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BMC Urology logoLink to BMC Urology
. 2022 Jun 15;22:86. doi: 10.1186/s12894-022-01036-1

Knowledge, attitudes, and practices of active surveillance in prostate cancer among urologists: a real-life survey from Brazil

Marcelo Langer Wroclawski 1,2,3,✉,#, Breno Santos Amaral 1,#, Paulo Priante Kayano 1, Wilson Francisco Schreiner Busato Jr 4, Sebastião José Westphal 5, Erik Montagna 3, Bianca Bianco 1,3, Andrey Soares 1,6,7, Fernando Cotait Maluf 1,2, Gustavo Caserta Lemos 1, Arie Carneiro 1
PMCID: PMC9199143  PMID: 35706024

Abstract

Background

Active surveillance (AS) is the preferred treatment for patients with very low-and low-risk prostate cancer (PCa), but it is underperformed worldwide. This study aimed to report knowledge, attitudes, and practices (KAP) of AS for PCa among urologists in Brazil.

Methods

This cross-sectional study used a questionnaire with 50 questions divided into participant characteristics, knowledge regarding inclusion criteria for AS, follow-up, intervention triggers, acceptance, and practice for an index patient. Data analysis comprises absolute and relative frequencies of the variables. After that, a logistic regression was performed in order to verify possible patterns of answers provided by the respondents in the index patient questionnaire.

Results

Questionnaires were sent through the SurveyMonkey® platform to 5,015 urologists using email addresses and through social media. A total of 600 (12%) questionnaires returned and 413 (8.2%) were completed and included in the analysis. Only 53% of urologists adopt AS for low- and very-low-risk PCa. Inclusion criteria were patients with age > 50 years (32.2%), prostate specific antigen (PSA) < 10 ng/mL (87.2%), T1 clinical stage (80.4%), Biopsy Gleason score ≤ 6, positive cores ≤ 2 (44.3%), positive core involvement < 50% (45.3%), and magnetic resonance imaging findings (38.7%). The PSA doubling time was still used by 60.3%. Confirmatory biopsy (55.9%), PSA level (36.6%), and digital rectal examination (34.4%) were considered by most urologists for follow-ups. Patient preference (85.7%), upgrade of Gleason score (73.4%), and increased number of positive cores (66.8%) were associated with conversion to definitive treatment. In an index patient, non-acceptance and active treatment request were the most cited reasons for not performing AS.

Conclusion

There is significant variability in the KAP of AS in Brazil, which indicates the need to reinforce AS, its inclusion and follow-up criteria, and the benefits for physicians and the general population.

Trial registration: Not applicable.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12894-022-01036-1.

Keywords: Active surveillance, Prostate cancer, Survey

Background

There were approximately 65,000 New cases of prostate cancer (PCa) in Brazil in 2020. In 2017, mortality due to neoplasia was 15,576 [1]. In the last two decades, PCa diagnosis has increased, especially in the low-risk category, mainly because of more widespread prostate specific antigen (PSA) screening [2].

Active surveillance (AS) is a safe option for low- and very low-risk PCa [3, 4]. Current guidelines from the European Association of Urology (EAU) [5], American Urological Association (AUA) [6], and National Comprehensive Cancer Network (NCCN) [7] recommend AS as the preferred treatment option for these patients. Intermediate-risk PCa patients present with poor outcomes when managed through AS, but its use should be considered in selected cases. Nevertheless, AS remains underperformed worldwide [8].

This study aimed to report the knowledge, attitudes, and practices (KAP) of AS for PCa among urologists in Brazil.

Methods

This cross-sectional study followed a checklist for reporting the E-Survey results [9].

An anonymous survey was created to assess KAP of AS for PCa among urologists in Brazil. Questionnaires were sent through the SurveyMonkey® platform to 5015 urologists from the Brazilian urological community using email addresses obtained from the Brazilian Society of Urology membership directory and through social media.

The instrument for data collection was developed ad hoc for this study and comprised two parts consisting in the mapping of fundamental concepts in AS and the validation of the categories identified. The first part adopted a delphi approach through semi-structured interviews until saturation, that is, when little or no variation is observed in the answers [10]. Participants were specialists in Urologic oncology. The interview consisted of three questions: (1) List the topics or knowledge that a doctor should already know about AS; (2) What are the typical and exclusive contents of AS? (3) List the most common misconceptions about AS. The common points mentioned were aggregated by equality, similarity or thematic coherence in order to reduce the number of conceptual categories. This procedure was carried out independently by two researchers with ties dismissed by a third participant. The saturation point was reached after three interviews, as the answers were similar, equivalent or complementary [11].

The survey consisted of 50 questions, divided into participant characteristics (five items), acceptance and inclusion criteria to select patients for AS (11 items), practice characteristics (nine items), follow-up protocol (five items), intervention triggers (11 items), and knowledge about index patient (65-year-old male without comorbidities, potent and continent, diagnosed with very low or low-risk PCa) (nine items) (Additional file 1).

The inclusion criteria included being a Brazilian urologist and signing an informed consent. Incomplete questionnaires were discarded.

