Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Breast cancer survival and its prognostic factors in the United Arab Emirates: A retrospective study

  • Yusra Elobaid,

    Roles Conceptualization, Data curation, Formal analysis, Validation, Writing – original draft, Writing – review & editing

    Affiliation Department of Medical and Health Sciences, Khawarizmi International College, Abu Dhabi, United Arab Emirates

  • Maria Aamir,

    Roles Conceptualization, Investigation, Validation

    Affiliations Department of Medical and Health Sciences, Khawarizmi International College, Abu Dhabi, United Arab Emirates, Cancer Registry, Tawam Hospital, SEHA, Al Ain, United Arab Emirates

  • Michal Grivna,

    Roles Conceptualization, Methodology, Resources, Supervision

    Affiliation Institute of Public Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates

  • Abubaker Suliman,

    Roles Data curation, Formal analysis, Investigation, Methodology, Validation

    Affiliation Institute of Public Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates

  • Samir Attoub,

    Roles Conceptualization, Methodology, Supervision, Writing – review & editing

    Affiliation Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates

  • Hussam Mousa,

    Roles Investigation, Methodology, Supervision, Validation, Writing – review & editing

    Affiliation Department of Surgery, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates

  • Luai A. Ahmed,

    Roles Formal analysis, Methodology, Supervision, Validation, Writing – review & editing

    Affiliation Institute of Public Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates

  • Abderrahim Oulhaj

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Software, Supervision, Validation, Writing – original draft, Writing – review & editing

    aoulhaj@uaeu.ac.ae

    Affiliations Institute of Public Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates, Zayed Center for Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates

Abstract

Background

Data on breast cancer survival and its prognostic factors are lacking in the United Arab Emirates (UAE). Sociodemographic and pathologic factors have been studied widely in western populations but are very limited in this region. This study is the first to report breast cancer survival and investigate prognostic factors associated with its survival in the UAE.

Methods

This is a retrospective cohort study involving 988 patients who were diagnosed and histologically confirmed with breast cancer between January 2008 and December 2012 at Tawam hospital, Al Ain, UAE. Patient were followed from the date of initial diagnosis until the date of death from any cause, lost-to-follow up or the end of December 2018. The primary outcome is overall survival (OS). The Kaplan-Meier method was used to estimate the survival curve along with the 2- and 5-year survivals. Different group of patients categorized according to prognostic factors were compared using the log-rank test. Multiple Cox proportional hazards models was used to examine the impact of several prognostic factors on the overall survival.

Results

The median study follow-up was 35 months. Of the 988 patients, 62 had died during their follow-up, 56 were lost to follow-up and 870 were still alive at the end of the study. The average age of patients was 48 years. The majority of patients presented to the hospital with grade II or III, 24% with at least stage 3 and 9.2% had metastasis. The 2-year and 5-year survivals were estimated to 97% and 89% respectively. Results of the multiple Cox proportional hazard model show that tumor grade, and stage of cancer at presentation are jointly significantly associated with survival.

Conclusion

The 2- and 5-year survival are within the norms compared to other countries. Significant clinical and pathological prognostic factors associated with survival were tumor grade, and the stage of cancer at presentation.

Introduction

Breast cancer is a significant global public health concern, since it is the most common cancer among women [1]. Survival rates differ across the globe with higher survival rates in developed compared to less developed countries. For instance, the 5-year survival rate in developed countries such as USA and UK was in the range of 85–90% between the years 2017–2019 [2, 3]. In developing countries this rate ranged between 40–60% [1, 4, 5]. The poorer survival in developing countries could be related to low awareness of screening needs, lack of early detection programs and lack of diagnosis and treatment facilities [6].

Many improvements have been made in the last 20 years in the management of breast cancer due to the identification of prognostic factors capable of providing information on the progression of the disease. These prognostic markers are usually indicators of growth, invasion, and metastatic potential [7]. These include tumor size, lymph nodes, histologic grade, stage, estrogen and progesterone receptors and HER2/neu (erB-2) oncogene alteration [8].

