Literature DB >> 35706024

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

Marcelo Langer Wroclawski1,2,3, Breno Santos Amaral4, Paulo Priante Kayano4, Wilson Francisco Schreiner Busato5, Sebastião José Westphal6, Erik Montagna7, Bianca Bianco4,7, Andrey Soares4,8,9, Fernando Cotait Maluf4,10, Gustavo Caserta Lemos4, Arie Carneiro4.   

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.
© 2022. The Author(s).

Entities:  

Keywords:  Active surveillance; Prostate cancer; Survey

Mesh:

Substances:

Year:  2022        PMID: 35706024      PMCID: PMC9199143          DOI: 10.1186/s12894-022-01036-1

Source DB:  PubMed          Journal:  BMC Urol        ISSN: 1471-2490            Impact factor:   2.090


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

VariablesN%
Age (years)a
45.8SD 11.2 (27–74)
Years of professional activitya
16.6SD 12.4 (0–52)
Major type of workplace
Outpatient clinic or non-university hospital of the public health system399.5
Exclusively Hospital and/or Private Clinic13131.7
50% Hospital and/or Private Clinic and 50% University-Hospital of the Public Health System23556.9
University Hospital of the Public Health System81.9
Continuing education
Residency in Urology413100
No other postgraduation course29872.1
Fellowship in Uro-oncology5212.6
Master degree307.3
Ph.D.338.0
Region of Brazil
North81.9
Northeast6315.3
Middle-west307.3
Southeast23657.1
South7618.4

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

Characteristics of the participants 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

QuestionItemsN%
Acceptance
Do you adopt AS in your practice for patients with low-risk and very-low risk prostate cancer?No225.3
Yes21953
Occasionally17241.7
Do you adopt any protocol for AS?No12430.0
John Hopkins17943.3
Toronto8219.9
Other286.8
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 informed9122.0
> 50 years13332.2
> 55 years143.4
> 60 years9322.5
> 70 years7117.2
> 80 years112.7
PSA level (ng/mL)Not considered276.5
< 10 ng/mL36087.2
Up to15 ng/mL122.9
Up to 20 ng/mL143.4
PSA density (ng/mL)Not considered22053.3
< 10 ng/mL358.5
< 15 ng/mL13031.5
< 20 ng/mL286.8
Doubling PSA timeNot considered16439.7
> 6 months5413.1
> 1 year9924.0
> 2 years6616.0
> 3 years204.8
> 4 years102.4
Clinical stagingNot considered153.6
T133280.4
T2a4811.6
T2b112.7
T2c61.5
T310.2
Gleason Score in the prostate biopsyNot considered41.0
≤ 638593.2
7 (3 + 4) only in selected cases225.3
7 (4 + 3) only in selected cases20.5
Number of positive coresNot considered266.3
≤ 2 fragments18344.3
≤ 3 fragments13733.2
≤ 34% of the total fragments419.9
≤ 50% of the total fragments266.3
Maximum involvement of each positive coreNot considered4711.4
< 20%12730.8
< 30%5212.6
< 50%18745.3
EligibilityNot considered8320.1
MRI16038.7
Slide review256.1
MRI e slide review11227.1
Other338.0

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

Acceptance and inclusion criteria to select patients for active surveillance 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 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

QuestionItemsN%
Practice characteristics
Considering the local where you practice most often
Do patients have easy access to MRI?No6515.7
Multiparametric MRI 1.5 Tesla16940.9
Multiparametric MRI 3.0 Tesla14134.2
Pelvic (unspecified)389.2
The prostate biopsyIt is performed at my service, by a urologist8119.6
It is performed at my service, by a radiologist14735.6
I do it myself7217.4
It is outsourced11327.4
What is the access of prostate biopsy?Transrectal41099.3
Perineal30.7
Number of cores retrievedSextant (6 cores)41.0
Sextant biopsies (12 cores with 2 of each area)17241.6
12 distinct cores of the peripheral zone5713.8
12 distinct cores of the peripheral zone plus 2–4 cores of the transition zone267.3
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)14234.4
Other122.9
Do you have access to biopsy with image fusion?No19747.7
Yes, with real-time software fusion9823.7
Yes, with cognitive fusion11828.6
How long do patients have to wait for a biopsy to be performed?Less than one month27767.1
1 to 3 months11928.8
3 to 6 months153.6
More than 6 months20.5
Does the histopathological report of the prostate biopsy product provide the Gleason score?Yes, of each fragment alone36387.9
Yes, but a general Gleason Score276.5
Yes, for right lobe fragments and another one for left lobe fragments235.6
Does the histopathological report of the prostate biopsy product specify how many fragments are positive?No71.7
Yes40698.3
Does the histopathological report of the prostate biopsy product specify the percentage of tumor involvement in each fragment?No153.6
Yes39896.4