The sample size for a population of unknown size, with non-random distribution, a 95% confidence level, and a 5% margin of error, required 385 respondents for a survey.

The data analysis pipeline comprised descriptive statistics steps in terms of the absolute and relative frequencies of the study variables. Categorical variables were compared using the chi-squared test. Pairwise comparisons were performed for all variables. Then, a chi-squared test of independence was used, where classes of respondents were the dependent variable and tested against items of the index patient knowledge part of the questionnaire. A logistic regression was performed in order to verify possible patterns of answers provided by the respondents in the “index patient knowledge questionnaire”. Considering that the variables of interest are categorical and that the analysis was based on the occurrence of responses instead of a yes/no response ratio, a binomial distribution was adopted for the logit (link function), with a non-robust covariance. The regression results were presented as non-adjusted regression coefficients (R). Statistical significance was set at p < 0.05. Statistical analyses were performed using the R Studio version 1.1.383.

Results

Participants characteristics

Questionnaires were sent to 5015 urologists. A total of 600 (600/5015, 12%) questionnaires returned and 413 (413/5015, 8.2%) were completed and included in the analysis. The characteristics of the respondents are listed in Table 1.

Table 1.

Characteristics of the participants

Variables N %
Age (years)a
45.8 SD 11.2 (27–74)
Years of professional activitya
16.6 SD 12.4 (0–52)
Major type of workplace
Outpatient clinic or non-university hospital of the public health system 39 9.5
Exclusively Hospital and/or Private Clinic 131 31.7
50% Hospital and/or Private Clinic and 50% University-Hospital of the Public Health System 235 56.9
University Hospital of the Public Health System 8 1.9
Continuing education
Residency in Urology 413 100
No other postgraduation course 298 72.1
Fellowship in Uro-oncology 52 12.6
Master degree 30 7.3
Ph.D. 33 8.0
Region of Brazil
North 8 1.9
Northeast 63 15.3
Middle-west 30 7.3
Southeast 236 57.1
South 76 18.4

aVariables presented as mean, standard deviation (SD) and minimum and maximum values (0 stands for residents in training)

Acceptance and Inclusion criteria to select patients for AS protocol

AS is the preferred treatment option for patients with low-risk and very low-risk PCa for 53% of urologists, while 5.3% do not recommend AS and consider any form of active treatment instead. Thirty percent of urologists reported that they did not use a predefined protocol for selecting patients who were candidates for AS. When a protocol was used (70% of the time), the one that was most frequently adopted was the one from John Hopkins (43.3%). Table 2 summarises the criteria considered for the AS indications.

Table 2.

Acceptance and inclusion criteria to select patients for active surveillance protocol

Question Items N %
Acceptance
Do you adopt AS in your practice for patients with low-risk and very-low risk prostate cancer? No 22 5.3
Yes 219 53
Occasionally 172 41.7
Do you adopt any protocol for AS? No 124 30.0
John Hopkins 179 43.3
Toronto 82 19.9
Other 28 6.8
Inclusion criteria to select patients for AS protocol

Do you use any of the following items in your practice to define eligibility for active surveillance?

*more than one answer per item was accepted

Age of the patient (years) Not informed 91 22.0
> 50 years 133 32.2
> 55 years 14 3.4
> 60 years 93 22.5
> 70 years 71 17.2
> 80 years 11 2.7
PSA level (ng/mL) Not considered 27 6.5
< 10 ng/mL 360 87.2
Up to15 ng/mL 12 2.9
Up to 20 ng/mL 14 3.4
PSA density (ng/mL) Not considered 220 53.3
< 10 ng/mL 35 8.5
< 15 ng/mL 130 31.5
< 20 ng/mL 28 6.8
Doubling PSA time Not considered 164 39.7
> 6 months 54 13.1
> 1 year 99 24.0
> 2 years 66 16.0
> 3 years 20 4.8
> 4 years 10 2.4
Clinical staging Not considered 15 3.6
T1 332 80.4
T2a 48 11.6
T2b 11 2.7
T2c 6 1.5
T3 1 0.2
Gleason Score in the prostate biopsy Not considered 4 1.0
≤ 6 385 93.2
7 (3 + 4) only in selected cases 22 5.3
7 (4 + 3) only in selected cases 2 0.5
Number of positive cores Not considered 26 6.3
≤ 2 fragments 183 44.3
≤ 3 fragments 137 33.2
≤ 34% of the total fragments 41 9.9
≤ 50% of the total fragments 26 6.3
Maximum involvement of each positive core Not considered 47 11.4
< 20% 127 30.8
< 30% 52 12.6
< 50% 187 45.3
Eligibility Not considered 83 20.1
MRI 160 38.7
Slide review 25 6.1
MRI e slide review 112 27.1
Other 33 8.0

AS active surveillance, MRI magnetic resonance imaging, PSA prostate-specific antigen