In the United Arab Emirates (UAE), breast cancer constitutes approximately 20% of all cases of cancer and is considered to be the second leading cause of death among women after cardiovascular diseases [9]. Although, the burden of breast cancer is not systematically investigated in the country, the available information indicates that the cumulative probability of developing breast cancer in the UAE increased over the past three decades, being 2% in 1980, 2.4% in 1990, 3.9% in 2000 and 5.2% in 2010 [10]. Although this rise in cumulative probability could be explained by the improvement in screening program, this rising incidence is not the only cause of concern in the UAE, but also the advanced stage at presentation [11]. Metastasis is also common among women in the UAE where around 15% of cases are metastatic [9].

Despite few studies have been published in the UAE on breast cancer research, there is still a gap of knowledge in this field. There is very limited data in the UAE and the region on the survival rates and prognostic factors for breast cancer. To the best of our knowledge, no study has been yet carried out in the UAE to estimate the survival rates of breast cancer. The aim of this study is to estimate the survival curve along with the 2-year and 5-year survival in breast cancer patients in the UAE, and also to evaluate the impact of multiple prognostic factors on the breast cancer survival. Knowledge of these prognostic factors in the UAE population will be the foundation for planning treatment and predicting the outcome for patients with breast cancer.

Methods

Population and study design

This is a retrospective cohort study involving all patients (n = 988) who were diagnosed (and histologically confirmed) with breast cancer between January 2008 and December 2012 at the department of oncology at Tawam hospital, a tertiary care and teaching hospital located in Al Ain (Eastern region of the Emirate of Abu Dhabi). Each patient was followed up from the date of initial diagnosis until the date of death from any cause or until 31st December, 2018. Data collected at baseline (date of diagnosis) included demographic variables (such as age and sex), anatomical site and quadrant (primary site), tumor size, pathological nodal status, clinical stage, histopathological type and grade and treatment modalities. The lymph node and tumor size status were pathologically evaluated. Outcome data (at follow-up) included date of death if occurred or date of last contact with the patient. This information was collected using a pre-formed questionnaire. Ethical approval to conduct the study was obtained from the Al Ain District Human Ethics Committee before the commencement of the study.

Determination of histological type, grade and stage using TNM classification.

Determination of histological type and grade was established by Modified Bloom-Richardson score system which scores for tubular formation, nuclear pleomorphic and mitotic rate within tumor cells. TNM was used to assign the clinical stage of the disease to each patient [12]. This is a staging system which is expression of anatomical extent of disease based on extent of primary tumor (T), absence or presence of and extent of regional lymph node metastasis (N) and absence or presence of distant metastasis (M).

Statistical analysis

Baseline characteristics were summarized using descriptive statistics including mean, median, and standard deviation for continuous measures, and frequencies tables for categorical variables. Categorical variables were compared using the chi square or Fisher’s exact test and continuous variables using the unpaired t-test. The primary outcome is overall survival (OS). The survival time was defined as the duration of time from the date of initial diagnosis until the date of death from any cause, date lost-to-follow up or the end of December 2018. Survival curves were estimated and plotted using the Kaplan-Meier method. Survival curves of different groups were compared using the log-rank test. Cox proportional hazards models were applied to examine the impact of prognostic factors on overall survival. These included the age at diagnosis, treatment delay (duration of time from the date of initial diagnosis to the date of starting the treatment), tumor grade, stage of cancer, metastasis, primary site and laterality. Pairwise associations between all these prognostic factors was first carried out, using the Goodman and Kruskal’s tau [13], in order to identify factors providing redundant or similar information on overall survival. This is done to avoid issues of multi-collinearity when fitting Cox proportional hazards models. Lasso procedure was used as a selection method to identify the set of risk factors that are jointly significantly associated with overall survival. The 2-year and 5-year chance of survival were derived from the fitted model. The results of Cox proportional hazard model are presented as hazard ratios along with their 95% confidence intervals. All statistical tests were two-sided, and p-values < .05 were considered statistically significant. All the analysis was conducted using R software version 3.6 [14].

