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X-ray mammography[]

Mammography is still the modality of choice for screening of early breast cancer, since it is relatively fast, reasonably accurate, and widely available in developed countries. Breast cancers detected by mammography are usually much smaller (earlier stage) than those detected by patients or doctors as a breast lump.[How to reference and link to summary or text]

Due to the high incidence of breast cancer among older women, screening is now recommended in many countries. Recommended screening methods include breast self-examination and mammography. Mammography has been estimated to reduce breast cancer-related mortality by 20-30%.[1] Routine (annual) mammography of women older than age 40 or 50 is recommended by numerous organizations as a screening method to diagnose early breast cancer and has demonstrated a protective effect in multiple clinical trials.[2] The evidence in favor of mammographic screening comes from eight randomized clinical trials from the 1960s through 1980s. Many of these trials have been criticised for methodological errors, and the results were summarized in a review article published in 1993.[3]

Improvements in mortality due to screening are hard to measure; similar difficulty exists in measuring the impact of Pap smear testing on cervical cancer, though worldwide, the impact of that test is likely enormous. Nationwide mortality due to cancer before and after the institution of a screening test is a surrogate indicator about the effectiveness of screening, and results of mammography are favorable.

File:Mammo breast cancer.jpg

Normal (left) versus cancerous (right) mammography image.

The U.S. National Cancer Institute recommends screening mammography every one to two years beginning at age 40.[4] In the UK, women are invited for screening once every three years beginning at age 50. Women with one or more first-degree relatives (mother, sister, daughter) with premenopausal breast cancer should begin screening at an earlier age. It is usually suggested to start screening at an age that is 10 years less than the age at which the relative was diagnosed with breast cancer.

A clinical practice guideline by the US Preventive Services Task Force recommended "screening mammography, with or without clinical breast examination (CBE), every 1 to 2 years for women aged 40 and older."[5] The Task Force gave a grade B recommendation.[6][verification needed]

In 2005, 67.9% of all U.S. women age 40–64 had a mammogram in the past two years (74.5% of women with private health insurance, 56.1% of women with Medicaid insurance, 38.1% of currently uninsured women, and 32.9% of women uninsured for > 12 months).[7]

Criticisms of screening mammography[]

Several scientific groups however have expressed concern about the public's perceptions of the benefits of breast screening.[8] In 2001, a controversial review published in The Lancet claimed that there is no reliable evidence that screening for breast cancer reduces mortality.[9] The results of this study were widely reported in the popular press.[10]

False positives are a major problem of mammographic breast cancer screening. Data reported in the UK Million Woman Study indicates that if 134 mammograms are performed, 20 women will be called back for suspicious findings, and four biopsies will be necessary, to diagnose one cancer. Recall rates are higher in the U.S. than in the UK.[11] The contribution of mammography to the early diagnosis of cancer is controversial, and for those found with benign lesions, mammography can create a high psychological and financial cost.

Mammography in women less than 50 years old[]

Part of the difficulty in interpreting mammograms in younger women stems from the problem of breast density. Radiographically, a dense breast has a preponderance of glandular tissue, and younger age or estrogen hormone replacement therapy contribute to mammographic breast density. After menopause, the breast glandular tissue gradually is replaced by fatty tissue, making mammographic interpretation much more accurate. Some authors speculate that part of the contribution of estrogen hormone replacement therapy to breast cancer mortality arises from the issue of increased mammographic breast density. Breast density is an independent adverse prognostic factor on breast cancer prognosis.

A systematic review by the American College of Physicians concluded "Although few women 50 years of age or older have risks from mammography that outweigh the benefits, the evidence suggests that more women 40 to 49 years of age have such risks".[12].

A report released November 27, 2007 by the Journal of the National Cancer Institute showed that the formula doctors use to calculate a woman's risk of breast cancer underestimates the danger for black women most of the time and especially for those age 50 and older — the age when they are most likely to benefit from screening tests and protective drugs, according to the first major reassessment of the widely used tool.[13]

Enhancements to mammography[]

In general, digital mammography and computer-aided mammography have increased the sensitivity of mammograms, but at the cost of more numerous false positive results.[How to reference and link to summary or text]

Computer-aided diagnosis(CAD) Systems may help radiologists to evaluate X-ray images to detect breast cancer in an early stage.[How to reference and link to summary or text] CAD is especially established in US and the Netherlands. It is used in addition to the human evaluation of the diagnostician.

Breast MRI[]

Magnetic resonance imaging (MRI) has been shown to detect cancers not visible on mammograms, but has long been regarded to have disadvantages. For example, although it is 27-36% more sensitive, it is less specific than mammography.[14] As a result, MRI studies will have more false positives (up to 5%), which may have undesirable financial and psychological costs. It is also a relatively expensive procedure, and one which requires the intravenous injection of a chemical agent to be effective. Proposed indications for using MRI for screening include:[15]

  • Strong family history of breast cancer
  • Patients with BRCA-1 or BRCA-2 oncogene mutations
  • Evaluation of women with breast implants
  • History of previous lumpectomy or breast biopsy surgeries
  • Axillary metastasis with an unknown primary tumor
  • Very dense or scarred breast tissue

However, two studies published in 2007 demonstrated the strengths of MRI-based screening:

  • In August 2007, an article published in The Lancet compared MRI breast cancer screening to conventional mammographic screening in 7,319 women. MRI screening was highly more sensitive (97% in the MRI group vs. 56% in the mammography group) in recognizing early high-grade Ductal Carcinoma in situ (DCIS), the most important precursor of invasive carcinoma. Despite the high sensitivity, MRI screening had a positive predictive value of 52%, which is totally accepted for cancer screening tests.[17] The author of a comment published in the same issue of The Lancet concludes that "MRI outperforms mammography in tumour detection and diagnosis."[18]

Breast ultrasound[]

Ultrasound alone is not usually employed as a screening tool but it is a useful additional tool for the characterization of palpable tumours and directing image-guided biopsies. Using an ultrasound allows a look at dense breast tissue which is not possible with digital mammmography. It is closely correlated with the digital mammography. The other significant advantage over digital mammography is that it is a pain-free procedure.