Concerning age, 22.5% of urologists considered AS only for patients aged above 60 years and 17.2% indicated it only for patients aged above 70 years. A PSA level of < 10.0 ng/mL was an inclusion criterion for 87.2% of the urologists. More than half (53%) of the urologists did not consider PSA density (PSA-D) to suggest AS. In contrast, 60.3% used PSA doubling time (PSAdt) as an inclusion criterion for AS. For clinical staging indications, AS is an option for 80.4% of urologists in T1 tumours, 11.6% in T2a tumours, 2.7% in T2b tumours, and 1.5% in T2c tumours. A Gleason score (GS) of 6 or less was an inclusion criterion for 93.2% of the urologists and 5.3% considered AS for some selected Gleason 7 (3 + 4) cases, while 0.5% considered it for Gleason 7 (4 + 3) cases. Two or fewer positive cores were used by 44.3% of urologists, 33.2% used ≤ 3 positive cores, 9.9% used < 34% of the cores involved, and 6.3% did not use this as a criterion to indicate AS. Approximately 30.8% of urologists use < 20% as the maximum involvement of each positive core as a criterion to indicate AS, while 45.3% used 50% as the threshold to indicate AS. Approximately 38.7% of urologists use magnetic resonance imaging (MRI) as an eligibility criterion to allocate a patient to an AS protocol (Table 2).

Practice characteristics

MRI is inaccessible to 15.7% of urologists, 9.2% have access to MRI of the pelvis, without a specific prostate protocol (multiparametric MRI (mpMR), and 1.5 and 3.0 Tesla mpMRI is available for 40.9% and 34.2% of urologists, respectively. Prostate biopsies are mostly performed at the same institution by the urologists (17.4%) who ordered it (17.4%), other urologists (19.6%), or radiologists (35.6%). The remaining 27.4% prostrate biopsies were performed elsewhere. The majority of biopsies were transrectal (99.3%). In terms of the number of cores retrieved, sextant biopsies (12 cores with two from each area) were the most common (41.6%). Fusion-guided biopsy was available for 52.3% of the urologists (23.7% with software, 28.6% cognitive), but 47.7% did not have access for their practice. The time interval between biopsy request and its execution was less than one month in most cases (67.1%). Biopsy histopathological reports provide GS in different ways. The vast majority provided Gleason for each specific fragment (87.9%). Occasionally, a unique GS is determined for fragments of the right lobe and another for fragments of the left lobe all together (5.6% of cases), and elsewhere only a single ‘general’ GS (6.5% of cases) is described. Histopathological reports do not indicate the number of positive cores and percentage of involvement of positive fragments in 1.7% and 3.6% of urologists’ practices, respectively (Table 3).

Table 3.

Practice characteristics

Question Items N %
Practice characteristics
Considering the local where you practice most often
Do patients have easy access to MRI? No 65 15.7
Multiparametric MRI 1.5 Tesla 169 40.9
Multiparametric MRI 3.0 Tesla 141 34.2
Pelvic (unspecified) 38 9.2
The prostate biopsy It is performed at my service, by a urologist 81 19.6
It is performed at my service, by a radiologist 147 35.6
I do it myself 72 17.4
It is outsourced 113 27.4
What is the access of prostate biopsy? Transrectal 410 99.3
Perineal 3 0.7
Number of cores retrieved Sextant (6 cores) 4 1.0
Sextant biopsies (12 cores with 2 of each area) 172 41.6
12 distinct cores of the peripheral zone 57 13.8
12 distinct cores of the peripheral zone plus 2–4 cores of the transition zone 26 7.3
12 distinct cores of the peripheral zone plus 2–4 cores of the transition zone plus additional cores of suspected area (nodule in US or MRI) 142 34.4
Other 12 2.9
Do you have access to biopsy with image fusion? No 197 47.7
Yes, with real-time software fusion 98 23.7
Yes, with cognitive fusion 118 28.6
How long do patients have to wait for a biopsy to be performed? Less than one month 277 67.1
1 to 3 months 119 28.8
3 to 6 months 15 3.6
More than 6 months 2 0.5
Does the histopathological report of the prostate biopsy product provide the Gleason score? Yes, of each fragment alone 363 87.9
Yes, but a general Gleason Score 27 6.5
Yes, for right lobe fragments and another one for left lobe fragments 23 5.6
Does the histopathological report of the prostate biopsy product specify how many fragments are positive? No 7 1.7
Yes 406 98.3
Does the histopathological report of the prostate biopsy product specify the percentage of tumor involvement in each fragment? No 15 3.6
Yes 398 96.4

MRI magnetic resonance imaging, US ultrasound

Follow-up

During follow-up, 26.6% of urologists did not perform a confirmatory biopsy. The remaining patients underwent a confirmatory biopsy, mainly between 6 and 12 months after diagnosis (55.9%). Approximately 63% of urologists perform additional biopsies after a confirmatory biopsy, every one to two years (37.3% and 25.7%, respectively). The remaining only perform it if a trigger point is reached, such as a PSA rise (29.5%) or an MRI modification (7.5%) (Table 4).

Table 4.

