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Preoperative Concurrent Chemotherapy and Intensity Modulated Radiotherapy (IMRT) in Locally Advanced Rectal Cancer

2011年4月20日 更新者:National University Hospital, Singapore

A Phase II Trial of Preoperative Concurrent Chemotherapy and (IMRT) in Locally Advanced Rectal Cancer

The hypothesis of this study is that dose escalated intensity modulated radiotherapy (IMRT) to a dose of 55Gy in 25# to primary rectal tumor concurrent with oral capecitabine results in an improved pathological response rate from 8% (German trial) to 25%.

研究概览

详细说明

This study aims to look at whether radiation dose escalation with intensity modulated radiotherapy can increase the rates of pathological complete response in patients with locally advanced rectal cancer treated with neoadjuvant chemoradiotherapy

研究类型

介入性

注册 (预期的)

63

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Singapore、新加坡、119074
        • 招聘中
        • National University Hospital
        • 接触:
        • 首席研究员:
          • Jeremy Tey, FRANZCR

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

21年 至 90年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Pathologically proven diagnosis of adenocarcinoma of the rectum
  • Clinically determined to be stage T3 or T4,N0-N2, and M0 -staged by MRI or transrectal ultrasound of the rectum
  • Patients who are medically operable and who have resectable adenocarcinoma of the rectum at least <15cm from the anal verge
  • Adequate liver/renal and haematological function.
  • Eastern Cooperative Oncology Group (ECOG) performance 0-2
  • Age ≥ 18 years
  • Full blood count obtained within 2 weeks prior to registration on study, with adequate bone marrow function defined as follows:

    • Absolute neutrophil count (ANC) ≥ 1,800 cells/mm3
    • Platelets ≥ 100,000 cells/mm3
    • Haemoglobin ≥ 8.0 g/dl
  • Serum creatinine within normal institutional limits or creatinine clearance ≥ 50 ml/min
  • Bilirubin within normal institutional limits
  • AST and ALT < 2.5 x the IULN
  • Patient must sign study specific informed consent prior to study entry

Exclusion Criteria:

Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years

  • Prior systemic chemotherapy for colorectal cancer; note that prior chemotherapy for a different cancer is allowable.
  • Prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields
  • Severe, active comorbidity, defined as follows:

    • Unstable angina and/or congestive heart failure requiring hospitalization within the last 12 months
    • Transmural myocardial infarction within the last 6 months
    • Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects
    • Acquired immune deficiency syndrome (AIDS) based upon current CDC definition; note, however, that HIV testing is not required for entry into this protocol.
    • Evidence of uncontrolled seizures, central nervous system disorders, or psychiatric disability judged by the investigator to be clinically significant, precluding informed consent, or interfering with compliance of oral drug intake.
    • Known, existing uncontrolled coagulopathy. Patients on therapeutic anticoagulation may be enrolled provided that they have been clinically stable on anti-coagulation for at least 2 weeks.
    • Major surgery within 28 days of study enrollment (other than diverting colostomy)
  • Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; this exclusion is necessary because the treatment involved in this study may be significantly teratogenic
  • Prior allergic reaction to capecitabine
  • Any evidence of distant metastases (M1)
  • A synchronous primary colon carcinoma
  • Extension of malignant disease into the anal canal
  • Lack of physical integrity of the gastrointestinal tract (i.e., severe Crohn's disease that results in
  • malabsorption; significant bowel resection that would make one concerned about the absorption of capecitabine) or malabsorption syndrome that would preclude feasibility of oral chemotherapy (capecitabine)
  • Participation in any investigational drug study within 28 days of study enrollment

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

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Intensity modulated Radiotherapy
Intensity modulated radiotherapy, dose escalation, rectal cancer, volumetric modulated arc therapy
Intensity modulated radiotherapy to a dose of 55Gy in 25 fractions
其他名称:
  • Intensity modulated radiotherapy. Dose escalation.

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
Pathological complete response rates
大体时间:8 weeks post chemoradiotherapy
Pathogical complete response rate 8 weeks post chemoradiotherapy at surgery according to Ryan's classification
8 weeks post chemoradiotherapy

次要结果测量

结果测量
措施说明
大体时间
Toxicity
大体时间:2 years
Toxicity including anorexia, nausea, vomiting, diarrhoea, dermatitis, proctitis, urinary frequency/urgency as per common toxicity criteria v3.0
2 years
Disease Free survival
大体时间:2 years
Time from study entry to disease recurrence or death
2 years
Downstaging rates
大体时间:8 weeks after chemoradiotherapy
percentage of patients who achieve downstaging 8 weeks post chemoradiotherapy at surgery according to TNM classification
8 weeks after chemoradiotherapy
Sphincter Preservation rates
大体时间:8 weeks after chemoradiotherapy
Sphincter Preservation rates 8 weeks post chemoradiotherapy at surgery.Percentage of patients who underwent sphincter salvage surgery after chemoradiotherapy
8 weeks after chemoradiotherapy

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。

调查人员

  • 首席研究员:Jeremy Tey, FRANZCR、National University Hospital, Singapore

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。

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

2011年1月1日

初级完成 (预期的)

2013年1月1日

研究完成 (预期的)

2013年1月1日

研究注册日期

首次提交

2011年4月18日

首先提交符合 QC 标准的

2011年4月20日

首次发布 (估计)

2011年4月22日

研究记录更新

最后更新发布 (估计)

2011年4月22日

上次提交的符合 QC 标准的更新

2011年4月20日

最后验证

2011年4月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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