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European Journal of Breast Health logoLink to European Journal of Breast Health
. 2018 Oct 1;14(4):225–228. doi: 10.5152/ejbh.2018.3870

Impact of The Method of Diagnosis on The Stage of Breast Carcinoma

Aylin Erdim 1,✉, Gülce Kayıkçı 2, Selin Doğu 2, Derya Zıvalı 2, Gizem Pehlivan 2, A Özdemir Aktan 1
PMCID: PMC6170021  PMID: 30288497

Abstract

Objective

Screening mammography is recommended to women at a certain age to achieve an early diagnosis. The purpose of this study is to find out how breast carcinoma was diagnosed and the impact of the method of diagnosis on the stage of the tumor.

Materials and Methods

In this study, 903 operated breast cancer patients, between 2010–2016, in a large volume Marmara University Istanbul Pendik Education and Research Hospital were analyzed retrospectively. Patients presenting with clinical symptoms and those diagnosed with screening were investigated separately. The percentage of the patients diagnosed with symptoms and the impact of the method of diagnosis on the stage of the tumor was the primary outcome of the study.

Results

738 patients fulfilling inclusion criteria with complete clinical records were analyzed. 126 patients (17%) were in the age range of 19–39 years, while 32% (236 patients) were 40–50 and 51% (376 patients) were older than 50 years.

485 patients (65.7%) were diagnosed with a mass in the breast, while 241 (32.6%) patients were diagnosed with screening with mammography. Twelve patients (1.7%) presented with nipple discharge. Median tumor sizes measured in the resected specimen were 22 mm, 21 mm, and 21 mm in patients diagnosed with a mass, screening, and nipple discharge respectively. The difference among the groups were not significant (p=0.460).

Axillary lymph nodes were positive in 210 (43.3%) of patients presenting with a mass in the breast while 85 patients (35.3%) diagnosed with screening had metastatic lymph nodes in the axilla. Three patients presenting with nipple discharge had positive axillary lymph nodes (p=0.137).

Conclusion

This study demonstrated that breast cancer screening programs in Turkey needs improvement and at the same time shows that screening with mammography after 40 years of age should be done annually despite Ministry of Health recommendations.

Keywords: Patient, breast cancer, mass, screening, discharge

Introduction

Breast cancer is the most prevalent malignant tumor among women in the world, accounting for almost 30% of all cancers in the female sex, with nearly 1.7 million new cases diagnosed in 2012. Breast cancer is the most common malignancy in United States, accounting for more than 40.000 female deaths each year (1, 2).

Mammography is the gold standard to detect breast cancer at an early stage and, when followed up with appropriate diagnosis and treatment, reduces mortality from breast cancer (3). However, meta-analysis of studies has revealed contradicting results (4).

Screening decisions should take into account an individual woman’s risks of breast cancer and her values and preferences, weighing the potential benefits and harms of screening (5). The characteristics of each country is important to identify the initial screening time and frequency. The majority of breast cancers in the United States are diagnosed as a result of an abnormal screening study, although a significant number cases are first brought to attention by a patient (6).

In Turkey, breast cancer awareness programs conducted by the Ministry of Health has been ongoing for almost 30 years and screening mammography for women 40–69 years of age, every two years, is recommended (7, 8). However, screening programs are far from perfect.

Estimating an individual woman’s absolute risk for breast cancer is essential for decision making about screening and preventive recommendations (9). Developing improved methods for breast cancer risk prediction could facilitate the targeting of interventions to women at highest risk, thereby reducing mortality, while sparing low-risk women the costs and inconvenience of unnecessary testing and procedures (10).

The purpose of this study is to find out how breast carcinoma was diagnosed and the impact of the method of diagnosis on the stage of the tumor. In this study, operated breast cancer patients in a large volume university hospital were analyzed retrospectively. Patients presenting with clinical symptoms and those diagnosed with screening were investigated separately. The percentage of the patients diagnosed with symptoms and the impact of the method of diagnosis on the stage of the tumor was the primary outcome of the study.

Materials and Methods

In this study, patients diagnosed and operated for breast carcinoma were analyzed retrospectively. 903 patients were operated in Marmara University Istanbul Pendik Education and Research Hospital, Istanbul, Turkey in 2010–2016. All female patients older than 18 years diagnosed with breast carcinoma were included in the study. Male breast carcinoma patients and patients receiving neoadjuvant treatment were excluded.

