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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)

Primary Purpose

Locally Advanced Rectal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
preoperative short-course radiotherapy
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Locally Advanced Rectal Cancer

Eligibility Criteria

19 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 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

  2. Between 19 and 80 years of age;
  3. Satisfactory performance status: ECOG≦2
  4. American Society of Anesthesiologists (ASA) physical status classification system class I~III
  5. Adequate hematologic function: white blood cell(WBC) counts≥4,000/mm3, neutrophils counts ≥ 1,500/mm3, platelet counts ≥ 100,000/µL, hemoglobin ≥ 9g/L;
  6. Adequate renal function: creatinine ≤ 1.5×upper normal limit

Exclusion Criteria:

  1. The evidence of relapse of distant metastasis
  2. Receiving treatment of other anti-cancer drug or methods
  3. Patients have low compliance and are not able to complete the entire trial
  4. Presence of uncontrolled life-threatening diseases
  5. cT4 with infiltration of anterior organ on pretreatment MRI
  6. 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

Arm Type

Experimental

Arm Label

Preoperative short-course radiotherapy

Arm Description

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)

Outcomes

Primary Outcome Measures

pathologic complete response (pCR) rate
According to pathological response criteria, a total regression is considered a complete response

Secondary Outcome Measures

Incidence of acute toxicities during radiation and chemotherapy
Incidence of acute toxicities during radiation and chemotherapy
Incidence of surgical complications
Incidence of surgical complications
Quality of life
QOL assessed using EORTC QLQ-CR29 survey form. The EORTC QLQ-CR29 is a 29-item colon and rectum cancer site-specific supplemental module that aims to enhance the sensitivity and specificity for colorectal cancer quality of life measures. The original English version comprises 4 multi-item scales (body image, urinary frequency, blood and mucus in stool, and stool frequency) and 17 functional/symptomatic single-items(anxiety, weight, sexual interest, urinary incontinence, dysuria, abdominal pain, buttock pain, bloating, dry mouth, hair loss, taste, flatulence, fecal incontinence, sore skin, embarrassment, stoma care problem, impotence or dyspareunia), with higher scores indicating better functional or worse symptomatic status. Of these 21 scales or items, only body image, anxiety, weight, and sexual interest are functional domain scales/items, and all the remaining are symptomatic.
Cost effectiveness
QALYs (quality adjusted life years) with treatment protocol

Full Information

First Posted
August 30, 2018
Last Updated
February 12, 2019
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT03676517
Brief Title
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)
Official Title
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)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
March 2019 (Anticipated)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
August 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Locally Advanced Rectal Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Enrolled patient receive 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). Short-term outcomes including complications, TME completeness, and tumor response will be investigated. EORTC-QLQ-C30 questionnaire scoring will be used to evaluate QoL during the treatment period and after surgery. Cost effectiveness will be assessed using cost-utility analysis.
Masking
None (Open Label)
Allocation
N/A
Enrollment
31 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Preoperative short-course radiotherapy
Arm Type
Experimental
Arm Description
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)
Intervention Type
Radiation
Intervention Name(s)
preoperative short-course radiotherapy
Intervention Description
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)
Primary Outcome Measure Information:
Title
pathologic complete response (pCR) rate
Description
According to pathological response criteria, a total regression is considered a complete response
Time Frame
Two weeks after surgery
Secondary Outcome Measure Information:
Title
Incidence of acute toxicities during radiation and chemotherapy
Description
Incidence of acute toxicities during radiation and chemotherapy
Time Frame
Three months
Title
Incidence of surgical complications
Description
Incidence of surgical complications
Time Frame
Four weeks after surgery
Title
Quality of life
Description
QOL assessed using EORTC QLQ-CR29 survey form. The EORTC QLQ-CR29 is a 29-item colon and rectum cancer site-specific supplemental module that aims to enhance the sensitivity and specificity for colorectal cancer quality of life measures. The original English version comprises 4 multi-item scales (body image, urinary frequency, blood and mucus in stool, and stool frequency) and 17 functional/symptomatic single-items(anxiety, weight, sexual interest, urinary incontinence, dysuria, abdominal pain, buttock pain, bloating, dry mouth, hair loss, taste, flatulence, fecal incontinence, sore skin, embarrassment, stoma care problem, impotence or dyspareunia), with higher scores indicating better functional or worse symptomatic status. Of these 21 scales or items, only body image, anxiety, weight, and sexual interest are functional domain scales/items, and all the remaining are symptomatic.
Time Frame
Baseline and QOL at 8 weeks after radiotherapy
Title
Cost effectiveness
Description
QALYs (quality adjusted life years) with treatment protocol
Time Frame
Three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Min Soo Cho, MD
Phone
82-2-2228-2107
Email
nagase96@yuhs.ac
Facility Information:
Facility Name
The Division of Colon and Rectal Surgery, Department of Surgery, Yonsei University College of Medicine
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Min Soo Cho, MD
Phone
82-2-2228-2107
Email
nagase96@yuhs.ac

12. IPD Sharing Statement

Learn more about this trial

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)

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