Skip to main content

Cancer mortality patterns in Ghana: a 10-year review of autopsies and hospital mortality



Cancer mortality pattern in Ghana has not been reviewed since 1953, and there are no population-based data available for cancer morbidity and mortality patterns in Ghana due to the absence of a population-based cancer registry anywhere in the country.


A retrospective review of autopsy records of Department of Pathology, and medical certificate of cause of death books from all the wards of the Korle-Bu Teaching Hospital (KBTH), Accra, Ghana during the 10-year period 1991–2000 was done.


The present study reviews 3659 cancer deaths at the KBTH over the 10-year period. The male-to-female ratio was 1.2:1. The mean age for females was 46.5 [Standard Deviation (SD), 20.8] years, whilst that of males was 47.8 (SD, 22.2) years. The median age was 48 years for females and 50 years for males.Both sexes showed a first peak in childhood, a drop in adolescence and young adulthood, and a second peak in the middle ages followed by a fall in the elderly, with the second peak occurring a decade earlier in females than in males. The commonest cause of cancer death in females was malignancies of the breast [Age-Standardized Cancer Ratio (ASCAR), 17.24%], followed closely by haematopoietic organs (14.69%), liver (10.97%) and cervix (8.47%). Whilst in males, the highest mortality was from the liver (21.15%), followed by prostate (17.35%), haematopoietic organs (15.57%), and stomach (7.26%).


Considering the little information available on cancer patterns in Ghana, this combined autopsy and death certification data from the largest tertiary hospital is of considerable value in providing reliable information on the cancer patterns in Ghana.

Peer Review reports


Knowledge of cancer patterns in Africa is woefully inadequate [17], and population-based epidemiological data on the occurrence of cancer in sub-Saharan Africa, especially, are sparse. Until recently, cancers and other non-communicable diseases were thought to be unimportant public health problems in developing countries, like Ghana, because of the overwhelming high prevalence of communicable diseases. The previous studies have focused on cancer morbidity data from the few established cancer registries in Africa, with very few reporting on cancer mortality data.

Malignant neoplasms accounted for 914 (2.6%) of all 34,598 admissions, and 141 (5.6%) of all 2,501 deaths at the Korle-Bu Teaching Hospital (KBTH) in the year 1996[8]. The case fatality risk from malignancies was thus 15.4%[8]. A review of the cancer register in the Department of Child Health, KBTH, over a 40-month period revealed that malignancies accounted for 1.67% of all admissions, with lymphomas (mainly Burkitt's lymphomas) being the commonest tumour (67%),followed by retinoblastoma (8.6%), leukaemia (8.2%) and Wilm's tumour (7.8%)[9]. The above cancer morbidity trend in the Ghanaian paediatric population is similar to the picture seen in West Africa and other developing African countries [922], with the exception of Namibia[23].

Previous reviews of cancer in Ghana have been mainly restricted to the study of single cancers, rather than the relative contributions of the various cancers to the disease burden because of the absence of a population-based registry. One of such reviews of autopsy material at the KBTH over the 10-year period from 1972–1981 (two decades earlier than this study), with emphasis on carcinoma of the pancreas, revealed that pancreatic cancers accounted for 5.8% of all cancer deaths over that period[24]. There has been no recent report on a systematic study of cancer mortality pattern across all age groups in Ghana. The problems of collecting cancer mortality statistics in developing countries have been described [17]. Knowledge of cancer patterns in Africa have largely been based on hospital series collected by clinicians and pathologists [17]. Despite the problems associated with interpreting data from hospital-based series, they are an invaluable source of information on cancer patterns where incidence and mortality data are unavailable. Ghana is on the threshold of starting a population-based cancer registry that will collect data on both morbidity and mortality. It is therefore an opportune time to attempt to present information on cancer mortality pattern before the advent of the registry to serve as the basis for future reference. This paper is partly hospital-based data and partly community-derived data to try and present as close a picture to the true situation as is possible now. This study was therefore carried out to establish the relative contributions of the various cancers to the cancer deaths certified and/or autopsied at the Korle-Bu Teaching Hospital, Accra, Ghana over a period of 10-years (1991–2000).


