Submit Your Article CMED MEACR meeting
Home Print this page Email this page Users Online: 275
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login 


 
 Table of Contents  
ORIGINAL ARTICLE
Year : 2020  |  Volume : 9  |  Issue : 4  |  Page : 155-158

Pancreatic cancer: Demographics and prevalence


Isfahan Kidney Transplantation Research Center, Isfahan University of Medical Sciences, Isfahan, Iran

Date of Submission25-Jan-2020
Date of Decision18-Apr-2020
Date of Acceptance15-May-2020
Date of Web Publication14-Aug-2020

Correspondence Address:
Zahra Tolou-Ghamari
Isfahan Kidney Transplantation Research Center, Isfahan University of Medical Sciences, Isfahan
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ccij.ccij_13_20

Rights and Permissions
  Abstract 


Background: The rapidly fatal cancer that called pancreatic cancer (PC) is the seventh primary source of cancer connected deaths globally. Its treatment is a big challenge with a relatively poor survival even after surgery. The aim of this study was to provide information associated with the PC prevalence, period prevalence (PP), and incidence rates (Irs) in Isfahan Province/Iran. Materials and Methods: Data from March 24, 2011 to March 19, 2015 were obtained from the Isfahan Cancer Registry. Irs and PP were calculated and expressed per 100,000 males. Statistical Analysis Used: The statistical analyses of d-Base were performed using Microsoft Excel and SPSS v. 20 (Chicago, IL, USA) for windows. Results: In all, there were 486 patients with PC. For the total population, the PP was calculated as 9.8 and Irs increased from 2.2 to 2.7/100,000 persons. The mean (standard deviation, min-max) age of the patients was 65.7 (13.0, 12–94) years. The total population was comprised of 150 alive and 336 deceased reported individuals. Conclusions: There was a 22.7% increase in the Irs over the study period. The PP was 58.9% higher in males than females. In 82%, PC occurred at the age between 40 and 80 years. Therefore, for the principal control of the disease, further consideration concerning etiology, pharmacotherapy, and recognizing all relevant features of the PC is crucial.

Keywords: Cancer, Iran, pancreas, pancreatic, prevalence


How to cite this article:
Tolou-Ghamari Z. Pancreatic cancer: Demographics and prevalence. Clin Cancer Investig J 2020;9:155-8

How to cite this URL:
Tolou-Ghamari Z. Pancreatic cancer: Demographics and prevalence. Clin Cancer Investig J [serial online] 2020 [cited 2020 Sep 21];9:155-8. Available from: http://www.ccij-online.org/text.asp?2020/9/4/155/292149




  Introduction Top


The significant but uncommon public health problem with an enormously high mortality rate is called pancreatic cancer (PC).[1] Based on GLOBOCAN, 2018 estimates, a total of 458,918 new cases with PC have been reported worldwide. The prediction for the year 2040 is an increase of 355,317 new cases. By increasing age, the incidence of PC is increasing in both sexes. Due to the report of PC in patients aged >70 years, it is defined as a disease of elderly populations. In the male population, PC is more common than the female population.[2],[3] As the 11th most common cancers, PC causes more than a quarter of a million deaths annually and is the seventh most frequent cause of death from cancer. As a tumor with the poorest survival, the mortality-to-incidence ratio is reported as 98%. With no metastasis to other organs, approximately 5-year survival could be achieved by resectional surgery in 20%. Although the cause of PC is multifaceted, cigarette smoking, alcohol consumption, chronic pancreatitis, obesity, diabetes mellitus, and genetic features have been mentioned as the main factors.[3],[4],[5]

For Europe, North America, and Oceania, the highest age-standardized rate (ASR) incidence was reported as 7.7, 7.6, and 6.4/100,000 people, respectively. Africa was reported the lowest ASR incidence of 2.2/100,000 persons. A 30-fold differences in ASR incidence were reported at the highest rate (Hungary; 10.8) and the lowest rate (Guinea; 0.35).[2] Republic of Moldova (12.3) and Uruguay (12.1) were reported the highest mortality rate associated with men. In women, the United Arab Emirates (10.0) and Uruguay reported the highest mortality rate. The least mortality rate in men was reported in Tanzania (0.3) and Malawi (0.32) and in women in Guinea (0.2) and Pakistan (0.3).[6],[7]

In Iran, a recent publication confirmed that smoking, aging, and lifestyle changes are the most important risk factors for PC.[8] Another study showed a gender difference between male and female with a higher mortality rate in males. The age of PC patients was reported 50 years or older.[9] In addition, for the years 1999–2004, a 20%–30% of deaths from the PC were reported in Iran.[10]

