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Treatment of Adenocarcinoma of the Rectum With Transanal Local Excision for Complete Responders

Primary Purpose

Rectal Cancer

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Standard of care chemotherapy with the change for avoidance of extensive surgery
Sponsored by
Ascension South East Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥ 18 years
  2. Diagnosis of rectal invasive adenocarcinoma
  3. Tumor in the low or mid rectum (up to 11 cm from the anal verge)
  4. Clinical stage T3/N0-N1M0. Patients with low T2 who will need abdominal perineal resection are also eligible.

1. Clinical staging will be estimated based on the combination of the following assessments:

  1. Physical examination by the primary surgeon
  2. Computed Tomography or Positron Emission Tomography/Computed Tomography scan of chest, abdomen and pelvis
  3. Pelvic MRI and endoscopic ultrasound

Exclusion Criteria:

  • Less than 18 years of age
  • Do not complete informed consent
  • Pregnant women

Sites / Locations

  • Ascension St. John HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Neoadjuvant Chemotherapy and Follow-up Surgery

Arm Description

All patients will receive standard of care therapy and based upon their response will either receive transanal local resection or full resection, based on pathologic response.

Outcomes

Primary Outcome Measures

Complete remission
Percent of patients who achieve complete remission
Partial remission
Percent of patients who achieve partial remission
Disease progression
Percent of patients with disease progression
Local resection
Percent of patients who require local resection only

Secondary Outcome Measures

Patient quality of life
Quality of life score on questionnaire
Patient health status
Patient self-reported health status

Full Information

First Posted
May 5, 2019
Last Updated
January 30, 2023
Sponsor
Ascension South East Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT03941366
Brief Title
Treatment of Adenocarcinoma of the Rectum With Transanal Local Excision for Complete Responders
Official Title
Treatment of T2-T3/NO-N+ Adenocarcinoma of the Rectum by Neoadjuvant Chemotherapy (FOLFOX) Followed by Preoperative Chemo (5FU/Capecitabine)-Radio Therapy (CRT) With Transanal Local Excision for Complete Responders
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 26, 2016 (Actual)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
January 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ascension South East Michigan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The current standard of care for rectal cancer has diminished local recurrence and enhanced survival. Quality of life, however, remains poor for many patients and the probability of distant recurrence is high. In this study, we will attempt to reduce the distant recurrence rate and improve quality of life by making changes in the timing and administration of chemotherapy and radiation and doing less invasive rectal surgery when indicated.
Detailed Description
The purpose of the study is to determine if neo-adjuvant FOLFOX therapy and lengthening the time interval between neo-adjuvant chemotherapy and transanal local excision will increase the percentage of patients with pathologic complete remission. This is a prospective pilot study to examine the impact of two variables: 1) addition of neo-adjuvant FOLFOX chemotherapy, and 2) increasing the time interval between completion of chemo-radiotherapy and subsequent surgery, on the rate of achieving pathologic complete remission with avoidance of radical resection while maintaining an excellent local control with improvement of quality of life. All procedures in this study are standard of care, the study question relates to the use of neo-adjuvant FOLFOX and the timing between the end of radiation and surgery.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients in the trial receive the intervention and are followed prospectively.
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Neoadjuvant Chemotherapy and Follow-up Surgery
Arm Type
Other
Arm Description
All patients will receive standard of care therapy and based upon their response will either receive transanal local resection or full resection, based on pathologic response.
Intervention Type
Procedure
Intervention Name(s)
Standard of care chemotherapy with the change for avoidance of extensive surgery
Intervention Description
All treatments (chemotherapy, radiation, surgery) are standard of care; however, the timing of the procedures is altered to allow for the possibility of local excision instead of more extensive surgery.
Primary Outcome Measure Information:
Title
Complete remission
Description
Percent of patients who achieve complete remission
Time Frame
18 months
Title
Partial remission
Description
Percent of patients who achieve partial remission
Time Frame
18 months
Title
Disease progression
Description
Percent of patients with disease progression
Time Frame
18 months
Title
Local resection
Description
Percent of patients who require local resection only
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Patient quality of life
Description
Quality of life score on questionnaire
Time Frame
18 months
Title
Patient health status
Description
Patient self-reported health status
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Diagnosis of rectal invasive adenocarcinoma Tumor in the low or mid rectum (up to 11 cm from the anal verge) Clinical stage T3/N0-N1M0. Patients with low T2 who will need abdominal perineal resection are also eligible. 1. Clinical staging will be estimated based on the combination of the following assessments: Physical examination by the primary surgeon Computed Tomography or Positron Emission Tomography/Computed Tomography scan of chest, abdomen and pelvis Pelvic MRI and endoscopic ultrasound Exclusion Criteria: Less than 18 years of age Do not complete informed consent Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lisa C Miller, BA
Phone
313-343-3166
Email
lisa.miller4@ascension.org
First Name & Middle Initial & Last Name or Official Title & Degree
Susan M Szpunar, PhD
Phone
313-343-7838
Email
susan.szpunar@ascension.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amr Aref, MD
Organizational Affiliation
Ascension SME
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ascension St. John Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48236
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lisa C. Miller, BA
Phone
313-343-3166
Email
lisa.miller@ascension.org
First Name & Middle Initial & Last Name & Degree
Amr Aref, MD
Phone
313-343-3166
Email
amr.aref@ascension.org

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Treatment of Adenocarcinoma of the Rectum With Transanal Local Excision for Complete Responders

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