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临床试验/NCT07314255
NCT07314255进行中(未招募)不适用

The Role of Trop2 in Radioactive Iodine-131 Therapy Sensitivity in Papillary Thyroid Carcinoma

Jiangxi Provincial Cancer Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年12月18日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
60
试验地点
1
主要终点
Tumor size;

研究概览

简要总结

Clinincal data and pathological specimens from patients who had undergone at least one radioactive iodine-131 (^131I) therapy in the Department of Nuclear Medicine at Jiangxi Cancer Hospital over the past 8-10 years were retrospectively collected (approximately 30-50 cases each in the ^131I treatment-responsive group vs. the ^131I treatment-resistant group). Patients in the ^131I treatment-resistant group underwent ^18F-Trop2 PET-CT imaging.

Inclusion criteria:

  1. History of total thyroidectomy with postoperative pathology confirming papillary thyroid carcinoma (PTC);
  2. At least one course of ^131I internal radiotherapy.

Exclusion criteria:

  1. Presence of other severe comorbidities;
  2. Incomplete clinical or follow-up data. The clinicopathological characteristics and Trop2 expression levels in tissue samples were compared between the ^131I treatment-responsive group and the ^131I treatment-resistant group.

Within the ^131I treatment-resistant group, comparisons were made between the rapidly progressing subgroup and the stable-disease subgroup under TSH-suppressive therapy in terms of clinicopathological features, tissue Trop2 expression levels, and SUVmax of metastatic lesions on ^18F-Trop2 PET-CT imaging. Factors influencing progression-free survival and overall survival in ^131I-resistant patients were analyzed.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ( 1) History of total thyroidectomy with postoperative pathology confirming papillary thyroid carcinoma (PTC); (2) At least one course of ^131I internal radiotherapy.

排除标准

  • (1) Presence of other severe comorbidities; (2) Incomplete clinical or follow-up data.

结局指标

主要结局

Tumor size;

时间窗: 6-60 months

Lesion size was determined using CT imaging. Lymph nodes were assessed based on their shortest diameter, while other target lesions were evaluated based on their longest diameter. Each measurable lesion underwent an average measurement derived from a minimum of three readings, with all measurements conducted by the same individual to minimize measurement discrepancies. Response Evaluation Criteria in Solid Tumors (RECIST 1.1) were used to assess treatment response

次要结局

  • Serological assessment(1-60months)

研究者

发起方
Jiangxi Provincial Cancer Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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