Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login 
Home Print this page Email this page Small font size Default font size Increase font size Users Online: 153


 
  Table of Contents  
ORIGINAL ARTICLE
Year : 2021  |  Volume : 27  |  Issue : 1  |  Page : 22-27  

Correlation between body mass index and gleason score in men with prostate cancer in Southeastern Nigeria


Department of Surgery, Division of Urology, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Anambra State, Nigeria

Date of Submission06-Jun-2020
Date of Decision29-Jun-2020
Date of Acceptance01-Jul-2020
Date of Web Publication09-Mar-2021

Correspondence Address:
Dr. Uchenna Victor Nwadi
Department of Surgery, Division of Urology, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Anambra State
Nigeria
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/njs.NJS_66_20

Rights and Permissions
  Abstract 


Introduction: Prostate cancer has an increasing global burden. The clinical course varies from an indolent disease to a rapidly aggressive cancer. It is associated with higher mortality in less developed nations due to late presentation. The Gleason scoring system for prostatic adenocarcinoma has prognostic implications in diagnosed cases. Obesity has been associated with the evolution of many cancers including prostate cancer. There are conflicting reports on the relationship between obesity, as measured by body mass index (BMI), and prostate cancer aggressiveness, as measured by Gleason score. This study is aimed to determine if a correlation exists between BMI and Gleason score in men with prostate cancer. Methodology: This was a prospective, hospital-based, cross-sectional study involving consecutive patients with prostate cancer. Clinical evaluation including anthropometry, digital rectal examination, and relevant investigations were done for each patient and data collected with pro forma. This was followed by prostate needle biopsy and those diagnosed with adenocarcinoma of the prostate had their Gleason grades and scores obtained. Data were analyzed statistically using Spearman Correlation. Results: The mean age of the patients was 69.54 ± 8.61 years (range 47–83 years). The BMI ranged from 16.98 to 36.45 kg/m2, with a mean of 27.03 ± 5.03 kg/m2. Twenty-six of the patients (36.1%) were overweight and 34.7% were obese. The mean total prostate-specific antigen was 118.65 ± 84.43 ng/ml, with a range of 31–406 ng/ml. The modal Gleason score was 9 with a range of 4–10. There was a strong positive correlation between BMI and Gleason score (r = 0.817, P = 0.0003). Conclusion: The BMI of patients with prostate cancer correlated positively with their Gleason score.

Keywords: Body mass index, Gleason score, Prostate cancer


How to cite this article:
Nwadi UV, Nwofor AM, Oranusi CK, Orakwe JC, Obiesie EA, Mbaeri TU, Abiahu JA, Mbonu OO. Correlation between body mass index and gleason score in men with prostate cancer in Southeastern Nigeria. Niger J Surg 2021;27:22-7

How to cite this URL:
Nwadi UV, Nwofor AM, Oranusi CK, Orakwe JC, Obiesie EA, Mbaeri TU, Abiahu JA, Mbonu OO. Correlation between body mass index and gleason score in men with prostate cancer in Southeastern Nigeria. Niger J Surg [serial online] 2021 [cited 2021 Apr 20];27:22-7. Available from: https://www.nigerianjsurg.com/text.asp?2021/27/1/22/311023




  Introduction Top


Difficulty with micturition is a common complaint in urology and is usually characterized by lower urinary tract symptoms (LUTS). Many men with LUTS have varying degrees of prostate enlargement often caused by prostate cancer, benign prostatic hyperplasia (BPH) and prostatitis as the most frequent pathologies.

Prostate cancer is the second-most common cancer among men and the fourth-most common malignancy worldwide.[1],[2],[3],[4] It has a clinical course that varies from an indolent disease to a rapidly aggressive cancer that metastasizes quickly, leading to severe pain and untimely death.[5],[6] Diagnosis is made through prostate biopsy and histology, which are prompted by clinical and/or biochemical features suggestive of the disease. The Gleason system is a histologic grading system for prostatic adenocarcinoma based on architectural patterns rather than cellular features.[7] In this system, histologic patterns called grades are defined. These range from Gleason grade 1, which represents the well-differentiated with the best prognosis to Gleason grade 5, which represents the poorly differentiated with the poorest prognosis.[7],[8] The addition of the two most common Gleason grades in a field gives the Gleason score, which ranges from 2 to 10 and represents the level of aggressiveness of prostate cancer.[7],[9]

