Preoperative Chemoradiotheray for Rectal Cancer
Primary Purpose
Rectal Neoplasm
Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
PCRT
Sponsored by
About this trial
This is an interventional treatment trial for Rectal Neoplasm focused on measuring Rectal neoplasm, Clinical stage, T3N0, Preoperative chemoradiotherapy, Laparoscopic, Open resection
Eligibility Criteria
Inclusion Criteria:
- Histologically demonstrated and cytologically evident rectal cancer (Glandular carcinoma: located on 4-12cm from anus), the case without remote metastasis
- Age: 18-70 years old
- The patients who did not undergo radiation therapy, surgery or antitumor agent therapy with the same disease medical history
- The patients with clinical stage of T3N0 identified by ultrasound or MRI
- Appropriate bone marrow, liver and renal function as follow; granulocyte ≥ 1500, platelet ≥ 80,000, bilirubin < 1.5 mg/dl , Serum Creatinine < 1.5 mg/dl, BUN < 30,
- The patients who understood the rights to withdraw the agreement at any time and signed on the informed consent form with or without their legal representatives.
Exclusion Criteria:
- Remote metastatic disease
- When the patient is concerned about the local recurrence if the preoperative chemo-radiation therapy is not undergone, or when the patient expects that the possibility of conservation of sphincter is improved owing to the preoperative chemo-radiotherapy.
- Pregnancy
- Radiotherapy, the past history of operation or chemotherapy
- Familial multiple polyp
- Uncontrolled psychiatric disorder, chronic alcohol disease or drug addiction and CNS(Central Nervous System) disorder
- Other malignant disorder
- After the radiotherapy or the case which remote metastasis is detected during the surgery
- The case which has splanchnemphraxis or the risk of progression to occlusion during the examination period
- Those patients who do not agree to participate in this study
- The patients who seemed to be likely to stop in the middle of clinical study.
- The patients who cannot undergo the regular follow-up owing to the following reasons. For instance, the patients who have psychologic, social, family or geographic reason or the patients who have difficulties in observing proper follow-up or clinical examination plan. Also, the patient who the doctor considers them as improper subjects of this study
Sites / Locations
- Korean Rectal Cancer Study Group
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Experimental
Active Comparator
Experimental
Arm Label
Open PCRT group
Open no PCRT group
LAP PCRT group
LAP no PCRT group
Arm Description
Patients who underwent preoperative chemoradiotherapy and open resection
Patients who did not undergo preoperative chemoradiotherapy and open resection
Patients who underwent preoperative chemoradiotherapy and laparoscopic resection
Patients who did not undergo preoperative chemoradiotherapy and laparoscopic resection
Outcomes
Primary Outcome Measures
Disease-free survival
Secondary Outcome Measures
Overall survival Local recurrence Early or late complication associated with preoperative radiotherapy Quality of life Accuracy of clinical staging Difference of surgical outcome between laparoscopic and open surgery
Full Information
NCT ID
NCT00819559
First Posted
January 7, 2009
Last Updated
January 8, 2009
Sponsor
Korean Rectal Cancer Study Group
1. Study Identification
Unique Protocol Identification Number
NCT00819559
Brief Title
Preoperative Chemoradiotheray for Rectal Cancer
Official Title
Role of Preoperative Chemoradiotherapy in Clinically T3No Mid and Low Rectal Cancer : Multi-Institute Clinical Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2009
Overall Recruitment Status
Unknown status
Study Start Date
March 2009 (undefined)
Primary Completion Date
February 2011 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Korean Rectal Cancer Study Group
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Hypothesis
Pre operative radio-chemotherapy might be not mandatory to improve local recurrent rate and survival rate in the mid-lower rectal cancer patients with T3N0 clinical stage, if surgical principals were kept.
Laparoscopic resection is not inferior to Open surgery in the treatment of rectal cancer.
