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临床试验/NCT00586326
NCT00586326已完成2 期

MammoSite Radiation Therapy System (RTS) as the Sole Radiation Therapy Technique for Ductal Carcinoma In-Situ (DCIS)

Hologic, Inc.23 个研究点 分布在 1 个国家目标入组 133 人开始时间: 2003年8月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
Hologic, Inc.
入组人数
133
试验地点
23
主要终点
Local Control Rate for Follow-up Period of 5 Years.

研究概览

简要总结

This study has been designed to compile information on the efficacy of the MammoSite RTS providing sole radiation therapy for patients with pure DCIS.

详细描述

Data relevant to the evaluation of the efficacy and safety of the MammoSite RTS system in providing radiation therapy to patients with DCIS will be collected. The MammoSite is a radionuclide applicator designed to deliver internal radiation therapy (brachytherapy) in patients with breast tumors following breast tumor resection surgery (lumpectomy).

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
45 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Pre-Surgery:
  • Unicentric pure DCIS
  • Lesions should have a greatest dimension of 3 cm or less as determined by pre-surgery mammography and MRI
  • Post-Surgery:
  • Negative histological margins confirmed prior to beginning radiation therapy.
  • Margins are positive if there is tumor at the inked margin.
  • Classified as low (NG1), intermediate (NG2) or high (NG3) nuclear grade DCIS, using the Philadelphia Consensus Conference Guidelines are eligible
  • Clinically node negative

排除标准

  • Distance from the balloon surface to the surface of the skin < 5mm as determined by CT imaging.
  • Distant metastases.
  • Invasive or in-situ lobular carcinoma (post-surgery assessment).
  • Nonepithelial breast malignancies such as sarcoma or lymphoma.
  • DCIS that is multicentric in the ipsilateral breast.
  • Pregnant or lactating.
  • Prior non-hormonal therapy for the present breast cancer, including radiation therapy and/or chemotherapy.
  • Collagen vascular diseases
  • Coexisting medical conditions with life expectancy < 2 years.
  • Serious psychiatric or addictive disorder
  • Previously treated contralateral breast carcinoma
  • Synchronous bilateral breast carcinoma.
  • Other malignancy, except non-melanoma skin cancer, < 5 years prior to participation in the study; the disease free interval from any prior carcinoma must be continuous.
  • Patients with diffuse disease

结局指标

主要结局

Local Control Rate for Follow-up Period of 5 Years.

时间窗: Data collected at the time of implant, radiation therapy, and at the patient's 3 month, 6 month, 1 year, 2 year, 3 year, 4 year and 5 year follow-up visits.

Failure of local control was defined as a histologically confirmed recurrence (invasive or non-invasive) within the prescription isodose volume. All recurrences were to have histological evaluation per the protocol; however, the case report forms did not provide space for this data to be captured. Ipsilateral axillary, infraclavicular, internal mammary, or supraclavicular recurrence or distant metastases were not considered treatment failures unless accompanied by ipsilateral breast failure.

次要结局

  • Overall Survival(At 5 Years)
  • Cause Specific Survival(At 5 Years)
  • Disease Free Survival(At 5 Years)
  • Cosmetic Evaluations Over Time(At 5 Years)

研究者

发起方
Hologic, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (23)

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