High body mass index (BMI) is a major global health problem. The BMI is derived from the weight of the individual in kilograms divided by the square of the height in meters (i.e., kg/m2).[10] Normal BMI ranges from 18.5 kg/m2 to 24.9 kg/m2, while overweight is defined as BMI ≥25 kg/m2 <30 kg/m2 and obesity is BMI ≥30 kg/m2.[10],[11]

Obesity has been shown by several studies to have a positive correlation with the more aggressive prostate cancers evidenced by high Gleason scores.[12],[13],[14] High BMI provides a favorable biological microenvironment for tumor onset and growth through some proposed mechanisms which involve alterations in the endocrine system, notably, the levels of testosterone, estrogen, and insulin-like growth factor-I.[14],[15],[16],[17],[18],[19],[20] However, this correlation was not found by some other studies. Gallina et al.[21] in a study of European men, and Chamie et al.[22] in California, the USA observed no relationship between BMI and high-grade prostate cancer.

With this disparity, it becomes necessary to ascertain if such a relationship exists in our environment where we have a high burden of the disease as well as obesity. The study, therefore, aims to determine the relationship between BMI and prostate cancer aggressiveness (Gleason score) in adult Nigerian males with histologically diagnosed prostate cancer.


  Methodology Top


This was a prospective, cross-sectional study conducted at the Urology Clinics of Nnamdi Azikiwe University Teaching Hospital, Nnewi from July 2018 to July 2019 following approval by the hospital's ethics committee.

All-new adult male patients that attended the Urology Clinics with LUTS and consented were enlisted into the study. The exclusion criteria included patients that could not stand erect, history of bariatric surgery, those on the medical program for weight reduction, immunosuppressive illnesses (e.g., TB, AIDS), prostatitis, BPH, and those currently on treatment for prostatic adenocarcinoma.

Detailed clinical assessment, including digital rectal examination, weight, and height measurements, were taken for each patient on presentation. Investigations included full blood count, serum electrolytes, urea and creatinine, serum prostate-specific antigen (PSA), urinalysis with urine microscopy, culture and sensitivity, and abdominopelvic ultrasound scan. The data obtained were entered into predesigned pro forma.

Patients were stratified into underweight, normal weight, overweight, and obesity groups using the World Health Organization classification of BMI.[11]

Patients suspected to have prostate cancer based on clinical and/or biochemical findings were counseled and informed consent obtained before subjecting them to digitally-guided transrectal prostate biopsy using size 18G semi-automated Tru-Cut® biopsy needle after adequate lubrication with 2% xylocaine gel. Specimens obtained were sent to a designated pathologist for histological examination and reporting using the Gleason Scoring System. Those diagnosed with prostate cancer were then stratified into three groups: low (Gleason score 2–4), intermediate (Gleason score 5–7), and high (Gleason score 8–10).

Data collected were analyzed with a multi-purpose computer analysis program, Statistical Package for the Social Sciences version 23 (IBM; SPSS, Chicago, IL, USA). Results obtained were expressed as tables and figures where necessary. Data were subjected to Spearman correlation. An r - value (Correlation coefficient) of either ≥−0.7 or ≥+0.7 was considered a high/strong correlation, whereas an r - value (Correlation coefficient) that ranged either from − 0.3 to <−0.7 or from + 0.3 to <+0.7 was considered moderate correlation and an r-value of either <−0.3 or <+0.3 was considered low correlation. Value of P ≤ 0.05 was considered statistically significant.


  Results Top


A total of 159 patients were recruited during the study period; however, only 72 patients who satisfied the criteria for inclusion were analyzed.

The age range of the participants was 47–83 years with a mean age of 69.54 ± 8.61 years and the median age of 71.50 years. The peak incidence of prostate cancer was in the eighth decade [Figure 1].
Figure 1: Age distribution of the patients

Click here to view


Most (80.6%) of the men were married. Widowers and single men made up 18.06% and 1.39% of the patients, respectively.

The most common educational attainment was a secondary school (48.6%), followed by primary school (19.4%), postsecondary (18.1%), whereas 13.9% had no formal education.