The classification of PC is based on four types. When the cancer is limited to the pancreas and has grown around 2 cm, then called stage one. In stage two, there is local spread of tumor with growth of >2 cm and <4 cm. When the tumor is widely spread and tumor cell expanded to the nearby blood vessels or nerves, but no metastasized to distant site called stage three. In stage four, cancer has spread to distant organs.[11],[12],[13],[14]

Beside with advanced native and detailed approaches, there is a need for further investigation associated with the mortality tendency of PC because there is still no certain treatment. Therefore, this study aimed to provide period prevalence (PP) and incidence rates (Irs) data of PC in Isfahan Province, Iran.


  Materials and Methods Top


PC data from March 2011 to March 2015 were obtained from the Isfahan Cancer Registry, located at the Isfahan Deputy of Health. The study was approved by the Institutional Review Board (extracted from the project with Code no. 295115). Demographic, clinical, and pathology data, with linkage to using of the de-identified patient name and surname, age and gender, final code for cancer diagnosis, and date of reported cancer were recorded in Microsoft Excel.

Statistical analysis

According to the International Classification of Diseases for Oncology (Third Edition), the cancer sites studied (C25) were defined. Microsoft Excel was used to arrange raw data before being inputted into the Statistical Package for the Social Science (SPSS® version 20; IBM Corp., Armonk, NY, USA) for analysis. Age, as a continuous variable, was expressed as mean ± standard deviation (SD). The total population of Isfahan was obtained from the Isfahan/Program and Budget Management Organization. PP was calculated as the proportion of the total cases over the period of the years 2011–2015/to populations at risk during the same time period ×100 000. The Irs were calculated by dividing new cases of cancer during a given time period/to the population at risk during the same time period × 100,000.[15],[16],[17],[18],[19],[20],[21]


  Results Top


Associated with the period of study, there were 486 patients with PC. For the total population, the PP was calculated as 9.8 which corresponded to a value of 7.5 for females and 11.9 for males/100,000 population. [Figure 1] shows the distribution of age, according to gender. With a minimum of 12 and a maximum of 94, the mean age ± SD was 65.7 ± 13.0 years. Ages related to PC from 10 to 40, 40–80, and 80–94 years of life in females versus males were as follows: 7, 34, and 25 (females) versus 12, 50, and 38 (males). [Figure 2] shows the Irs for the related years of study. The calculated Irs for each year were as follows: 2 (2011–2012), 2.2 (2012–2013), 2.8 (2013–2014), and 2.7 (2014–2015), correspondingly. As shown in [Figure 3], death reported data were associated with 336 records out of the total population (n = 486). One sample Kolmogorov–Smirnov test confirmed normal distribution of age among deceased patients (P = 0.03) with a mean ± SD of 67.2 ± 13.3 years (ranged 12–94 years).
Figure 1: Distribution of age in pancreatic cancer

Click here to view
Figure 2: Incidence of pancreatic cancer

Click here to view
Figure 3: Death/alive reported data on pancreatic cancer

Click here to view



  Discussion Top


The prevalence and incidence of PC differs significantly across regions and populations. Available reports indicate an increase in mortality in the United States, European countries, Japan, and China.[22],[23],[24]

In addition to geographic variations and genetic differences[25],[26],[27],[28] and in agreement with previous publications, associated with the PC mortality,[1],[2],[3] this investigation indicated a 69% mortality rate, with a 22.7% increase in the trend of PC incidence.

The PP of PC was 9.8 that corresponded to a value of 7.5 for females and 11.9 for males/100,000 persons in Isfahan Province/Iran. This is in agreement with previously published articles that confirmed ethnicity, male sex, cigarette smoking, daily diet based on a low amount of vegetables and fruits, high consumption of red meat, obesity, diabetes mellitus, and chronic pancreatitis have been mentioned as the main risk factors.[8],[9],[10],[29],[30],[31]

In this study, the mean age of patients was 65.7 years, and this is in agreement with previous publication that confirmed an age of >60 years as a risk factor for PC.[22] Other publications confirmed that PC is rarely identified before 55 years of age, and it can be distinct as a disease of elderly populations, since the maximum occurrence is reported in people over 70 years.[2],[3],[22] In this study, PC occurred at the ages between 10 and 50 years in 9% of the total population.

