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临床试验/NCT06635096
NCT06635096尚未招募不适用

A Prospective, Single-center, Single-arm Phase II Clinical Trial to Evaluate the Safety and Efficacy of Multimodal Thermal Therapy in the Treatment of Early-stage Invasive Breast Cancer

Fudan University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月8日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Complete ablation rate

研究概览

简要总结

Multimodal thermal therapy (MTT), as an initiative integration of cryotherapy and radiofrequency heating, has been applied to treat various solid tumors. However, the feasibility and safety for MTT in the treatment of breast cancer is unknown. This prospective, open-label, single-arm phase II clinical study aimed to evaluate the efficacy and safety of MTT in the treatment of early-stage invasive breast cancer, and to explore the ablation-induced immune activating response.

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 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female,age 18-80 years.
  • Invasive carcinoma confirmed by core biopsy.
  • Newly diagnosed breast cancer patients, without neoadjuvant therapy.
  • Imaging findings showed an unifocal breast tumor with a maximum diameter of 2 cm, with no distant metastasis, no calcification, no skin or nipple adhesion, and no invasion of chest wall.
  • The functional level of major organs must meet the following requirements: blood routine: neutrophil (ANC)≥1.5×10^9/L; platelet count (PLT) ≥ (PLT)≥90×10^9/L; hemoglobin (Hb) ≥90g/L; coagulation: international normalized ratio (INR) or prothrombin time (PT) ≤1.5×ULN; activated partial thromboplastin time (APTT) ≤1.5×ULN.

排除标准

  • Tumor involving skin, ulceration, inflammatory breast cancer patients.
  • Tumor involving the superficial layer of the skin.
  • KPS score < 70, or ECOG score > 2
  • Prior radiotherapy or prior use of investigational drugs or other immunosuppressive agents.
  • Heart, brain, lung, kidney and other vital organ failure.
  • Uncorrectable severe coagulopathy
  • Patient is pregnant or lactating
  • Poor glycemic control in diabetes
  • Patients with foreign body implantation around the tumor (such as breast augmentation injections or prostheses).
  • Patients with severe scars on the skin of the treatment area (protruding from the skin surface, width ≥ 1 cm)
  • Human immunodeficiency virus (HIV) infection, active hepatitis B (hepatitis B indicates antigen positive and HBV DNA ≥ 500 IU/ml), hepatitis C (hepatitis C antibody positive and HCV-RNA above the lower limit of detection of the analytical method).
  • Concurrent medical conditions that, in the judgment of the investigator, would jeopardize the subject's safety, could confound the study results, or affect the subject's completion of this study.

结局指标

主要结局

Complete ablation rate

时间窗: 3 months

The complete ablation rate was confirmed by core needle biopsy 3 months after multimodal thermal therapy. Complete ablation was defined as: tissue section at the ablation margin that was negative by histochemical staining.

次要结局

  • Safety of Multimodal Tumor Thermal Therapy(In 1 year)
  • Breast MRI confirmed complete ablation.(In 6 months)
  • Breast self evaluation(In 1 year)
  • Assessment of immune activating response(In 1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhimin Shao

Director of General Surgery of Fudan Shanghai Cancer Center

Fudan University

研究点 (1)

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