All patients had a preoperative diagnosis with core needle biopsy. Patients were either treated with mastectomy or breast conserving surgery. Sentinel lymph node (SLN) biopsy was done to all patients without palpable lymph nodes after staining with isosulfan blue. Patients with a positive SLN biopsy underwent axillary dissection. Patients with clinically palpable nodes were treated with axillary dissection.

Patients with complete records were analyzed retrospectively regarding their clinical presentation before diagnosis. Patients were grouped as those presenting with a mass in the breast, presenting with nipple discharge, and those diagnosed with screening mammography. Tumor size, tumor grade, and axillary lymph node status were recorded for each patient.

Ethics committee approval was received for this study from the ethics committee of Marmara University Institute of Health Science.

Statistical analysis

Data was evaluated using the “Statistical Package for the Social Sciences for Windows 17.0” (SPSS Inc., Chicago, IL, USA) software. Patients’ data were defined as percentages, mean ± standard deviation (SD), and median (minimum-maximum). The independent student test was used to compare categorical data. The results were evaluated in confidence interval of 95% and significance level of p<0.05.

Results

Out of 903 patients, 8 male breast carcinoma patients and 130 patients receiving neoadjuvant treatment were excluded. 27 patients having their first operations elsewhere and scheduled for reoperation were also excluded.

738 patients fulfilling inclusion criteria with complete clinical records were analyzed. The mean age of the patients was 52.7 (±11.9) years. 126 patients (17%) were in the age range of 19–39 years, while 32% (236 patients) were 40–50. and 51% (376 patients) were older than 50 years.

485 patients (65.7%) were diagnosed with a mass in the breast, while 241 (32.6%) patients were diagnosed with screening with mammography. Twelve patients (1.7%) presented with nipple discharge. Median tumor sizes measured in the resected specimen were 22 mm (1–170), 21 mm (0–90), and 21 mm (6–86) in patients diagnosed with a mass, screening, and nipple discharge respectively. The difference among the groups were not significant (p=0.460).

Axillary lymph nodes were positive in 210 (43.3%) of patients presenting with a mass in the breast while 85 patients (35.3%) diagnosed with screening had metastatic lymph nodes in the axilla. Three patients presenting with nipple discharge had positive axillary lymph nodes. There was no significant difference among the groups (p=0.137).

A great majority of patients in all groups had either grade III or IV tumors. Tumor grades were not significant among the groups (p=0.123) (Table 1).

Table 1.

Tumor characteristics of patients

VISIT MOTIVE MASS N=485 SCREENING N=241 NIPPLE DISCHARGE N=12 TOTAL N=738 p

n % n % n % n %
TUMOR SIZE (mm) Median 22 21 21
Min.– max. 1 – 170 0 – 90 6 – 86 0.460
AXILLARY LYMPH NODE POSITIVE 210 43 85 35 3 25 298 45.4
NEGATIVE 275 57 156 65 9 75 440 54.6 0.137
GRADE G0 35 7 12 5 0 0 47 6
G1 45 9 24 10 3 25 72 10
G2 240 50 123 51 7 58 370 50 0.123

126 patients were younger than 40 years. Considering that mammography is not indicated or ineffective for these patients, of the remaining 612 patients’ diagnosis was made with a mass in the breast in 391 (63.9%) (Table 2).

Table 2.

Tumor characteristics of patients aged 40–69

VISIT MOTIVE MASS N=391 SCREENING N=210 NIPPLE DISCHARGE N=11 TOTAL N=612 p

n % n % n % n %
TUMOR SIZE (mm) Median 23 21 21
Min.– max. 0 – 170 0 – 90 6 – 80 0.460
AXILLARY LYMPH NODE POSITIVE 184 47 88 42 4 36 276 45
NEGATIVE 207 53 122 58 7 64 336 55 0.138
GRADE G0 36 9 25 12 0 0 61 10
G1 64 16 47 22 4 36 115 19
G2 291 75 138 66 7 64 436 71 0.125

Discussion and Conclusion

This study revealed that majority of patients (65.7%) operated for breast carcinoma in a large volume Marmara University Istanbul Pendik Education and Research Hospital were diagnosed with a mass in the breast, while only 32.6% of patients were diagnosed with screening mammography. Median tumor sizes measured in the resected specimens were 22 mm, 21 mm, and 21 mm in patients diagnosed with a mass, screening, and nipple discharge respectively without any significant differences.