The patients generally had LUTS of varying degrees. In 38.9% of the patients, the symptoms were present for over 12 months before the presentation. The rest had their symptoms for 6–12 months (37.3%) and for <6 months (23.6%).

There was a family history of prostate cancer in 6 (8.3%) of the patients. This was seen in their fathers (2 patients), brothers (3 patients), and first cousin (1 patient).

The mean total PSA of the patients was 118.65 ± 84.43 ng/mL with a range of 31–406 ng/mL and a median of 85.86 ng/mL. The mean percentage Free PSA was 9.03% ± 6.23%, with a range of 0.52%–29.37%.

The mean weight of the participants was 75.75 ± 13.08 kilograms, with a range of 48–95 kilograms. The mean height of the participants was 1.68 ± 0.063 m, with a range of 1.56–1.78 m. The mean BMI was 27.03 ± 5.03 kg/m2 with a range of 16.98–36.45 kg/m2 and a median of 27.85 kg/m2. Twenty-six (36.1%) of the participants were overweight and 34.7% were obese (Class I obesity: 23 patients [31.9%]; Class II Obesity: 2 patients [2.8%]) [Table 1].
Table 1: Distribution of body mass index of the participants

Click here to view


The mean, median, and modal Gleason Scores were 7.5 ± 0.80, 7.0, and 9, respectively, with a range of 4–10. Forty-one (56.9%) of the patients had Gleason Scores within the Intermediate group, whereas 29 (40.3%) of the patients had Gleason scores within the high group [Table 2].
Table 2: Distribution of the Gleason scores of the participants

Click here to view


There was a significant association between Normal BMI and Low Gleason score (χ2 = 14.098; P = 0.003) after stratifying the patients into High (Gleason score >7) and low (Gleason score ≤7) Gleason Score groups [Table 3]. The obesity Class II patients had a low Gleason Score though not statistically significant (χ2 = 1.547; P = 0.216), as shown in [Table 3]. On further analysis by stratifying the patients into high (≥25 kg/m2), normal (18.5–24.9 kg/m2), and low (<18.5 kg/m2) BMI groups, there was a significant association between high Gleason score and high BMI (χ2 = 4.771; P = 0.03), as shown in [Table 4].
Table 3: Relationship between body mass index and Gleason score of the patients

Click here to view
Table 4: Analysis of the relationship between high Gleason score and body mass index of the patients

Click here to view


There was a strong positive correlation between BMI and Gleason Score (r = 0.817; P = 0.0003), as shown in [Table 5].
Table 5: Correlation between body mass index and Gleason score

Click here to view



  Discussion Top


Cancer of the prostate is a frequent diagnosis made at urologic consultations, and attempts at early diagnosis and prediction of prognosis using several patient parameters are usually made to institute aggressive but appropriate treatment. Several clinical and nonclinical parameters, including BMI, have been used to predict the aggressiveness of tumor and outcome of treatment. In this study, we have tried to establish if there is a correlation between BMI and the aggressiveness of prostate cancer.

The age distribution of the patients from this study is in keeping with the facts that prostate cancer is not commonly diagnosed in men <50 years and its incidence continues to increase with advancing age.[4],[23] There is a slight drop in the frequency of the patients after the age group of 70–79 years, which could be attributed to the life expectancy of the study population. The mean age of 69.54 ± 8.61 years found in this study is similar to the findings of other Nigerian studies.[24],[25],[26] The age range of 47–83 years and the peak incidence of the 8th decade from this study compares fairly with 44–92 years found earlier by Nwofor and Oranusi[24] in the same centre. Secondary education was the most common highest educational attainment among patients. This may be attributed to the fact that Nnewi, Southeastern Nigeria, is a commercial hub with mainly traders as inhabitants.

