跳至主要内容
临床试验/NCT00681993
NCT00681993已完成不适用

"A Feasibility Trial of Partial Breast Irradiation With Various Concurrent Chemotherapy Regimens (PBIC)"

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2008年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
35
试验地点
2
主要终点
Subcutaneous tissue toxicities of PBIC

研究概览

简要总结

Breast conserving therapy, (BCT), which consists of wide local excision of the tumor followed by 6 weeks of whole breast irradiation, (WBI), is integral to the management of breast cancer. Evidence now suggests that WBI may not be necessary and treatment to the involved area only, partial breast irradiation, (PBI), may suffice. PBI can be achieved by interstitial or intracavitary brachytherapy, intra-op, or post op external beam radiation therapy. The feasibility, toxicity and efficacy of PBI are currently being studied in both the U.S. and Europe. Review of smaller studies suggests that PBI will prove to be comparable to WBI. Chemotherapy combined with radiation has been shown to increase local control in BCT when compared to radiation alone. However there is little data on how sequencing or timing of these therapies with respect to one another affect outcome. As a result there is no consensus about the optimal combination. There are real and potential benefits to concurrent chemo-radiation therapy. Concurrent therapy 1) allows both treatments to start closer to surgery, theoretically maximizing the benefits of each modality; 2) shortens the overall treatment program; and 3) may also improve local control via chemo-sensitization of residual cancer cells. However, concurrent chemotherapy and WBI have been associated with prohibitive skin toxicity. Since less breast tissue is treated with PBI, this skin toxicity may no longer be prohibitive. We have shown in J0381 that PBI and concurrent dose dense AC is safe. As a follow-up, we propose a phase I/II trial addressing the toxicity and efficacy associated with PBI delivered concurrently with various chemotherapy regimens.

详细描述

  1. Partial Breast Irradiation with concurrent chemotherapy (various regimens. Subjects will receive Segmental Mastectomy (Lumpectomy)
  2. Medical Oncology Evaluation
  3. Consent/Registration Pre-RT evaluation
  4. Simulation/Treatment Planning
  5. Chemo-Radiation Therapy:

ddAC, Std AC, TAC, TC, TCH or TH Concurrent with PBI - (270 cGy per fraction for 15 fractions). RT may start up to 7days prior to C1D1, but no later than 7 days after C1D1 (+/- 7 days of C1D1 radiation may start) 6. Further chemotherapy, hormonal therapy or biologic therapy at the medical oncologist's discretion 7. F/U Schedule

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Standard ddAC chemotherapy with concurrent radiation therapy

Active Comparator

Standard dose-dense Adriamycin and Cyclophosphamide (ddAC) chemotherapy and concurrent radiation therapy (RT)

干预措施: Standard Dose Dense Doxorubucin and Cyclophosphamide (Other)

Standard AC chemotherapy with concurrent RT

Active Comparator

Standard Adriamycin and Cyclophosphamide (AC) chemotherapy and concurrent radiation therapy

干预措施: Standard Doxorubucin and Cyclophosphamide (Other)

Standard TCarbo H chemotherapy with concurrent RT

Active Comparator

Standard Taxotere, Carboplatin and Herceptin (TCarbo H) chemotherapy and concurrent radiation therapy

干预措施: Standard Docetaxel, Carboplatin, and Herceptin (Other)

Standard TAC chemotherapy with concurrent RT

Active Comparator

Standard Taxotere, Adriamycin and Cyclophosphamide (TAC) chemotherapy with concurrent radiation therapy

干预措施: Standard Docetaxel, Doxorubucin and Cyclophosphamide (Other)

Standard TC chemotherapy with concurrent RT

Active Comparator

Standard Taxotere and Cyclophosphamide (TC) chemotherapy with concurrent radiation therapy

干预措施: Standard Docetaxel and Cyclophosphamide (Other)

结局指标

主要结局

Subcutaneous tissue toxicities of PBIC

时间窗: up to 5 years post-intervention

Subcutaneous tissue toxicity will be scored on a scale ranging from 0-4, where a higher score reflects more severe toxicity: 0= none; 1= slight induration (fibrosis) and loss of subcutaneous fat; 2= moderate fibrosis but asymptomatic; slight field contracture; \<10% linear reduction; 3= severe induration and loss subcutaneous tissue; field contracture \>10% linear reduction; 4= necrosis

Late skin toxicities of PBIC

时间窗: up to 5 years post-intervention

Late Skin toxicity will be scored on a scale ranging from 0-4, where a higher score reflects more severe toxicity: 0= none; 1= slight atrophy, pigmentation change, some hair loss; 2= patchy atrophy, moderate telangiectasias, total hair loss; 3= marked atrophy, gross telangiectasias; 4= ulceration

Acute skin toxicities of partial breast irradiation concurrent with chemotherapy (PBIC)

时间窗: up to 5 years post-intervention

Acute Skin toxicity will be scored on a scale ranging from 0-4, where a higher score reflects more severe toxicity: 0= no change; 1= follicular, fain or dull erythema/epilation/dry/desquamation/decreased swelling; 2= tender or bright erythemal patchy moist desquamation/moderate edema; 3= confluent moist desquamation other than skin folds, pitting edema; 4= ulceration, hemorrhage, necrosis.

次要结局

  • Cosmetic effect of PBIC(up to 5 years post-intervention)
  • Local control rate of patients treated with PBIC.(up to 5 years post-intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验