All cancer deaths diagnosed at autopsy in the 10-year period from the beginning of January 1991 to the end of December 2000 were retrieved from the autopsy logbooks of the Department of Pathology, and all certified cancer deaths for which medical certificates of cause of death were issued in all the wards and units of the Korle-Bu Teaching Hospital over the same period were also collected and reviewed retrospectively to find all cancer deaths seen from 1991 to 2000 inclusive. All cases were entered into a database using the Paradox for workgroups microcomputer software (Boreland International, Inc) and later transferred into the EPI-INFO microcomputer software version 3.3 (Centres for Disease Control, Atlanta, USA.). Three thousand, six hundred and fifty-nine (3659) cases were retrieved and reviewed. Information collected on each case included the name, age, sex, date of death and the site of the primary tumour. To avoid double enumeration of autopsied cases for which certificates of cause of death were subsequently issued in the hospital, the database programme was set up to reject any case that had the same name, age, sex and site as an already registered case until this had been proved to be an entirely new case.

The primary site and morphology data were coded using the International Classification of Diseases (10th Edition, ICD-10, World Health Organization)[25]. The ages were grouped according to the format used by International Agency for Research on Cancer (IARC, Lyon, France) for cancer reporting [17], namely 0–14, 15–24, 25–34, 35–44, 45–54, 55–64, and ≥65 years. Cases were analyzed according to sex and age distribution for all cases, and sex and age distribution for selected sites. The relative frequency (RF)of different cancer types varies greatly in relation to the age group studied, and thus the proportion of different cancers in a particular series is strongly influenced by the age composition of the series. This poses a problem when comparing summary statistics derived from populations of different age structures[1]. To overcome this problem and allow for comparison of proportions derived from this study with those derived from case series of different age structures, the age-standardized cancer ratio (ASCAR) was chosen as the standardization method. The reference case standard distribution used to calculate ASCAR was the standard age distribution of cancer cases for developing countries, namely 0–14 (5%), 15–24 (5%), 25–34 (5%), 35–44 (10%), 45–54 (20%), 55–64 (25%), and ≥ 65 (30%) years[1]. Tumours of the skin were excluded in calculating the ASCARaccording to convention [17]. The protocol for the study was approved by the Ethical and Protocol Review Committee of the University of Ghana Medical School, Accra, Ghana.


There were 1651 (45.1%) females and 2008 (54.9%) males in the series, making a total of 3659 cases. The male to female ratio is thus 1.2:1. The mean age for females was 46.5 years (SD, 20.8) and that of males was 47.8 years (SD, 22.2). The median age was 48 years for females and 50 years for males. The ages were not stated for 1 female and 4 males. Both sexes showed a peak in childhood with a drop in adolescence and young adulthood, and a rise to another peak in the middle ages followed by a fall in the elderly. The second peak occurs a decade earlier in females than in males.

The number of cases from each primary cancer site by age group, the summary RFrates of these sites and the ASCAR in females and males are shown in Tables 1 and 2, respectively. In females, malignancies of the breast (ASCAR, 17.24%) are the commonest cause of deaths, followed by the haematopoietic organs (lymphomas and leukaemias, 14.69%), and then the liver (10.97%), and the cervix (8.47%). In males, the highest mortality is from the liver (ASCAR, 21.15%), followed by the prostate (17.35%), and the haematopoietic organs (15.57%), and the stomach (7.26%). Deaths from tumours of the anus and eyes are uncommon in both sexes, while deaths from laryngeal cancers in female (ASCAR, 0.1%) are much less common than in males (2.75%), and deaths from stomach cancers in males (7.26%) are much more common than in females (4.76%).

Table 1 Number of cases by age group and summary frequency rates in females
Table 2 Number of cases by age group and summary frequency rates in males

There were 375 children (< 15 years), of which 209 (55.7%) were males and 166 (44.3%) were females, giving a paediatric male to female ratio of 1.26:1. Figure 1 shows the gender distribution of the various sites involved by tumours in children. In both sexes, the malignancies with the highest mortalityare those of the haematopoietic system, 57.8% of all paediatric cases in females and 60.3% among males. These are followed by brain and renal tumours. Liver and eye tumours feature in the top six death-causing malignancies in male children, but appear to be of less importance among female children, while bone tumours seem more important in female than male children.

