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)
1 other identifier
interventional
31
1 country
1
Brief Summary
Multimodality treatment including surgery and radiotherapy is the current standard of care in locally advanced rectal cancer. Most clinical trials comparing short course radiotherapy (SCRT) with long course chemoradiotherapy(LCRT) did not find significant differences in oncological outcomes and short-term outcomes even though some debates. Recently, Stockholm III trial comparing SCRT plus delayed surgery with SCRT plus immediate surgery and LCRT demonstrated no differences with respect to short-term outcomes such as complications, mortality, and acute toxicity. However, overall quality of life (QoL) after curative treatment for rectal cancer is still major concern in both SCRT and LCRT. Furthermore, daily hospital visits for 5 weeks may be the cause of the increase of total medical cost due to indirect medical expense in patients with LCRT, especially in rural area. SCRT plus chemotherapy followed by delayed surgery may have the possibility of reducing total hospital costs as well as increasing QoL by proving non-inferiority in terms of perioperative outcomes. The present prospective single-arm phase 2 trial was designed to validate the efficacy, quality of life and cost effectiveness of preoperative short-course radiotherapy plus XELOX chemotherapy followed by delayed surgery for high-risk rectal cancer patient based on magnetic resonance imaging.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2019
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 30, 2018
CompletedFirst Posted
Study publicly available on registry
September 18, 2018
CompletedStudy Start
First participant enrolled
March 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2023
CompletedFebruary 15, 2019
February 1, 2019
4.4 years
August 30, 2018
February 12, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
pathologic complete response (pCR) rate
According to pathological response criteria, a total regression is considered a complete response
Two weeks after surgery
Secondary Outcomes (4)
Incidence of acute toxicities during radiation and chemotherapy
Three months
Incidence of surgical complications
Four weeks after surgery
Quality of life
Baseline and QOL at 8 weeks after radiotherapy
Cost effectiveness
Three months
Study Arms (1)
Preoperative short-course radiotherapy
EXPERIMENTAL1-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)
Interventions
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)
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Division of Colon and Rectal Surgery, Department of Surgery, Yonsei University College of Medicine
Seoul, 03722, South Korea
Related Publications (1)
Lee JM, Lee J, Kim T, Kim NK, Cho MS. Long-Term Outcomes of Long-Course Chemoradiotherapy vs. Short-Course Radiotherapy Followed by Consolidation Chemotherapy in Rectal Cancer. Yonsei Med J. 2025 Dec;66(12):891-896. doi: 10.3349/ymj.2025.0216.
PMID: 41287502DERIVED
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 30, 2018
First Posted
September 18, 2018
Study Start
March 1, 2019
Primary Completion
August 1, 2023
Study Completion
August 1, 2023
Last Updated
February 15, 2019
Record last verified: 2019-02