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CompletedNCT03401034Updated Jan 17, 2018

Influence of Lifestyle, Inflammatory Biomarkers, and Genetic Factors on Long-term Breast Cancer Prognosis

An observational study in Breast Cancer, Breast Cancer Mortality and Breast Cancer Survival, sponsored by German Cancer Research Center. Completed. Open to female participants aged 50 Years to 74 Years. Per ClinicalTrials.gov, last updated 2018-01-17.

Sponsored by German Cancer Research Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
3,813
Ages
50 Years to 74 Years
Sex
Female
01

Study summary

The MARIEplus study is a prospective cohort of breast cancer patients recruited into the MARIE (Mamma Carcinoma Risk factor InvEstigation) study, a population-based case-control study of breast cancer conducted in two German study regions, Hansestadt Hamburg and Rhine-Neckar-Karlsruhe (RNK) region. Participants were identified through participating clinics and the Hamburg cancer registry between January 1st, 2001 and September 30th, 2005 in Hamburg and between August 1st, 2002 and July 31st, 2005 in the RNK study region. Patients were aged 50-74 years at histologically confirmed primary invasive (stages I to IV) or in situ breast tumor (stage 0). Comprehensive information on demographic, socio-economic, and lifestyle factors was collected at multiple time points: at recruitment by a standardized face-to-face interview and at follow-up median 6 years as well as 11 years later using computer assisted telephone interview.

Vital status was assessed in 2009 and again in 2015 via the population registries and causes of death were obtained from death certificates and coded according to the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10).

Information on the clinical course was abstracted from medical records to verify clinical events either self-reported in follow-up interviews or reported by treating physicians.

The studies were approved by the ethics committee of the University of Heidelberg and the University of Hamburg and conducted in agreement with the Helsinki Declaration. Written informed consent was provided by all participants at baseline and during follow-up.

The primary objectives of this study are

  • To assess the association of modifiable lifestyle factors and personal factors, including BMI, diet, physical activity, tobacco and alcohol use, menopausal hormone therapy, socioeconomic status, with breast cancer survival, overall and according to tumor type, after accounting for established prognostic factors.
  • To examine the influence of genetic variants on breast cancer relapse and survival
  • To assess the association of lifestyle factors and their changes in the course of survivorship on subsequent breast cancer prognosis.
  • To assess the individual and combined association of inflammation/metabolic biomarkers as well as changes in their serum levels with subsequent breast cancer prognosis overall and according to tumor type.
  • To assess whether and to what extent the associations between breast cancer prognosis and lifestyle factors and/or their changes are mediated by circulating biomarker levels.
02

Conditions studied

  • Breast Cancer
  • Breast Cancer Mortality
  • Breast Cancer Survival
  • Postmenopausal Breast Cancer
  • Lifestyle
  • Genetic Factors
  • Inflammation
  • Inflammatory Biomarkers
  • Hormone Therapy
  • Phytoestrogens
03

Who can participate

Ages eligible
50 Years to 74 Years
Sexes eligible
Female
Sampling method
Probability sample

Study population

Patients with histologically confirmed primary invasive or in situ breast tumors aged 50-74 years at diagnosis recruited in the city and state of Hamburg or the Rhine-Neckar-Karlsruhe region

Inclusion criteria

  • Histologically confirmed Primary invasive (ICD-10 C50) (stage I-IV) or in-situ (ICD-10 D05) breast cancer
  • 50 to 74 years at diagnosis
  • Patients in the city and state of Hamburg in northern Germany and the Rhine-Neckar-Karlsruhe region in southern Germany
  • German-speaking
  • Physically and mentally ability to participate in a personal interview of about 90 minutes

Exclusion criteria

Exclusion Criteria:

  • Previous diagnosis of breast cancer
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
3,813 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna
05

What researchers measure

Primary outcomes

  1. Mortality after breast cancer diagnosis

    Risk of mortality (all-cause, breast cancer specific)

    Time frame: Median follow-up time 6 and 11 years

Secondary outcomes

  1. Risk of recurrence

    Risk of recurrence

    Time frame: Median follow-up time 6 and 11 years

06

Study locations

No study locations are listed for this record.

07

Registry details

Key details

Study ID
NCT03401034
Lead sponsor
German Cancer Research Center
Responsible party
Sponsor
First posted
Jan 17, 2018
Start date
Aug 1, 2002
Primary completion
Jun 30, 2015
Completion
Jun 30, 2015
Last update
Jan 17, 2018

Study contacts

Jenny Chang-Claude, Prof. Dr.
principal investigator · German Cancer Research Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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This study is completed, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

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