Previous publication reported 220,000 deaths annually for PC[3] in which, among industrialized countries, mentioned as the fifth leading cause of death from cancer.[23] In this study, dead/alive reported data were 69%, which is in agreement with previously published articles that mentioned PC as one of the most deadly common cancer types.[22],[23] Previous publication reported a higher mortality from PC in males when compared to females.[24] In Isfahan Province/Iran, mortality from PC in both genders was 129/184 in females versus 207/302 in males. Regarding to sex, as similar as other studies, we found male and female differences in Ir (11.9 vs. 7.5) per 100,000 persons, respectively.

The burden of the PC is increasing, and based on the estimation of the International Agency for Research on Cancer, global PC rates tend to increase.[31],[32],[33],[34] Therefore, from this survey, plan for a change in strategy based on the prevention and early diagnosis, lifestyle changes, awareness campaigns, and advanced pharmacotherapy management recommended for health authorities and policymakers in Iran.


  Conclusions Top


With a closer distance between the incidence and mortality rates, the worldwide problem, PC necessitates a comprehensive determination. Many risk factors have been identified as the cause of PC in patients.

In Isfahan Province/Iran, the PP associated with PC was with a value of 9.8/100,000 persons with a significant increase in the incidence from 2011 to 2015. These outcomes highlighted a greater effort toward advanced pharmacotherapy, prevention, and early diagnosis of PC in Iran.

Financial support and sponsorship

Nil.

Conflicts of interest

We extend our thanks to Isfahan University of Medical Sciences for supporting this study.



 
  References Top

1.
Thapa P. Epidemiology of pancreatic and periampullary cancer. Indian J Surg 2015;77:358-61.  Back to cited text no. 1
    
2.
Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68:394-424.  Back to cited text no. 2
    
3.
Rawla P, Sunkara T, Gaduputi V. Epidemiology of pancreatic cancer: Global trends, etiology and risk factors. World J Oncol 2019;10:10-27.  Back to cited text no. 3
    
4.
Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics. CA Cancer J Clin 2002;55:74-108.  Back to cited text no. 4
    
5.
Baradaran B, Shahbazi R, Khordadmehr M. Dysregulation of key microRNAs in pancreatic cancer development. Biomed Pharmacother 2019;109:1008-15.  Back to cited text no. 5
    
6.
Oberstein PE, Olive KP. Pancreatic cancer: Why is it so hard to treat? Therap Adv Gastroenterol 2013;6:321-37.  Back to cited text no. 6
    
7.
Levi F, Lucchini F, Negri E, La Vecchia C. Pancreatic cancer mortality in Europe: The leveling of an epidemic. Pancreas 2003;27:139-42.  Back to cited text no. 7
    
8.
Siri FH, Salehiniya H. Pancreatic cancer in Iran: An epidemiological review. J Gastrointest Cancer 2020;51:418-24.  Back to cited text no. 8
    
9.
Pourhoseingholi MA, Pourhoseingholi A, Vahedi M, Ashtari S, Safaee A, Moghimi-Dehkordi B, et al. Decreased trend of pancreatic cancer mortality in Iran. Asian Pac J Cancer Prev 2011;12:153-5.  Back to cited text no. 9
    
10.
Taghavi A, Fazeli Z, Vahedi M, Baghestani AR, Zali MR, Pourhoseingholi MA. Pancreatic cancer mortality and misclassification-Bayesian analysis. Asian Pac J Cancer Prev 2011;12:2271-4.  Back to cited text no. 10
    
11.
Torgeson A, Tao R, Garrido-Laguna I, Willen B, Dursteler A, Lloyd S. Large database utilization in health outcomes research in pancreatic cancer: An update. J Gastrointest Oncol 2018;9:996-1004.  Back to cited text no. 11
    
12.
Capasso M, Franceschi M, Rodriguez-Castro KI, Crafa P, Cambiè G, Miraglia C, et al. Epidemiology and risk factors of pancreatic cancer. Acta Biomed 2018;89:141-6.  Back to cited text no. 12
    
13.
McGuigan A, Kelly P, Turkington RC, Jones C, Coleman HG, McCain RS. Pancreatic cancer: A review of clinical diagnosis, epidemiology, treatment and outcomes. World J Gastroenterol 2018;24:4846-61.  Back to cited text no. 13
    
14.
Weledji FP, Enoworock G, Mokake M, Sinju M. How Grim is Pancreatic Cancer? Oncol Rev 2016;10:294.  Back to cited text no. 14
    