Detailed Description
It is known that 20-60% of the rectal cancer patients treated with radical resection have the local recurrence. Therefore, chemo-radiotherapy before or after operation have been the standard treatment protocol in the rectal cancer patients to reduce the local recurrence, preserve more surrounding pelvic viscera, improve the prognosis and eventually quality of life. The preoperative chemo-radiotherapy was introduced by the German Rectal Cancer study, which compared pre- and postoperative chemo and radiotherapy. In this study, the authors reported that preoperative chemo-radiotherapy reduced local recurrent rate and 3 or 4 degree toxicity and improved the compliance for treatment. Since the introduction of chemo and radiotherapy in the treatment of rectal cancer, there have been numerous controversies on the guidelines or protocols of chemo-radiotherapy. In 1990, National Institute of Health (NIH) recommended postoperative chemo- radiotherapy to all the pT3 or pN1 rectal cancer patients at the consensus conference. In some studies, they reported that good clinical outcome and low local recurrence rate were obtained by only surgical treatment in the pT3N0 rectal cancer patients with favourable pathological characteristics. They also insisted that the effectiveness of postoperative chemo- radiotherapy was not evident. Gunderson, et al. retrospectively evaluated the five-year survival rate of the pT3N0 patients. They reported that the patients with surgery and chemotherapy showed the similar survival rate with the patients who underwent surgery and postoperative chemo-radiotherapy. National Cancer Data Base showed the similar report. However, there are some problems to apply theses results to the decision of preoperative therapeutic options. Moreover, some papers showed the low local recurrent rate (less than 5%) in the stage II without the supplement therapy, when the TME was precisely performed. All these results present the controversies on the radio-chemotherapy on all the T3N0 patients in terms of the clinical outcomes and the prognosis. In Korea, numerous clinical trials have been performed on the rectal cancer patients, however there has been no clinical study for preoperative chemo- radiotherapy in the T3N0 rectal cancer patients. In this reason, the protocols are different among institutions without unified standard treatment protocol. In this study, the authors compare the accuracy of diagnosis, the functional differences according to the preoperative chemo- radiotherapy, the local recurrent rate and survival rate between the two groups of T3N0 patients; one group with preoperative chemo-radiotherapy vs. the other without. In addition, the authors evaluate the advantage of the laparoscopic surgery, such as an extensive vision, so that laparoscopy can help rectal surgery as well as the surgical outcome.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Neoplasm
Keywords
Rectal neoplasm, Clinical stage, T3N0, Preoperative chemoradiotherapy, Laparoscopic, Open resection
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1160 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Open PCRT group
Arm Type
Active Comparator
Arm Description
Patients who underwent preoperative chemoradiotherapy and open resection
Arm Title
Open no PCRT group
Arm Type
Experimental
Arm Description
Patients who did not undergo preoperative chemoradiotherapy and open resection
Arm Title
LAP PCRT group
Arm Type
Active Comparator
Arm Description
Patients who underwent preoperative chemoradiotherapy and laparoscopic resection
Arm Title
LAP no PCRT group
Arm Type
Experimental
Arm Description
Patients who did not undergo preoperative chemoradiotherapy and laparoscopic resection
Intervention Type
Radiation
Intervention Name(s)
PCRT
Other Intervention Name(s)
preoperative chemoradiotherapy
Intervention Description
Preoperative chemoradiotherapy
Primary Outcome Measure Information:
Title
Disease-free survival
Time Frame
5 year
Secondary Outcome Measure Information:
Title
Overall survival Local recurrence Early or late complication associated with preoperative radiotherapy Quality of life Accuracy of clinical staging Difference of surgical outcome between laparoscopic and open surgery
Time Frame
Up to 2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically demonstrated and cytologically evident rectal cancer (Glandular carcinoma: located on 4-12cm from anus), the case without remote metastasis
Age: 18-70 years old
The patients who did not undergo radiation therapy, surgery or antitumor agent therapy with the same disease medical history
The patients with clinical stage of T3N0 identified by ultrasound or MRI
Appropriate bone marrow, liver and renal function as follow; granulocyte ≥ 1500, platelet ≥ 80,000, bilirubin < 1.5 mg/dl , Serum Creatinine < 1.5 mg/dl, BUN < 30,
The patients who understood the rights to withdraw the agreement at any time and signed on the informed consent form with or without their legal representatives.
Exclusion Criteria:
Remote metastatic disease
When the patient is concerned about the local recurrence if the preoperative chemo-radiation therapy is not undergone, or when the patient expects that the possibility of conservation of sphincter is improved owing to the preoperative chemo-radiotherapy.
Pregnancy
Radiotherapy, the past history of operation or chemotherapy
Familial multiple polyp
Uncontrolled psychiatric disorder, chronic alcohol disease or drug addiction and CNS(Central Nervous System) disorder
Other malignant disorder
After the radiotherapy or the case which remote metastasis is detected during the surgery
The case which has splanchnemphraxis or the risk of progression to occlusion during the examination period
Those patients who do not agree to participate in this study
The patients who seemed to be likely to stop in the middle of clinical study.
The patients who cannot undergo the regular follow-up owing to the following reasons. For instance, the patients who have psychologic, social, family or geographic reason or the patients who have difficulties in observing proper follow-up or clinical examination plan. Also, the patient who the doctor considers them as improper subjects of this study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
InJa Park, M.D.
Phone
82-2-519-8975
Email
ijpark7@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gyu-Seog Choi, M.D.
Organizational Affiliation
School of Medicine, Kyungpook National University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Korean Rectal Cancer Study Group
City
Daegu
ZIP/Postal Code
700-721
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
InJa Park, M.D.
Phone
82-2-519-8975
Email
ijpark7@gmail.com
First Name & Middle Initial & Last Name & Degree
InJa Park, M.D.
12. IPD Sharing Statement
Learn more about this trial
Preoperative Chemoradiotheray for Rectal Cancer
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