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Organ Preservation in Elderly Patients With Rectal Cancer

Primary Purpose

Rectal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Radiochemotherapy or radiotherapy
Sponsored by
Maria Sklodowska-Curie National Research Institute of Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring Rectal cancer, Chemoradiation, Complete pathological response

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

The initial eligibility criteria

  • Age ≥70 years or <70 years in patients with ASA 3+
  • Tumour accessible by digital rectal examination
  • Maximal tumour size (usually length) not more than 5 cm
  • Circumferential bowel wall involvement not larger than 60%

There will be two groups of patients:

  1. Candidates for preoperative (chemo)radiotherapy and local excision: tumour ≤3 cm, non-polipoid cT1, or cT2 or borderline cT3, cN0.
  2. Candidates for preoperative (chemo)radiotherapy and total mesorectal excision: cT2 tumors requiring abdominoperineal excision, or cT3 or resectable cT4 (slight involvement of vagina, prostate or seminal vesicles); cN+ is allowed.

The final eligibility criterion

• Complete clinical response obtained 8 weeks after chemoradiation or 10 weeks after short-course radiation

Exclusion Criteria:

  • Distant metastases
  • Fixed tumour on digital rectal examination

Sites / Locations

  • M. Sklodowska-Curie Memorial Cancer CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Clinical complete responders.

Arm Description

Patients with complete clinical response obtained 8 weeks after chemoradiation or 10 weeks after short-course radiation.

Outcomes

Primary Outcome Measures

The final three-year rate of local and distant recurrences taking into consideration results of rescue surgery for pelvic recurrence.

Secondary Outcome Measures

The rate of local recurrence at one year without taking into consideration results of rescue surgery.
The rate of local and distant recurrences after rescue surgery of pelvic recurrence.
Overall survival at three years.
Disease-free survival at three years
Cancer specific survival at three years.
Evaluation of anorectal function by using self-administered questionnaire in patients without local recurrence.
Multivariable analysis of prognostic factors associated with clinical complete response.

Full Information

First Posted
May 14, 2013
Last Updated
March 28, 2019
Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology
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1. Study Identification

Unique Protocol Identification Number
NCT01863862
Brief Title
Organ Preservation in Elderly Patients With Rectal Cancer
Official Title
Organ Preservation in Elderly Patients With Rectal Cancer: a Prospective Observational Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
January 2020 (Anticipated)
Study Completion Date
January 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In elderly patients postoperative mortality measured 3-6 months after total mesorectal excision is high. Thus, less toxic treatments may lead to a survival benefit for elderly patients even if a risk of local recurrence is slightly higher compared to the open surgery. The investigators addressed the question whether watch and wait policy is safe in clinical complete responders after (chemo)radiation for elderly patients with small or moderately advanced tumours.
Detailed Description
There are two steps of selection. In the first step, the elderly patients with small or moderately advanced tumours who should routinely receive neoadjuvant chemoradiation (or radiation alone in those unfit for chemotherapy) prior to full-thickness local excision using transanal endoscopic microsurgery or prior to total mesorectal excision will be included. In the next step, only patients with clinical complete response obtained 8-10 weeks from completion of (chemo)radiation are selected. Those patients constitute study group and will be observed without further treatment. The remaining patients with residual cancer will proceed to routine management, namely transanal endoscopic microsurgery or total mesorectal excision. Patients undergoing transanal endoscopic microsurgery and having poor response to (chemo)radiation (ypT2-3 disease or positive margin) will proceed to the conversion to total mesorectal excision. Neoadjuvant chemoradiation: 50 Gy total dose over 5 weeks with 2 Gy per fraction delivered with simultaneous chemotherapy consisting of three cycles of 5-Fu 200 mg/m2 i.v. bolus and leucovorin 100 mg/m2 i.v. short infusion over 2 days given during 1-2, 15-16, and 29-30 days of radiotherapy. Patients unfit for chemotherapy will receive 25 Gy total dose over 5 days with 5 Gy per fraction. The study hypothesis is that in clinical complete responders after (chemo)radiation treated without initial surgery, the local recurrence rate will be less than 25% and results of the rescue surgery (local and distant recurrence rate) will be not worse (or only slightly worse) than that seen after up-front total mesorectal excision in patients with similar stage of the disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer
Keywords
Rectal cancer, Chemoradiation, Complete pathological response

