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临床试验/CTRI/2023/03/051025
CTRI/2023/03/051025尚未招募2 期

Somatostatin receptor (SSTR) imaging with 68Ga-DOTATATE PET/CT and its comparison with 18F-FDG PET/CT in patients with estrogen receptor positive (ER positive) metastatic breast cancer (mBC)

All India Institute of Medical Sciences, New Delhi1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年4月15日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
68Ga-DOTATATE PET/CT imaging

研究概览

简要总结

Breast cancer is the most commonly diagnosed malignancy worldwide and is the leading cause of cancer-related mortality in women. Hormone receptor status is an important biomarker in breast cancer influencing management strategy. Majority (~70-75%) of breast cancers are reported to be ER+. The mortality of breast cancer correlates with disease extent. The presence of distant metastases is associated with poor survival outcomes. The median five-year survival rate in ER+ mBC is less than 30%, suggesting the need for newer diagnostic and therapeutic techniques to improve patient outcomes in this population.

Identification of specific tumor-associated antigens and receptors has led to a paradigm shift in the fields of molecular imaging and targeted cancer therapy. Immunohistochemistry studies have reported SSTR expression in breast cancer tissue samples with higher rates of expression in ER+ breast cancer. There is a dearth of published literature evaluating the role of SSTR-targeted PET imaging in ER+ breast cancer patients. This phase II trial will determine if SSTR-targeted imaging with 68Ga-DOTATATE PET/CT can visualize malignancy in patients with ER+ mBC. The results of this study will also guide the feasibility of SSTR-targeted radionuclide therapy in progressive ER+ mBC patients having limited therapeutic options.

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Open Label

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • Biopsy proven estrogen receptor positive metastatic breast cancer
  • Patients who have undergone 18F-FDG PET/CT for staging/re-staging within the last 3 weeks
  • At least one site of known active disease on imaging within 3 months
  • If a woman is of childbearing potential, a negative urine pregnancy test before administration of SSTR-targeted PET radiotracer would be mandatory.

排除标准

  • Pregnant and lactating females
  • Patients who refuse to give written informed consent
  • Unable to give informed consent or withdrawal of consent any point of time
  • Recent anti-cancer chemotherapy/surgery in less than four weeks or radiotherapy in less than eight weeks
  • Use of long-acting SSTR-targeting agents (example: lanreotide) within 28 days of SSTR-targeted imaging
  • Use of short-acting SSTR-targeting agents (example: sandostatin) within 24 hours of SSTR-targeted imaging
  • Concurrent primary malignancy other than known metastatic breast cancer, except adequately treated carcinoma in situ, non-melanoma carcinoma of the skin or any other curatively treated malignancy that has achieved complete response and is not expected to require treatment for recurrence during participation in the study
  • Subjects with allergy/hypersensitivity to SSTR-targeted imaging agents
  • Current use of high-dose glucocorticoids (≥ 20 mg prednisone per day or equivalent) 10.

结局指标

主要结局

68Ga-DOTATATE PET/CT imaging

时间窗: 45 minutes to 1 hour from time of injection

(Assessment of 68Ga-DOTATATE PET/CT imaging to detect lesions in patients with estrogen receptor positive metastatic breast cancer)

时间窗: 45 minutes to 1 hour from time of injection

次要结局

未报告次要终点

研究者

发起方
All India Institute of Medical Sciences, New Delhi
申办方类型
Research institution and hospital

研究点 (1)

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