Results

Baseline characteristics of the patients

The final data set includes 988 breast cancer female patients having complete information on their demographic, prognosis factors and follow-up duration. Of these 988 patients, 62 had died during the follow-up, 56 were lost to follow-up and 870 were still alive at their last follow-up. The maximum follow-up time was 125 months and the median follow-up was of 35 months.

The average age at diagnosis was 48 years. The distribution of demographics, clinical and pathological characteristics at baseline, overall and according to the age group of diagnosis (< 50 years versus > 50 years) are presented in Table 1. The majority of patients are non-Emirati (81%). The average duration of time between the date of initial diagnosis and the date of first treatment was 18 days.

thumbnail
Table 1. Demographic, clinical and pathological characteristics at baseline, overall and by age groups.

https://doi.org/10.1371/journal.pone.0251118.t001

The majority of patients (88%) were presented with grade II or III and approximately 54% had left laterality. Regarding the stage of breast cancer, 80% of the patients were diagnosed with stage 2 at least. There was no statistically significant association between the tumor grade and the age at diagnosis. The distribution of tumor grades was similar in younger (< 50 years) compared to older woman (> 50 years) (P-value = 0.204). The same conclusions apply to other prognostic factors such as metastasis and stage of cancer except for laterality where older women were found to be more likely to have breast cancer in the left side compared to younger women.

Survival curves.

The unadjusted survival curve of patients, estimated using Kaplan-Meier method, is illustrated in Fig 1. Unadjusted survival curve. The 2-years survival was 97% (95% CI; 96%-99%) meaning that 97% of breast cancer women survived beyond 2 the first two years after their initial diagnosis and the 5-years survival was estimated to 89% (95% CI; 86%-92%).

Fig 2 shows the estimated survival functions according to the stage of cancer, tumor grade and metastasis. The log-rank test shows significant differences in survival curves between groups of each prognosis factor (all p-values were < 0.001). Patients with tumor grade I were observed to have higher 5-years survival of 99% (95% CI; 96%-100%) compared to those with tumor grade III who had a low 5-years survival rate of 85% (95% CI; 80%-90%). Similarly, patients with M0 metastasis had higher 5-years survival of 93% (95% CI; 90%-95%) compared to patients with M1 metastasis who had a 5-years survival of 48% (95% CI; 33%-70%). Regarding the stage of breast cancer, it is clear that those diagnosed with advanced stage have worse survival diagnosis 48% (95% CI; 33%-70%) in comparison to those with stage 1 or less 97% (95% CI; 94%-100%).

thumbnail
Fig 2. Overall survival curve according to selected prognostic factors.

https://doi.org/10.1371/journal.pone.0251118.g002

Cox proportional hazard model.

The hazard ratios obtained from separate univariate cox proportional hazard models fitted for each potential prognosis factor show no evidence for the survival curve to be affected by the age at diagnosis or the relative delay in treatment (in months). However, among clinical and pathological factors investigated, only the tumor grade and stage of cancer were statistically significantly associated with the survival (Table 2).

thumbnail
Table 2. Crude hazard ratio of overall survival associated with several prognostic factors.

https://doi.org/10.1371/journal.pone.0251118.t002

The final multiple Cox proportional hazard model, derived from the stepwise backward and the lasso variable selection procedures, retained two prognosis factors that are jointly significantly associated with survival. These include tumor grade and the stage of cancer. The results of the fit of the final Cox proportional hazard model, along with the estimated hazard ratio and their corresponding 95% confidence intervals are provided in Table 3.

thumbnail
Table 3. Results of final multivariate of the Cox proportional hazard model.

https://doi.org/10.1371/journal.pone.0251118.t003

The hazard ratio of death in patients with tumor grade III was 10.24 compared to those with Grade I. Patients presented at earlier stage were more likely to survive compared to those presented at late stage. More specifically, the hazard ratio was 4.85 for patients with stage 3 and 25.76 in patients with stage 4 compared to those with stage I.