Obesity and overweight have remained a global health concern. The global burden of high BMI is worse off in developing nations where there is attendant poor health facilities. Nigeria, the most populous nation in Africa, is one of such developing countries.[27] In Nigeria, prevalence ranges of 20.3% to 35.1% and 8.1% to 22.2% have been noted for obesity and overweight, respectively.[27] The mean BMI of 27.03 ± 5.03 kg/m2 noted in this study compares well with the findings of Okafor et al.[28] who studied the relationship between obesity and blood pressure in Southeastern Nigeria and Goris-Gbenou et al.[29] who studied an American population. Furthermore, studies by Freedland et al.[20] in Europe and Su et al.[18] in an African–American population reported similar findings. The median BMI of 27.85 kg/m2 in this study compares well with that of a European study (27.6 kg/m2) while it is at variance with a study in Asia (23.9 kg/m2).[20],[30] As much as 36.1% of the participants in this study were overweight, while obesity was seen in 25 (34.7%) patients (Class I: 23 patients [31.9%]; Class II: 2 patients [2.8%]). This is similar to the findings by Bai et al.[30] who studied the association between BMI, Gleason score and risk of biochemical recurrence following radical prostatectomy in Chinese men.

The predominant Gleason score of 9 and the mean Gleason score of 7.5 ± 0.80 in this study are in contrast with the reported predominant Gleason score of 6 by Liang et al.[31] and a mean Gleason score of 5.87 ± 1.17 by Goris-Gbenou et al.[29] This could be due to early presentation of the patients used in those studies and thus, lesser tumor burden. Furthermore, it has been observed that men of African descent are more likely to have higher Gleason scores and present with more advanced disease.[32],[33],[34],[35]

This study found a strong positive correlation between BMI and the Gleason score of patients with prostate cancer. The two patients with Class II Obesity had a low Gleason Score, though not statistically significant, this may have arisen as a result of a low number. Also found from this study was a significant association between high BMI and high Gleason score and between normal BMI and low Gleason score similar to the observations of Gioia et al.[14] in a study of Caucasian men, and Liang et al.[31] in a study using a cohort from Selenium and Vitamin E Cancer Prevention Trial (SELECT). They noted an association between high BMI and risk of high-grade prostate cancer, especially in men with a family history of prostate cancer. Similarly, Jayachandran et al.[19] observed in a retrospective analysis of 1,415 men treated with radical prostatectomy that obesity was a risk factor for aggressive prostate cancer and tumor recurrence irrespective of the race while high BMI was found to be independently associated with high-grade prostate cancer by Freedland et al.[20] in their analysis of 2,302 men in America. There was a higher proportion (72.4%) of the patients with high Gleason score in the high BMI group, similar to the finding in the study by Zhou et al.[13] In another study by Kryvenko et al.,[12] 5118 patients who underwent robotic radical prostatectomy in America were analyzed and they observed that the Gleason score and the number of positive cores were higher in overweight and obese men.

In all, it seems that BMI correlates positively with the Gleason score.


  Conclusion Top


There was a significant association between high BMI and high Gleason score as well as between normal BMI and low Gleason score from this study. The study showed a strong positive correlation between BMI and Gleason score in men with prostate cancer. Thus, the higher the BMI the higher the chances of aggressive disease.

Ascertaining the BMI of patients with prostate cancer should be encouraged and there is a need for more public campaign efforts to tackle high BMI through lifestyle and dietary modifications. Obese and overweight men should be encouraged to get screened for prostate cancer earlier than their normal-weight counterparts. Further, multi-center studies are necessary as these will be more representative of the picture in the general population.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer 2015;136:E359-86.  Back to cited text no. 1
    
2.
Baade PD, Youlden DR, Krnjacki LJ. International epidemiology of prostate cancer: Geographical distribution and secular trends. Mol Nutr Food Res 2009;53:171-84.  Back to cited text no. 2
    
3.
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer 2010;127:2893-917.  Back to cited text no. 3
    
4.
Abouassaly R, Thompson IM Jr., Platz EA, Klein EA. Epidemiology, etiology and prevention of prostate cancer. In: Wein AJ, kavoussi LR, Novick AC, Partin AW, Peters CA, editors. Campbell-Walsh Urology. Ch. 95., 10th ed. Philadelphia: Elsevier Saunders; 2012. p. 2704-25.  Back to cited text no. 4
    
5.
Eastham JA, Scardino PT. Expectant management of prostate cancer. In: Wein AJ, Kavoussi LR, Novick AC, Partin AW, Peters CA, editors. Campbell-Walsh Urology. Ch. 101., 10th ed. Philadelphia: Elsevier Saunders; 2012. p. 2789-800.  Back to cited text no. 5
    
