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临床试验/NCT01289353
NCT01289353已完成1 期

Phase I-II Study of Concurrent Adjuvant Systemic Therapy and Accelerated Radiotherapy (Over 3 Weeks)

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2009年3月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
92
试验地点
1
主要终点
Number of Patients Who Developed Grade 2-3 Acute Radiation Dermatitis Within 60 Days Post-RT

研究概览

简要总结

The purpose of this study is to determine the safety and effectiveness of a combination of chemotherapy and radiotherapy in breast cancer patients after breast surgery.

详细描述

Preliminary experience in the neo-adjuvant setting of Locally Advanced Breast Cancer (LABC) has recently demonstrated that hormone receptors negative patients have approximately 50% chance to achieve a pathological response after concurrent chemo-radiation. In a multi-institutional collaboration of 105 patients it was found that triple negative (TN) tumor carriers achieved pathological response in 54% of the cases and that the response reflected on 5-year disease free survival and overall survival. Our group has speculated that these effects on the risk of distant recurrence could depend on the recovery of antitumor immunity among the patients achieving pathological response, after tumor cell death induced by concurrent chemo-radiation.

The investigators are proposing a novel study that translates these findings to the adjuvant setting of TN tumors. TN breast cancer is a more aggressive form of the disease often coinciding with basal-like tumors. BRCA mutated-cancer is more frequently TN.

The current protocol converges the experience NYU has developed in accelerated prone breast radiotherapy with encouraging finding from the use of concurrent chemoradiation in LABC.

The investigators will study the feasibility of combining weekly carboplatin with concurrent 3-weeks prone breast radiotherapy in the adjuvant setting of 35 women with TN tumors, after segmental mastectomy and nodal assessment. Primary endpoint of the study is acute toxicity of the combined regimen, with a target of < 25% of grade II-III dermatitis.

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

入选标准

  • Age older than 18
  • Pre- or post-menopausal women with Stage I and II breast cancer, triple negative tumors
  • Biopsy-proven invasive breast cancer, excised with negative margins of at least 1 mm
  • Status post segmental mastectomy, after sentinel node biopsy and/or axillary node dissection (Tumors < 5 mm in size do not require nodal assessment) or after mastectomy
  • No previous chemotherapy
  • Patient needs to be able to understand and demonstrate willingness to sign a written informed consent document

排除标准

  • Previous radiation therapy to the ipsilateral breast
  • Active connective tissue disorders, such as lupus or scleroderma
  • Pregnant or lactating women

研究组 & 干预措施

ChemoRT

Experimental

Concurrent Carboplatin and Radiotherapy

干预措施: Carboplatin (Drug)

ChemoRT

Experimental

Concurrent Carboplatin and Radiotherapy

干预措施: 3D-RT or IMRT (Radiation)

结局指标

主要结局

Number of Patients Who Developed Grade 2-3 Acute Radiation Dermatitis Within 60 Days Post-RT

时间窗: 60 days post-RT

次要结局

  • Number of Patients Who Experience Grade 2 or Higher Late Toxicities at or More Than 6 Months After Completion of Radiation Treatment (RT)(6 months to 5 years post-RT)
  • Number of Patients Who Experience Acute Toxicities at or More Than 6 Months After Completion of Radiation Treatment (RT)(6 months to 5 year post-RT)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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