Figure 1
figure 1

Gender distribution of cases in children.

The number of females in the adolescent and young adult age group (15–24 years) was 106 (42.7%), while males were 142 in number (57.3%), giving a male to female ratio of 1.3:1. Again, malignancies of the haematopoietic system dominate the picture, causing 43.4% of cancer deaths in females and 50.7% of the male cancer deaths. These are followed in the females by brain and then hepatic followed by ovarian tumours. In the males, haematopoietic malignancies were followed by hepatic, bone and brain tumours in that order. While in the children, bone tumours appeared more important as a cause of death in females than in males, in the adolescents and young adults the converse is found. Tumours of the eye continue to be more important in males than in female adolescents and young adults, as they were in children. An interesting finding is the occurrence of deaths due to endometrial tumours in this young age group, all of which were found to be due to choriocarcinoma, and the RF of mortality from pancreatic tumours of 4.2% in males and 0% in females. In this series, these pancreatic tumours occurred mainly in young adults (mean age 20 years). Bladder cancers contributed to 1.4% of cancer deaths in male adolescents and young adults, but 0% in females of the same age group. Conversely, soft tissue cancers contributed to 2.8% of cancer deaths in female adolescents and young adults, but 0% in males of the same age group.

The gender distribution of the RF of mortality from the various primary cancer sites in older adults, including the elderly, showed that the commonest fatal malignancies in females are those arising in the breast, while in males hepatic tumours are the commonest. Other gender differences in the pattern of cancer mortality in older adults that clearly stand out include laryngeal tumours which are about 27 times, oesophageal cancers which are about 6 times, and liver cancers which are about twice as common in males as in females. Additionally, lung and bladder cancers are about twice as common in male than female older adults. Gallbladder cancers are 5 times commoner in female than male older adults. The RF of pancreatic cancer deaths are similar between male and female older adults, in contrast to the 4.2% relative frequency in male adolescents and young adults and 0% in females of that age group.


Cancer is a worldwide public health problem. It accounts for 12.5% of all deaths, more than the percentage of deaths caused by HIV/AIDS, tuberculosis and malaria put together, is the second leading cause of death in developed countries, and is among the three leading causes of death for adults in developing countries[26]. In 2002, there were 6.7 million cancer deaths worldwide with less than 5% of these in sub-Saharan Africa. It is estimated that by 2020, cancer could kill 10.3 million people worldwide, with a 50 to 75 percentage increase in cancer mortality in sub-Saharan Africa[26]. This is the first report of cancer mortality patterns in Ghana, since the report of Edington in 1953[27]. The data used in the study were collected from two sources, namely medical certificates of cause of death issued in the hospital for deaths occurring in the hospital and autopsy records of the Department of Pathology of the hospital. Information from these sources was combined in an attempt to overcome some of the bias inherent in using data from either source. The Department of Pathology carries out an average of 5,000 autopsies annually, the vast majority (75%) of which are referred for autopsy by the coroner. Such coroner-referred deaths normally occur in the community (outside any hospital facility) or in the hospital usually in less than 24 hours of admission, when a firm cause of death would not have been determined. However, all hospital-based data on cancer are biased by selective factors that operate in hospitals[1]. The hospital may not comprehensively cover the population of interest. Thus hospital data may not completely reflect what happens at the community level as comparisons based on relative frequency of different cancers in hospital-based series will be biased in terms of the probability that the different cancers occurring in the community will be included.