6.
Spahn M, Kneitz S, Scholz CJ, Stenger N, Rüdiger T, Ströbel P, et al. Expression of microRNA-221 is progressively reduced in aggressive prostate cancer and metastasis and predicts clinical recurrence. Int J Cancer 2010;127:394-403.  Back to cited text no. 6
    
7.
Chen N, Zhou Q. The evolving Gleason grading system. Chin J Cancer Res 2016;28:58-64.  Back to cited text no. 7
    
8.
Montironi R, Mazzuccheli R, Scarpelli M, Lopez-Beltran A, Fellegara G, Algaba F. Gleason grading of prostate cancer in needle biopsies or radical prostatectomy specimens: Contemporary approach, current clinical significance and sources of pathology discrepancies. BJU Int 2005;95:1146-52.  Back to cited text no. 8
    
9.
Yakar D, Debats OA, Bomers JG, Schouten MG, Vos PC, van Lin E, et al. Predictive value of MRI in the localization, staging, volume estimation, assessment of aggressiveness, and guidance of radiotherapy and biopsies in prostate cancer. J Magn Reson Imaging 2012;35:20-31.  Back to cited text no. 9
    
10.
World Health Organization. Obesity and Overweight. Fact Sheet. World Health Organization; 2020. Availablefrom:http://www.who.int/mediacentre/factsheets/fs311/en/.[Last accessed on 2020 May 22].  Back to cited text no. 10
    
11.
World Health Organization. Body Mass Index-BMI. Denmark: World Health Organization; 2017. Available from: http://www.euro.who.int/en/health-topics/disease-prevention/nutrition/a-healthy-lifestyle/body-mass-index-bmi. [Last accessed on 2017 Nov 08].  Back to cited text no. 11
    
12.
Kryvenko ON, Epstein JI, Meier FA, Gupta NS, Menon M, Diaz M. Correlation of high body mass index with more advanced localized prostate cancer at radical prostatectomy is not reflected in PSA level and PSA density but is seen in PSA mass. Am J Clin Pathol 2015;144:271-7.  Back to cited text no. 12
    
13.
Zhou F, Chen X, Pu J, Ouyang J, Li G, Ping J, et al. Correlation between body mass index (BMI) and the Gleason score of prostate biopsies in Chinese population. Oncotarget 2016;7:63338-41.  Back to cited text no. 13
    
14.
Gioia A, Manco R, Tenaglia RL, Tirabassi G, Balercia G. Relationship between BMI, PSA and histopathological tumor grade in a Caucasian population affected by prostate cancer. Global J Med Clin Case Rep 2014;2:14-9.  Back to cited text no. 14
    
15.
Hu MB, Bai PD, Wu YS, Zhang LM, Xu H, Na R, et al. Higher body mass index increases the risk for biopsy-mediated detection of prostate cancer in Chinese men. PLoS One 2015;10:e0124668.  Back to cited text no. 15
    
16.
Massengil JC, Sun L, Moul JW, Wu H, McLeod DG, Amling C, et al. Pretreatment total testosterone level predicts pathological stage in patients with localized prostate cancer treated with radical prostatectomy. J Urol 2003;169:1670-5.  Back to cited text no. 16
    
17.
Schatzl G, Madersbacher S, Thurridl T, Waldmüller J, Kramer G, Haitel A, et al. High-grade prostate cancer is associated with low serum testosterone levels. Prostate 2001;47:52-8.  Back to cited text no. 17
    
18.
Su LJ, Arab L, Steck SE, Fontham ET, Schroeder JC, Bensen JT, et al. Obesity and prostate cancer aggressiveness among African and Caucasian Americans in a population-based study. Cancer Epidemiol Biomarkers Prev 2011;20:844-53.  Back to cited text no. 18
    
19.
Jayachandran J, Bañez LL, Aronson WJ, Terris MK, Presti JC Jr, Amling CL, et al. Obesity as a predictor of adverse outcome across black and white race: Results from the Shared Equal Access Regional Cancer Hospital (SEARCH) Database. Cancer 2009;115:5263-71.  Back to cited text no. 19
    
20.
Freedland SJ, Bañez LL, Sun LL, Fitzsimons NJ, Moul JW. Obese men have higher-grade and larger tumors: An analysis of the duke prostate center database. Prostate Cancer Prostatic Dis 2009;12:259-63.  Back to cited text no. 20
    