Follow-up protocol

Question Items N %
Follow-up protocol
In the follow-up of patients under AS:
After the inclusion of a patient in an active surveillance protocol, do you perform a confirmatory biopsy? No 110 26.6
Yes, up to 3 months 18 4.4
Yes, between 3 and 6 months 54 13.1
Yes, between 6 and 12 months 231 55.9
In addition to the confirmatory biopsy, how often do you have new biopsies? Yearly 154 37.3
Biennial 106 25.7
Only if PSA levels increase 122 29.5
If there is a worsening in the imaging exam 31 7.5
In the first 5 years, how often do you evaluate PSA levels? Quarterly 131 31.7
Half-yearly 151 36.6
Quarterly in the first two years and half-yearly between 2 and 5 years 117 28.3
Annually 14 3.4
How often do you perform a digital rectal examination? I do not use routinely 32 7.7
Quarterly 41 9.9
Quarterly in the first two years and half-yearly between 2 and 5 years 75 18.2
Half-yearly measure 142 34.4
Annually 123 29.8
In addition to ultrasound for biopsy, do you use other imaging tests? No 93 22.5
MRI occasionally 177 42.9
MRI periodically 143 34.6

AS active surveillance, MRI magnetic resonance imaging, PSA prostate-specific antigen

Intervention triggers

Triggers for active treatment during follow-up are presented in Table 5. More than one answer was permitted.

Table 5.

Intervention trigger

Question N %
Intervention trigger

Which of the following options do you use to recommend conversion from active surveillance to definitive treatment?

*more than one answer was accepted

Patient’s preference 354 85.7
Change in rectal examination (worsening of clinical staging) 250 60.5
Single rising PSA level (PSA > 10 ng/mL) 133 32.0
Two or more consecutive rising in PSA levels (PSA > 10 ng/mL) 225 54.5
PSA doubling time < 3 years 110 26.4
Rising PSA density (> 15%) 78 18.9
Gleason score upgrading to 7 (3 + 4) 228 55.2
Gleason score upgrading to 7 (3 + 4) or greater on re-biopsy 303 73.4
Increased tumor volume on imaging (MRI) 167 40.4
Higher number of positive cores in re-biopsy (> 1/3) 276 66.8
Involvement > 50% in at least 1 core in re-biopsy 189 45.8

MRI magnetic resonance imaging, PSA prostate-specific antigen

Knowledge about index patient

The reasons for not performing AS in an index patient (65-year-old male without comorbidities, potent and continent, diagnosed with very low or low-risk PCa) are listed in Table 6. More than one answer was provided.

Table 6.

Knowledge about index patient

Question N %

Knowledge about index patient

*more than one answer was accepted

Reasons for not performing active surveillance (AS) in an index-patient
I don't know enough about this type of treatment to properly follow-up the patients 5 1.3
I believe that AS is an inappropriate approach for patients with prostate cancer, even at low or very-low risk 12 3.1
Morbidity associated with multiple biopsies 68 17.4
Patient does not accept the AS and requests active treatment 344 88.0
I would like to indicate, but the biopsy performed is inadequate 16 4.1
I would like to indicate, but I do not trust the team responsible for performing the biopsy 14 3.6
I would like to indicate, but the histopathological report does not provide the necessary data 17 4.3
I would like to indicate, but I do not trust the team responsible for the histopathological evaluation 20 5.1
I would like to indicate, but I cannot schedule laboratory tests and/or biopsy and/or outpatient return with the appropriate interval 42 10.7

Response patterns

The logistic regression among ‘Indication of AS’ versus ‘Index Patient Knowledge’ was statistically significant for the following items: Considering those who did not indicate AS, there was a direct relation to ‘I don't know enough about this type of treatment to properly follow-up the patients’ (p = 0.030, R = 2.19) and ‘I believe that AS is an inappropriate approach for patients with prostate cancer, even at low or very-low risk’ (p = 0.004, R = 2.14), while an inverse relation was observed with ‘Patient does not accept AS and requests active treatment’ (p = 0.018, R = − 1.21). Considering those who indicate AS occasionally, there is a direct relation to ‘I would like to indicate, but I cannot schedule laboratory tests and/or biopsy and/or outpatient return with the appropriate interval’ (p = 0.026, R = 0.83), while an inverse relation was observed with ‘Morbidity associated with multiple biopsies’ (p = 0.001, R = -1.01) and ‘I would like to indicate, but the histopathological report does not provide the necessary data’ (p = 0.012, R = − 2.72). Finally, considering those who indicated AS, there was an inverse relation to ‘I believe that AS is an inappropriate approach for patients with PCa, even at low or very-low risk’ (p = 0.024, R = − 2.42), ‘Morbidity associated with multiple biopsies’ (p = 0.001, R = − 1.06), and ‘I would like to indicate, but I cannot schedule laboratory tests and/or biopsy and/or outpatient return with the appropriate interval’ (p = 0.048, R = − 0.74).

Regarding the region of Brazil and the indication of AS, multiple logistic regression showed a significant difference in the southern region (p = 0.028, R = 1.87).

Discussion

AS has been proposed as the preferred treatment option for low- and very low-risk PCa; however, the inclusion criteria and follow-up schedules present great variability [3, 5, 1217]. The features that vary most are the number of positive cores, proportion of cancer in each positive core, PSA cut-off, and use of PSA-D and PSAdt. The absence of homogeneous recommendations affects urological practice.

