Evaluation of Efficacy, Quality of Life and Cost Effectiveness of Short-course Radiotherapy Followed by Capecitabine Plus Oxaliplatin chemotheRapy and TME for High-risk Rectal Cancer (ESCORT Trial)
Locally Advanced Rectal Cancer
About this trial
This is an interventional treatment trial for Locally Advanced Rectal Cancer
Eligibility Criteria
Inclusion Criteria:
High-risk patients of rectal cancer on pretreatment MRI using the following risk stratification system Location of the lower part of the tumor is measured below less than 10 cm on the anal verge and lower part of the tumor is located below the lower limit of the peritoneal reflection.
If there is more than one, classify as a high risk group Positive CRM threatening: 5mm ≦ Extramural depth Positive EMVI.
cN2: Positive Lateral pelvic LN metastasis
- Between 19 and 80 years of age;
- Satisfactory performance status: ECOG≦2
- American Society of Anesthesiologists (ASA) physical status classification system class I~III
- Adequate hematologic function: white blood cell(WBC) counts≥4,000/mm3, neutrophils counts ≥ 1,500/mm3, platelet counts ≥ 100,000/µL, hemoglobin ≥ 9g/L;
- Adequate renal function: creatinine ≤ 1.5×upper normal limit
Exclusion Criteria:
- The evidence of relapse of distant metastasis
- Receiving treatment of other anti-cancer drug or methods
- Patients have low compliance and are not able to complete the entire trial
- Presence of uncontrolled life-threatening diseases
- cT4 with infiltration of anterior organ on pretreatment MRI
- cT4 with infiltration of internal or external anal sphincter on pretreatment MRI
Sites / Locations
- The Division of Colon and Rectal Surgery, Department of Surgery, Yonsei University College of Medicine
Arms of the Study
Arm 1
Experimental
Preoperative short-course radiotherapy
1-week short-course radiation (5 Gy x 5) plus 6-week XELOX (capecitabine 1,000mg/m2 and oxaliplatin 130mg/m2 every 3 weeks) chemotherapy before total mesorectal excision (TME)