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ORIGINAL RESEARCH article
Front. Urol. , 17 March 2025
Sec. Urologic Oncology
Volume 5 - 2025 | https://doi.org/10.3389/fruro.2025.1496951
Introduction: In Africa, prostate cancer poses significant diagnostic and treatment challenges due to limited access to diagnostic tools and healthcare resources. This survey aimed to assess current prostate biopsy practices, patient classification methods, and available therapeutic means among African urologists to propose strategies for improved screening, diagnosis, and management.
Methods: A web-based self-administered questionnaire was distributed to urologists in 58 African centres, focusing on biopsy practices, cancer diagnosis, management, and treatment protocols. After pretesting and validation, data collection spanned six weeks, followed by duplicate elimination and arithmetical analysis, with results expressed in absolute, mean, or percentage values.
Results: Feedback was received from 58 centres across diverse African regions, including Central, Southern, West, East Africa, and Madagascar, comprising general, private, and university hospitals. Prostate cancer emerged as the most frequent urological cancer in all regions studied. The assay for prostate-specific antigen (PSA) was available in nearly all centres. Biopsy techniques varied, with ultrasound-guided biopsies being the most common (30 centres), followed by digital-guided (20 centres) and MRI-guided biopsies (5 centres). One centre lacked the expertise to perform biopsies. Radiological workup availability was high, with CT available in 56 centres, MRI in 54, PET scans in 14, and scintigraphy in 29. Treatment capabilities varied, with 53.4% of centres able to perform radical prostatectomies, 86.2% offering radiotherapy, and 94.8% providing medical castration. Among the centres, 56 performed fewer than 5 radical prostatectomies per month, while only 2 centres performed between 5 and 10 per month.
Conclusion: It is important to standardise prostate cancer diagnosis and treatment protocols across Africa while improving access to advanced diagnostic technologies and treatment facilities. Implementing these changes could enhance early detection, improve treatment outcomes, and reduce the burden of prostate cancer in Africa.
Prostate cancer is the second most common cancer and the fifth leading cause of cancer death in men in 2020, according to global cancer statistics. Its incidence varies from country to country (1). This variation can even exist within a single country. In the United States, it has been shown that the incidence of prostate cancer is higher in African-Americans than in Americans of other origins (2). Prostate cancer is also the leading cause of cancer death among men in 48 countries, including many in sub-Saharan Africa (1). In many countries or geographical areas, population-based epidemiological data are available (3–5). In Africa, only a few countries have population-based cancer registries, and these are not well equipped or regularly updated (6, 7).
The diagnosis of prostate cancer is traditionally based on a combination of clinical, biological and histological data. Clinically, diagnosis is made by digital rectal examination, which assesses the shape, regularity and consistency of the prostate (8). Any abnormality of the prostate on digital rectal examination is an indication for prostate biopsy (9). Biologically, prostate cancer is suspected on the basis of elevated plasma levels of prostate-specific antigen. Prostate-specific antigen is a glycoprotein normally expressed by prostate tissue and can also be elevated in men even when there is no prostate cancer involvement (10). In the PSA-based screening program, most patients diagnosed with prostate cancer have a normal digital rectal examination (8). Thus, for diagnostic confirmation of prostate cancer, a prostate biopsy is mandatory. The standard technique is ultrasound-guided needle biopsy of the prostate, taking 12 cores per extended sextant (8).In selected patients, magnetic resonance imaging may be required for targeted biopsy (11). MRI-ultrasound fusion biopsy, especially in those patients with previous negative prostate biopsy but with persistent clinical signs and symptoms of prostate cancer. Biopsy protocols covering indications, preparation, procedure and management of complications are well defined by various national and international urology societies (12, 13). However, there are still wide differences in prostate biopsy practice patterns, according to a survey of 51 Nigerian urologists, which revealed variation in practice. The authors of this publication concluded that practice standardisation is required to increase consistency in patient treatment (14).
On the basis of a range of clinical, biological and histological data, a classification system has been proposed, stratifying patients into groups and guiding the performance of an extensive workup (thoraco-abdomino-pelvic CT and bone scan) (15). Depending on D’Amico’s classification and the presence or absence of metastases on imaging, several learned societies have defined recommendations for practice (12, 13).
There has been a reported rise in the cancer burden in sub-Saharan Africa (16). In terms of incidence and mortality, prostate cancer is the most common cancer among men in sub-Saharan Africa (17). In addition to this huge burden, diagnosing and treating prostate cancer is challenging in sub-Saharan Africa. This is due to lack of access to diagnostic tools and limited healthcare resources. PSA testing, magnetic resonance imaging and biopsy are often limited. Treatment options are often limited by a lack of qualified human and material resources (18). Given the above, we have asked 3 questions within the context of sub-Saharan:
1. What is the current practice of urologists regarding prostate biopsy across Africa?
2. How do urologists classify patients to frame a therapeutic plan?
3. What therapeutic means are available, and what are the selection criteria?
To answer these questions, we surveyed urologists practicing in hospitals in various African countries. The aim of this survey is to give a general overview of the current practice, to compare and contrast the various practice protocols and to propose strategies and recommendations for better screening, diagnosis and management of prostate cancer.
The Modern Urology for Africa (MUFA) association is a recently established continental initiative aimed at advancing urological care in Africa. MUFA conducted this qualitative multicentric survey as one of its diversified scopes of research activities. A web-based, self-administered questionnaire targeting Africa’s prostate biopsy and cancer management practices was designed and electronically disseminated to urologists in 45 African urology centres. These were mainly African public health care institutions with a functioning urology unit or a surgery unit with an attending urologist.
The questionnaire contained the following questions specific to prostate cancer:
● Prostate biopsy practice: patient consent, prostate biopsy preparation, monthly biopsies performed on average, biopsy technique and post-biopsy management.
● Prostate cancer diagnosis, staging and imaging modalities.
● Prostate cancer management: MDT meetings, management protocol, therapeutic modalities.
● Prostate cancer treatment: androgen deprivation therapy (medical or surgical), chemotherapy, radiotherapy, and immunotherapy.
After pretesting and validation of the form by the authors, a Google Form was prepared and sent out through email and WhatsApp to African urologists for automatic data collection. The study was launched on February 12, 2024 and lasted for 6 consecutive weeks. Following data collection, a double check was carried out by authors to eliminate duplicates, and an arithmetical analysis was done. Results were expressed as absolute, mean or percentage values. No correlations were performed.
We received feedback from 58 centres spanning diverse African regions, such as Central Africa, Southern Africa, West Africa, East Africa, and Madagascar, like indicated in Figure 1.
These institutions comprised general community hospitals, academic affiliated hospitals, and university hospitals. Table 1 displays the breakdown of participating hospitals categorised by their respective African regions.
In all subregions of Africa, i.e., Western, Eastern, Central, and Southern, prostate cancer ranks first in terms of prevalence among the studied urological cancers. Regarding the available screening and diagnostic modalities, the assay for prostate-specific antigen (PSA) is available in almost all the mentioned hospital centres. The majority of centres (n=30, 50%) perform ultrasound-guided biopsies while 20 centres (35%) rely on finger-guided prostate biopsies. Only a smaller number of centres perform MRI-guided biopsies (5 centres). Surprisingly, one centre reported an inability to perform prostate biopsies due to a lack of expertise (Figure 2).
The cross-sectional diagnostic imaging modalities available in the various countries were CT scans (56 centres), followed by MRIs (54 centres). For extensive workup, it was possible to do scintigraphy in 29 centres, while only 14 centres could do PET scans. The distribution of imaging modalities is in Figure 3.
In general, at least 1 therapeutic modality for prostate cancer could be proposed to patients in the centres involved in our survey. The distribution of these modalities varies from one centre to another. The distribution of those various modes of treatment being practiced in the surveyed urology centres is shown in Table 2.
Radical prostatectomy was performed in 53.4% of the centres among the surveyed centres. Out of those 37 centres performing RP, 29 centres do <5 RP per month, while 2 centres do between 5 and 10 RP monthly.
Concerning nonsurgical therapeutic modalities, they were distributed as shown in Table 3.
Table 3. Availability of non-surgical therapeutic modalities and their distribution among represented hospitals and countries.
In regards to radiotherapy, 50 responders (86.2%) reported it was available within their country. We could identify a radiotherapy unit/centre in 18 centres within 18 countries. Mainly, external beam therapy was possible; only 4 centres could offer brachytherapy.
Either surgical or chemical hormonal suppression was possible in all centres, except 3 centres where medical castration was not available. So, only 94.8% of the centres could propose chemical androgen deprivation to patients.
Immunotherapy was offered by 14 centres in 13 countries.
Cryotherapy was only in 2 countries with 1 centre each.
The diagnosis and management of prostate cancer in Africa is of growing concern to the urology community. Although prostate cancer is one of the most common cancers in men, diagnostic and therapeutic practices vary considerably across the continent, influenced by economic, cultural and infrastructural factors. This survey of urologists in various African hospitals provides an overview of current approaches to screening, diagnosis and treatment. By comparing these practices with international standards, this discussion aims to identify specific challenges encountered in Africa, regional variations in management approaches, and opportunities for improving patient outcomes.
In western practice, digital rectal exam (DRE) is often performed during screening of prostate cancer and is used as a supporting but not definitive tool to detect prostate cancer. Its capabilities are limited due to its questionable reliability, reduced sensitivity, and inability to explore the entire surface of the prostate, especially when dealing with small tumours that have not yet developed to the point of reaching the prostatic capsule (19). The prostate-specific antigen (PSA) blood test is also another clinical evidence that is used to assess suspicion of prostate cancer (20). In high-income countries, the use of technologies such as MRI is beginning to have a place in prostate cancer screening and surveillance (21). In Africa, DRE and PSA are almost always used for screening and diagnosing PCA. Determining PSA levels depends on the availability of a biomedical analysis laboratory. The results of this survey clearly demonstrated the unavailability of MRI in several centres that responded to the survey.
In 2021, the National Comprehensive Cancer Network (NCCN) developed several harmonised consensus guidelines for sub-Saharan Africa in collaboration with the Africa Cancer Coalition (ACC). One of these guidelines is about early detection of prostate cancer. In this guideline, the NCCN acknowledges that the recommendations on prostate cancer screening methods and intervals are based on expert opinion, and a unanimous consensus has not been reached. Guidelines on when to start and stop screening, screening intervals and when to perform a biopsy are included in the guideline and should be used after the patient has been properly counselled (22). Just recently, the Lancet commission on prostate cancer published an article that draws attention to the increasing number of cases. Among the key points of this publication, it was made clear that late diagnosis of prostate cancer is widespread throughout the world, but particularly in low-income countries. Therefore, they recommended an urgent need to set up earlier diagnosis systems in low- and middle-income countries. For men of African descent, the case for prostate cancer screening lies between the ages of 45 and 70 (21).
Screening for PCa is an area of frequent debate. Screening practices and guidelines aim to balance the early detection of clinically significant cancers against the risk of potential overdiagnosis and resulting overtreatment of clinically insignificant PCa.
The diagnosis of prostate cancer, like any other cancer type, is highly dependent on histopathological confirmation. The decision to perform a prostate biopsy is made by a urologist based on abnormalities identified during routine screening protocols or after clinical examination of a symptomatic patient (23, 24).