Cancers are emerging as a significant health problem in several parts of Africa[8, 9, 1318], though infections remain the leading cause of morbidity and mortality. Indeed, cancers accounted for 2.6% of all admissions, and 5.6% of all deaths at the KBTH in the year 1996 [8]. In the current study, malignancies of the breast were the leading cause of deaths in females, followed closely by the haematopoietic organs, liver and the cervix. In males, the highest mortality was from the liver, followed closely by the prostate, the haematopoietic organs and the stomach. The relatively high position of liver, haematopoietic and pancreas cancers in both sexes may be partly as a result of their high case mortality rate in Ghana. A recent review of cancer morbidity in adults in Ibadan, Nigeria showed prostate cancer as the most common cancer in males, whilst breast cancer topped the list in females[28]. The first such review in the same population reported that cancers of the reticuloendothelial system topped the list[29], while the second observed that liver cancer was commonest among males and cervical cancer was commonest among females[30]. Cancer mortality figures can be used as a good approximation of incidence of cancers for which mortality is high, such as hepatocellular carcinoma. Cancers with high survival rates will be underrepresented in such series. Hospital autopsy series, although having good diagnostic information, suffer from selective factors that operate in causing admission to a hospital and in having an autopsy. Thus they are not representative of deaths in a population[1].

The International Agency for Research on Cancer (IARC) has recently published GLOBOCAN 2002 estimates of cancer incidence, mortality and prevalence for Ghana, with the acknowledgement that the degree of detail and quality of this source of data (both the accuracy of the recorded cause of death and the completeness of the registration) vary considerably[26]. The GLOBOCAN 2002 estimates for Ghana are therefore a mixture of real data, extrapolations from limited samples, and informed guesses[26]. In contrast, this series is based on only actual data and is the best contemporary information on the cancer mortality pattern in Ghana, though it is not derived from a nationally-based cancer registry and therefore may not be representative of the national cancer mortality pattern.

GLOBOCAN 2002[26] reported that the top 10 causes of cancer mortality in descending order in females in Ghana were cervix, breast, liver, haematopoietic organs, stomach, colorectal, ovary, bladder, with pancreas and Kaposi sarcoma tied for the 9th and 10th position. In this series, the top 10 causes of cancer mortality in descending order in females in Ghana were breast, haematopoietic organs, liver, cervix, ovary, pancreas, stomach, colorectal, gall bladder and brain. Therefore, both GLOBOCAN and this series concur that the top 4 causes of cancer deaths in Ghanaian females are undoubtedly breast, cervix, haematopoietic organs and liver, though cervix in 1st position for GLOBOCAN was 4th in this series and haematopoietic organs in 2nd position in this series was in 4th position for GLOBOCAN for Ghanaian females.

GLOBOCAN 2002 [26]reported that the top 10 causes of cancer mortality in descending order in males in Ghana were prostate, liver, haematopoietic organs, colorectal, bladder, Kaposi sarcoma, stomach, lung, larynx and oral cavity. In this series, the top 10 causes of cancer mortality in descending order in males in Ghana were liver, prostate, haematopoietic organs, stomach, pancreas, bladder, lung, colorectal, brain and larynx. Therefore, both GLOBOCAN and this series concur that the top 3 causes of cancer deaths in Ghanaian males are undoubtedly liver, prostate and haematopoietic organs, with haematopoietic cancers in 3rd position for both, and liver and prostate cancers swapping positions in the two series for Ghanaian males.

In both sexes of Ghanaian children combined, themalignancies with the highest mortality are those of the haematopoietic system, followed by brain, kidney, eyes, liver and bone tumours in that order. This cancer mortality picture is comparable to the reported cancer morbidity trend in the Ghanaian paediatric population[9] and other developing African countries [1022], with a preponderance of Burkitt's lymphomas, followed by retinoblastoma, nephroblastoma and soft tissue sarcomas as the commonest malignancies, and a low relative frequency of leukaemias and intracranial tumours [922]. This is in contrast to the situation in Europe and North America, with their high leukaemia and intracranial tumour frequency ratios, and low lymphoma frequency ratio. However, a report of frequency rates of childhood cancers in Namibia, a developing African country, showed an intermediate or mixed picture with tumours of the central nervous system occurring most commonly (18%), followed by renal tumours (14%), leukaemia (12%) and lymphoma (11.5%)[23]. One obvious departure though, is the second position of brain tumours in this paediatric malignancy mortality series, compared to the low relative frequency of intracranial tumours in most paediatric malignancy morbidity series from developing African counties [922], with the exception of Namibia[23]. The reasons for these differences require further investigation, though the high position of brain tumours in this mortality series may be as a result of its relatively higher case mortality rate in Ghana, and thus its possible over-representation in this mortality series.


