跳至主要内容
临床试验/NCT04108117
NCT04108117已完成不适用

Surgical and Oncologic Outcomes After Robotic Nipple Sparing Mastectomy and Immediate Reconstruction : an International Multicenter Pooled Analysis

Severance Hospital1 个研究点 分布在 1 个国家目标入组 659 人开始时间: 2020年5月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
659
试验地点
1
主要终点
Postoperative complication rates in 30 days

研究概览

简要总结

Robotic mastectomy with immediate reconstruction was introduced by Toesca et al. in 2015. Since then, several studies have reported the safety and feasibility of robotic nipple-sparing mastectomy with immediate reconstruction. However, most studies were conducted by single centers and had small samples. Furthermore, there is a lack of studies comparing surgical and oncologic outcomes between robotic nipple-sparing mastectomy and conventional nipple-sparing mastectomy. For this reason, this study evaluates surgical and oncologic outcomes of robotic nipple-sparing mastectomy with immediate reconstruction using international multi-center data.

详细描述

This study is an international multi-center pooled analysis using prospective and retrospective studies to evaluate surgical and oncologic outcomes of robotic nipple-sparing mastectomy with immediate reconstruction.

Raw data for robotic or conventional nipple-sparing mastectomy from Severance Hospital, Samsung Medical Center, the European Institute of Oncology, Changhua Christian Hospital, and Gustave Roussy is collected. Among them, Severance Hospital takes the lead at performing analysis from the data. Storage and disposal of patients' records are managed by each researcher. In the analysis process, although the collaborators can request records from Severance Hospital if necessary, they are only supposed to be provided computerized data which were originally clinical data from patients who already ended treatments. In this case, individual identifying data and medical records are not shown.

Clinicopathologic variables including operation times, hospital stay, medical history, smoking history, family history, BMI, menopausal status, specimen weight, TNM stage, grade, histological type, estrogen receptor, progesterone receptor, HER2, Ki 67, and perivascular involvement are analyzed.

Postoperative complications within 30 days are collected and classified by the Clavien-Dindo grade. Locoregional recurrence-free survival and local and systemic recurrences are examined. Patients whose data have been retrospective for at least one month are to be examined.

Patient's and surgeon's satisfaction using Breast Q is evaluated. Categorical variables are examined using the chi-square test or Fisher's exact test if indicated.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Women who underwent nipple sparing mastectomy and immediate reconstruction
  • Women with early breast cancer
  • Women with germline BRCA 1/2 mutation or germline mutations in genetic susceptibility genes
  • Women with interstitial mastopathy
  • Women with risk-reducing mastectomy or contralateral mastectomy

排除标准

  • Male patients
  • Women with stage IV disease at diagnosis
  • Women who underwent previous breast cancer surgery
  • Women who received prior radiotherapy for the ipsilateral breast

结局指标

主要结局

Postoperative complication rates in 30 days

时间窗: Postoperative 30 days

Postoperative complication rates are calculated as total number of postoperative complication cases per total operation cases.

Recurrence free survival (RFS)

时间窗: Postoperative 5 years

Events of RFS includes locoregional recurrence, distant recurrence, and death. Contralateral breast cancer and second primary malignancy are considered to be censored data.

Clavien-Dindo grade of postoperative complications

时间窗: Postoperative 30 days

Clavien-Dindo grade of postoperative complications is evaluated. The highest grade of postoperative complications are used for the analysis.

Nipple necrosis rates

时间窗: Postoperative 30 days

Nipple necrosis rates are calculated as number of total nipple necrosis cases per total operation cases.

次要结局

  • Locoregional recurrence-free survival (LRFS)(Postoperative 5 years)
  • Operation times(Time during operation)

研究者

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

Hyung Seok Park, MD, PhD

Clinical Associate Professor

Severance Hospital

研究点 (1)

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