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Breast cancer screening programs have the potential to catch breast cancer at a less advanced stage, with a better chance of survival. However, experience with screening programmes in a number of countries, show screening is not without risks. For example in the UK screening women aged 50 for the next 20 years, for every 10,000 women screened approximately 43 deaths will be prevented, however 129 will be overdiagnosed (Independent UK Panel on Breast Cancer Screening, 2011). That translates to 1 breast cancer death being prevented for about every 3 overdiagnosed cases identified and treated. Overdiagnosis is where screening identifies a tumour, which is then treated (possibly with surgery, radiotherapy and medication), but which would otherwise have remained undetected for the rest of the woman’s life, without causing illness, if it had not been detected by screening.
Menu: Breast Cancer Screening
Information for Patients and the Public
Information for Health Professionals / Researchers
Latest Research Publications
Breast CancerInformation Patients and the Public (8 links)
- Breast Cancer Screening
National Cancer Institute
PDQ summaries are written and frequently updated by editorial boards of experts Further info. - Mammograms in breast screening
Cancer Research UK
CancerHelp information is examined by both expert and lay reviewers. Content is reviewed every 12 to 18 months. Further info.
This page covers what mammograms are, after the mammogram, if you are called back, what a mammogram can show and possible risks of breast screening. - Breast cancer (female) - Screening
NHS Choices - Breast Cancer NHS Breast Screening Controversey
Genesis Appeal
Interview with Dr Mary Wilson, Director of the Greater Manchester Breast Cancer Screening Programme. - Breast Screening Information for Provinces and Territories in Canada
Breast Cancer Society of Canada
All of the provinces and territories in Canada offer screenings for women aged 50 - 69. The eligibility for women outside of this age group varies from province to province. This page list links to the regional breast cancer screening programmes. - BreastScreen Australia Program
Australian Government Department of Health and Ageing
A national screening programme established in 1991 targeted at well women without symptoms aged 50-69. - NHS Breast Screening Programme
NHSBSP
Women between the ages of 50 and 70 are invited for regular breast screening (every three years) under this national programme. This is intended to detect breast cancer at an early stage. - The benefits and harms of breast cancer screening: an independent review
Lancet; 380: 1778-86, November 2012
Abstract from the report by the Independent UK Panel on Breast Cancer Screening. Whilst there is some uncertainty with the statistics, screening UK women aged 50 for the next 20 years, for every 10,000 women screened approximately 43 deaths will be prevented but 129 will be overdiagnosed (1 breast cancer death will be prevented for about every 3 overdiagnosed cases identified and treated).
Information for Health Professionals / Researchers (6 links)
- PubMed search for publications about Breast Cancer Screening - Limit search to: [Reviews]
PubMed Central search for free-access publications about Breast Cancer Screening
US National Library of Medicine
PubMed has over 22 million citations for biomedical literature from MEDLINE, life science journals, and online books. Constantly updated. - Breast Cancer Screening
National Cancer Institute
PDQ summaries are written and frequently updated by editorial boards of experts Further info. - Breast Cancer Surveillance Consortium
BCSC
The BCSC is a collaborative network of seven mammography registries with linkages to tumor and/or pathology registries in the USA. The network is supported by a central Statistical Coordinating Center and supports studies designed to assess the delivery and quality of breast cancer screening. - CTFPHC: Breast Cancer Screening 2011 Guideline
Canadian Task Force on Preventive Health Care
Video aimed at physicians to help them better understand and communicate guidelines from the task force reviewing the use of mammography, magnetic resonance imaging, breast self exam and clinical breast exam to screen for breast cancer. These recommendations apply only to women at average risk of breast cancer aged 40 to 74 years. They do not apply to women at higher risk due to personal/family history of breast cancer. - NHS Breast Screening Programme
NHSBSP
Women between the ages of 50 and 70 are invited for regular breast screening (every three years) under this national programme. This is intended to detect breast cancer at an early stage. - The benefits and harms of breast cancer screening: an independent review
Lancet; 380: 1778-86, November 2012
Abstract from the report by the Independent UK Panel on Breast Cancer Screening. Whilst there is some uncertainty with the statistics, screening UK women aged 50 for the next 20 years, for every 10,000 women screened approximately 43 deaths will be prevented but 129 will be overdiagnosed (1 breast cancer death will be prevented for about every 3 overdiagnosed cases identified and treated).