Discussion

Clinical and histological information of a large number of breast cancer patients recruited from a tertiary hospital-based cancer registry in the UAE were analyzed. The aim of the study is to estimate the overall survival curve and the 2- and 5-year survival in breast cancer patients, and also to identify the set of important prognostic factors affecting survival in these patients. The average age of diagnosis was 48 years with the majority of patients presenting to the hospital with grade II or grade III, 24% with at least stage 3, and 9.2% had metastasis. We showed that among the clinical and pathological risk factors investigated, the tumor grade and the stage of cancer at presentation and metastasis were statistically significantly associated with the overall survival when analyzed separately. However, when added together into the Cox proportional hazard model, only tumor grade and stage of cancer were found to be jointly significantly associated with overall survival. The 5-year risk of death from breast cancer was estimated to 11% and the 2-year risk to 3%.

Based on the CONCORD 3 study [15], in the gulf region, breast cancer survival rates increased between 1995–1999 and 2010–2014. In Saudi Arabia, between 1995–1999 and 2005–2009 the overall 5- year’s survival increased from 70.9% to 78.4%. In Bahrain, between 2000 and 2004 the survival was reported to be 63%. In Kuwait, between 2000–2004 and 2010–2014, the survival increased from 68.3% to 75.2% and in Qatar, it has increased from 59.2% to 71.9%. In the UAE, there is no previously reported disease survival rate, this is the first study to report it. Based on our findings, the 5 years survival of breast cancer in the UAE was 89%, this is similar to western countries such as Australia 89.5% and Canada 88.2% [15]. The 5 year survival rate is also good compared to other countries in the same region such as Qatar (71.95%) and Kuwait (75.2%). This may reflect improved treatment and intensified efforts to tackle the burden of breast cancer in the country through the introduction of the national screening program. Previous studies have established numerous prognostic factors of breast cancer survival including age at diagnosis, tumor size, axillary lymph node involvement, tumor grade, stage of cancer, and metastasis. In our study, the average age at diagnosis of women was 48 years supporting the findings of other studies from the region claiming that Arab women are more likely to develop breast cancer at an earlier age [16, 17]. In fact, the median age at diagnosis of breast cancer in the UAE is 10 to 15 years younger than in North America and Europe [18]. Women at younger ages generally suffer from a more aggressive type of breast cancer, an advanced stage at presentation, and worse outcome [19]. A study conducted in southern Iran showed a relatively low 5-year survival (58%) of breast cancer [20]. However, in our data set, the hazard ratios obtained from separate univariate cox proportional hazard models fitted for each variable show no evidence for the survival function to be affected by age at diagnosis. In this study, the median patient delay in seeking treatment was 18 days, this is relatively similar to other studies in Europe [21, 22]. The percentage of stage 1 and II breast cancer in Australia, Canada, Denmark, Norway, Sweden, and the United Kingdom was 61–62% between 2000–2007 [23]. In our study, around 66% of patients were diagnosed at stage I or II versus 34% in stage III or IV. This was comparable to data from developed countries.

In this study, tumor stage was related to decreased survival, similar to other researches [2426]. Saadatmand et al (2015) reported that in univariable and multivariable analyses, both stage and lymph node status had major influence on overall survival. Stage at diagnosis still influence overall survival considerably [27].

In our study, the hazard ratio for death in patients with grade III compared to those with Grade I was 10.59 (95% CI 1.45–77.44). This finding is in agreement with the literature, suggesting that more advanced grading has worse prognoses for breast cancer [28, 29].

This is the first study to report estimates of survival rates and prognostics factors of breast cancer based on cancer registry data in the UAE. The study was based on robust cancer registry data. The follow-up duration was sufficient to capture and adequately estimate the 2-year and 5-year risk of death due to the fact that 50% of subjects were followed up for more than 35 months and 25% of patients followed up for more than 56 months. However, as this was hospital-based registry, generalizability of the study findings should be interpreted with caution. The sample does not represent the whole UAE, but it captures a good proportion of breast cancer patients referred to Tawam Hospital as it is used to be the main referral center for oncology cases in the UAE and has the only breast health center in the country. Moreover, as the analysis was based on secondary data, other potential confounding factors such as presenting symptoms and signs, family history, and lifestyle factors including diet and physical activity were unavailable and could not be included in the study analysis.