The patterns observed from this study, despite the obvious limitation of not being population-based, provide reliable information on cancer mortality patterns in Ghana. Whether the above observed patterns actually reflect parallel patterns in cancer morbidity and mortality in the general Ghanaian population will have to await further studies from the just established population-based cancer registry in Accra, Ghana.



Korle-Bu Teaching Hospital


Standard Deviation


Age-Standardized Cancer Ratio


Confidence Interval


Relative Frequency


International Agency for Research on Cancer


  1. Parkin DM, Arslan A, Bieber A, Bouvy O, Muir CS, Owor R, Whelan S: Cancer Occurrence in Developing Countries. International Agency for Research on Cancer (IARC) Scientific Publication No. 75. 1986, Lyon, France: IARCPress

    Google Scholar 

  2. Waterhouse J, Muir CS, Shanmugaratnam K, Powell J: Cancer Incidence in Five Continents. IARC Scientific Publication No. 42. 1982, Lyon, France: IARCPress, IV:

    Google Scholar 

  3. Parkin DM, Bray F, Ferlay J, Pisani P: Global Cancer Statistics, 2002. CA Cancer J Clin. 2005, 55: 74-108.

    Article  PubMed  Google Scholar 

  4. Parkin DM, Pisani P, Ferlay J: Global Cancer Statistics, 1998. CA Cancer J Clin. 1999, 49: 33-64.

    Article  CAS  PubMed  Google Scholar 

  5. Pisani P, Bray F, Parkin DM: Estimates of the worldwide prevalence of cancer for twenty-five sites in the adult population. Int J Cancer. 2002, 97: 72-81. 10.1002/ijc.1571.

    Article  CAS  PubMed  Google Scholar 

  6. Parkin DM, Pisani P, Ferlay J: Estimates of the worldwide incidence of twenty-five major cancers in 1990. Int J Cancer. 1999, 80: 827-841. 10.1002/(SICI)1097-0215(19990315)80:6<827::AID-IJC6>3.0.CO;2-P.

    Article  CAS  PubMed  Google Scholar 

  7. Pisani P, Parkin DM, Bray F, Ferlay J: Estimates of the worldwide mortality from twenty-five cancers in 1990. Int J Cancer. 1999, 83: 18-29. 10.1002/(SICI)1097-0215(19990924)83:1<18::AID-IJC5>3.0.CO;2-M.

    Article  CAS  PubMed  Google Scholar 

  8. Biritwum RB, Gulaid J, Amaning AO: Pattern of diseases or conditions leading to hospitalization at the Korle-Bu Teaching Hospital, Ghana in 1996. Ghana Medical Journal. 2000, 34: 197-205.

    Google Scholar 

  9. Welbeck JE, Hesse AA: Pattern of childhood malignancy in Korle-Bu Teaching Hospital, Ghana. West Afr J Med. 1998, 17: 81-84.

    CAS  PubMed  Google Scholar 

  10. Akang EE: Tumors of childhood in Ibadan, Nigeria (1973–1990). Pediatr Pathol Lab Med. 1996, 16: 791-800. 10.1080/107710496175408.

    Article  CAS  PubMed  Google Scholar 

  11. Ekanem IA, Asindi AA, Ekwere PD, Ikpatt NW, Khalil MI: Malignant childhood tumours in Calabar, Nigeria. Afr J Med Med Sci. 1992, 21: 63-69.

    CAS  PubMed  Google Scholar 

  12. Teka K: Childhood malignancies in an Ethiopian teaching hospital. Ethiop Med J. 1992, 30: 159-162.

    CAS  PubMed  Google Scholar 

  13. Hussain MAM, Abbass FEM, Ahmed HM: Malignant disease in Sudanese children. East Afr Med J. 1988, 65: 507-514.

    CAS  PubMed  Google Scholar 

  14. Agugua NEN, Okeahialam T: Malignant disease of childhood seen at the University of Nigeria Teaching Hospital, Enugu, Nigeria. East Afr Med J. 1986, 63: 717-723.