Abnormal findings on DRE, elevation of PSA and a suspicious nodule on mp-MRI are the three most common scenarios that prompt a urologist to perform a prostate biopsy. There is no debate among urologists and oncologists on the need to analyse prostatic tissue samples before diagnosing prostate cancer and planning on the treatment options. However, the question is how these tissue samples are obtained (25). There is certain global variation in practice in this regard, and our study attempted to highlight the practice pattern in Africa.
Until recently, a twelve-core transrectal ultrasound (TRUS)-guided core needle biopsy has been the standard according to the American Urological Association (AUA) and European Association of Urology (EAU) guidelines (26). Recently, a TRUS-guided transperineal biopsy has been recommended by these guidelines mainly to reduce the risk of infection, which is higher in a transrectal biopsy.
Efficient diagnosis and staging of prostate cancer require exhaustive testing techniques specifically designed for the African environment. A prostate biopsy is a crucial diagnostic procedure that is frequently carried out blindly in many African nations. Our results illustrate that biopsy practices vary between regions. According to them, 20 centres were still practicing digital-guided biopsies, and 1 centre in particular could not perform biopsies. On the other hand, switching to image-guided biopsies—ideally using fusion methods that combine MRI and ultrasound—can greatly improve accuracy. We found out that only 5 centres could perform MRI-guided biopsies, but noted a shift toward ultrasound-guided biopsies, which were available in 30 centres. This makes single-use biopsy trocars, biopsy guidance devices, and endorectal ultrasonography probes necessary.
Because image-guided prostate biopsy is a very simple operation to learn, urologists may find it easier to embrace if they participate in short-term training programs in these procedures.
A study reported that twelve procedures are necessary to perform high-quality TRUS-guided prostate biopsies without compromising prostate cancer detection; therefore, they strongly recommended training under direct supervision for a minimum of 12 cases before allowing TRUS-guided biopsy without supervision (27).
In the era of imaging-guided biopsy of the prostate, finger-guided prostate biopsy still has a role in low- to middle-income countries. Concerning finger-guided biopsy and TRUS-biopsy practices in Africa, even if the first one is far from gold-standard, it remains a suitable alternative in resource-limited settings, especially when the prostate is clinically abnormal (28). Perhaps in patients with palpable disease, the addition of finger-guided prostate biopsy of these areas increased the positive predictive value over transrectal ultrasound prostate biopsies alone (29). Also, many countries are still practicing ‘out-of-pocket’ healthcare, and something as simple as a TRUS-guided prostate biopsy may be totally unaffordable. Therefore, in low- to middle-income countries, the cost of a prostate biopsy needs to be considered, as well as the cost to the patient, which may include time off work and travel costs.
We did not distinguish between transrectal and transperineal ultrasound or MRI-guided biopsy technique in our survey; therefore, we could not discuss or compare the advantages of one over the other, including a reduction in infectious complications, improved quality of prostate sampling, and rebiopsy rates, which were reported in a systematic review on biopsy approaches as 15.4% in transrectal vs. 5.26% in transperineal (30).
Even though we did not evaluate prostate biopsy antibiotic prophylaxis protocols applied by each centre in our survey, following a literature review on the topic, we found a study dedicated to analysing post-biopsy complications in relation to antibiotic prophylactic protocols conducted by Tulone et al. They observed that prophylaxis based on the use of fluoroquinolones appears to be associated with a lower risk of infectious complications following transrectal prostate biopsy, compared to other prophylactic regimens, such as those involving cephalosporins or trimethoprim/sulfamethoxazole (31). In addition, another study on the topic conducted in Nigeria comparing two groups of patients among whom Group 1 patients received a single dose of 1 g of amikacin intravenously 30 minutes prior to the procedure, followed by the immediate administration of 500 mg of oral ciprofloxacin after the transrectal ultrasound-guided prostate biopsy (TRUS-PB), while Group 2 patients were given the same antibiotics, but with a notable difference: ciprofloxacin was initiated one day before the procedure. Both patient groups were subsequently administered ciprofloxacin twice daily for a total duration of five days (32). They found a significant reduction in the incidence and severity of sepsis in the second group. In this study, it was requested that antibiotics be used. We wanted to see clinical habits and compare them with the recommendations of learned societies.
Recommendations on prostate cancer screening and early detection from main international urology societies, including AUA, EAU and NCCN guidelines, are highlighted and summarised in Table 4 (22, 33).
The commonly used prostate-specific antigen (PSA) screening is not widely accessible or affordable in this region. To address this, alternative screening methods like risk assessment approaches and cost-effective PSA tests are being explored to target high-risk individuals and improve screening access (18).
Clinical practice guidelines (CPGs) serve as frameworks to unify diagnostic criteria and guide clinical decision-making and to promote the highest standards of urological clinical care through education, research and the formation of health care policy. In Africa, the limited resources may preclude urologists from strictly adhering to international guidelines and recommendations. In addition, screening practices and guidelines for PCa and their availability vary across Africa (24). So, some countries have developed their own national guidelines. The American Urological Association (AUA), the European Urological Association (EAU), and the National Comprehensive Cancer Network (NCCN) have standardised guidelines for the management of prostate cancer. From those guidelines, African management of prostate cancer is extrapolated. As an example in South Africa, local practitioners were commissioned to revise international CPGs with a view to applicability to South African clinical practice (34). Prostate cancer screening consists of systematic screening for the disease in an asymptomatic population. This early screening aims at early detection of these diseases and risk stratification; unfortunately, the major challenge experienced in low- and lower-middle-income countries (LLMICs) is the late presentation of PC patients in health facilities due partly to lack of screening, highlighting the need for accessible and affordable early detection programs (35). Despite the fact that mass screening is not recommended compared to individualised informed screening due to the risk of overdiagnosis and overtreatment, many African countries, especially in SSA, still practice population-based screening, often initiated by local hospitals through public health campaigns. For example, in a community-based screening program in Nigeria, 10% of men 50 years of age and over had a PSA over 4 mg/ml, and most had a PSA greater than 10 mg/ml. 8.5% were biopsied, and 1% had histologically confirmed prostate cancer; no information was provided about treatments and outcomes (36). South African guidelines recommend that PCa screening (PSA and digital rectal examination [DRE]) should be performed in all men from 45 years onwards in the absence of identifiable risk factors and from 40 years in black men, where there is a family history of PCa and other identifiable risk factors (37).