21.
Gallina A, Karakiewicz PI, Hutterer GC, Chun FK-H, Briganti A, Walz J, et al. Obesity does not predispose to more aggressive prostate cancer either at biopsy or radical prostatectomy in European men. Int J Cancer 2007;121:791-5.  Back to cited text no. 21
    
22.
Chamie K, Oberfoell S, Kwan L, Labo J, Wei JT, Litwin MS. Body mass index and prostate cancer severity: Do obese men harbor more aggressive disease on prostate biopsy? Urology 2013;81:949-55.  Back to cited text no. 22
    
23.
Cooperberg MR, Presti JC, Shinohera K, Carroll PR. Neoplasms of the prostate gland. In: McAninch JW, Lue TF, editors. Smith & Tanagho's General Urology. Ch. 23., 18th ed.. California: The McGraw-Hill Co; 2013. p. 350-79.  Back to cited text no. 23
    
24.
Nwofor AM, Oranusi CK. Cancer of the prostate: Experience at Nnewi, Southeast, Nigeria. Niger J Clin Pract 2004;7:65-8.  Back to cited text no. 24
    
25.
Badmus TA, Adesunkanmi AR, Yusuf BM, Oseni GO, Eziyi AK, Bakare TI, et al. Burden of prostate cancer in southwestern Nigeria. Urology 2010;76:412-6.  Back to cited text no. 25
    
26.
Ekwere PD, Egbe SN. The changing pattern of prostate cancer in Nigerians: Current status in the southeastern states. J Natl Med Assoc 2002;94:619-27.  Back to cited text no. 26
    
27.
Chukwuonye II, Chuku A, John C, Ohagwu KA, Imoh ME, Isa SE, et al. Prevalence of overweight and obesity in adult Nigerians-a systematic review. Diabetes Metab Syndr Obes 2013;6:43-7.  Back to cited text no. 27
    
28.
Okafor C, Anyaehie U, Ofoegbu E. The magnitude of obesity and its relationship to blood pressure among the residents of Enugu metropolis in South East Nigeria. Ann Med Health Sci Res 2014;4:624-9.  Back to cited text no. 28
[PUBMED]  [Full text]  
29.
Goris Gbenou MC, Peltier A, Schulman CC, Velthoven Rv. Increased body mass index as a risk factor in localized prostate cancer treated by radical prostatectomy. Urol Oncol 2016;34:254.e1-6.  Back to cited text no. 29
    
30.
Bai PD, Hu MB, Xu H, Zhu WH, Hu JM, Yang T, et al. Body mass index is associated with higher Gleason score and biochemical recurrence risk following radical prostatectomy in Chinese men: A retrospective cohort study and meta-analysis. World J Surg Oncol 2015;13:311.  Back to cited text no. 30
    
31.
Liang Y, Ketchum NS, Goodman PJ, Klein EA, Thompson IM Jr., Is there a role for body mass index in the assessment of prostate cancer risk on biopsy? J Urol 2014;192:1094-9.  Back to cited text no. 31
    
32.
Haas GP, Delongchamps N, Brawley OW, Wang CY, de la Roza G. The worldwide epidemiology of prostate cancer: Perspectives from autopsy studies. Can J Urol 2008;15:3866-71.  Back to cited text no. 32
    
33.
Moul JW. Targeted screening for prostate cancer in African-American men. Prostate Cancer Prostatic Dis 2000;3:248-55.  Back to cited text no. 33
    
34.
Delongchamps NB, Singh A, Haas GP. Epidemiology of prostate cancer in Africa: Another step in the understanding of the disease? Curr Probl Cancer 2007;31:226-36.  Back to cited text no. 34
    
35.
Rebbeck TR, Devesa SS, Chang BL, Bunker CH, Cheng I, Cooney K, et al. Global patterns of prostate cancer incidence, aggressiveness, and mortality in men of african descent. Prostate Cancer 2013;2013:560857.  Back to cited text no. 35
    


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5]



 

Top
   
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
Abstract
Introduction
Methodology
Results
Discussion
Conclusion
References
Article Figures
Article Tables

 Article Access Statistics
    Viewed292    
    Printed2    
    Emailed0    
    PDF Downloaded17    
    Comments [Add]    

Recommend this journal