Total PSA up to 10 ng/dL is an inclusion criterion used by Klotz et al. [4], Tosoian et al. [3], Godtman et al. [12], and Bokhorst et al. [15]. Selvadurai et al. [13] accepted patients with PSA levels up to 15 ng/dL. Findings showed that the vast majority of urologists in Brazil use PSA < 10 ng/dL (87.2%) as the cut-off limit to propose AS.

Tosoian et al. [3] and Bokhorst et al. [15] considered PSA-D as an inclusion criterion. During follow-up, PSA-D is an important risk factor for progression of PCa [18]. In this study, up to 53.3% of urologists did not use it as an inclusion criterion. For those who adopt it, PSA-D < 15%, as in Johns Hopkins [3], is the cut-off for 31.5% and < 20%, as in PRIAS [15], is the cut-off for 6.8%.

In contrast, PSAdt has not been used by most of the AS protocols because this feature is a weak stage upgrading predictor in the specimen analysis after surgery [19]. Conversely, more than 60% of the responders still used PSAdt to indicate AS where 13.1% will offer AS if PSAdt is more than six months, and 24% will consider AS only if PSAdt is more than 12 months.

The number of positive cores and maximum tumour involvement in each core were both considered as inclusion criteria by Tosoian et al. [3], Welty et al. [20], Thomsen et al. [6], and Soloway et al. [7]. These characteristics are also linked to unfavourable evolution during follow-up and a higher chance of tumour reclassification [21]. The EAU [5] and NCCN guidelines [7] define very low-risk PCa when up to two cores are involved, as described by Epstein et al. [22]. However, AUA guidelines [6] classify very-low risk when there are < 34% positive cores, as the number of cores retrieved in a prostate biopsy has risen from the original six to a much greater sampling. In this study, 44.3% of urologists considered ≤ 2 positive cores, and 9.9% considered < 34% of the total cores as an inclusion criterion. A considerable number of urologists (33.2%) adopted a criterion of ≤ 3 positive cores, which was used by Thomsen [16].

Less than 50% maximum involvement of a positive core to include patients in an AS protocol was considered by 45.3% of the urologists, as used by Tosoian et al. [3], Welty et al. [20], and Thomsen et al. [16]. Notably, 43.4% of urologists used other cut-off limits as part of the inclusion criteria. Less than 20% of tumours in each core, as in Soloway et al. [17], was adopted by 30.8% urologists and less than 30% of tumours in each core, as in Thompson et al. [14], was used by 12.6%.

The follow-up management is also different in terms of the interval of digital rectal exam and PSA evaluation, and the role of confirmatory and re-biopsy indications varies among studies [3, 4, 1317, 20]. This study also revealed similar differences in responses in terms of follow-up management preferences.

Although Brazil is a country with limited resources and a lack of MRI availability, a significant number of urologists order it to manage AS, even though its use during follow-up is still under investigation and has conflicting results [23, 24]. Also, it is has been demonstrated that MRI targeted biopsies can cause a “grade inflation” and this should be considered during the risk assessment [25]. The availability of MRI in Brazil varies according to the working environment (private versus public). In the public environment, mpMRI is accessible to 56.7% of urologists, and in almost two-thirds of these cases, only 1.5 Tesla equipment is available. In contrast, mpMRI can be easily ordered by 80% of urologists in private institutions, and half of them are 3 Tesla. The use of MRIs also varies according to geography, being less available in the northern and north-eastern regions, considered as economically disadvantaged areas compared to the rest of the country.

Since there is not a validated Brazilian guideline regarding the management of patients under AS, Brazilian urologists adapt their practice according to their own convenience, mixing criteria from diverse international guidelines, as demonstrated by our survey.

There was a direct relationship between the response of the urologists who did not indicate AS and the lack of knowledge about AS because they considered this type of treatment inappropriate for the index patient. While analysing those that indicated AS occasionally, we found that they did not consider the biopsy to be harmful and they have good pathology reports; however, they do not indicate AS regularly because of lack of access to scheduled laboratory tests and/or biopsy and/or outpatient return with the appropriate interval. As expected, urologists who indicated AS agreed to the harmfulness of biopsy were able to follow-up patients and had access to good pathology reports.

This study demonstrated that AS remains underused in Brazil. Only 53% of respondents considered it the preferred option for low- and very low-risk PCa in most cases. In developed countries, AS has gained traction in recent years. In the United States, up to 75% of very low-risk cases are initially treated with AS [26]. In Sweden, use of AS is even greater, reaching 91% for very-low-risk and 74% for low-risk cases [27].

Findings showed that economically less-favoured regions presented worse AS indications and acceptance rates when compared to more developed areas (South Region). This has also been observed in other studies. A survey demonstrated that AS is underused in Lebanon due to patient non-compliance and discrete acceptance among physicians [28]. Although the use of AS varies based on geographic location, county-level socioeconomic factors in the United States did not influence its indication [29].