While international guidelines are shifting toward transperineal prostate biopsy and MRI-fusion biopsy, in our context, TRUS-guided biopsy as well as finger-guided biopsy are still commonly done (14).
Treatment with curative intent is not widely available and is often very costly in SSA. Currently, there is no consensus on the management of prostate cancer in Africa, as most of the treatment options are directly adopted from international guidelines. The availability of treatment modalities, namely, androgen-deprivation therapy, chemotherapy, radical prostatectomy, external beam radiotherapy and brachytherapy, varied widely among the countries. Notwithstanding, several authors have proposed prostate cancer updates depending on the stage and African subregion (18, 24, 38–40).
Diagnosis of prostate cancer in Sub-Saharan Africa is challenging due to limited access to diagnostic tools and healthcare resources, in addition to a low level of awareness by the community and the myths and misconceptions associated with it. The misconceptions include denial of conjugal rights if diagnosed with PCa, and one of the prevention methods is having multiple sexual partners, which predisposes for sexually transmitted disease and often judgement from the community (41). Clinical evaluation and digital rectal examination are commonly used, but PSA testing, magnetic resonance imaging, and biopsy are often restricted to a few locations. Consequently, many men in this region are diagnosed with advanced-stage cancer (39). The data from our study demonstrate an unequal and insufficient distribution of medical devices in healthcare facilities across Africa necessary for the diagnosis and management of prostate cancer. For example, 22 countries have centres capable of performing a computerised tomography (CT) scan, 21 countries have centres with MRI facilities, 10 respondents’ countries have centres equipped with scintigraphy, and only 5 countries have centres capable of performing a positron emission tomography (PET) scan. This aligns with data obtained from the Global Health Observatory in 2014 (42), which showed the limited availability of cancer care equipment in Africa like mammography units, radiotherapy units, CT scanners, gamma camera units, MRI machines, and PET scanners. Radiotherapy centres are also scarce, especially in sub-Saharan Africa. The availability of multimodal PCa treatment in various African countries is key to effectively managing this disease and adhering to standard recommendations. Countries such as Burundi, Guinea-Bissau, Liberia, and the Central African Republic, according to this study finding, do not have radiotherapy centres, forcing eligible patients to seek treatment in neighbouring countries with associated economic costs. In Eswatini, the costs associated with prostate cancer (PCa) management are overwhelming. Due to the absence of radiation therapy in the country, the government must refer PCa patients to private hospitals in South Africa. While surgical procedures like transurethral resection can be performed locally, most patients also seek chemotherapy treatment in South Africa. The total annual cost of PCa to Eswatini is estimated at $6 million, including direct expenses for treatments and non-medical costs like transportation and lodging, which impose a significant financial burden on patients (43).
Urologists in Africa may encounter difficulties adhering to international recommendations due to these resource and knowledge limitations. In our study, it was observed that not all urological centres perform radical prostatectomy due to a lack of technical expertise and adequate equipment. Furthermore, among those centres that do perform this procedure, the average monthly number of prostatectomies conducted by centres indicating affirmative responses was approximately 5.33 cases per year. Our findings also highlight there are centres that do not offer radical prostatectomy services, which significantly impacts both the quality of patient care and training of urologists.
The difficulty for African urological centres to accurately diagnose different stages of prostate cancer, due to limitations in existing diagnostic tests, can result in either underdiagnosis or overtreatment, posing a barrier to the implementation of the best international recommendations. Furthermore, the lack of attention given to the severity of prostate cancer in men compared to other types of cancer in women, such as breast and cervical cancer, can lead to a lack of attention and resources for the screening and early management of prostate cancer. The fact that many cases of prostate cancer in Africa remain undiagnosed and untreated reflects systemic barriers to accessing healthcare and standard treatment. In particular, the centralisation of oncology facilities (including investigations, radiotherapy, and chemotherapy) in urban areas and the shortage of specialised urologists and oncologists make access to care even more difficult for patients in rural areas. Public health expenditures are only $8 per capita, significantly below the recommended $34. Most healthcare costs are paid out-of-pocket, comprising around 70% of total health spending (44). The National Health Insurance Scheme (NHIS) mainly covers civil servants, leaving a large portion of the population uninsured. Endemic poverty exacerbates the situation, making healthcare unaffordable for many patients and leading to delays in seeking medical care (45). These systemic and organisational challenges can affect the quality of urological practices in Africa and explain why they may not always meet international standards. Aligning with international standards for prostate cancer management requires an upgrade of the technical infrastructure in African hospitals for prostate cancer diagnosis, improving the accessibility of these technical platforms to all patients, as well as strengthening training programs for healthcare professionals, including urologists, oncologists, and radiotherapists, to ensure they have the skills and expertise needed to provide quality care to prostate cancer patients.
With the recent advancement in the standardised reporting of prostatic MRI and the wide availability of it in higher-income countries, it has been used for the detection, localisation, and characterisation of clinically significant prostate cancers (46). This recent development of using MRI as a screening tool in the detection of prostate cancer has aided urologists and oncologists in performing targeted biopsies and also avoiding unnecessary biopsies. The impact of these targeted biopsies is very high, especially in patients with prior negative biopsy results and still suspicious DRE and PSA results. In this survey, 46.7% (n=21) centres only have access to MRI, which will affect the quality of service provided, resulting in underdiagnosis by missing the cancer on biopsy or increased performance of biopsies.
