跳至主要内容
临床试验/NCT06725940
NCT06725940招募中不适用

Clinical Study on the Evaluation of Neoadjuvant Therapy Efficacy in Breast Cancer Using PET/CT With Granzyme B Imaging Probe

Shanghai Jiao Tong University School of Medicine1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
1
主要终点
Optimal SUVmax threshold of 68Ga-GZMB PET/CT for predicting pCR

研究概览

简要总结

To explore the efficacy of 68Ga-GZMB PET/CT in assessing the response to neoadjuvant therapy for breast cancer, and to investigate the optimal SUVmax threshold of 68Ga-GZMB PET/CT for predicting pathological complete response (pCR), aiming to provide a new and effective means for accurately and non-invasively evaluating the efficacy of neoadjuvant therapy.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 16-65
  • histologically confirmed unilateral primary invasive breast cancer
  • Tumor size≥2cm, axillary lymph node positive, treated with neoadjuvant therapy
  • complete clinical and histo-pathological information
  • ECOG 0-1 within 10 days from the beginning of the study
  • Normal Bone Marrow Reserve: White blood cell count ≥ 3.0×10^9/L, Neutrophil count ≥ 1.5×10^9/L, Hemoglobin level ≥ 90g/L; Platelet count (PLT) ≥ 80×10^9/L; Normal Liver and Kidney Function: Blood aspartate aminotransferase (AST) ≤ 2.5 times the upper limit of normal, Total bilirubin ≤ 1.5 times the upper limit of normal, Serum creatinine ≤ 1.5 times the upper limit of normal, and Creatinine clearance rate > 50ml/min.
  • The patient has good compliance with the planned treatment, understands the research procedures, and has signed a written informed consent form

排除标准

  • bilateral or metastatic (stage IV) breast cancer
  • There has been a history of other malignancies within the past 5 years, except for cured cervical carcinoma in situ and non-melanoma skin cancer
  • Severe systemic infection or other uncontrolled diseases
  • Patients with psychiatric disorders or those unable to comply with treatment due to other reasons
  • Known allergy or intolerance to the drug or its excipients
  • Having received cytotoxic chemotherapy, endocrine therapy, biological therapy, or radiotherapy for any reason in the past
  • Patients who are pregnant or lactating, as well as patients of reproductive age who refuse to take appropriate contraceptive measures during the course of this trial.
  • Patients deemed unsuitable for participation in this study by the investigator.

结局指标

主要结局

Optimal SUVmax threshold of 68Ga-GZMB PET/CT for predicting pCR

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

Optimal SUVmax threshold of 68Ga-GZMB PET/CT for predicting pathological complete response after neoadjuvant therapy in breast cancer

次要结局

  • Sensitivity and specificity of 68Ga-GZMB PET/CT for pCR(through study completion, an average of 1 year)
  • Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 after 68Ga-GZMB PET/CT(through study completion, an average of 1 year)
  • Correlation between the efficacy of 68Ga-GZMB PET/CT in predicting pathological complete response and tumor-infiltrating lymphocytes(through study completion, an average of 1 year)

研究者

发起方
Shanghai Jiao Tong University School of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kunwei Shen

Professor

Shanghai Jiao Tong University School of Medicine

研究点 (1)

Loading locations...

相似试验