Organ Preservation in Elderly Patients With Rectal Cancer

Not Applicable

• Conditions: Rectal Cancer
• Interventions: Radiation: Radiochemotherapy or radiotherapy

• Registration Number: NCT01863862
• Lead Sponsor: Maria Sklodowska-Curie National Research Institute of Oncology

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.

Study Timeline

• Study Start: 2012-08
• Study First Submitted: 2013-05-14
• Study First Submitted QC: 2013-05-23
• Study First Posted: 2013-05-29
• Status Verified: 2019-03
• Last Update Submitted: 2019-03-28
• Last Update Posted: 2019-03-29
• Primary Completion: 2020-01
• Study Completion: 2020-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 90

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

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Exclusion Criteria

• Distant metastases
• Fixed tumour on digital rectal examination

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Clinical complete responders.	Radiochemotherapy or radiotherapy	Patients with complete clinical response obtained 8 weeks after chemoradiation or 10 weeks after short-course radiation.

Primary Outcome Measures

Name	Time	Method
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

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

Trial Locations

Locations (1)

M. Sklodowska-Curie Memorial Cancer Center; 🇵🇱 Warsaw, Poland