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Clinical complete responders.
Arm Type
Experimental
Arm Description
Patients with complete clinical response obtained 8 weeks after chemoradiation or 10 weeks after short-course radiation.
Intervention Type
Radiation
Intervention Name(s)
Radiochemotherapy or radiotherapy
Intervention Description
50 Gy, 2 Gy per fraction with simultaneous 5-Fu and leucovorin or 5 x 5 Gy for patients unfit for chemotherapy. Patients with complete clinical response 8-10 weeks after radiotherapy will be closely observed and rescue surgery will be performed in a case of local recurrence. Patients with persistent tumour 8-10 weeks after radiotherapy will undergo transanal endoscopic microsurgery or total mesorectal excision. After transanal endosciopic microsurgery, patients with ypT0-1 disease and negative surgical margins will be closely observed and rescue total mesorectal excision will be performed in a case of local recurrence; those with ypT2-3 disease or with positive margin will undergo immediate conversion to total mesorectal excision.
Primary Outcome Measure Information:
Title
The final three-year rate of local and distant recurrences taking into consideration results of rescue surgery for pelvic recurrence.
Time Frame
After 3 years of median follow-up for living patients.
Secondary Outcome Measure Information:
Title
The rate of local recurrence at one year without taking into consideration results of rescue surgery.
Time Frame
up to 20 months
Title
The rate of local and distant recurrences after rescue surgery of pelvic recurrence.
Time Frame
After 3 years of median follow-up for living patients.
Title
Overall survival at three years.
Time Frame
After 3 years of median follow-up for living patients.
Title
Disease-free survival at three years
Time Frame
After 3 years of median follow-up for living patients.
Title
Cancer specific survival at three years.
Time Frame
After 3 years of median follow-up for living patients.
Title
Evaluation of anorectal function by using self-administered questionnaire in patients without local recurrence.
Time Frame
1 year after treatment
Title
Multivariable analysis of prognostic factors associated with clinical complete response.
Time Frame
After 3 years of median follow-up for living patients.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The initial eligibility criteria Age ≥70 years or <70 years in patients with ASA 3+ Tumour accessible by digital rectal examination Maximal tumour size (usually length) not more than 5 cm Circumferential bowel wall involvement not larger than 60% There will be two groups of patients: Candidates for preoperative (chemo)radiotherapy and local excision: tumour ≤3 cm, non-polipoid cT1, or cT2 or borderline cT3, cN0. Candidates for preoperative (chemo)radiotherapy and total mesorectal excision: cT2 tumors requiring abdominoperineal excision, or cT3 or resectable cT4 (slight involvement of vagina, prostate or seminal vesicles); cN+ is allowed. The final eligibility criterion • Complete clinical response obtained 8 weeks after chemoradiation or 10 weeks after short-course radiation Exclusion Criteria: Distant metastases Fixed tumour on digital rectal examination
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Krzysztof Bujko, Prof.
Phone
+48 601207466
Email
bujko@coi.waw.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Krzysztof Bujko, Prof.
Organizational Affiliation
M. Sklodowska-Curie memorial Cancer Centre in Warsaw
Official's Role
Principal Investigator
Facility Information:
Facility Name
M. Sklodowska-Curie Memorial Cancer Center
City
Warsaw
ZIP/Postal Code
02-781
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Krzysztof Bujko, Prof.
Phone
+48 601207466
Email
bujko@coi.waw.pl
First Name & Middle Initial & Last Name & Degree
Krzysztof Bujko, Prof.

12. IPD Sharing Statement

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Organ Preservation in Elderly Patients With Rectal Cancer

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