DOI: 10.12809/hkmj185079
© Hong Kong Academy of Medicine. CC BY-NC-ND 4.0
EDITORIAL
    Is now the right time to abolish breast cancer
      screening in Hong Kong?
    Lorraine CY Chow, MB, BS, FRCSEd
    Private Practice
    Corresponding author: Dr Lorraine CY Chow (drlorrainechow@gmail.com)
    In a recent article by the Cancer Expert Working
      Group on Cancer Prevention and Screening,1
      screening for breast cancer in the general female population was not
      recommended based on the lack of evidence for its survival benefit and the
      imminent cause of patient anxiety. The criticisms of implementing a
      population-based screening programme for breast cancer include
      overexposure to radiation and increment in the number of invasive
      investigations and treatments for breast lesions that may never become
      malignant. Nonetheless it is important to recognise that the primary aim
      of screening in breast cancer is to facilitate timely detection of
      early-stage disease, and hence improve survival. In contrast to this
      notion, several large-scale studies using nationwide data showed that
      screening could only prevent one to two cancer deaths in every one to 2000
      women screened at the expense of 20% overdiagnosis rates as well as
      induction of anxiety in every one to 2000 women.2
      3 Nonetheless a more in-depth
      analysis would reveal major weaknesses in these studies including their
      methodology, inclusion criteria for screening, level of expertise in the
      evaluation of screening results, and the standard of equipment used for
      screening. For instance, the Canadian National Breast Screening Study was
      the only randomised controlled trial that did not show any survival
      benefit for screening, but a 35% increment in the overdiagnosis of ductal
      carcinoma in situ.4 Nonetheless
      randomisations were not blinded and with pitfalls. Women with symptomatic
      palpable breast masses were also recruited into the ‘screening’ arm, and
      the quality of mammography was suboptimal and evaluation of mammographic
      images deficient.
    On the contrary, many studies have shown that
      treatment for smaller tumours without nodal involvement confers better
      oncological outcomes as well as a better chance of undergoing breast
      conserving surgery, and fewer postoperative morbidities.5 6 7 This is an important issue that was often not addressed
      by these large-scale population studies such as the Swiss Medical Board
      study and the Cochrane review.2 3 The primary end-point of these
      studies was reduced mortality. They paid no regard to the short-term
      physical and psychological impact of cancer treatment. The current trend
      in treatment for breast cancer is multifaceted. A smaller tumour size
      increases the chances of breast conserving surgery with consequently less
      postoperative morbidity compared with standard mastectomy.8 Applying the same principle, the advent of sentinel
      lymph node mapping in the management of the axillary area implied a
      substantially reduced need for axillary dissection in early tumours, and
      hence lower risk of lymphoedema and its associated morbidities.9 10 Moreover,
      advances in imaging techniques may further improve the accuracy of
      screening. In the Norwegian nationwide study of over 40 000 women with
      breast cancer, screening led to a reduction in mortality by 4.8 deaths per
      100 000 person-years when compared with the non-screened group.11 Furthermore, screening in the ‘modern’ era further
      reduced mortality by 7.2 deaths per 100 000 person-years compared with
      screening in the ‘historical’ era implying that changes to breast cancer
      awareness, advances in imaging techniques, and improved treatments in
      recent years could all contribute to the survival benefit of a screening
      programme. Such finding was also in line with the evidence provided by the
      National Health Service Screening Programme in which there was a steady
      decline in mortality for women with breast cancer aged between 50 and 79
      years as the screening programme evolved over a 10-year period from 1990
      to 2000.12 In Hong Kong, there has
      been a steady increment in the number of new cases of breast cancer over
      the last three decades. According to the Hong Kong Cancer Registry, breast
      cancer is now the most common female cancer with over 3500 new cases
      diagnosed annually.13 Public
      awareness of breast cancer has substantially improved in recent years
      following promotion by local media and other non-profitable organisations
      such as the Hong Kong Breast Cancer Foundation, Well Women Clinic of the
      Tung Wah Group of Hospitals, and the Family Planning Association. In fact,
      breast screening in our local population has been shown to be feasible and
      well accepted.14 Advanced imaging
      technology such as three-dimensional mammography has been introduced as an
      alternative efficient assessment tool for screening as well as
      multidisciplinary management of breast cancer in clinical practice. It may
      be premature to conclude that screening for the general female population
      in Hong Kong is of little clinical value.
    Declaration
    The author has no conflicts of interest to
      disclose.
    References
    1. Cancer Expert Working Group on Cancer
      Prevention and Screening. Recommendations on prevention and screening for
      breast cancer in Hong Kong. Hong Kong Med J 2018;24:298-306. Crossref
    2. Gøtzsche PC, Jørgensen KJ. Screening for
      breast cancer with mammography. Cochrane Database Syst Rev
      2013;(6):CD001877. Crossref
    3. Biller-Andorno N, Jüni P. Abolishing
      mammography screening programs? A view from the Swiss Medical Board. N
      Engl J Med 2014;370:1965-7. Crossref
    4. Miller AB, Baines CJ, To T, Wall C.
      Canadian National Breast Screening Study: 2. Breast cancer detection and
      death rates among women aged 50 to 59 years. CMAJ 1992;147:1477-88.
    5. Cossetti RJ, Tyldesley SK, Speers CH,
      Zheng Y, Gelmon KA. Comparison of breast cancer recurrence and outcome
      patterns between patients treated from 1986 to 1992 and from 2004 to 2008.
      J Clin Oncol 2015;33:65-73. Crossref
    6. Metzger-Filho O, Sun Z, Viale G, et al.
      Patterns of recurrence and outcome according to breast cancer subtypes in
      lymph node-negative disease: results from international breast cancer
      study group trials VIII and IX. J Clin Oncol 2013;31:3083-90. Crossref
    7. Jacobson JA, Danforth DN, Cowan KH, et
      al. Ten-year results of a comparison of conservation with mastectomy in
      the treatment of stage I and II breast cancer. N Engl J Med
      1995;332:907-11. Crossref
    8. Eby PR. Evidence to support screening
      women annually. Radiol Clin North Am 2017;55:441-56.
    9. Veronesi U, Paganelli G, Viale G, et al.
      A randomized comparison of sentinel-node biopsy with routine axillary
      dissection in breast cancer. N Engl J Med 2003;349:546-53. Crossref
    10. Bromham N, Schmidt-Hansen M, Astin M,
      Hasler E, Reed MW. Axillary treatment for operable primary breast cancer.
      Cochrane Database Syst Rev 2017;(1):CD004561. Crossref
    11. Kalager M, Zelen M, Langmark F, Adami
      HO. Effect of screening mammography on breast-cancer mortality in Norway.
      N Engl J Med 2010;363:1203-10. Crossref
    12. Blanks RG, Moss SM, McGahan CE, Quinn
      MJ, Babb PJ. Effect of NHS breast screening programme on mortality from
      breast cancer in England and Wales, 1990-8: comparison of observed with
      predicted mortality. BMJ 2000;321:665-9. Crossref
    13. Hong Kong Cancer Registry. Available
      from: http://www3.ha.org.hk/cancereg/. Accessed Jun 2018.
    14. Kwong A, Cheung PS, Wong AY, et al.
      The acceptance and feasibility of breast cancer screening in the East.
      Breast 2008;17:42-50. Crossref