Radical prostatectomy has undergone a very rapid change from an open approach to a laparoscopic and robotic approach. From initial reports of both laparoscopic and robotic approaches in the beginning of 2000, it has gained wide popularity (47, 48). Now, minimally invasive radical prostatectomy, specifically robotic, is the standard. 91.5% of radical prostatectomies and more than 84% of prostatectomies in England and the USA, respectively, were done robotically (49). In Sub-Saharan Africa, few centres are able to perform radical prostatectomies, and usually it is an open approach. The eligibility of patients for this curative approach is also dependent on early presentation, proper staging, and the availability of skilled urologists who can offer the surgery.
South Africa is the first African country to perform robotic radical prostatectomy and also has many robotic surgery centres (50). The price of acquiring robots and the running cost per procedure have made it unthinkable for most African centres. In addition to its expensiveness, the unavailability of training centres in Africa and the difficulty of securing on-hand training in high-income countries make even the disparity in radical prostatectomy an ongoing challenge. The Vattikuti Foundation has played a significant role in training more than 50 fellows in robotic surgery in India (51). Africa also needs collaboration from this type of foundation and international stakeholders to train and equip the urologists with the necessary skills.
It is important for urologists to remain up-to-date regarding research and clinical guidelines within their specialty. Prostate cancer rarely involves a single treatment; patient care can be as diverse as the disease itself. Its management often requires a multispecialty team dedicated to managing the diagnosis, evaluation, and treatment. This approach has been reported to improve quality-of-life issues for these patients. The availability of primary treatment modalities, namely, radical prostatectomy, external beam radiotherapy and brachytherapy, varied widely among the countries in which the urologists practiced based on their referral patterns.
Uro-oncology has emerged as a subspecialty that plays an important role in the daily practice and care of urologic malignancies. Its role is so important in standardising the care and in a continuation of urologic oncology training, especially with updated guidelines, changing treatment modalities, new oncological drugs, developments in advanced technology, and the increasing use of laparoscopic, robotic, and endoscopic techniques. A study showed that 40.54% of the urologists did not find the uro-oncology training in their own country to be sufficient, so there is a need for training after residency to be supported by not only the authorities but also the urologists in the field to strengthen their skills (52). Also, surgery training is essential; this is illustrated by the results of multi-institutional analysis, which showed that only 11% of patients treated by high-volume surgeons experienced a biochemical recurrence at five years, compared to 18% of patients treated by low-volume surgeons (53). Performing radical prostatectomy is a key tool for urologists dealing with prostate cancer, especially for eligible patients. Mastering this technique comes with training and practice. Postoperative morbidity in high-volume centres has a 6% absolute reduction in postoperative complication rates (26% vs. 32%), an 8% absolute reduction in late urinary complications (20% vs. 28%), and a 4% absolute reduction in long-term incontinence (16% vs. 20%), compared to those treated by low-volume surgeons (54). Apart from fellowship, urologists indicated an interest in taking courses designed to educate them on prostate cancer care even after residency. Consequently, they should be encouraged to participate in continuous medical education and workshops, to be members of different societies and groups, to subscribe to journals or newsletters, to attend scientific meetings and programs, and to collaborate with other fields. Guidelines are developed to improve the quality of patient care.
This study has shown a significant disparity in diagnostic and treatment resources between different centres, not only based on the country but also within the same country. This situation has a considerable practical impact, particularly on the reliability of diagnosis, the quality of disease staging, and especially patient management. Even though many efforts have been made to improve diagnostic means, as highlighted by our study (all centres perform prostate biopsies except one), many patients are diagnosed at a late metastatic stage, mainly due to the absence of early screening or the unavailability of tests. Digital rectal examination and PSA testing are available in almost all centres. In a review, Jalloh et al. reported that the unavailability of certain equipment, the lack of expertise among human resources, and the high cost of exams and treatments result in each centre operating according to the available means (18). Similarly, it was reported by Tanzanian authors that there is a significant disparity in the prices of diagnostics and treatments between different centres in the country, and these prices remain relatively high compared to the patients’ means (55). It would be beneficial to establish or encourage collaboration between different centres within the same country and the sub-region, which would increase the level of detection and patient management.
There was no systematic sampling for selecting the hospitals involved in this study, and therefore the possibility of sampling errors exists, and the results may not reflect the overall picture of prostate cancer diagnostic and treatment modalities in Africa. Our sample size and unknown response rate may not represent the population for which the survey was intended.
These may mean our results may be subject to the influence of chance factors. Although there was a mixture of different African country representatives, information about the unrepresented countries may have changed our result significantly. It is also important to recognise that the responding urologist may have limited knowledge about the countries he is practicing in. The questions were not competency-based and did not assess deficiencies of skills or knowledge in PCa. Therefore, it was not possible to determine whether any deficiencies in skills or knowledge were significant enough to affect their response. Furthermore, the possibility of response bias cannot be completely eliminated in this study.
The diagnosis and management of prostate cancer in Africa face significant challenges due to late diagnosis, inadequate manpower, poor health facilities, and limited treatment options. Our survey highlights disparities in diagnostic capabilities, with some centres lacking essential imaging modalities and biopsy techniques. Treatment options also vary widely, with only a few centres offering comprehensive care, including surgery and advanced therapies. There’s a need to improve early detection and patient outcomes by increasing public awareness, developing screening programs, and investing in novel diagnostic and treatment options. Strengthening technical skills through continuous education and training, enhancing infrastructure, and fostering collaboration among healthcare centres are essential steps toward reducing the burden of prostate cancer in sub-Saharan Africa.
