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临床试验/NCT06757621
NCT06757621招募中3 期

Hypofractionated Postoperative Regional Nodal Irradiation for Patients With Intermediate-risk Breast Cancer: A Multicenter Prospective Randomized Phase III Trial and Cohort Study.

Cancer Institute and Hospital, Chinese Academy of Medical Sciences1 个研究点 分布在 1 个国家目标入组 3,142 人开始时间: 2024年10月10日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
3,142
试验地点
1
主要终点
Disease-Free Survival Rate

研究概览

简要总结

The role of postoperative regional nodal irradiation (RNI) for T1-2N1 intermediate-risk breast cancer is controversial, and there is a lack of class I evidence of a survival benefit from RNI. A number of retrospective studies of breast cancer patient been undertaken to risk stratify, analyse site of recurrence and assess the role of radiotherapy. RNI is currently recommended for patients at high risk of recurrence, but prospective studies in other patients are needed to assess the role of RNI. Two randomised phase III trials have confirmed the safety and efficacy of 15-fraction hypofractionated radiotherapy, while 5-fraction super-hypofractionated radiotherapy to further shorten the course of radiotherapy is a hotspot of current research. The present study aimed to investigate whether RNI improves the outcome of intermediate-risk breast cancer patients; and to assess the efficacy and toxicity of 15-fraction hypofractionated and 5-fraction super-hypofractionated radiotherapy.

研究设计

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

入选标准

  • •≥45 years old
  • •Receiving breast-conserving surgery or total mastectomy and axillary lymph node dissection or sentinel lymph node biopsy
  • •Negative surgical margins
  • •Tumor staging: A. patients without neoadjuvant chemotherapy: pT1-2N1M0, axillary lymph node dissection with 1-3 metastatic lymph nodes, at least 1 lymph node with macroscopic metastasis, and a score of 0-2 according to the following risk factors: ≤40 years of age (1 point), tumour located in the inner quadrant (1 point), 2-3 lymph nodes positive in the axilla (1 point), presence of choroidal tumour thrombus (1 point), and restaging according to the 8th edition of the staging criteria (IB-IIA 1 point, and IIB-IIIA 2 points) B. patients without neoadjuvant chemotherapy: pT1-2N1M0, sentinel lymph node biopsy with 1-2 metastatic lymph nodes, at least 1 lymph node with macroscopic metastasis, and a score of 0-2 according to the following risk factors: ≤40 years of age (1 point), tumour located in the inner quadrant (1 point), 2-3 lymph nodes positive in the axilla (1 point), presence of choroidal tumour thrombus (1 point), and restaging according to the 8th edition of the staging criteria (IB-IIA 1 point, and IIB-IIIA 2 points) C. patients with neoadjuvant chemotherapy: cT1-2N1-2M0→ypT0-2N0M0, requiring positive clinical lymph nodes with pathological confirmation, receiving ≥6 cycles of neoadjuvant chemotherapy, and ≥3 sentinel lymph nodes detected for those with simple sentinel lymph node biopsy
  • •Signed informed consent

排除标准

  • •Distant metastases
  • •Metastasis to ipsilateral internal breast, supraclavicular or subclavicular lymph nodes
  • •Previous radiotherapy to the chest
  • •Bilateral breast cancer
  • •Pregnancy, breastfeeding
  • •Previous or concurrent other malignancy with tumor-free survival <5 years (but excluding skin cancer with non-malignant melanoma, papillary/follicular thyroid cancer, cervical carcinoma in situ)

研究组 & 干预措施

Without Hypofractionated Postoperative Regional Nodal Irradiation

No Intervention

Hypofractionated Postoperative Regional Nodal Irradiation

Experimental

干预措施: Regional Nodal Irradiation (Radiation)

结局指标

主要结局

Disease-Free Survival Rate

时间窗: through study completion, an average of 10 year

次要结局

  • Locoregional Recurrence Rate(through study completion, an average of 10 year)
  • Distant Metastasis Rate(through study completion, an average of 10 year)
  • Incidence of acute and late adverse reactions(through study completion, an average of 10 year)
  • Quality of life Questionnaire (EORTC QLQ-C30)(through study completion, an average of 2 year)
  • European Organization for Research and Treatment of Cancer Breast Cancer-Specific Quality-of-Life Questionnaire (QLQ-BR23)(through study completion, an average of 2 year)
  • Overall Survival Rate(through study completion, an average of 10 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Shulian Wang

Professor

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

研究点 (1)

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