Continuous medical education programmes and patient awareness campaigns are essential to reinforce AS and reduce the overtreatment of PCa and its potential complications. It is important to address the advantages of AS as a treatment option for the public, since the main reason for not performing AS was patient non-acceptance (88%).

This is the largest worldwide survey to evaluate AS and the first large-scale survey in low- to middle-income countries. Despite this, the response rate was 12% in the lower tier of what can be expected in voluntary e-mail-based surveys [3032]. Another aspect that may represent a selection bias is that responders average age was 46.8 years old, maybe being more web/IT oriented, and prone to follow international guidelines and be updated to current practices.

We believe that this study described in detail Brazilian urologists’ knowledge, attitude, and practice regarding AS. Based on this data, public authorities and medical societies may have an instrument to guide the construction of a national guideline.

Conclusions

PCa management through AS in a low-middle-income country presents many challenges. Many urologists do not adopt AS for a number of reasons. Continuous medical education and population awareness programmes are the most important methods to disseminate evidence-based knowledge in medical and general populations and to reduce overtreatment of PCa.

Supplementary Information

12894_2022_1036_MOESM1_ESM.docx (34.2KB, docx)

Additional file 1. Survey about knowledge, acceptance, and practice of urologists concerning active surveillance for prostate cancer in Brazil.

Acknowledgements

We would like to thank the assistance provided by Ms. Maria Beatriz Lemos (Research Nurse, HIAE), and Mr. Ricardo de Morais (Technical editor, SBU).

Abbreviations

AS

Active surveillance

AUA

American Urological Association

EUA

European Association of Urology (EAU)

GS

Gleason score

KAP

Knowledge, attitudes, and practices (KAP)

mpMRI

Multiparametric magnetic resonance imaging

MRI

Magnetic resonance imaging

NCCN

National Comprehensive Cancer Network (NCCN)

PCa

Prostate cancer PC

PSA

Prostate specific antigen

PSA-D

PSA density

PSAdt

PSA doubling time

Author contributions

Conceptualization, M.L.W., B.S.A. and A.C.; Methodology, M.L.W., B.S.A., P.P.K., W.B., S.W., A.S., F.C.M., G.C.L., and A.C.; Software, M.L.W. and B.S.A.; Validation, M.L.W., B.S.A. and E.M.; Formal Analysis, M.L.W., B.S.A., and E.M.; Investigation, M.L.W., B.S.A., P.P.K., W.B., S.W., A.S., F.C.M., G.C.L., and A.C.; Resources, M.L.W.; Data Curation, M.L.W., B.S.A. and E.M.; Writing—Original Draft Preparation, M.L.W., B.S.A. and B.B.; Writing—Review & Editing, M.L.W., B.S.A., P.P.K., B.B. and A.C.; Supervision, A.C.; Visualization, M.L.W., P.P.K. and B.B; Project Administration, M.L.W., B.S.A. and A.C. All authors critical review of the manuscript and approved the final version of the manuscript.

Funding

Not applicable.

Availability of data and materials

The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.

Declarations

Ethics approval and consent to participate

The study was approved by the Research Ethics Commit-tee of the “Hospital Israelita Albert Einstein” (Approve Code CAAE: 15032919.1.0000.0071and date of approval 01/08/2019) and was performed in accordance with relevant guidelines and regulations. Each participant enrolled in this study signed an informed consent for the survey and to allow analysis for research purposes.

Consent for publication

Informed consent was obtained from all subjects involved in the study.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Marcelo Langer Wroclawski and Breno Santos Amaral have contributed equally to this work.

