Surgery for Locally Advanced Colon Cancer: is it Worth it? A Multicenter Retrospective Analysis. (LACC)
2020年11月30日 更新者：Francesca Cravero、Santo Spirito Hospital, Italy
Surgery for Locally Advanced Colon Cancer: is it Worth it? A Multicenter Retrospective Analysis. (LACC Trial)
The aim of the present study is to assess the post-operative outcomes (morbidity and mortality) in relation to preoperative data and the oncological outcomes (overall and disease-free survival) in patients with a locally advanced colon cancer (LACC) with the necessity of a multivisceral resection (MVR).
研究概览
详细说明
All patients that meet the inclusion criteria will be registered in a retrospective database from 2014 to 2019 (5 years) Data will be reported for every patients with colon cancer to have had either a resection of another organ or structure in addition to resection of the primary tumor, or to have had a T4 (a or b) tumour on postoperative histopathology.
Data included are patient demographics, ASA score, tumor localization, preoperative imaging, neoadjuvant treatments, type of bowel resection and adjacent organs resected, tecnique (laparoscopic/laparotomic), postoperative complications and 30-day mortality, histopathology data including TNM scoring, completeness of surgical procedure (R0 to R2) and infiltration of tumor cells in resected tissues, adjuvant oncological treatments, and long term follow-up data on local and distant recurrence and survival.
研究类型
观察性的
注册 (预期的)
100
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Patients with a locally advanced colon cancer (LACC) with the necessity of a multivisceral resection (MVR).
描述
Inclusion criteria
- > 18 aa
- Patients with a locally advanced colon cancer (LACC) with the necessity of a multivisceral resection (MVR).
Exclusion criteria
- Stage IV
- Rectal cancer
- Emergency surgery (<48 hours from admission)
- ASA > III
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Postoperative morbidity
大体时间：30 days
|
I evaluate peri and post-operative surgical (e.g.
intraabdominal collection, fistula, anastomotic leak) and medical (e.g.
pneumoniae, deep vein thrombosis) complications
|
30 days
|
|
Postoperative mortality
大体时间：30 days
|
I evaluate in-hospital and 30-day mortality correlate to the intervention
|
30 days
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Overall Survival
大体时间：5 years
|
The length of time from the intervention that patients diagnosed with a T4 colon cancer are still alive.
|
5 years
|
|
Disease Free Survival
大体时间：5 years
|
The measure of time after treatment during which no sign of recurrence (local or metastatic) is found.
|
5 years
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
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研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (预期的)
2021年1月1日
初级完成 (预期的)
2021年1月1日
研究完成 (预期的)
2021年6月30日
研究注册日期
首次提交
2020年11月17日
首先提交符合 QC 标准的
2020年11月23日
首次发布 (实际的)
2020年11月30日
研究记录更新
最后更新发布 (实际的)
2020年12月1日
上次提交的符合 QC 标准的更新
2020年11月30日
最后验证
2020年11月1日
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
IPD 计划说明
Data will retrospectively collected from a maintained database in each center, created by the.
A local study manager will be identified for each participating center.
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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