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OpenTrials
Completed

NCT Number: NCT03877029

Long-term Effects of Breast Cancer Treatment

The objective of this project is to generate evidence about quality of life related to side effects of treatment of women with screen-detected versus symptomatic breast cancer. The project will investigate the impact of detection mode (by screening or by symptoms) versus tumor characteristics as a predictor of quality of life among breast cancer survivors. The burden of long-term effects, measured as quality of life at specific points after diagnosis, will be compared between these groups. The results will also be compared with a control group of women, who have attended screening, but never been diagnosed with breast cancer.

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Key information

Age range

50 year–69 year

Sex eligibility

Female

Study type

Observational

Primary location

Cancer Registry of Norway

Oslo, 0304, Norway

About this study

The project will include a retrospective information which will be collected by using a self-administered questionnaire about the treatment women received and their quality of life at certain time points after a breast cancer diagnosis. Women aged 50-69 years at the time of diagnosis are the target group of BreastScreen Norway and also for this project.

The women will be identified from the Cancer Registry databases. The questionnaire will be based on EQ-5D-5L and will be developed in close collaboration with breast cancer survivors who have personally experienced the long-term effects of breast cancer treatment, whether resulting from screen-detected or symptomatic breast cancer.

The questionnaire will cover topics related to demographics, treatment, and information required to estimate health related quality of life (HRQoL) and quality-adjusted life years (QALY). Information about detection mode and disease stage at diagnosis will be extracted from the Cancer Registry.

Study I - a review of the literature in a paper describing and analyzing the current evidence on quality of life among women diagnosed with breast cancer and treated for this disease, with a focus on disease stage at diagnosis. Due to substantial changes in treatment during the last decades, only studies reporting on women who have received treatment in 1995 or later will be included. Solely studies written in English will be included.

For studies II and III, data collected from the self-administered questionnaire will be used. In addition, information about screening history and tumor characteristics will be obtained from the Cancer Registry of Norway.

In Study II, quality of life will be compared between about 1000 women treated for screen-detected, about 1000 women treated for symptomatic, about 1000 women treated for interval cancer and about 1000 women without any diagnosis of breast cancer. The main hypothesis is that women with screen-detected breast cancer have a higher quality of life than women diagnosed with symptomatic breast cancer.

Study III will be a continuation of Study II, and will aim to investigate the impact of detection mode versus tumor characteristics and treatment types as the main predictor of long-term quality of life among women diagnosed and treated for breast cancer among the two groups of women, those diagnosed with screen-detected breast cancer versus those diagnosed with interval breast and symptomatic breast cancer.

Who can participate

Healthy volunteers accepted: Yes

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

Study II

Inclusion criteria

  • Screened in BreastScreen Norway and diagnosed with breast cancer between 2006 and 2017
  • Diagnosed with symptomatic breast cancer between 2006 and 2017 and never attended screening
  • Screened in BreastScreen Norway and diagnosed with interval breast cancer between 2006 and 2017
  • Screened in BreastScreen Norway and have never been diagnosed with breast cancer

Exclusion criteria

  • Death after recruitment

Study III

Inclusion criteria

  • Screened in BreastScreen Norway and diagnosed with breast cancer between 2006 and 2017
  • Screened in BreastScreen Norway and diagnosed with interval breast cancer between 2006 and 2017
  • Diagnosed with symptomatic breast cancer between 2006 and 2017 and never attended screening

Exclusion criteria

  • Death after recruitment

Treatment and study plan

Primary outcomes

  1. Quality of life score

    Time frame: 2006-2017

    Quality of life measure from 0 to 100 on a visual analogue scale

  2. QALY (Quality-Adjusted-Life-Year)

    Time frame: 2006-2017

    QALY is calculated by estimating the years of life remaining for a woman following a particular treatment or intervention and weighting each year with her corresponding health related quality of life score

Sponsors and collaborators

Lead sponsor

Norwegian Institute of Public Health

Other Gov

Collaborators

  • The Dam Foundation

Registry information

Official study title

Long-term Effects Following Treatment of Women With Screen-detected Versus Symptomatic Breast Cancer

Important dates

Study start
2019
Primary completion
2024
Study completion
2025
First posted
Mar 15, 2019
Registry last updated
Mar 9, 2026

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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