References

  • 1.Instituto Nacional do Câncer. https://www.inca.gov.br/campanhas/cancer-de-prostata/2020/saude-do-homem. Accessed 24 June 2020.
  • 2.Ploussard G, Epstein JI, Montironi R, Carroll PR, Wirth M, Grimm MO, et al. The contemporary concept of significant versus insignificant prostate cancer. Eur Urol. 2011;60:291–303. doi: 10.1016/j.eururo.2011.05.006. [DOI] [PubMed] [Google Scholar]
  • 3.Tosoian JJ, Mamawala M, Epstein JI, Landis P, Wolf S, Trock BJ, Carter HB. Intermediate and longer-term outcomes from a prospective active-surveillance program for favorable-risk prostate cancer. J Clin Oncol. 2015;33:3379–3385. doi: 10.1200/JCO.2015.62.5764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Klotz L, Vesprini D, Sethukavalan P, Jethava V, Zhang L, Jain S, Yamamoto T, Mamedov A, Loblaw A. Long-term follow-up of a large active surveillance cohort of patients with prostate cancer. J Clin Oncol. 2015;33:272–277. doi: 10.1200/JCO.2014.55.1192. [DOI] [PubMed] [Google Scholar]
  • 5.Mottet N, van den Bergh R, Briers CN, et al.: EAU—ESTRO—ESUR—SIOG guidelines on prostate cancer 2020. In: European Association of urology guidelines. 2020 Edition. Arnhem, The Netherlands: European Association of Urology Guidelines Office, vol presented at the EAU Annual Congress Amsterdam 2020.
  • 6.Sanda MG, Cadeddu JA, Kirkby E, Chen RC, Crispino T, Fontanarosa J, Freedland SJ, Greene K, Klotz LH, Makarov DV, Nelson JB, Rodrigues G, Sandler HM, Taplin ME, Treadwell JR. Clinically localized prostate cancer: AUA/ASTRO/SUO guideline. Part II: recommended approaches and details of specific care options. J Urol. 2018;199:990–997. doi: 10.1016/j.juro.2018.01.002. [DOI] [PubMed] [Google Scholar]
  • 7.NCCN Prostate Cancer Guidelines, 2020. https://www.nccn.org/professionals/physician_gls/default.aspx. Accessed 24 June 2020.
  • 8.Musunuru HB, Yamamoto T, Klotz L, Ghanem G, Mamedov A, Sethukavalan P, Jethava V, Jain S, Zhang L, Vesprini D, Loblaw A. Active surveillance for intermediate risk prostate cancer: survival outcomes in the Sunnybrook experience. J Urol. 2016;196:1651–1658. doi: 10.1016/j.juro.2016.06.102. [DOI] [PubMed] [Google Scholar]
  • 9.Eysenbach G. Improving the quality of Web surveys: the Checklist for Reporting Results of Internet E-Surveys (CHERRIES) J Med Internet Res. 2004;6:e34. doi: 10.2196/jmir.6.3.e34. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.McMillan SS, King M, Tully MP. How to use the nominal group and Delphi techniques. Int J Clin Pharm. 2016;38:655–662. doi: 10.1007/s11096-016-0257-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Lynn MR. Determination and quantification of content validity. Nurs Res. 1986;35(382):385. [PubMed] [Google Scholar]
  • 12.Godtman RA, Holmberg E, Khatami A, Pihl CG, Stranne J, Hugosson J. Long-term results of active surveillance in the Göteborg randomized, population-based prostate cancer screening trial. Eur Urol. 2016;70:760–766. doi: 10.1016/j.eururo.2016.03.048. [DOI] [PubMed] [Google Scholar]
  • 13.Selvadurai ED, Singhera M, Thomas K, Mohammed K, Woode-Amissah R, Horwich A, Huddart RA, Dearnaley DP, Parker CC. Medium-term outcomes of active surveillance for localised prostate cancer. Eur Urol. 2013;64:981–987. doi: 10.1016/j.eururo.2013.02.020. [DOI] [PubMed] [Google Scholar]
  • 14.Thompson JE, Hayen A, Landau A, Haynes AM, Kalapara A, Ischia J, Matthews J, Frydenberg M, Stricker PD. Medium-term oncological outcomes for extended vs saturation biopsy and transrectal vs transperineal biopsy in active surveillance for prostate cancer. BJU Int. 2015;115:884–891. doi: 10.1111/bju.12858. [DOI] [PubMed] [Google Scholar]
  • 15.Bokhorst LP, Valdagni R, Rannikko A, Kakehi Y, Pickles T, Bangma CH, Roobol MJ, PRIAS study group A decade of active surveillance in the PRIAS study: an update and evaluation of the criteria used to recommend a switch to active treatment. Eur Urol. 2016;70:954–960. doi: 10.1016/j.eururo.2016.06.007. [DOI] [PubMed] [Google Scholar]
  • 16.Thomsen FB, Berg KD, Røder MA, Iversen P, Brasso K. Active surveillance for localized prostate cancer: an analysis of patient contacts and utilization of healthcare resources. Scand J Urol. 2015;49:43–50. doi: 10.3109/21681805.2014.970572. [DOI] [PubMed] [Google Scholar]
  • 17.Soloway MS, Soloway CT, Eldefrawy A, Acosta K, Kava B, Manoharan M. Careful selection and close monitoring of low-risk prostate cancer patients on active surveillance minimizes the need for treatment. Eur Urol. 2010;58:831–835. doi: 10.1016/j.eururo.2010.08.027. [DOI] [PubMed] [Google Scholar]
  • 18.Soeterik TFW, van Melick HHE, Dijksman LM, Biesma DH, Witjes JA, van Basten JA. Active surveillance for prostate cancer in a real-life cohort: comparing outcomes for PRIAS-eligible and PRIAS-ineligible patients. Eur Urol Oncol. 2018;1:231–237. doi: 10.1016/j.euo.2018.03.015. [DOI] [PubMed] [Google Scholar]