    CAS  PubMed  Google Scholar 

  15. Molyneux EM: Childhood malignancies in Malawi, 1967–76. East Afr Med J. 1979, 56: 15-25.

    CAS  PubMed  Google Scholar 

  16. Sinnette CH: Childhood malignancies: report from a West African teaching hospital with special emphasis on Burkitt's tumor. Clin Pediatr. 1976, 15: 721-727.

    Google Scholar 

  17. Williams AO: Tumors of childhood in Ibadan, Nigeria. Cancer. 1975, 36: 370-378. 10.1002/1097-0142(197508)36:2<370::AID-CNCR2820360212>3.0.CO;2-K.

    Article  CAS  PubMed  Google Scholar 

  18. Brown RE, Wright BI: Malignancies in African children: how do these differ from malignancies in the United States?. Clin Pediatr . 1967, 6: 106-115.

    Article  CAS  Google Scholar 

  19. Miller RW: Geographic and ethnic differences in the occurrence of childhood cancer. IARC Scientific Publication No. 87. 1988, IARCPress, Lyon, France, 37-44.

    Google Scholar 

  20. Tijani SO, Elesha SO, Banjo : Morphological patterns of paediatric solid cancer in Lagos, Nigeria. West Afr J Med. 1995, 14: 174-180.

    CAS  PubMed  Google Scholar 

  21. Makata AM, Toriyama K, Kamidigo NO, Eto H, Itakura H: The pattern of pediatric solid malignant tumors in western Kenya, East Africa, 1979–1994: an analysis based on histopathologic study. Am J Trop Med Hyg. 1996, 54: 343-347.

    CAS  PubMed  Google Scholar 

  22. Macharia WM: Childhood cancers in a referral hospital in Kenya: a review. East Afr Med J. 1996, 73: 647-650.

    CAS  PubMed  Google Scholar 

  23. Wessels G, Hesseling PB: Incidence and frequency rates of childhood cancer in Namibia. South Afr Med J. 1997, 87: 885-889.

    CAS  Google Scholar 

  24. Dankwa KE, Anim JT: Carcinoma of the pancreas: a review of autopsy material at the Korle-Bu Teaching Hospital for the period 1972–1981. Ghana Medical Journal. 1988, 22: 17-20.

    Google Scholar 

  25. World Health Organization (WHO): International Statistical Classification of Diseases and Related Health Problems (10th Revision). 1989, Geneva, Switzerland

    Google Scholar 

  26. Ferley J, Bray F, Pisani P, Parkin DM: GLOBOCAN 2002: Cancer Incidence, Mortality and Prevalence Worldwide. IARC CancerBase No.5 version 2.0. 2004, IARCPress, Lyon, France

    Google Scholar 

  27. Edington GM: Malignant disease in the Gold Coast. Br J Cancer. 1956, 10: 595-608.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Ogunbiyi JO: Epidemiology of cancer in Ibadan: tumours in Adults. Archives of Ibadan Medicine. 1999, 1: 1-3.

    Google Scholar 

  29. Edington GM, Maclean CMU: A cancer rate survey in Ibadan, Western Nigeria. Br J Cancer. 1965, 19: 471-481.

    Article  PubMed Central  Google Scholar 

  30. Abioye AA: The Ibadan Cancer Registry. Cancer in Africa. Proceedings of a workshop of the West African College of Physicians. Edited by: Olatunbosun DA. 1981, WACP press,Lagos,Nigeria, 1-33.

    Google Scholar 

Pre-publication history

Download references


We thank the staff of the Department of Pathology whose work generated much of the data, and the nursing staff of all the wards in the hospital and the personnel of the Medical Records Unit of the Korle-Bu Teaching Hospital, Accra, Ghana for their cooperation and assistance during the data collection for this study.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Edwin K Wiredu.

Additional information

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

EKW conceived and designed the study, provided guidance to all aspects of this study, and was the senior author. HBA was responsible for data collection and data entry. Both authors did the quality assessment of the data, data analysis, and data preparation. Both authors collaborated intensely on all aspects of the preparation of the manuscript, and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Wiredu, E.K., Armah, H.B. Cancer mortality patterns in Ghana: a 10-year review of autopsies and hospital mortality. BMC Public Health 6, 159 (2006).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: