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Time dependent effects of adjuvant tamoxifen therapy on cerebrovascular disease : results from a randomised trial

Rosell, Johan (author)
Östergötlands Läns Landsting,Linköpings universitet,Onkologi,Hälsouniversitetet,Onkologiska kliniken US
Nordenskjöld, Bo (author)
Östergötlands Läns Landsting,Linköpings universitet,Onkologi,Hälsouniversitetet,Onkologiska kliniken US
Bengtsson, Nils-Olof (author)
Umeå universitet,Onkologi,Department of Oncolog, Umea University Hospital, Sweden
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Fornander, T. (author)
Karolinska Institutet,Department of Oncology, Karolinska University Hospital, Stockholm, Sweden
Hatschek, T. (author)
Karolinska Institutet,Department of Oncology, Karolinska University Hospital, Stockholm, Sweden
Lindman, Henrik (author)
Uppsala universitet,Enheten för onkologi,Department of Oncology, Uppsala University Hospital, Uppsala, Sweden
Malmström, Per (author)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Department of Oncology, Lund University Hospital, Lund, Sweden
Wallgren, A. (author)
Department of Oncology, Sahlgrenska University Hospital, Göteborg, Sweden
Stål, Olle (author)
Östergötlands Läns Landsting,Linköpings universitet,Onkologi,Hälsouniversitetet,Onkologiska kliniken US
Carstensen, John (author)
Linköpings universitet,Hälsa och samhälle,Hälsouniversitetet
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 (creator_code:org_t)
2011-02-22
2011
English.
In: British Journal of Cancer. - : Springer Science and Business Media LLC. - 0007-0920 .- 1532-1827. ; 104:6, s. 899-902
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Tamoxifen has been associated with an increased risk of stroke. There is, however, little information on the effect in the post-treatment period. Using data from the Swedish Breast Cancer Group adjuvant trial of 5 vs 2 years of tamoxifen treatment, we now report both short-term and long-term effects on morbidity as well as mortality because of cerebrovascular disease. METHODS: Data from the Swedish National Hospital Discharge Registry combined with information from the Swedish Cause of Death Registry was used to define events of disease. Hazard ratios (HRs) were estimated using Cox regression. RESULTS: Comparing patients randomised to 5 years of tamoxifen with patients randomised to 2 years of tamoxifen, the incidence of cerebrovascular diseases was increased (HR 1.70, 95% CI 1.05-2.75) during the active treatment phase and reduced after the active treatment period (HR 0.78, 95% CI 0.63-0.96), and the difference in HR between the two time-periods was significant (P 0.0033). The mortality from cerebrovascular diseases was increased during the treatment period (HR 3.18, 95% CI 1.03-9.87) and decreased during the post-treatment period (HR 0.60, 95% CI 0.40-0.90) with a significant difference in HR between the two periods of follow-up (P=0.0066). Similar results were seen for subgroups of cerebrovascular diseases, such as stroke and ischaemic stroke. CONCLUSION: In an adjuvant setting, tamoxifen was associated with an increased risk of cerebrovascular disease during treatment, but a decreased risk in the post-treatment period.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

breast cancer
tamoxifen
adjuvant treatment
adverse events
cerebrovascular disease
MEDICINE
MEDICIN
breast cancer
tamoxifen
adjuvant treatment
adverse events
cerebrovascular disease
SOCIAL SCIENCES

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