  • 19.Ross AE, Loeb S, Landis P, Partin AW, Epstein JI, Kettermann A, Feng Z, Carter HB, Walsh PC. Prostate-specific antigen kinetics during follow-up are an unreliable trigger for intervention in a prostate cancer surveillance program. J Clin Oncol. 2010;28:2810–2816. doi: 10.1200/JCO.2009.25.7311. [DOI] [PubMed] [Google Scholar]
  • 20.Welty CJ, Cowan JE, Nguyen H, Shinohara K, Perez N, Greene KL, Chan JM, Meng MV, Simko JP, Cooperberg MR, Carroll PR. Extended followup and risk factors for disease reclassification in a large active surveillance cohort for localized prostate cancer. J Urol. 2015;193:807–811. doi: 10.1016/j.juro.2014.09.094. [DOI] [PubMed] [Google Scholar]
  • 21.Petrelli F, Vavassori I, Cabiddu M, Coinu A, Ghilardi M, Borgonovo K, Lonati V, Barni S. Predictive factors for reclassification and relapse in prostate cancer eligible for active surveillance: a systematic review and meta-analysis. Urology. 2016;91:136–142. doi: 10.1016/j.urology.2016.01.034. [DOI] [PubMed] [Google Scholar]
  • 22.Epstein JI, Egevad L, Amin MB, Delahunt B, Srigley JR, Humphrey PA, Grading Committee The 2014 International Society of Urological Pathology (ISUP) consensus conference on Gleason grading of prostatic carcinoma: definition of grading patterns and proposal for a new grading system. Am J Surg Pathol. 2016;40:244–252. doi: 10.1097/PAS.0000000000000530. [DOI] [PubMed] [Google Scholar]
  • 23.Klotz L, Loblaw A, Sugar L, Moussa M, Berman DM, Van der Kwast T, Vesprini D, Milot L, Kebabdjian M, Fleshner N, Ghai S, Chin J, Pond GR, Haider M. Active surveillance magnetic resonance imaging study (ASIST): results of a randomized multicenter prospective trial. Eur Urol. 2019;75:300–309. doi: 10.1016/j.eururo.2018.06.025. [DOI] [PubMed] [Google Scholar]
  • 24.Jayadevan R, Felker ER, Kwan L, Barsa DE, Zhang H, Sisk AE, Delfin M, Marks LS. Magnetic resonance imaging-guided confirmatory biopsy for initiating active surveillance of prostate cancer. JAMA Netw Open. 2019;2:e1911019. doi: 10.1001/jamanetworkopen.2019.11019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Mesko S, Marks L, Ragab O, Patel S, Margolis DA, Demanes DJ, Kamrava M. Targeted prostate biopsy gleason score heterogeneity and implications for risk stratification. Am J Clin Oncol. 2018;41(5):497–501. doi: 10.1097/COC.0000000000000308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Shelton JB, Buffington P, Augspurger R, Gaylis F, Cohen T, Mehlhaff B, Suh R, Bradford TJ, Kwan L, Koo AS, Shore N. Contemporary management of incident prostate cancer in large community urology practices in the United States. Urology. 2019;129:79–86. doi: 10.1016/j.urology.2019.01.061. [DOI] [PubMed] [Google Scholar]
  • 27.Loeb S, Folkvaljon Y, Curnyn C, Robinson D, Bratt O, Stattin P. Uptake of active surveillance for very-low-risk prostate cancer in Sweden. JAMA Oncol. 2017;3:1393–1398. doi: 10.1001/jamaoncol.2016.3600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.El Sebaaly R, Mansour M, Labban M, Jaafar RF, Armache A, Mukherji D, El Hajj A. Survey on the practice of active surveillance for prostate cancer from the Middle East. Prostate Int. 2020;8:41–48. doi: 10.1016/j.prnil.2019.11.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Washington SL, 3rd, Jeong CW, Lonergan PE, Herlemann A, Gomez SL, Carroll PR, Cooperberg MR. Regional variation in active surveillance for low-risk prostate cancer in the US. JAMA Netw Open. 2020;3:e2031349. doi: 10.1001/jamanetworkopen.2020.31349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Gudaru K, Gonzalez Padilla DA, Castellani D, Tortolero Blanco L, Tanidir Y, Ka Lun L, Wroclawski ML, Maheshwari PN, Figueiredo FCA, Yuen-Chun TJ. A global knowledge, attitudes and practices survey on anatomical endoscopic enucleation of prostate for benign prostatic hyperplasia among urologists. Andrologia. 2020;52:e13717. doi: 10.1111/and.13717. [DOI] [PubMed] [Google Scholar]
  • 31.Teoh JY, Ong WLK, Gonzalez-Padilla D, Castellani D, Dubin JM, Esperto F, Campi R, Gudaru K, Talwar R, Okhunov Z, Ng CF, Jain N, Gauhar V, Wong MC, Wroclawski ML, Tanidir Y, Rivas JG, Tiong HY, Loeb S, UroSoMe Working Group A global survey on the impact of COVID-19 on urological services. Eur Urol. 2020;78:265–275. doi: 10.1016/j.eururo.2020.05.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Gomes CM, Favorito LA, Henriques JVT, Canalini AF, Anzolch KMJ, de Carvalho Fernandes R, Bellucci CHS, Silva CS, Wroclawski ML, Pompeo ACL, de Bessa J. Impact of COVID-19 on clinical practice, income, health and lifestyle behavior of Brazilian urologists. Int Braz J Urol. 2020;46:1042–1071. doi: 10.1590/s1677-5538.ibju.2020.99.15. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

12894_2022_1036_MOESM1_ESM.docx (34.2KB, docx)

Additional file 1. Survey about knowledge, acceptance, and practice of urologists concerning active surveillance for prostate cancer in Brazil.

Data Availability Statement

The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.


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