Latest Research Publications
This list of publications is regularly updated (Source: PubMed).
Screening, imaging, and image-guided biopsy techniques for breast cancer.
Surg Clin North Am. 2013; 93(2):309-27 [PubMed]
Determinants of breast cancer screening uptake in women, evidence from the British Household Panel Survey.
Soc Sci Med. 2013; 82:108-14 [PubMed]
An interesting case of screen-detected breast cancer encasing a ventriculoperitoneal shunt.
BMJ Case Rep. 2013; 2013 [PubMed]
Women's views on overdiagnosis in breast cancer screening: a qualitative study.
BMJ. 2013; 346:f158 [PubMed] Free Access to Full Article
DESIGN: Qualitative study using focus groups that included a presentation explaining overdiagnosis, incorporating different published estimates of its rate (1-10%, 30%, 50%) and information on the mortality benefit of screening, with guided group discussions
SETTING: Sydney, Australia
PARTICIPANTS: Fifty women aged 40-79 years with no personal history of breast cancer and with varying levels of education and participation in screening.
RESULTS: Prior awareness of breast cancer overdiagnosis was minimal. Women generally reacted with surprise, but most came to understand the issue. Responses to overdiagnosis and the different estimates of its magnitude were diverse. The highest estimate (50%) made some women perceive a need for more careful personal decision making about screening. In contrast, the lower and intermediate estimates (1-10% and 30%) had limited impact on attitudes and intentions, with many women remaining committed to screening. For some women, the information raised concerns, not about whether to screen but whether to treat a screen detected cancer or consider alternative approaches (such as watchful waiting). Information preferences varied: many women considered it important to take overdiagnosis into account and make informed choices about whether to have screening, but many wanted to be encouraged to be screened.
CONCLUSIONS: Women from a range of socioeconomic backgrounds could comprehend the issue of overdiagnosis in mammography screening, and they generally valued information about it. Effects on screening intentions may depend heavily on the rate of overdiagnosis. Overdiagnosis will be new and counterintuitive for many people and may influence screening and treatment decisions in unintended ways, underscoring the need for careful communication.
Parameter estimates for invasive breast cancer progression in the Canadian National Breast Screening Study.
Br J Cancer. 2013; 108(3):542-8 [PubMed] Article available free on PMC after 19/02/2014
METHODS: We describe invasive breast cancer progression in the Canadian National Breast Screening Study and construct progression models with and without covariates. The effect of risk factors on transition intensities and false-negative probability is investigated. We estimate the transition rates, the sojourn time and sensitivity of diagnostic tests for women aged 40-49 and 50-59.
RESULTS: Although younger women have a slower transition rate from healthy state to preclinical, their screen-detected tumour becomes evident sooner. Women aged 50-59 have a higher mortality rate compared with younger women. The mean sojourn times for women aged 40-49 and 50-59 are 2.5 years (95% CI: 1.7, 3.8) and 3.0 years (95% CI: 2.1, 4.3), respectively. Sensitivity of diagnostic procedures for older women is estimated to be 0.75 (95% CI: 0.55, 0.88), while women aged 40-49 have a lower sensitivity (0.61, 95% CI: 0.42, 0.77). Age is the only factor that affects the false-negative probability. For women aged 40-49, 'age at entry', 'history of breast disease' and 'families with breast cancer' are found to be significant for some of the transition rates. For the age-group 50-59, 'age at entry', 'history of breast disease', 'menstruation length' and 'number of live births' are found to affect the transition rates.
CONCLUSION: Modelling and estimating the parameters of cancer progression are essential steps towards evaluating the effectiveness of screening policies. The parameters include the transition rates, the preclinical sojourn time, the sensitivity, and the effect of different risk factors on cancer progression.
Perceived experiences of discrimination in health care: a barrier for cancer screening among American Indian women with type 2 diabetes.
Womens Health Issues. 2013; 23(1):e61-7 [PubMed] Article available free on PMC after 01/01/2014
METHODS: Data were collected from patient report and medical records. Prevalence of breast and cervical cancer screening were assessed. Unadjusted and adjusted logistic regression analyses were used to assess associations between perceived discrimination, cancer screening status, and patients' health care-seeking behaviors.