High median tumor sizes in those patients diagnosed with screening implicate that screening is not being done effectively. Most commonly, patients seek for medical help with pain in the breast and physicians direct them for mammography which in fact should not be considered as screening. With such high median tumor sizes, with careful examination, most of these tumors should be palpable. Unfortunately, most unexperienced physicians depend on mammography rather than clinical examination. Furthermore, the high patient load in many hospitals prohibits appropriate clinical examination (11, 12).

The percentage of patients having axillary lymph node metastasis was also similar in groups diagnosed with a mass in the breast and diagnosed with screening (43.3% and 35.3% respectively, p=0.213). When the similar sizes of tumors diagnosed are considered, this result is to be expected. Furthermore, the tumor grades were found to be similar in the groups studied (p=0.123).

This study clearly demonstrates that screening for breast carcinoma in Turkey is far from perfect. Causes are probably multifactorial. Poor educational status and inadequate public awareness are the two leading causes. As this study was done in a Marmara University Istanbul Pendik Education and Research Hospital in the most populated city in Turkey, access to health care should not be a limiting factor. However, health care is given to patients paying their premiums to Social Security Institution (SGK). Considering the high unemployment rate and high number of unregistered work force in Turkey, this may be a contributing factor even in a large metropole as Istanbul.

The median size of the tumors diagnosed with screening is also alarming. As the median size is 21 mm, most of these tumors should be clinically detectable. Diagnosis with radiological and biochemical investigation is the current trend sometimes prohibiting careful history taking and clinical examination. Turkey has a very high yearly doctor visit rate when compared with other OECD countries (8.5 vs 6.6) (12, 13). This is even more surprising as Turkey has the youngest population among these countries. The physician workload is high reaching 50–100 consultations a day and consultation lengths of less than ten minutes (11).

49% of patients operated for breast carcinoma in this study group were 50 years old or younger. This finding is important because The Ministry of Health recommends screening with mammography after 40 years every two years. Considering the high number of young patients diagnosed with breast carcinoma, a span of 40–50 years needs special attention. When diagnosed with a mass in the breast or nipple discharge usually tumor stage increases. Late diagnosis is most commonly associated with higher tumor stage and worse prognosis.

Although, this study is from a single center and represents a small sample, the same results were found in the national database. Ozmen analyzed 20 000 patients in the National Database and the mean age was 51.8 years for patients with breast carcinoma. 47% were younger than 50 years. The results are almost identical (14). Our findings and national database clearly indicate that screening for breast carcinoma should begin before 50 years in Turkey.

In this study, the prognosis and recurrence rates were not investigated. Therefore, the impact of late diagnosis and big tumor sizes on prognosis is not given. Considering high number of positive lymph nodes in the axilla and big tumor sizes, early diagnosis with appropriate screening programs may improve prognosis.

This study indicates that breast cancer screening programs in Turkey needs improvement and at the same time shows that screening with mammography after 40 years of age should be done annually despite Ministry of Health recommendations.

Acknowledgements

The authors would like to thank Dr. M.Ümit Uğurlu for allowing us to use his database.

Footnotes

This study was presented in part at the National Breast Surgery Congress, 2–4 March 2017, Antalya, Turkey.

Ethics Committee Approval: Ethics committee approval was received for this study from the ethics committee of Marmara University Institute of Health Science.

Informed Consent: Informed consent was not taken due to retrospective design of the study.

Peer-review: Externally peer-reviewed.

Author Contributions: Concept - A.E., G.K., S.D., D.Z., G.K., A.Ö.A.; Design - A.E., G.K., S.D., D.Z., G.K., A.Ö.A.; Supervision - A.E, A.Ö.A.; Resource - A.E., G.K., S.D., D.Z., G.K.; Materials - M.Ü.U.; Data Collection and/or Processing - G.K., S.D., D.Z., G.K.; Analysis and/or Interpretation - A.E., G.K., S.D., D.Z., G.K., A.Ö.A.; Literature Search - G.K., S.D., D.Z., G.K.; Writing Manuscript - A.E., G.K., S.D.,D.Z., G.K., A.Ö.A.; Critical Reviews - A.E., G.K., S.D.,D.Z., G.K., A.Ö.A.

Conflict of Interest: The authors have no conflicts of interest to declare.