Conclusion

The 2-year survival was estimated to 97% and the 5-year survival to 89%. Tumor grade and the stage of cancer were found to be jointly significantly associated with survival. The findings of this research enable the estimate of the long-term breast cancer survival, as well as reemphasizes the importance of early diagnosis and screening through mammography which can prevent local systemic metastasis and therefore advanced stage diagnosis.

Acknowledgments

We would like to acknowledge Tawam Hospital Cancer registry staff for their cooperation.

References

  1. 1. WHO | Breast cancer: prevention and control. (2019). Retrieved October 15, 2019, from WHO website: http://www.who.int/cancer/detection/breastcancer/en/
  2. 2. American Cancer Society. Cancer Facts & Figures 2019
  3. 3. Cancer survival in England: national estimates for patients followed up to 2017. Office for National Statistics (2019). Retrieved October 16, 2019, from https://www.ons.gov.uk/peoplepopulationandcommunity/healthandsocialcare/conditionsanddiseases/bulletins/cancersurvivalinengland/nationalestimatesforpatientsfollowedupto2017
  4. 4. Hamdi Cherif M et al. Cancer estimation of incidence and survival in Algeria 2014. J Cancer Res Ther 2015, 3(9):100–104. http://dx.doi.org/10.14312/2052-4994.2015-14
  5. 5. GLOBOCAN, 784-united-arab-emirates-fact-sheets.pdf. (2018). Retrieved on March 15, 2020 from http://gco.iarc.fr/today/data/factsheets/populations/784-united-arab-emirates-fact-sheets.pdf
  6. 6. Elobaid Y. E., Aw T. C., Grivna M., & Nagelkerke N. Breast Cancer Screening Awareness, Knowledge, and Practice among Arab Women in the United Arab Emirates: A Cross-Sectional Survey. PLoS ONE 2014, 9(9). https://doi.org/10.1371/journal.pone.0105783
  7. 7. Foukakis, T., & Bergh, j. Prognostic and predictive factors in early, non-metastatic breast cancer. UptoDate 2013. Retreived on 15/12/2013 from http://www.uptodate.com/contents/prognostic-and-predictive-factors-in-early-non-metastatic-breast-cancer
  8. 8. Rubin E., & Reisner H. Essentials of Rubin’s Pathology (5th ed.). Lippincott Williams & Wilkins, 2009, Philadelphia, USA.
  9. 9. Cancer Incidence in United Arab Emirates Annual Report of the UAE National Cancer Registry- 2017 www.mohap.gov.ae Statistics and Research Center https://www.mohap.gov.ae/Files/MOH_OpenData/1585/CANCER%20INCIDENCE%20IN%20UNITED%20ARAB%20EMIRATES%20ANNUAL%20REPORT%20OF%20THE%20UAE%20-%20NATIONAL%20CANCER%20REGISTRY%20-%202017.pdf
  10. 10. Forouzanfar M., Foreman K., Delossantos A., Lozano R., Lopez A., Murray C., et al. Breast and cervical cancer in 187 countries between 1980 and 2010: a systematic analysis. Lancet. 2011, 378(9801), 1461–1484. pmid:21924486
  11. 11. Elobaid, Y. (2014). Breast Cancer Presentation Delay among Women in the United Arab Emirates. Thesis. United Arab Emirates University. Available at: https://scholarworks.uaeu.ac.ae/all_dissertations/31/ (Accessed: 18 October 2020).
  12. 12. American Joint Committee: AJCC Cancer Staging Manual. 5th edition. Philadelphia, New York. Lippincott-Raven; 1997.
  13. 13. Strobl C., Boulesteix A.-L., Kneib T., Augustin T., & Zeileis A. Conditional variable importance for random forests. BMC Bioinformatics. 2008, 9(1), 307. pmid:18620558
