"Watch and Wait" After Neo-adjuvant Chemoradiotherapy for Primary Locally Advanced Rectal Cancer.
NCT ID: NCT03402477
Last Updated: 2024-04-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
86 participants
OBSERVATIONAL
2018-01-10
2024-04-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients who have completed neoadjuvant treatment according to national guidelines for rectal cancer, i.e., radiotherapy or chemo-radiotherapy (at least 40 Gy) or short-course radiotherapy combined with chemotherapy
* Patients aged ≥18 years of age are eligible for inclusion. However, patients aged ≤40 years are recommended to undergo surgery on the theoretical base of a possibly more aggressive tumour disease in this age group, and will be asked to participate in the study by consenting to recording of data. Those patients who insist on W\&W approach after careful consideration and well-documented informed consent are eligible for entering the W\&W protocol.
* Given informed consent
* Stage I-III rectal cancer; however, patients with limited liver metastases who undergo primary liver surgery as part of a "liver first" treatment approach may be included
Exclusion Criteria
* Patients unable to give informed consent
* Patients with short course radiotherapy (5x5 Gy) without additional chemotherapy, or patients receiving less than 40 Gy in long course CRT
* Patients with cCR but with increasing tumour growth on MRI after preoperative treatment
* Patients with metastatic disease at the time of diagnosis with the exception of those who are eligible for "liver first" treatment approach as part of an intention to cure approach.
* Patients previously diagnosed and treated for malignant disease in the pelvic region with radio- or chemoradiotherapy
* Other circumstances that may interfere with successful participation in the W\&W protocol
18 Years
ALL
No
Sponsors
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University Hospital of North Norway
OTHER
St. Olavs Hospital
OTHER
Helse-Bergen HF
OTHER
Sorlandet Hospital HF
OTHER_GOV
Oslo University Hospital
OTHER
University Hospital, Akershus
OTHER
Norwegian Institute of Public Health
OTHER_GOV
Helse Stavanger HF
OTHER_GOV
Responsible Party
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Principal Investigators
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Hartwig Kørner, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Helse Stavanger HF
Locations
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Haukeland University Hospital
Bergen, , Norway
Sørlandet Hospital Kristiansand
Kristiansand, , Norway
Akershus University Hospital
Lørenskog, , Norway
Oslo University Hospital
Oslo, , Norway
Stavanger University Hospital
Stavanger, , Norway
University Hospital Northern Norway
Tromsø, , Norway
St. Olavs Hospital
Trondheim, , Norway
Countries
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Other Identifiers
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SUSID674
Identifier Type: -
Identifier Source: org_study_id
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