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Clinical Trials/NCT02572362
NCT02572362CompletedNot Applicable

Estimation of Second Cancer Risk in Patients Planned With Different Radiotherapy Regimes for Rectal Cancer - A Planning Study and Model-based Analysis

Kantonsspital Graubuenden1 site in 1 country25 target enrollmentStarted: August 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
25
Locations
1
Primary Endpoint
Calculation of the organ-specific excess lifetime attributable risk (LAR) (%)

Study Overview

Brief Summary

Retrospective study comparing dose distribution of 3D conformal radiotherapy (3DCRT) and volumetric-modulated arc therapy (VMAT) to estimate secondary cancer risk for patients having had radiation therapy for rectal cancer. Twenty-five patients are included in this study. Planning CT scans are used for comparison of dose distribution and calculation of second cancer risk.

Detailed Description

A model-based Analysis calculating the organ-specific excess lifetime attributable risk using the planning CT data sets of 25 patients to estimate second cancer risk for patients after radiotherapy for rectal cancer comparing conventional 3DCRT with VAMT techniques.

Study Design

Study Type
Observational
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male/Female > 18 years of age
  • pre or postoperative radiation therapy for rectal cancer
  • Planning CT

Exclusion Criteria

  • Planning CT not available

Outcomes

Primary Outcomes

Calculation of the organ-specific excess lifetime attributable risk (LAR) (%)

Time Frame: 60 years (model-based calculation)

LAR is calculated for variable Ages at exposure

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Kantonsspital Graubuenden
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Daniel Rudolf Zwahlen

MD, MBA

Kantonsspital Graubuenden

Study Sites (1)

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