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Corrigendum| Volume 96, P131-132, June 2018

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Corrigendum to “An association study of established breast cancer reproductive and lifestyle risk factors with tumour subtype defined by the prognostic 70-gene expression signature (MammaPrint®)” [Eur J Cancer 75 (April 2017) 5–13]

  • M. Makama
    Affiliations
    Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands

    Division of Molecular Pathology, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
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  • C.A. Drukker
    Affiliations
    Department of Surgery, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands

    Albert Schweitzer Hospital, Department of Surgery, Dordrecht, The Netherlands
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  • E.J.Th. Rutgers
    Affiliations
    Department of Surgery, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
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  • L. Slaets
    Affiliations
    Department of Statistics, European Organization for Research and Treatment of Cancer, Brussels, Belgium
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  • F. Cardoso
    Affiliations
    Breast Unit, Champalimaud Clinical Center, Lisbon, Portugal
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  • M.A. Rookus
    Affiliations
    Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
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  • K. Tryfonidis
    Affiliations
    Medical Department, European Organization for Research and Treatment of Cancer, Brussels, Belgium
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  • L.J. Van't Veer
    Affiliations
    Division of Molecular Pathology, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
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  • M.K. Schmidt
    Correspondence
    Corresponding author: Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066CX, Amsterdam, The Netherlands.
    Affiliations
    Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands

    Division of Molecular Pathology, Netherlands Cancer Institute – Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
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Published:April 12, 2018DOI:https://doi.org/10.1016/j.ejca.2018.03.017
      The authors regret a typographical error was made in table one in the original document, the time between diagnosis and questionnaire indicated there should have stated “years”, instead of “months”.
      The correct table now shows below and the authors would like to apologise for any inconvenience caused.
      Table 1Distribution of breast cancer risk factors and patient characteristics by the 70-gene MammaPrint® signature result.
      Values are means ± standard deviation or percentages.
      N
      Missing data vary by variable.
      Low-risk tumourN
      Missing data vary by variable.
      High-risk tumourP
      P < 0.05; differences tested between patients with low-risk and high-risk tumours using chi-square for categorical variables and Wilcoxon rank-sum test for continuous variables.
      Age at enrolment (years)90956.5 ± 8.664554.8 ± 9.80.003
      Risk factors investigated
      Current BMI (Kg/m2)87725.7 ± 4.661925.9 ± 4.80.65
      Age at menarche (years)87613.0 ± 1.561913.0 ± 1.50.96
      Hormonal contraceptive use0.60
       Never (%)11513.67211.2
       Former (%)58464.243567.4
       Current (%)19121.012419.2
       Missing (%)202.2142.2
      Parity0.74
       Nulliparous (%)18720.614322.2
       Parous (%)68375.147573.6
       Missing (%)404.4274.2
      Age at first birth (years)66126.5 ± 4.745526.9 ± 4.70.13
      Breastfeeding duration (months)8705.5 ± 7.96185.7 ± 9.00.44
      Age at menopause (years)70648.7 ± 5.848947.9 ± 6.20.03
      HRT use0.81
       Never (%)75983.453883.4
       Former (%)636.9497.6
       Current (%)677.4416.4
       Missing (%)212.3172.6
      Others
      Birth weight (grams)4983097 ± 7703523070 ± 6210.90
      Current height (cm)881168.5 ± 6.4622168.2 ± 6.60.48
      Education level0.68
       Low38041.827442.5
       Intermediate22024.216926.2
       High27830.618128.1
       Missing323.5213.3
      Family history of breast cancer0.56
       No (%)68174.849777.1
       Yes (%)19020.912519.4
       Missing (%)394.3233.6
      BRCA1/2 germline mutation (in family)0.0006
       Yes91.0274.2
       No42947.129946.4
       Unknown37140.824838.5
       Missing10111.17111.0
      BRCA1/2 germline mutation (patient)
       Yes80.9345.3<0.0001
       No51056.033852.4
       Unknown28931.819930.9
       Missing10311.37411.5
      Time interval from diagnosis to filling questionnaire (years)9091.7 ± 1.16451.5 ± 1.00.002
      Breast cancer characteristics
      Age at diagnosis (years)91054.3 ± 8.664552.8 ± 9.80.007
      Tumour histology<0.0001
       Ductal (%)71879.058490.5
       Lobular (%)12213.4325.0
       Mixed (%)374.181.2
       Other (%)323.5213.3
      Lymph node status0.08
       Negative (%)76183.654484.3
       Positive (%)14916.410115.7
      Tumour size (mm)91016.5 ± 8.964518.9 ± 8.4<0.0001
      Tumour grade<0.0001
       Well differentiated (%)32335.5314.8
       Moderately differentiated (%)47652.320832.3
       Poorly/undifferentiated (%)10811.940562.8
       Undefined (%)30.310.2
      Oestrogen receptor (ER) status
      Measured by immunohistochemistry, and for HER2 additionally by an in situ hybridisation method.
      <0.0001
       Negative (%)121.322835.4
       Positive (%)89898.741764.7
      Progesterone receptor (PR) status
      Measured by immunohistochemistry, and for HER2 additionally by an in situ hybridisation method.
      <0.0001
       Negative (%)11412.532548.1
       Positive (%)78185.831050.4
       Missing (%)151.7101.6
      Human epidermal growth factor receptor 2 receptor (HER2) status
      Measured by immunohistochemistry, and for HER2 additionally by an in situ hybridisation method.
      <0.0001
       Negative (%)84292.549076.0
       Positive (%)667.315423.9
       Unknown (%)20.210.2
      a Values are means ± standard deviation or percentages.
      b Missing data vary by variable.
      c P < 0.05; differences tested between patients with low-risk and high-risk tumours using chi-square for categorical variables and Wilcoxon rank-sum test for continuous variables.
      d Measured by immunohistochemistry, and for HER2 additionally by an in situ hybridisation method.

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