15.
Mazdak H, Tolou-Ghamari Z. Preliminary study of prevalence for bladder cancer in Isfahan Province, Iran. Arab J Urol 2018;16:206-10.  Back to cited text no. 15
    
16.
Tolou Ghamari Z. Prevalence of lung cancer in Isfahan Province, Iran. J Egypt Natl Canc Inst 2018;30:57-9.  Back to cited text no. 16
    
17.
Tolou Ghamari Z, Tadayon F, Mazdak H. Prevalence of liver cancer in Isfahan province, Iran. Indonesian J Cancer 2018;12:56-9.  Back to cited text no. 17
    
18.
Tolou Ghamari Z. Prevalence of breast cancer in Isfahan province, Iran. Women Health 2018;5:e82678.  Back to cited text no. 18
    
19.
Tolou Ghamari Z. Prevalence of skin cancer in Isfahan province, Iran. Jentashapir J Health Res 2018;9:e82743.  Back to cited text no. 19
    
20.
Ghamari ZT. Prevalence of stomach cancer in Isfahan province, Iran. Gulf J Oncolog 2018;1:42-5.  Back to cited text no. 20
    
21.
Mazdak H, Tolou-Ghamari Z, Gholumpour M. Investigation of bladder cancer incidence in Isfahan, Iran. Tehran Univ Med J 2019;77:252-6.  Back to cited text no. 21
    
22.
Ilic M, Ilic I. Epidemiology of pancreatic cancer. World J Gastroenterol 2016;22:9694-705.  Back to cited text no. 22
    
23.
Malvezzi M, Carioli G, Bertuccio P, Rosso T, Boffetta P, Levi F, et al. European cancer mortality predictions for the year 2016 with focus on leukaemias. Ann Oncol 2016;27:725-31.  Back to cited text no. 23
    
24.
Qiu D, Katanoda K, Marugame T, Sobue T. A Joinpoint regression analysis of long-term trends in cancer mortality in Japan (1958-2004) Int J Cancer 2009;124:443-8.  Back to cited text no. 24
    
25.
Wang L, Yang GH, Lu XH, Huang ZJ, Li H. Pancreatic cancer mortality in China (1991-2000). World J Gastroenterol 2003;9:1819-23.  Back to cited text no. 25
    
26.
Apte MV, Pirola RC, Wilson JS. Pancreas: Alcoholic pancreatitis-it's the alcohol, stupid. Nat Rev Gastroenterol Hepatol 2009;6:321-2.  Back to cited text no. 26
    
27.
Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C, et al. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11. Lyon, France: International Agency for Research on Cancer; 2013.  Back to cited text no. 27
    
28.
Silverman DT, Schiffman M, Everhart J, Goldstein A, Lillemoe KD, Swanson GM, et al. Diabetes mellitus, other medical conditions and familial history of cancer as risk factors for pancreatic cancer. Br J Cancer 1999;80:1830-7.  Back to cited text no. 28
    
29.
Lowenfels AB, Maisonneuve P. Risk factors for pancreatic cancer. Cell Biochem 2005;95:649-56.  Back to cited text no. 29
    
30.
Schwartz GG, Reis IM. Is cadmium a cause of human pancreatic cancer? Cancer Epidemiol Biomarkers Prev 2000;9:139-45.  Back to cited text no. 30
    
31.
Sant M, Aareleid T, Berrino F, Bielska Lasota M, Carli PM, Faivre J, et al. EUROCARE-3: Survival of cancer patients diagnosed 1990-94-results and commentary. Ann Oncol 2003;14 Suppl 5:v61-118.  Back to cited text no. 31
    
32.
Coleman MP, Forman D, Bryant H, Butler J, Rachet B, Maringe C, et al. Cancer survival in Australia, Canada, Denmark, Norway, Sweden, and the UK, 1995-2007 (the International Cancer Benchmarking Partnership): An analysis of population-based cancer registry data. Lancet 2011;377:127-38.  Back to cited text no. 32
    
33.
Tolou-Ghamari Z. Prevalence and demographic characteristics of cancers. CCIJ 2020;9:13-9.  Back to cited text no. 33
    
34.
Tolou-Ghamari Z, Mazdak H, Saboori M, Mohammadi Sichani M. Genitourinary tract cancers. Frequency and demographic characteristics. CCIJ 2019;8:232-5.  Back to cited text no. 34
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

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
Materials and Me...
Results
Discussion
Conclusions
References
Article Figures

 Article Access Statistics
    Viewed98    
    Printed1    
    Emailed0    
    PDF Downloaded0    
    Comments [Add]    

Recommend this journal