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
Ethical review and approval was not required for this study in accordance with the local legislation and institutional requirements. Written informed consent was not required from participants of this study in accordance with the national legislations and institutional requirements.
MB: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. KG: Conceptualization, Investigation, Project administration, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. NS: Conceptualization, Formal analysis, Investigation, Methodology, Project administration, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. OZ: Conceptualization, Formal analysis, Investigation, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. NS: Conceptualization, Investigation, Writing – original draft, Writing – review & editing. AK: Conceptualization, Investigation, Writing – original draft, Writing – review & editing. NT: Investigation, Writing – original draft, Writing – review & editing. TM: Investigation, Writing – original draft, Writing – review & editing. AC: Writing – original draft, Writing – review & editing. BY: Writing – original draft, Writing – review & editing. SI: Conceptualization, Investigation, Writing – original draft, Writing – review & editing. OM: Conceptualization, Investigation, Writing – original draft, Writing – review & editing. MM: Investigation, Writing – original draft, Writing – review & editing. RR: Investigation, Validation, Visualization, Writing – original draft, Writing – review & editing. AN: Supervision, Validation, Writing – original draft, Writing – review & editing. OO: Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. FA: Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing.
The author(s) declare that no financial support was received for the research and/or publication of this article.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
ACC, Africa Cancer Coalition; ADT, Androgen deprivation therapy; AUA, American Urological Association ; CPGs, Clinical practice guidelines; CT, Computed tomography; CT Scan, computed tomography scan; DRE, Digital Rectal Examination; EAU, European Urological Association; LLMICs, Low- and Lower-Middle-Income Countries; LMICs, low- and middle-income countries; MDT, Multidisciplinary team; mpMRI, Multiparametric Magnetic Resonance Imaging; MRI, Magnetic Resonance Imaging; MUFA, Modern Urology for Africa; NCCN, National Comprehensive Cancer Network; NHIS, The National Health Insurance Scheme; PCa, Prostate Cancer; PET Scan, positron emission tomography scan; PSA, Prostate-Specific Antigen; SSA, Sub Saharan Africa; TRUS, Transrectal Ultrasound.
>1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. (2021) 71:209–49. doi: 10.3322/caac.21660
2. Eeles R, Goh C, Castro E, Bancroft E, Guy M, Al Olama AA, et al. The genetic epidemiology of prostate cancer and its clinical implications. Nat Rev Urol. (2014) 11:18–31. doi: 10.1038/nrurol.2013.266
3. Brawley OW. Prostate cancer epidemiology in the United States. World J Urol. (2012) 30:195–200. doi: 10.1007/s00345-012-0824-2
4. Baade PD, Youlden DR, Cramb SM, Dunn J, Gardiner RA. Epidemiology of prostate cancer in the Asia-Pacific region. Prostate Int. (2013) 1:47–58. doi: 10.12954/PI.12014
5. Crocetti E. Epidemiology of prostate cancer in Europe Vol. 2015. London, UK: Centre for Parliamentary Studies (CfPS (2015). Available at: https://publications.jrc.ec.europa.eu/repository/handle/JRC101382 (Accessed July 11, 2024).
6. Baade PD, Youlden DR, Krnjacki LJ. International epidemiology of prostate cancer: Geographical distribution and secular trends. Mol Nutr Food Res. (2009) 53:171–84. doi: 10.1002/mnfr.200700511
7. Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: A systematic analysis for the Global Burden of Disease Study 2010. Lancet. (2012) 380:2095–128. doi: 10.1016/S0140-6736(12)61728-0
8. Descotes JL. Diagnosis of prostate cancer. Asian J Urol. (2019) 6:129–36. doi: 10.1016/j.ajur.2018.11.007
9. Loeb S, Catalona WJ. What is the role of digital rectal examination in men undergoing serial screening of serum PSA levels? Nat Clin Pract Urol. (2009) 6:68–9. doi: 10.1038/ncpuro1294
10. Rawla P. Epidemiology of prostate cancer. World J Oncol. (2019) 10:63–89. doi: 10.14740/wjon1191
11. Marks L, Young S, Natarajan S. MRI-ultrasound fusion for guidance of targeted prostate biopsy. Curr Opin Urol. (2013) 23:43–50. doi: 10.1097/MOU.0b013e32835ad3ee
12. Lowrance W, Dreicer R, Jarrard DF, Scarpato KR, Kim SK, Kirkby E, et al. Updates to advanced prostate cancer: AUA/SUO guideline (2023). J Urol. (2023) 209:1082–90. doi: 10.1097/JU.0000000000003452
13. EAU Guidelines. Edn. presented at the EAU Annual Congress Paris (2024), ISBN. ISBN 978-94-92671-23-3 Arnhem, the Netherlands: EAU Guidelines Office.
