitivity to study drugs
  • Pregnancy or lactation period

研究组 & 干预措施

metformin and chemotherapy

Experimental

干预措施: metformin and chemotherapy (Drug)

结局指标

主要结局

Tumor metabolic pathway

时间窗: Through study completion, an average of 1 year

To compare the changes of tumor metabolic pathway of pre-chemotherapy endoscopic biopsy samples and post-chemotherapy surgical resection samples

Tumor microenvironment

时间窗: Through study completion, an average of 1 year

To compare the changes of tumor microenvironment of pre-chemotherapy endoscopic biopsy samples and post-chemotherapy surgical resection samples

次要结局

  • Rate of pathologic complete response(pCR)(Through study completion, an average of 1 year)

研究者

发起方
Peking University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Shen Lin

Clinical Professor

Peking University

研究点 (1)

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