Financial Disclosure: The authors declared that this study has received no financial support.

References

  • 1.Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D, Bray F. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136:E359–E386. doi: 10.1002/ijc.29210. [DOI] [PubMed] [Google Scholar]
  • 2.Siegel RL, Miller KD, Jemal A. Cancer statistics 2017. CA Cancer J Clin. 2017;67:7–30. doi: 10.3322/caac.21387. [DOI] [PubMed] [Google Scholar]
  • 3.Tabar L, Vitak B, Chen HH, Duffy SW, Yen MF, Chiang CF, Smith RA, et al. The Swedish Two-County Trial twenty years later. Updated mortality results and new insights from long-term follow-up. Radiol Clin North Am. 2000;38:625–651. doi: 10.1016/S0033-8389(05)70191-3. [DOI] [PubMed] [Google Scholar]
  • 4.Gotzsche PC, Jorgensen KJ. Screening for breast cancer with mammography. The Cochrane Library. 2013 doi: 10.1002/14651858.CD001877.pub5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Welch HG, Prorok PC, O’Malley AJ, Kramer BS. Breast-cancer tumor size, overdiagnosis, and mammography screening effectiveness. N Engl J Med. 2016;375:1438–1447. doi: 10.1056/NEJMoa1600249. [DOI] [PubMed] [Google Scholar]
  • 6.Bleyer A, Welch HG. Effect of three decades of screening mammography on breast-cancer incidence. N Engl J Med. 2012;367:1998–2005. doi: 10.1056/NEJMoa1206809. [DOI] [PubMed] [Google Scholar]
  • 7.Ozmen V, Fidaner C, Aksaz E, Bayol U, Dede I, Goker E, Gulluoglu BM, Işıkdoğan A, Topa U, Uhri M, Utkan Z, Zengin N, Tuncer M. Organizing Early Diagnosis and Screening Programs for Breast Cancer in Turkey “ The report of breast cancer early detection and screening Sub-Comittiee, National Cancer Advisory Board The Ministry of Health of Turkey”. Eur J Breast Health. 2009;5:125–134. [Google Scholar]
  • 8.Ozmen V, Gurdal SO, Cabioglu N, Ozcinar B, Ozaydın AN, Kayhan A, Aribal E, Sahin C, Saip P, Alagoz O. Cost-Effectiveness of Breast Cancer Screening in Turkey, a Developing Country: Results from Bahçeşehir Mammography Screening Project. Eur J Breast Health. 2017;13:117–122. doi: 10.5152/ejbh.2017.3528. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Saslow D, Boetes C, Burke W, Harms S, Leach MO, Lehman CD, Morris E, Pisano E, Schnall M, Sener S, Smith RA, Warner E, Yaffe M, Andrews KS, Russell CA American Cancer Society Breast Cancer Advisory Group. American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. CA Cancer J Clin. 2007;57:75–89. doi: 10.3322/canjclin.57.2.75. [DOI] [PubMed] [Google Scholar]
  • 10.Gierach GL, Yang XR, Figueroa JD, Sherman ME. Emerging concepts in breast cancer risk prediction. Curr Obstet Gynecol Rep. 2013;2:43–52. doi: 10.1007/s13669-012-0034-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Akman M, Sakarya S, Sargın M, Unluoglu I, Egici MT, Boerma WG, Schäfer WL. Changes in primary care provision in Turkey: A comparison of 1993 and 2012. Health Policy. 2017;121:197–206. doi: 10.1016/j.healthpol.2016.11.016. [DOI] [PubMed] [Google Scholar]
  • 12.Reinhardt UE, Hussey PS, Anderson GF. Cross-national comparisons of health systems using OECD data, 1999. Health Aff (Millwood) 2002;21:169–181. doi: 10.1377/hlthaff.21.3.169. [DOI] [PubMed] [Google Scholar]
  • 13.Anderson GF, Hussey PS. Comparing health system performance in OECD countries. Organization for Economic Cooperation and Development. Health Aff (Millwood) 2001;20:219–232. doi: 10.1377/hlthaff.20.3.219. [DOI] [PubMed] [Google Scholar]
  • 14.Ozmen V, editor. Incidence, distribution, mortality, risk factors. Istanbul: 2017. Breast Cancer in Turkey: An analysis of 20 000 patients; pp. 45–49. [Google Scholar]

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