FINDINGS: Substantial proportions of AI women in our sample were behind the recommended schedules of screening for breast and cervical cancer. Adjusted estimates revealed that perceived discrimination was significantly associated with not being current for clinical breast examination and Pap test, and was close to statistical significance with not being current for mammography. The number of suboptimal health care-seeking behaviors increased with higher mean levels of perceived discrimination.
CONCLUSIONS: Among AI women, perceived discrimination in health care may negatively influence use of breast and cancer screening services, and health care-seeking behaviors. More research is needed among AIs to examine features of health care systems related to the phenomenon patients perceived experience of discrimination.
Physicians' beliefs about breast cancer surveillance testing are consistent with test overuse.
Med Care. 2013; 51(4):315-23 [PubMed] Article available free on PMC after 01/04/2014
METHODS: During 2009-2010, a cross-sectional survey of US medical oncologists and primary care physicians (PCPs) was carried out. Physicians responded to a clinical vignette ascertaining beliefs about appropriate breast cancer surveillance testing. Multivariable analyses examined the extent to which test beliefs were consistent with overuse and associated with physician and practice characteristics and physician perceptions, attitudes, and practices.
RESULTS: A total of 1098 medical oncologists and 980 PCPs completed the survey (response rate 57.5%). Eighty-four percent of PCPs [95% confidence interval (CI), 81.4%-86.5%] and 72% of oncologists (95% CI, 69.8%-74.7%) reported beliefs consistent with blood test overuse, whereas 50% of PCPs (95% CI, 47.3%-53.8%) and 27% of oncologists (95% CI, 23.9%-29.3%) reported beliefs consistent with imaging test overuse. Among PCPs, factors associated with these beliefs included smaller practice size, lower patient volume, and practice ownership. Among oncologists, factors included older age, international medical graduate status, lower self-efficacy (confidence in knowledge), and greater perceptions of ambiguity (conflicting expert recommendations) regarding survivorship care.
CONCLUSIONS: Beliefs consistent with breast cancer surveillance test overuse are common, greater for PCPs and blood tests than for oncologists and imaging tests, and associated with practice characteristics and perceived self-efficacy and ambiguity about testing. These results suggest modifiable targets for efforts to reduce surveillance test overuse.
Challenges in the management of breast cancer in low- and middle-income countries.
Future Oncol. 2012; 8(12):1575-83 [PubMed]
Application of breast tomosynthesis in screening: incremental effect on mammography acquisition and reading time.
Br J Radiol. 2012; 85(1020):e1174-8 [PubMed] Article available free on PMC after 01/12/2013
METHODS: We prospectively examined the effect on radiographers' and radiologists' workload of implementing 3D mammography in screening by comparing image acquisition time and screen-reading time for two-dimensional (2D) mammography with that of combined 2D+3D mammography. Radiologists' accuracy was also calculated.
RESULTS: Average acquisition time (measured from start of first-view breast positioning to compression release at completion of last view) for seven radiographers, based on 20 screening examinations, was longer for 2D+3D (4 min 3 s; range 3 min 53 s-4 min 18 s) than 2D mammography (3 min 13 s; range 3 min 0 s-3 min 26 s; p<0.01). Average radiologists' reading time per screening examination (three radiologists reading case-mix of 100 screens: 10 cancers, 90 controls) was longer for 2D+3D (77 s; range 60-90 s) than for 2D mammography (33 s; range 25-46 s; p<0.01). 2D+3D screen-reading was associated with detection of more cancers and with substantially fewer recalls than 2D mammography alone.
CONCLUSION: Relative to standard 2D mammography, combined 2D+3D mammography prolongs image acquisition time and screen-reading time (at initial implementation), and appears to be associated with improved screening accuracy. ADVANCES IN KNOWLEDGE: These findings provide relevant information to guide larger trials of integrated 3D mammography (2D+3D) and its potential implementation into screening practice.
Effect of three decades of screening mammography on breast-cancer incidence.
N Engl J Med. 2012; 367(21):1998-2005 [PubMed]
METHODS: We used Surveillance, Epidemiology, and End Results data to examine trends from 1976 through 2008 in the incidence of early-stage breast cancer (ductal carcinoma in situ and localized disease) and late-stage breast cancer (regional and distant disease) among women 40 years of age or older.