  14. 14. R Development Core Team. (2013). a language and environment for statistical computing: reference index. R Foundation for Statistical Computing. http://www.polsci.wvu.edu/duval/PS603/Notes/R/fullrefman.pdf
  15. 15. Allemani C., Weir H. K., Carreira H., Harewood R., Spika D., Wang X.-S., et al. Global surveillance of cancer survival 1995–2009: analysis of individual data for 25 676 887 patients from 279 population-based registries in 67 countries (CONCORD-2). The Lancet. 2015, 385(9972), 977–1010. Retrieved on March 15, 2020 from https://doi.org/10.1016/S0140-6736(14)62038-9
  16. 16. Najjar H, Easson A. Age at diagnosis of breast cancer in Arab nations. Int J Surg. 2010, 8, 448–452. pmid:20601253
  17. 17. World Health Statistics by World Health Organization. Electronic version http://www.who.int.whosis/whostat/EN_WHSo8_Full.pdf (2008). Google Scholar
  18. 18. National Cancer Registry (UAE). (2015). Retrieved April 11, 2020, from https://smartapps.moh.gov.ae/ords/f?p=105:512:10387122530459::NO:RP,RP,RIR,512:IR_YEAR_OF_DIAGNOSIS:2015&cs=1glSOv-Qci-yb_CJ3qHk9Q0O_YJc
  19. 19. Swanson G., & Lin C. Survival patterns among younger women with breast cancer: the effects of age, race, stage, and treatment. J Natl Cancer Inst Monogr. 1994, 16, 69–77.
  20. 20. Rezaianzadeh A, Peacock J, Reidpath D, Talei A, Hosseini SV, Mehrabani D. Survival analysis of 1148 women diagnosed with breast cancer in Southern Iran. BMC Cancer. 2009 Jun 5;9:168. pmid:19497131; PMCID: PMC2699348.
  21. 21. Innos K., Padrik P., Valvere V. et al. Identifying women at risk for delayed presentation of breast cancer: a cross-sectional study in Estonia. BMC Public Health 13, 947 (2013). pmid:24107190
  22. 22. Hansen RP, Vedsted P, Sokolowski I, Sondergaard J, Olesen F: Time intervals from first symptom to treatment of cancer: a cohort study of 2,212 newly diagnosed cancer patients. BMC Health Serv Res. 2011, 11: 284– pmid:22027084
  23. 23. Walters S, Maringe C, Butler J, Rachet B, Barrett-Lee P, Bergh J, et al.; ICBP Module 1 Working Group (2013a). Breast cancer survival and stage at diagnosis in Australia, Canada, Denmark, Norway, Sweden and the UK, 2000–2007: a population-based study. Br J Cancer, 108(5):1195–208. Cancer.net [Internet]. pmid:23449362
  24. 24. Fidler IJ. The pathogenesis of cancer metastasis: the ‘seed and soil’ hypothesis revisited. Nat Rev Cancer. 2003, 3:453–458. pmid:12778135.
  25. 25. Weigelt B, Peterse JL, van‘t Veer LJ. Breast cancer metastasis: markers and models. Nat Rev Cancer. 2005, 5:591–602. pmid:16056258.
  26. 26. Sopik V., & Narod S. A. The relationship between tumour size, nodal status and distant metastases: on the origins of breast cancer. Breast Cancer Research and Treatment, 2018, 170(3), 647–656. Retrieved on March 15, 2020 from pmid:29693227
  27. 27. Saadatmand S, Bretveld R, Siesling S, Tilanus-Linthorst M M A. Influence of tumour stage at breast cancer detection on survival in modern times: population based study in 173 797 patients BMJ 2015; 351:h4901 pmid:26442924
  28. 28. Kashi ASY, Yazdanfar S, Akbari M-E, Rakhsha A. Triple negative breast cancer in iranian women: Clinical profile and survival study. International Journal of Cancer Management. 2017; 10(8).
  29. 29. Carey LA, Perou CM, Livasy CA, Dressler LG, Cowan D, Conway K, et al. Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study. JAMA. 2006; 295(21):2492–502. Epub 2006/ 06/08. pmid:16757721.