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临床试验/NCT05253170
NCT05253170尚未招募3 期

A Randomized Phase III Trial of Hypofractionated Versus Conventionally Fractionated Radiotherapy in Breast Cancer Patients With Reconstruction After Mastectomy

Seoul National University Bundang Hospital0 个研究点目标入组 622 人开始时间: 2022年4月1日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
622
主要终点
Major Complication Rate

研究概览

简要总结

This randomized Phase III study aims to show major complication rate of hypofractionation radiation therapy is not inferior, compared to conventional fractionation radiation therapy in breast cancer patients undergoing mastectomy and reconstruction surgery.

详细描述

This study is a multicenter, randomized, phase 3 clinical trial. For breast cancer patients who underwent breast reconstruction after mastectomy, the hypofractionation radiotherapy group (experimental group) and the conventional fractionation radiotherapy group (control group) were divided 1:1 and compared to reveal the non-inferiority with hypofractionation in terms of major complication rate.

I. Primary Objective

  • To show the non-inferiority of major complication rate in reconstructed-breast between the hypofractionation radiotherapy group (experimental group) and the conventional fractionation radiotherapy group (control group) at 2 years after radiation therapy.
  • The main complications are defined at those requiring hospitalization or surgery among complications.

II. Secondary Objective:

  • Comparison of other side effects between the two groups.
  • Comparison of complication rate stratified by reconstruction timing and type of reconstruction

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
Single (Outcomes Assessor)

入排标准

年龄范围
19 Years 至 85 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patient who underwent mastectomy for invasive breast cancer
  • Patients who have undergone breast reconstruction after mastectomy or who have inserted a tissue expander
  • (y)p patients with stage IIIA or lower (excluding T4 and N3 patients) who need adjuvant radiation therapy
  • Eastern Cooperative Oncology Group Performance ≤ 2
  • Age ≥ 19 years
  • Patients who agreed to participate in the study

排除标准

  • Patients who already had implants at the time of diagnosis of breast cancer or who have already undergone reconstructive surgery
  • Patients who underwent reconstruction after partial resection or breast conserving surgery rather than mastectomy
  • Patients who are using or planning to use an air expander
  • Patients receiving radiation therapy for salvage or palliative purposes
  • Patients with distant metastases at the time of diagnosis
  • Patients who are scheduled to undergo concurrent chemoradiation therapy
  • Patients with bilateral breast cancer
  • Male breast cancer patients
  • Patients who have previously received radiation therapy for the ipsilateral breast or supraclavicular area
  • Patients with history of cancers other than thyroid cancer, intraepithelial cancer of the cervix, or skin cancer
  • Patients diagnosed with ductal breast carcinoma in situ, lobular carcinoma in situ, phyllodes, metaplastic cancer, or other benign tumors based on histological diagnosis

结局指标

主要结局

Major Complication Rate

时间窗: Up to 2 years after the completion of radiation therapy

* Unplanned re-hospitalization or re-operation for intervention * Implant removal due to infection, autologous flap total failure (reconstruction failure)

Capsular Contracture (If implant-based recontruction is performed)

时间窗: Up to 2 years after the completion of radiation therapy

• Baker Scale * G1: the breast is normally soft and appears natural in size and shape * G2: the breast is a little firm, but appears normal * G3: the breast is firm and appears abnormal * G4: the breast is hard, painful to the touch, and appears abnormal

次要结局

  • Hematoma(Up to 2 years after the completion of radiation therapy)
  • Wound Dehiscence(Up to 2 years after the completion of radiation therapy)
  • Wound infection(Up to 2 years after the completion of radiation therapy)
  • Seroma(Up to 2 years after the completion of radiation therapy)

研究者

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

In Ah Kim

Professor

Seoul National University Bundang Hospital

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