STUDIES IN THYROID DISEASE
甲状腺疾病研究
基本信息
- 批准号:3876402
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:cancer risk combination cancer therapy dosage doxorubicin drug adverse effect endocrine disorder chemotherapy hormone inhibitor human subject human therapy evaluation hypothyroidism iodine lithium mood disorders neoplasm /cancer chemotherapy neoplasm /cancer radionuclide diagnosis neoplasm /cancer radionuclide therapy radiation dosage radionuclide imaging /scanning radiosensitizer radiotracer thyroid disorder thyroid neoplasm thyroxine tissue /cell culture triiodothyronine
项目摘要
Two forms of adjuvant therapy designed to improve the effectiveness of
I-131 radiation in thyroid cancer are under study. The first is lithium
ion, which is used to prolong the retention of I-131 in the cancer.
Preliminary findings have been described in previous annual reports. The
second is the use of doxorubicin (adriamycin) as a radiosensitizing agent.
To evaluate its effectiveness, we have begun a randomized study of
high-risk thyroid cancer patients who receive standard I-131 therapy with
or without the administration of low-dose adriamycin (10mg/square m) 30 min
preceding each I-131 treatment dose. To our knowledge, this is the first
attempt to randomize patients in a therapy protocol for thyroid cancer
employing I-131.
Other patients with negative I-131 whole body scans but elevated
concentration of thyroglobulin in blood are given I-131 therapy in an
attempt to localize the cancer by post-therapy scanning. Most patients have
been found to have positive post-therapy scans and they are under
evaluation for possible beneficial effects of the therapy.
两种形式的辅助治疗,旨在提高有效性,
甲状腺癌的I-131辐射正在研究中。首先是锂
离子,其用于延长I-131在癌症中的保留。
初步调查结果已在以往的年度报告中作了说明。的
第二种是使用阿霉素(阿霉素)作为放射增敏剂。
为了评估其有效性,我们已经开始了一项随机研究,
接受标准I-131治疗的高危甲状腺癌患者,
或不给予小剂量阿霉素(10 mg/m2)30 min
在每次I-131治疗剂量之前。据我们所知,这是第一个
尝试在甲状腺癌治疗方案中随机分配患者
使用I-131。
其他I-131全身扫描阴性但升高的患者
血液中的甲状腺球蛋白浓度给予I-131治疗,
试图通过治疗后扫描定位癌症。大多数患者有
被发现有积极的治疗后扫描,他们是根据
评估治疗的可能有益效果。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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