Organ Preservation in Elderly Patients With Rectal Cancer

Organ Preservation in Elderly Patients With Rectal Cancer: a Prospective Observational Study

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.

Study Overview

• Status: Unknown
• Conditions: Rectal Cancer
• Intervention / Treatment: Radiation: Radiochemotherapy or radiotherapy

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.

• Study Type: Interventional
• Enrollment (Anticipated): 90
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Krzysztof Bujko, Prof.; Phone Number: +48 601207466; Email: bujko@coi.waw.pl

Study Locations

• Poland
  • Warsaw, Poland, 02-781
    • Recruiting
    • M. Sklodowska-Curie Memorial Cancer Center
    • Contact: Krzysztof Bujko, Prof.; Phone Number: +48 601207466; Email: bujko@coi.waw.pl

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 70 years and older (OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Clinical complete responders.; Patients with complete clinical response obtained 8 weeks after chemoradiation or 10 weeks after short-course radiation.

Radiation: Radiochemotherapy or radiotherapy; 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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
The final three-year rate of local and distant recurrences taking into consideration results of rescue surgery for pelvic recurrence.	After 3 years of median follow-up for living patients.

Secondary Outcome Measures

Outcome Measure	Time Frame
The rate of local recurrence at one year without taking into consideration results of rescue surgery.	up to 20 months
The rate of local and distant recurrences after rescue surgery of pelvic recurrence.	After 3 years of median follow-up for living patients.
Overall survival at three years.	After 3 years of median follow-up for living patients.
Disease-free survival at three years	After 3 years of median follow-up for living patients.
Cancer specific survival at three years.	After 3 years of median follow-up for living patients.
Evaluation of anorectal function by using self-administered questionnaire in patients without local recurrence.	1 year after treatment
Multivariable analysis of prognostic factors associated with clinical complete response.	After 3 years of median follow-up for living patients.

Collaborators and Investigators

• Sponsor: Maria Sklodowska-Curie National Research Institute of Oncology
• Investigators: Principal Investigator: Krzysztof Bujko, Prof., M. Sklodowska-Curie memorial Cancer Centre in Warsaw

Study record dates

Study Major Dates

• Study Start: August 1, 2012
• Primary Completion (Anticipated): January 1, 2020
• Study Completion (Anticipated): January 1, 2020

Study Registration Dates

• First Submitted: May 14, 2013
• First Submitted That Met QC Criteria: May 23, 2013
• First Posted (Estimate): May 29, 2013

Study Record Updates

• Last Update Posted (Actual): March 29, 2019
• Last Update Submitted That Met QC Criteria: March 28, 2019
• Last Verified: March 1, 2019

More Information

Terms related to this study

• Keywords: Chemoradiation; Rectal cancer; Complete pathological response
• Additional Relevant MeSH Terms: Digestive System Diseases; Neoplasms; Neoplasms by Site; Gastrointestinal Neoplasms; Digestive System Neoplasms; Gastrointestinal Diseases; Intestinal Diseases; Intestinal Neoplasms; Rectal Diseases; Colorectal Neoplasms; Rectal Neoplasms
• Other Study ID Numbers: PGBRJG0113