RESULTS: The introduction of screening mammography in the United States has been associated with a doubling in the number of cases of early-stage breast cancer that are detected each year, from 112 to 234 cases per 100,000 women--an absolute increase of 122 cases per 100,000 women. Concomitantly, the rate at which women present with late-stage cancer has decreased by 8%, from 102 to 94 cases per 100,000 women--an absolute decrease of 8 cases per 100,000 women. With the assumption of a constant underlying disease burden, only 8 of the 122 additional early-stage cancers diagnosed were expected to progress to advanced disease. After excluding the transient excess incidence associated with hormone-replacement therapy and adjusting for trends in the incidence of breast cancer among women younger than 40 years of age, we estimated that breast cancer was overdiagnosed (i.e., tumors were detected on screening that would never have led to clinical symptoms) in 1.3 million U.S. women in the past 30 years. We estimated that in 2008, breast cancer was overdiagnosed in more than 70,000 women; this accounted for 31% of all breast cancers diagnosed.
CONCLUSIONS: Despite substantial increases in the number of cases of early-stage breast cancer detected, screening mammography has only marginally reduced the rate at which women present with advanced cancer. Although it is not certain which women have been affected, the imbalance suggests that there is substantial overdiagnosis, accounting for nearly a third of all newly diagnosed breast cancers, and that screening is having, at best, only a small effect on the rate of death from breast cancer.
Socio-economic and health access determinants of breast and cervical cancer screening in low-income countries: analysis of the World Health Survey.
PLoS One. 2012; 7(11):e48834 [PubMed] Article available free on PMC after 01/12/2013
PURPOSE: To assess the influence of household socio-economic status (SES), healthcare access and country level characteristics on breast and cervical cancer screening among women in developing countries.
METHODS: Women ages 18-69 years (cervical cancer screening) and 40-69 years (breast cancer screening) from 15 developing countries who participated in the 2003 World Health Survey provided data for this study. Household SES and healthcare access was assessed based on self-reported survey responses. SAS survey procedures (SAS, Version 9.2) were used to assess determinants of breast and cervical cancer screening in separate models.
RESULTS: 4.1% of women ages 18-69 years had received cervical cancer screening in the past three years, while only 2.2% of women ages 40-69 years had received breast cancer screening in the past 5 years in developing countries. Cancer screening rates varied by country; cervical cancer screening ranged from 1.1% in Bangladesh to 57.6% in Congo and breast cancer screening ranged from 0% in Mali to 26% in Congo. Significant determinants of cancer screening were household SES, rural residence, country health expenditure (as a percent of GDP) as well as healthcare access.
DISCUSSION: A lot more needs to be done to improve screening rates for breast and cervical cancer in developing countries, such as increasing health expenditure (especially in rural areas), applying the increased funds towards the provision of more, better educated health providers as well as improved infrastructure.
Update on emerging technologies in breast imaging.
J Natl Compr Canc Netw. 2012; 10(11):1355-62 [PubMed]
Supplementary breast ultrasound screening in Asian women with negative but dense mammograms-a pilot study.
Ann Acad Med Singapore. 2012; 41(10):432-9 [PubMed]
MATERIALS AND METHODS: The study was approved by the hospital's Institutional Review Board. A prospective clinical trial was performed between September 2002 and November 2004. Asymptomatic Asian women with negative and dense mammograms were offered supplementary ultrasound screening for breast cancer. Ultrasound assessment was categorised as U1 to U4. U1 and U2 cases were recommended routine interval screening mammography. U3 cases were recommended follow-up ultrasound in 6 months and routine interval screening mammography and U4 cases were recommended biopsy.
RESULTS: One hundred and forty-one women with mean age of 45.1 years were enrolled into the study. Mean scan time was 13.0 minutes (± 5.6 minutes) for bilateral vs 11.0 minutes (± 1.4 minutes) for unilateral scans. There were 10 patients and 14 patients in the in the U3 and U4 categories, respectively. Two U4 category patients were diagnosed with malignancy-a-6 mm ductal carcinoma-in-situ and a 13- mm invasive ductal carcinoma. The breast cancer detection rate was 1.4%. Sensitivity and specifi city were 100% (2/2) and 88.5% (92/104) respectively. The positive predictive value was 14.3% (2/14) and the negative predictive value was 100% (92/92).
