跳至主要内容
临床试验/NCT01995942
NCT01995942Unknown不适用

Molecular, Pathologic and MRI Investigation of the Prognostic and Redictive Importance of Extramural Venous Invasion in Rectal Cancer

Royal Marsden NHS Foundation Trust19 个研究点 分布在 1 个国家目标入组 246 人开始时间: 2013年6月7日最近更新:
适应症

试验速览

阶段
不适用
入组人数
246
试验地点
19
主要终点
The primary endpoint will be time to relapse pertaining to the primary objective of relapse rate at 1 year and 3 years.

研究概览

简要总结

Extramural venous invasion (EMVI) is the spread of microscopic tumour cells into the veins around the tumour. Rectal cancer treatment has improved greatly over recent years. However, it is important for us to learn as much about the tumours as possible in order to develop newer therapies. Current treatments may benefit from new genetic information relating to the cancer. We hope to identify genetic differences in certain types of rectal cancer which will allow future treatments.

详细描述

Neoadjuvant chemoradiotherapy (CRT) is widely accepted as beneficial to selected patients in terms of decreased risk of local recurrence and overall survival. Current management of rectal cancer involves risk stratification through pre-operative staging leading to formulation of treatment strategy. Very little is known about the long-term outcomes and response to CRT on MRI detected extramural venous invasion (mrEMVI). Although mrEMVI is accepted as a marker of poor prognosis, whether it has a predictive value and should be specifically treated is not known.

Molecular and genetic profiling provides us with an opportunity to understand the underlying mechanisms which govern clinical behaviour in rectal cancer. Using high-throughput technology such as tissue microarray analysis allows large-scale analysis of specimens in a relatively short amount of time. It offers the ability to compare the molecular profiles of different subtypes of rectal cancer such as mrEMVI-positive and -negative tumours and whether any changes are observed following CRT. This can then be correlated with clinical behaviour over the medium and long-term with regards to local recurrence, distant metastases and overall survival.

This study will identify important differences between key rectal cancer tumour subtypes. Identification of reliable pathological markers of EMVI pathways (from both the primary tumour sample, but more importantly from the pre-operative biopsies) has real potential for taking us a step closer to more personalised management of rectal cancer by establishing prognostic biomarkers reflective of disease type, but also through the underlying biology that may be highlighted (with its promise of therapeutic translation).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Locally advanced primary rectal cancer (requiring pre-operative treatment); diagnosed on tissue biopsy
  • Adult patients - over 18 years
  • Able to undergo curative (TME) surgery
  • Able to undergo MRI and CT with relevant contrast agent
  • Able to undergo LCRT
  • Exclusion Criteria
  • Metastatic disease at presentation
  • Emergency diagnosis/treatment
  • Unable to undergo staging (MRI and CT) or treatment procedures (LCRT/surgery)

排除标准

  • 未提供

结局指标

主要结局

The primary endpoint will be time to relapse pertaining to the primary objective of relapse rate at 1 year and 3 years.

时间窗: 3 years

次要结局

  • Response rates (in terms of mrTstage, mrN stage, involvement of CRM (circumferential resection margin) and mrTRG (tumour regression grade)) in addition to recurrence rates at 1 year and 3 years.(3 years)
  • Measurement of the change in mrEMVI from pre to post pre-operative therapy, will be based on a new proposed EMVI-TRG classification (EMVI TRG 1-5).(5 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (19)

Loading locations...

相似试验

Molecular, Pathologic and MRI Investigation of the... | 临床试验