14. Mohammed TO, Ajape AA, Kuranga SA, Olanipekun HB, Ogunfowora TT. Prostate biopsy: a survey of practice among Nigerian urologists. Afr J Urol. (2021) 27:135. doi: 10.1186/s12301-021-00240-z
15. D’Amico AV, Whittington R, Malkowicz SB, Schultz D, Blank K, Broderick GA, et al. Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer. JAMA. (1998) 280:969–74. doi: 10.1001/jama.280.11.969
16. Bray F, Parkin DM, African Cancer Registry Network. Cancer in sub-Saharan Africa in 2020: a review of current estimates of the national burden, data gaps, and future needs. Lancet Oncol. (2022) 23:719–28. doi: 10.1016/S1470-2045(22)00270-4
17. Seraphin TP, Joko-Fru WY, Kamaté B, Chokunonga E, Wabinga H, Somdyala NIM, et al. Rising prostate cancer incidence in sub-saharan africa: A trend analysis of data from the African cancer registry network. Cancer Epidemiol Biomarkers Prev. (2021) 30:158–65. doi: 10.1158/1055-9965.EPI-20-1005
18. Jalloh M, Cassell A, Niang L, Rebbeck T. Global viewpoints: updates on prostate cancer in Sub-Saharan Africa. BJU Int. (2024) 133:6–13. doi: 10.1111/bju.16178
19. Gambert SR. Screening for prostate cancer. Int Urol Nephrol. (2001) 33:249–57. doi: 10.1023/a:1015290429403
20. Ilic D, Neuberger MM, Djulbegovic M, Dahm P. Screening for prostate cancer. Cochrane Database Syst Rev. (2013) 2013:CD004720. doi: 10.1002/14651858.CD004720
21. James ND, Tannock I, N’Dow J, Feng F, Gillessen S, Ali SA, et al. The Lancet Commission on prostate cancer: planning for the surge in cases. Lancet. (2024) 403:1683–722. doi: 10.1016/S0140-6736(24)00651-2
22. National Comprehensive Cancer Network. NCCN clinical practice guidelines in oncology (NCCN Guidelines®). (Prostate cancer early detection 2.2024 – March 6, 2024. (2024). Available online at: https://www.nccn.org/professionals/physician_gls/pdf/prostate_detection.pdf.
23. Onyeodi IA, Akintelure S, Oladipo AT, Fashola TO. Knowledge, attitude and screening practices of prostate cancer among men in an urban community in Lagos, Nigeria. J Community Med Primary Health Care. (2022) 34:82–97. doi: 10.4314/jcmphc.v34i3.7
24. Makau-Barasa LK, Manirakiza A, Carvalho AL, Rebbeck TR. Prostate cancer screening, diagnostic, treatment procedures and costs in sub-saharan Africa: a situational analysis. Cancer Control. (2022) 29:10732748221084932. doi: 10.1177/10732748221084932
25. Durkan GC, Sheikh N, Johnson P, Hildreth AJ, Greene DR. Improving prostate cancer detection with an extended-core transrectal ultrasonography-guided prostate biopsy protocol. BJU Int. (2002) 89:33–9. doi: 10.1016/j. afju.2014.12.002
26. Wei JT, Barocas D, Carlsson S, Coakley F, Eggener S, Etzioni R, et al. Early detection of prostate cancer: AUA/SUO guideline part I: prostate cancer screening. J Urol. (2023) 210:45–53. doi: 10.1097/JU.0000000000003491
27. Benchikh El Fegoun A, El Atat R, Choudat L, El Helou E, Hermieu JF, Dominique S, et al. The learning curve of transrectal ultrasound-guided prostate biopsies: implications for training programs. Urology. (2013) 81:12–5. doi: 10.1016/j.urology.2012.06.084
28. Jehle KS, Lazarus JM, Barnes RD. A review of transrectal ultrasound guided prostate biopsies: Is there still a role for finger guided prostate biopsies? Afr J Urol. (2015) 21:62–6. doi: 10.1016/j.afju.2014.12.002
29. Huynh CC, Awad N, Fulton M. The advantage of finger guided prostate biopsies in addition to transrectal ultrasound guided prostate biopsies in patients with palpable disease. BJU Int. (2006) 97:19. doi: 10.1111/j.1464-410X.2006.06085_66.x
30. Marenco Jimenez JL, Claps F, Ramón-Borja JC, Mascarós Martinez JM, Gutierrez AW, Lozano ÁGF, et al. Rebiopsy rate after transperineal or transrectal prostate biopsy. Prostate Int. (2021) 9:78–81. doi: 10.1016/j.prnil.2020.10.001
31. Tulone G, Giannone S, Mannone P, Tognarelli A, Di Vico T, Giaimo R, et al. Comparison of fluoroquinolones and other antibiotic prophylaxis regimens for preventing complications in patients undergoing transrectal prostate biopsy. Antibiotics (Basel). (2022) 11:415. doi: 10.3390/antibiotics11030415
32. Faty M, Saleh SM, El-Nahas AR, Al-Shaiji TF, Al-Terki A. Antibiotic prophylaxis for transrectal ultrasound-guided prostatic biopsies: a comparison of two regimens. Afr J Urol. (2020) 26:11. doi: 10.1186/s12301-020-00026-9
33. Cornford P, van den Bergh RC, Briers E, Van den Broeck T, Brunckhorst O, Darraugh J, et al. EAU-EANM-ESTRO-ESUR-ISUP-SIOG guidelines on prostate cancer—2024 update. Part I: screening, diagnosis, and local treatment with curative intent. Eur Urol. (2024) 86(2):148–63. doi: 10.1016/j.eururo.2024.03.027
34. McCaul M, Ernstzen D, Temmingh H, Draper B, Galloway M, Kredo T. Clinical practice guideline adaptation methods in resource constrained settings: Four case studies from South Africa. BMJ Evid Based Med. (2020) 25:193–8. doi: 10.1136/bmjebm-2019-111192
35. Cassell A, Yunusab B, Jalloh M, Mbodji MM, Diallo A, Ndoye M, et al. A review of localized prostate cancer: an African perspective. World J Oncol. (2019) 10:162–8. doi: 10.14740/wjon1221
36. Ikuerowo SO, Omisanjo OA, Bioku MJ, Ajala MO, Mordi VP, Esho JO. Prevalence and characteristics of prostate cancer among participants of a community-based screening in Nigeria using serum prostate specific antigen and digital rectal examination. Pan Afr Med J. (2013) 15:129. doi: 10.11604/pamj.2013.15.129.2489
37. Anderson D, Barnes R, Meshack B, Bigalke M, Bongers M, Chetty P, et al. Prostate cancer diagnostic and treatment guidelines. Johannesburg: The Prostate Cancer Foundation of South Africa (2017).