CONCLUSION: This pilot study reveals the usefulness of supplementary ultrasound screening in detecting early stage mammographically and clinically occult breast cancers in Asian women with dense breasts. A larger long-term study is, however, needed to assess its feasibility and impact on breast cancer prognosis.
Applying the Stress and 'Strength' Hypothesis to Black women's breast cancer screening delays.
Stress Health. 2012; 28(5):389-96 [PubMed]
Three-dimensional thermoacoustic imaging for early breast cancer detection.
Med Phys. 2012; 39(11):6738-44 [PubMed]
METHODS: A fast TAT system, which based on three 128-elements transducers, a 384-64ch switch and a parallel data acquisition system (DAS), was developed to reconstruct the three-dimensional (3D) image of a breast model with similar microwave absorption coefficient to breast tissue. A novel method to explore the ability of TAT system to distinguish absorption coefficient was introduced and the minimum absorption coefficient difference that can be distinguished clearly by our TAT system is 12 m(-1).
RESULTS: The potential applications of the TAT system were clearly demonstrated by successfully mapping breast model with mimicked tumors and microcalcification. An imaging experiment of human breast tumor embedding in the breast model was performed and the tumor was visualized by the 3D thermoacoustic volume.
CONCLUSIONS: The thermoacoustic images match well with the samples and achieve penetration depth of 6 cm. The experimental results indicate that TAT has a great potential to be used for detecting early-stage breast cancers with high contrast and high resolution.
The benefits and harms of breast cancer screening: an independent review.
Lancet. 2012; 380(9855):1778-86 [PubMed]
Characteristics of HER2-positive breast cancer diagnosed following the introduction of universal HER2 testing.
Breast. 2012; 21(6):724-9 [PubMed]
Health care reform and women's insurance coverage for breast and cervical cancer screening.
Prev Chronic Dis. 2012; 9:E159 [PubMed] Article available free on PMC after 01/12/2013
METHODS: We used the nationally representative 2009 American Community Survey to estimate the determinants of insurance status for women in Massachusetts, assuming full implementation of the ACA. We extrapolated findings to simulate the effects of the ACA on each state. We used individual-level predicted probabilities of being uninsured to generate estimates of the number of women who would gain health insurance after implementation of the ACA and to predict demand for NBCCEDP services.
RESULTS: Approximately 6.8 million low-income women would gain health insurance, potentially increasing the annual demand for NBCCEDP cancer screenings initially by about 500,000 mammograms and 1.3 million Papanicolaou tests. Despite a 60% decrease in the number of low-income uninsured women, the NBCCEDP would still serve fewer than one-third of the estimated number of women eligible for services. The NBCCEDP-eligible population would comprise a larger number of women with language and literacy-related barriers to care.
CONCLUSION: Implementation of the ACA would increase insurance coverage and access to cancer screening for millions of women, but the NBCCEDP will remain essential for the millions who will remain uninsured.
Identifying women's knowledge about risk factors of breast cancer and reasons for having mammography.
Asian Pac J Cancer Prev. 2012; 13(8):4191-7 [PubMed]
The African American Women and Mass Media campaign: a CDC breast cancer screening project.
J Womens Health (Larchmt). 2012; 21(11):1107-13 [PubMed]
Follow-up and timeliness after an abnormal cancer screening among underserved, urban women in a patient navigation program.
Cancer Epidemiol Biomarkers Prev. 2012; 21(10):1691-700 [PubMed] Article available free on PMC after 01/10/2013
METHODS: Women with an abnormal breast (n = 352) or cervical (n = 545) cancer screening test were recruited for the quasi-experimental study. Navigation subjects originated from five federally qualified health center sites and one safety net hospital. Records-based concurrent control subjects were selected from 20 sites. Control sites had similar characteristics to the navigated sites in terms of patient volume, racial/ethnic composition, and payor mix. Mixed-effects logistic regression and Cox proportional hazard regression analyses were conducted to compare navigation and control patients reaching diagnostic resolution by 60 days and time to resolution, adjusting for demographic covariates and site.
