NCT03676517

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
31

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2019

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Completed
19 days until next milestone

First Posted

Study publicly available on registry

September 18, 2018

Completed
5 months until next milestone

Study Start

First participant enrolled

March 1, 2019

Completed
4.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2023

Completed
Last Updated

February 15, 2019

Status Verified

February 1, 2019

Enrollment Period

4.4 years

First QC Date

August 30, 2018

Last Update Submit

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

EXPERIMENTAL

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)

Radiation: preoperative short-course radiotherapy

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)

Preoperative short-course radiotherapy

Eligibility Criteria

Age19 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

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.

Central Study Contacts

Min Soo Cho, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: 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.
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

Locations