38. Bosland MC, Shittu OB, Ikpi EE, Akinloye O. Potential new approaches for prostate cancer management in resource- limited countries in Africa. Ann Global Health. (2023) 89:14, 1–7. doi: 10.5334/aogh.3994
39. Marima R, Mbeje M, Hull R, Demetriou D, Mtshali N, Dlamini Z. Prostate cancer disparities and management in southern Africa: insights into practices, norms and values. Cancer Manag Res. (2022) 14:3567–79. doi: 10.2147/CMAR.S382903
40. Swanson W, Samba RN, Lavelle M, Elzawawy A, Sajo E, Ngwa W, et al. Practical guidelines on implementing hypofractionated radiotherapy for prostate cancer in Africa. Front Oncol. (2021) 11:725103. doi: 10.3389/fonc.2021.725103
41. Mbugua RG, OluChina S, Karanja S. Prostate cancer awareness and screening among men in a rural community in Kenya: a cross-sectional study. Afr J Urol. (2021) 27:7. doi: 10.1186/s12301-020-00108-8
42. Dosanjh M, Ristova M, Gershan V, et al. Availability of technology for managing cancer patients in the Southeast European (SEE) region. Clin Trans Radiat Oncol. (2022) 34:57–66. doi: 10.1016/j.ctro.2022.03.004
43. Ngcamphalala C, Östensson E, Ginindza TG. The economic burden of prostate cancer in Eswatini. BMC Health Serv Res. (2022) 22:483. doi: 10.1186/s12913-022-07817-6
44. Okeke CJ, Obi AO, Ojewola RW, Jeje EA, Okorie CO, Afogu EN, et al. Prostate cancer and challenges in management in a semi-urban centre: A 10-year experience. J West Afr Coll Surg. (2022) 12:44–8. doi: 10.4103/jwas.jwas_140_22
45. Akinyemi OO, Owopetu OF, Agbejule IO. NATIONAL HEALTH INSURANCE SCHEME: PERCEPTION AND PARTICIPATION OF FEDERAL CIVIL SERVANTS IN IBADAN. Ann Ib Postgrad Med. (2021) 19:49–55.
46. Park JJ, Kim CK. Paradigm shift in prostate cancer diagnosis: pre-biopsy prostate magnetic resonance imaging and targeted biopsy. Korean J Radiol. (2022) 23:625–37. doi: 10.3348/kjr.2022.0059
47. Guillonneau B, Vallancien G. Laparoscopic radical prostatectomy: the Montsouris experience. J Urol. (2000) 163:418–22. doi: 10.1016/s0022-5347(05)67890-1
48. Pasticier G, Rietbergen JBW, Guillonneau B, Fromont Gaëlle, Menon M, Vallancien G. Robotically assisted laparoscopic radical prostatectomy: feasibility study in men. Eur Urol 1 July. (2001) 40:70–4. doi: 10.1159/000049751
49. Pessoa RR, Maroni P, Kukreja J, Kim SP. Comparative effectiveness of robotic and open radical prostatectomy. Transl Androl Urol. (2021) 10:2158–70. doi: 10.21037/tau.2019.12.01
50. Forgan T, Lazarus J. Embracing the future: the necessity of implementing robotic surgery in South African training institutions. S Afr J Surg. (2023) 61:144–9. doi: 10.36303/SAJS.4111
51. Ecosystem for Robotic Surgery: Fellowships, awards, grants. Vattikuti Foundation (2024). Available at: https://vattikutifoundation.com/ (Accessed May 07, 2024).
52. Karagöz MA, Bağcıoğlu M, Demirbaş A, Özcan S, Taş T, Huri E. Current status of uro-oncology training during urology residency and the need for fellowship programs: An international questionnaire study. Turk J Urol. (2020) 46:455–9. doi: 10.5152/tud.2020.20276
53. Barocas DA, Mitchell R, Chang SS, Cookson MS. Impact of surgeon and hospital volume on outcomes of radical prostatectomy. Urol Oncol. (2010) 28:243–50. doi: 10.1016/j.urolonc.2009.03.001
54. Begg CB, Riedel ER, Bach PB, Kattan MW, Schrag D, Warren JL, et al. Variations in morbidity after radical prostatectomy. N Engl J Med. (2002) 346:1138–44. doi: 10.1056/NEJMsa011788
Keywords: prostate, prostate-specific antigen, urologist, prostate cancer, Africa
Citation: Biyouma MDC, Gebreselassie KH, Abdelkerim Nedjim S, Ziba OJD, Makon AMN, Kifle AT, Mohammed TO, Cassell AK III, Youssef B, Idrissa S, Mbwambo OJ, Mahamat MA, Aboutaieb R, Ngwa‐Ebogo TT, Ndoye AK, Olapade-Olaopa EO and Angwafo FF III (2025) Prostate cancer diagnosis and management: current practices in Africa a consultant-based survey. Front. Urol. 5:1496951. doi: 10.3389/fruro.2025.1496951
Received: 16 September 2024; Accepted: 28 January 2025;
Published: 17 March 2025.
Edited by:
Mihai Dorin Vartolomei, University of Bern, SwitzerlandReviewed by:
Biagio Barone, ASL Napoli 1 Centro, ItalyCopyright © 2025 Biyouma, Gebreselassie, Abdelkerim Nedjim, Ziba, Makon, Kifle, Mohammed, Cassell, Youssef, Idrissa, Mbwambo, Mahamat, Aboutaieb, Ngwa‐Ebogo, Ndoye, Olapade-Olaopa and Angwafo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Marcella Derboise Christelle Biyouma, bWFyY2VsbGFiaXlvdW1hQGdtYWlsLmNvbQ==
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