RESULTS: Compared with controls, the breast navigation group had shorter time to diagnostic resolution (aHR = 1.65, CI = 1.20-2.28) and the cervical navigation group had shorter time to diagnostic resolution for those who resolved after 30 days (aHR = 2.31, CI = 1.75-3.06), with no difference before 30 days (aHR = 1.42, CI = 0.83-2.43). Variables significantly associated with longer time to resolution for breast cancer screening abnormalities were being older, never partnered, abnormal mammogram and BI-RADS 3, and being younger and Black for cervical abnormalities.
CONCLUSIONS: Patient navigation reduces time from abnormal cancer finding to definitive diagnosis in underserved women.
IMPACT: Results support efforts to use patient navigation as a strategy to reduce cancer disparities among socioeconomically disadvantaged women.
Boston Patient Navigation Research Program: the impact of navigation on time to diagnostic resolution after abnormal cancer screening.
Cancer Epidemiol Biomarkers Prev. 2012; 21(10):1645-54 [PubMed] Article available free on PMC after 01/10/2013
METHODS: Boston Patient Navigation Research Program conducted a quasi-experimental patient navigation intervention across six federally qualified inner-city community health centers, three assigned to a breast cancer navigation intervention and three assigned to a cervical cancer navigation intervention; each group then served as the control for the other. Eligible women had an abnormal breast or cervical cancer screening test conducted at one of the participating health centers during a baseline (2004-2005) or intervention period (2007-2008). Kaplan-Meier survival curves and proportional hazards regression examined the effect of patient navigation on time to definitive diagnosis, adjusting for covariates, clustering by clinic and differences between the baseline and intervention period.
RESULTS: We enrolled 997 subjects in the baseline period and 3,041 subjects during the intervention period, of whom 1,497 were in the navigated arm, and 1,544 in the control arm. There was a significant decrease in time to diagnosis for subjects in the navigated group compared with controls among those with a cervical screening abnormality [aHR 1.46; 95% confidence interval (CI), 1.1-1.9]; and among those with a breast cancer screening abnormality that resolved after 60 days (aHR 1.40; 95% CI, 1.1-1.9), with no differences before 60 days.
CONCLUSIONS: This study documents a benefit of patient navigation on time to diagnosis among a racially/ethnically diverse inner city population.
IMPACT: Patient navigation may address cancer health disparities by reducing time to diagnosis following an abnormal cancer-screening event.
Breast cancer and clinical outcome among women over 60 years of age: a plead for more screening and alternative treatments.
Anal Quant Cytol Histol. 2012; 34(4):189-94 [PubMed]
STUDY DESIGN: A consecutive sample of 311 breast cancer patients > or = 60 years of age from 1991 were analyzed according to tumor size at diagnosis, frequencies of lymph node metastasis, tumor histological grade and stage, ploidy, proliferation index, stem-line-scatter index and survival rate in breast cancer and other causes of death. Tumor size was compared to a patient group aged 60-69 from 1987, before the introduction of mammography screening in Sweden.
RESULTS: In the screening group a significant reduction in tumor size was found at diagnosis compared to the sample from 1987 (p < 0.001) and to the older group > or = 70 years (p < 0.02). In the latter group a higher death rate appeared for breast cancer.
CONCLUSION: Older women would have a better outcome if included in the mammography screening program.
Sonographic features of triple-negative and non-triple-negative breast cancer.
J Ultrasound Med. 2012; 31(10):1531-41 [PubMed]
METHODS: Data from 315 consecutive breast cancer cases were collected. The images were reevaluated by an examiner blinded to the patients' characteristics and histologic results according to the Breast Imaging Reporting and Data System. The sonographic features of TNBC (n = 33) and non-TNBC (n = 282) were compared.
RESULTS: Triple-negative breast cancer was significantly correlated with a younger patient age (P = .002) and was associated with higher tumor grades (P < .001), more lymph node involvement (P = .014), and a trend toward a larger tumor size. With regard to sonographic features, the margin of TNBC was more frequently described as lobulated or microlobulated (75.8% versus 49.5% in non-TNBC; P = .005). The echoic halo was observed significantly less often in TNBC than in non-TNBC(39.4% versus 62.8%; P = .014). Cooper ligaments were displaced rather than disrupted in TNBC compared to non-TNBC (P = .003). Regarding the posterior acoustic features, enhancement was observed significantly more often in TNBC (36.4% versus 13.0% in non-TNBC; P = .031).
