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Completed

NCT Number: NCT00952926

Watchful Waiting. An Observational Study of Patients With Rectal Cancer After Concomitant Radiation and Chemotherapy

The purpose of this study is to investigate if operation and permanent stoma can be omitted in patients with cancer in the lower part of the rectum.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Vejle Hospital

Vejle, DK-7100, Denmark

About this study

Patients entering this study are offered the possibility of avoiding an extensive operation and a permanent stoma.

Over the past 2 years Vejle Hospital examined patients with rectal cancer during their course of treatment and we have developed a method to predict complete response.

Patients in this study are treated with chemotherapy and external irradiation supplemented with an endorectal boost (2 fractions). At the start of treatment and weeks 2, 4, and 6 of the treatment course an endoscopy is performed to evaluate the response. The final evaluation is performed 6 weeks after end of treatment. Patients with complete remission are offered observation. Patients with residual tumor are advised to be operated.

Follow-up is performed every 2 months the first year and every 3 months the second year. 2 follow-up visits are planned for the third year. A yearly follow-up is scheduled for the fourth and fifth year.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histopathologically verified adenocarcinoma in the rectum
  • Planned APR or ultra low resection
  • Primary resectable T2 or T3 tumor
  • Distance from anus to lower edge of tumor ≤ 6 cm
  • Suited for curative intended radiation and chemotherapy
  • Accept taking of biopsy and blood samples for translational research
  • Age ≥ 18 years
  • Normal function of bone marrow
  • leukocytes ≥ 3 x 10^9/l
  • thrombocytes ≥ 100
  • Normal liver function
  • ALAT < 2.5 x upper normal value
  • bilirubin < 2.5 x upper normal value
  • Renal function
  • Serum creatinin < 1.5 x upper normal value
  • Written and orally informed consent

Exclusion criteria

  • Other malignant disease within the last 5 years apart from basocellular skin cancer and carcinoma in situ cervicis uteri
  • Distant metastases
  • Pregnant or breast feeding patients

Treatment and study plan

Primary outcomes

  1. Frequency of local recurrence

    Time frame: 1 year

Secondary outcomes

  1. Frequency of cumulative local recurrence

    Time frame: Up to 5 years

  2. Frequency of distant metastases verified by planned PET/CT scans

    Time frame: Up to 5 years.

  3. Overall survival

    Time frame: Up to 5 years.

Sponsors and collaborators

Lead sponsor

Vejle Hospital

Other

Registry information

Official study title

A Prospective Observational Study of Patients With Rectal Cancer After Concomitant Radiation and Chemotherapy

Important dates

Study start
2009
Primary completion
2014
Study completion
2019
First posted
Aug 6, 2009
Registry last updated
Feb 5, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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