Rectal Cancer
Conditions
Keywords
Ultra-low rectal cancer, Intersphincteric resection, IORT
Brief summary
To study the application of Intersphincteric Resection（ISR）combined with intraoperative radiation therapy(IORT) for ultra-low rectal cancer,and to broaden the surgical indications of Intersphincteric Resection（ISR. The study is aimed to assess the postoperative acute complication and the short-term acute efficacy on the patients with middle and low rectal cancer by treated with intraoperative radiotherapy,especially those with peritoneal inversion rectal cancer.
Detailed description
Abstract objective: To study the application of Intersphincteric Resection（ISR）combined with intraoperative radiation therapy(IORT) for ultra-low rectal cancer,and to broaden the surgical indications of Intersphincteric Resection（ISR）. Methods: Patients, who were diagnosed with ultra-low rectal cancer and had strong desire of preserving anal function, will take part in the research,whose tumor invading the levator ani muscle or above, the diameter less than 6cm, the lower tumor margin away from the anal verge by less than 5cm and away from the dentate line by less than 3cm.They will undergo total mesorectal excision(TME) and ISR combined with IORT and prophylactic ileostomy. Outcomes Measures:The evaluation of short term effects includes complications such as anastomotic leakage, acute radiation injury ,urinary dysfunction ,dysfunction of anal sphincter ,sexual dysfunction ,local recurrence , total life expectancy and expectancy without metastasis. The postoperative pathological examination reported to be moderately differentiated adenocarcinoma .We wili assess their postoperative acute complications and short-term efficacy .Their time of follow up visit wil be 1 year or more.
Interventions
RADIATIONIntraoperative radiotherapy by Intrabeam（Zeiss Meditech，Jena，Germany）
We confirmed that if the patients had the distant metastasis before IORT. The median radiation dose was 5.00 Gy (range: 5.00-10.00Gy), the average dose was 6.00 Gy. The median radiation time was 0:33:24 (range: 0:21:45-1:06:23), which was the same with the patients'. All patients' surface dose ranged from 15.00 to 28.50 Gy.
Sponsors
Second Hospital of Jilin University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Inclusion Criteria: * Aged 40 to 80 years old, gender not limited. * Be diagnosed as colorectal cancer by coloscopy. * Patients with middle and low rectal cancer,whose preoperative staging evaluation is T3 ,T4 or N+. * Accept surgery and intraoperative radiotherapy. * Signed informed consent
Exclusion criteria
* the patients whose preoperative evaluation is below T3 stage with middle and rectal cancer. * Active internal bleeding (such as gastrointestinal bleeding), urogenital system, or have not cure of peptic ulcer in four weeks * Severe liver and kidney dysfunction * Intracranial tumor, suspicious aortic dissection, arteriovenous malformation, aneurysm * Thrombolysis treatment in one week * Allergies of thrombolysis drug or contrast * Participated in any clinical trials within three months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Decide and record the region of radiotherapy | Intraoperation | The operator will confirm and record the range of intrabeam after removal of tumor such as the length and height to modify the dose and the time of intrabeam. |
| The basic information and medical history achieved (questionnaire) | baseline | Investigators will take a overall information about the patients including the physical condition,history of present illness,family genetic history etc;Then the information will be recorded in a format to develop a statistic analysis. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Major Adverse Events | 1 year after operation | The local relapse (pelvic pain, bleeding and intestinal obstruction included)or metastasis will be recorded by the investigator |
| The short-term complications | 1 year after operation | The short-term complications(seroma,wound dehiscence and bleeding hematomas)will be followed up by investigator. |
Countries
China
Contacts
Primary ContactMin Wang, M.D.
Backup ContactWangsheng Xue
Outcome results
None listed