Breast-specific gamma imaging[]

File:Miraluma.jpg

Miraluma scan with cancer

Breast-Specific Gamma Imaging (BSGI, also called Miraluma) is a breast imaging procedure that reflects the metabolic activity of breast lesions. Most (not all) malignant tumors show a higher metabolic activity than normal tissue, a reflection of their faster growth rate and of their abnormal metabolism (see the Warburg hypothesis). A small amount of Technetium 99 linked to six molecules of MIBI (Tc99m-sestamibi) is injected intravenously to a patient. The highly metabolic tumors absorb a greater amount of the tracing agent and appear as "hot spots" on the image produced by a gamma camera. At best, sestamibi complements mammography — it will not replace it. [19]


See also[]

[[Preventative medicine

  1. Elwood J, Cox B, Richardson A. The effectiveness of breast cancer screening by mammography in younger women.. Online J Curr Clin Trials Doc No 32: [23,227 words; 195 paragraphs]. PMID 8305999.
  2. Fletcher S, Black W, Harris R, Rimer B, Shapiro S (1993). Report of the International Workshop on Screening for Breast Cancer.. J Natl Cancer Inst 85 (20): 1644-56. PMID 8105098.
  3. Fletcher SW, Black W, Harris R, Rimer BK, Shapiro S (1993). Report of the International Workshop on Screening for Breast Cancer. J. Natl. Cancer Inst. 85 (20): 1644-56.
  4. NCI Statement on Mammography Screening - National Cancer Institute. URL accessed on 2007-09-11.
  5. (2002)Screening for breast cancer: recommendations and rationale. Ann. Intern. Med. 137 (5 Part 1): 344-6.
  6. Cite error: Invalid <ref> tag; no text was provided for refs named USPSTF Ratings
  7. Ward E, Halpern M, Schrag N, Cokkinides V, DeSantis C, Bandi P, Siegel R, Stewart A, Jemal A (Jan-Feb 2008). Association of insurance with cancer care utilization and outcomes. CA Cancer J Clin 58 (1).
  8. includeonly>"Women 'misjudge screening benefits'", BBC, Monday, 15 October, 2001. Retrieved on 2007-04-04.
  9. Olsen O, Gøtzsche P (2001). Cochrane review on screening for breast cancer with mammography. Lancet 358 (9290): 1340-2.
  10. includeonly>"New concerns over breast screening", BBC, Thursday, 18 October, 2001. Retrieved on 2007-04-04.
  11. Smith-Bindman R, Ballard-Barbash R, Miglioretti DL, Patnick J, Kerlikowske K (2005). Comparing the performance of mammography screening in the USA and the UK. Journal of medical screening 12 (1): 50-4.
  12. Armstrong K, Moye E, Williams S, Berlin JA, Reynolds EE (2007). Screening mammography in women 40 to 49 years of age: a systematic review for the American College of Physicians. Ann. Intern. Med. 146 (7): 516-26.
  13. Chlebowski RT, Anderson GL, Lane DS, Aragaki AK, Rohan T, Yasmeen S, Sarto G, Rosenberg CA, Hubbell FA (2007). Predicting risk of breast cancer in postmenopausal women by hormone receptor status.. J. Natl. Cancer Inst. 99 (22): 1695–705.
  14. Hrung J, Sonnad S, Schwartz J, Langlotz C (1999). Accuracy of MR imaging in the work-up of suspicious breast lesions: a diagnostic meta-analysis.. Acad Radiol 6 (7): 387-97. PMID 10410164.
  15. Morrow M (2004). Magnetic resonance imaging in breast cancer: one step forward, two steps back?. JAMA 292 (22): 2779-80. PMID 15585740.
  16. Lehman CD, Gatsonis C, Kuhl CK, Hendrick RE, Pisano ED, Hanna L, Peacock S, Smazal SF, Maki DD, Julian TB, DePeri ER, Bluemke DA, Schnall MD (2007). MRI evaluation of the contralateral breast in women with recently diagnosed breast cancer.. N Engl J Med. 356 (13): 1295-1303. PMID 17392300.
  17. Kuhl CK, Schrading S, Bieling HB, Wardelmann E, Leutner CC, Koenig R, Kuhn W, Schild HH (2007). MRI for diagnosis of pure ductal carcinoma in situ: a prospective observational study. The Lancet 370 (9586): 485-492. PMID.
  18. Boetes C, Mann RM (2007). Ductal carcinoma in situ and breast MRI. The Lancet 370 (9586): 459-460. PMID.
  19. Sestamibi (Miraluma), online article at www.breastcancer.org
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