CONCLUSIONS: Triple-negative breast cancer and non-TNBC have different sonographic features. This finding can be explained by the pathologic profile of this breast cancer subtype. Some of the distinct sonographic criteria for TNBC are more likely to be associated with benign masses. Knowledge of the distinct sonographic features of TNBC would help the examiner avoid false-negative classification of this tumor type.
Breast cancer screening: are we seeing the benefit?
BMC Med. 2012; 10:106 [PubMed] Article available free on PMC after 01/10/2013
Sensitivity and specificity of mammographic screening as practised in Vermont and Norway.
Br J Radiol. 2012; 85(1020):e1226-32 [PubMed] Article available free on PMC after 01/12/2013
METHODS: Incident screening data from 1997 to 2003 for female patients aged 50-69 years from the Vermont Breast Cancer Surveillance System (116 996 subsequent screening examinations) and the Norwegian Breast Cancer Screening Program (360 872 subsequent screening examinations) were compared. Sensitivity and specificity estimates for the initial (based on screening mammogram only) and final (screening mammogram plus any further diagnostic imaging) interpretations were directly adjusted for age using 5-year age intervals for the combined Vermont and Norway population, and computed for 1 and 2 years of follow-up, which ended at the time of the next screening mammogram.
RESULTS: For the 1-year follow-up, sensitivities for initial assessments were 82.0%, 88.2% and 92.5% for 1-, 2- and >2-year screening intervals, respectively, in Vermont (p=0.022). For final assessments, the values were 73.6%, 83.3% and 81.2% (p=0.047), respectively. For Norway, sensitivities for initial assessments were 91.0% and 91.3% (p=0.529) for 2- and >2-year intervals, and 90.7% and 91.3%, respectively, for final assessments (p=0.630). Specificity was lower in Vermont than in Norway for each screening interval and for all screening intervals combined, for both initial (90.6% vs 97.8% for all intervals; p<0.001) and final (98.8% vs 99.5% for all intervals; p<0.001) assessments.
CONCLUSION: Our study showed higher sensitivity and specificity in a biennial screening programme with an independent double reading than in a predominantly annual screening program with a single reading. ADVANCES IN KNOWLEDGE: This study demonstrates that higher recall rates and lower specificity are not always associated with higher sensitivity of screening mammography. Differences in the screening processes in Norway and Vermont suggest potential areas for improvement in the latter.
Can missed breast cancer be recognized by regular peer auditing on screening mammography?
J Chin Med Assoc. 2012; 75(9):464-7 [PubMed]
METHODS: Between 2004 and 2007, a total of 311,193 free nationwide biennial mammographic screenings were performed for 50- to 69-year-old women in Taiwan. Retrospectively comparing the records in Taiwan's Cancer registry, 1283 cancers were detected (4.1 per 1000). Of the total, 176 (0.6 per 1000) initial mammographic negative assessments were reported to have cancers (128 traditional films and 48 laser-printed digital images). We selected 186 true negative films (138 traditional films and 48 laser-printed ones) as control group. These were seeded into 4815 films of 2008 images to be audited in 2009. Thirty-four auditors interpreted all the films in a single-blind, randomized, pair-control study. The performance of 34 auditors was analyzed by chi-square test. A p value of < 0.05 was considered significant.
RESULTS: Eight (6 traditional and 2 digital films) of the 176 false negative films were not reported by the auditors (missing rate of 4.5%). Of this total, 87 false negatives were reassessed as positive, while 29 of the 186 true negatives were reassessed as positive, making the overall performance of the 34 auditors in interpreting the false negatives and true negatives a specificity of 84.4% and sensitivity of 51.8%. The specificity and sensitivity in traditional films and laser-printed films were 98.6% versus 43.8% and 41.8% versus 78.3%, respectively. Almost 42% of the traditional false negative films had positive reassessment by the auditors, showing a significant difference from the initial screeners (p < 0.001). The specificity of their reinterpretation of laser-printed films was obviously low.
CONCLUSION: Almost 42% of the false negative traditional films were judged as missed cancers in this study. A peer auditing should reduce the probability of missed cancers.
Benefits and harms of detecting clinically occult breast cancer.
J Natl Cancer Inst. 2012; 104(20):1542-7 [PubMed]
Should we individualize breast cancer screening?
Maturitas. 2012; 73(3):202-5 [PubMed]
This page last updated: 22nd May 2013
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