MRI magnetic resonance imaging, US ultrasound

Practice characteristics 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

QuestionItemsN%
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?No11026.6
Yes, up to 3 months184.4
Yes, between 3 and 6 months5413.1
Yes, between 6 and 12 months23155.9
In addition to the confirmatory biopsy, how often do you have new biopsies?Yearly15437.3
Biennial10625.7
Only if PSA levels increase12229.5
If there is a worsening in the imaging exam317.5
In the first 5 years, how often do you evaluate PSA levels?Quarterly13131.7
Half-yearly15136.6
Quarterly in the first two years and half-yearly between 2 and 5 years11728.3
Annually143.4
How often do you perform a digital rectal examination?I do not use routinely327.7
Quarterly419.9
Quarterly in the first two years and half-yearly between 2 and 5 years7518.2
Half-yearly measure14234.4
Annually12329.8
In addition to ultrasound for biopsy, do you use other imaging tests?No9322.5
MRI occasionally17742.9
MRI periodically14334.6

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

Follow-up protocol 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

QuestionN%
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 preference35485.7
Change in rectal examination (worsening of clinical staging)25060.5
Single rising PSA level (PSA > 10 ng/mL)13332.0
Two or more consecutive rising in PSA levels (PSA > 10 ng/mL)22554.5
PSA doubling time < 3 years11026.4
Rising PSA density (> 15%)7818.9
Gleason score upgrading to 7 (3 + 4)22855.2
Gleason score upgrading to 7 (3 + 4) or greater on re-biopsy30373.4
Increased tumor volume on imaging (MRI)16740.4
Higher number of positive cores in re-biopsy (> 1/3)27666.8
Involvement > 50% in at least 1 core in re-biopsy18945.8

MRI magnetic resonance imaging, PSA prostate-specific antigen

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 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

QuestionN%

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 patients51.3
I believe that AS is an inappropriate approach for patients with prostate cancer, even at low or very-low risk123.1
Morbidity associated with multiple biopsies6817.4
Patient does not accept the AS and requests active treatment34488.0
I would like to indicate, but the biopsy performed is inadequate164.1
I would like to indicate, but I do not trust the team responsible for performing the biopsy143.6
I would like to indicate, but the histopathological report does not provide the necessary data174.3
I would like to indicate, but I do not trust the team responsible for the histopathological evaluation205.1
I would like to indicate, but I cannot schedule laboratory tests and/or biopsy and/or outpatient return with the appropriate interval4210.7
Knowledge about index patient Knowledge about index patient *more than one answer was accepted

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, 12–17]. 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, 13–17, 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 [30-32]. 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. Additional file 1. Survey about knowledge, acceptance, and practice of urologists concerning active surveillance for prostate cancer in Brazil.
  29 in total

1.  Extended followup and risk factors for disease reclassification in a large active surveillance cohort for localized prostate cancer.

Authors:  Christopher J Welty; Janet E Cowan; Hao Nguyen; Katsuto Shinohara; Nannette Perez; Kirsten L Greene; June M Chan; Maxwell V Meng; Jeffry P Simko; Matthew R Cooperberg; Peter R Carroll
Journal:  J Urol       Date:  2014-09-28       Impact factor: 7.450

2.  A global knowledge, attitudes and practices survey on anatomical endoscopic enucleation of prostate for benign prostatic hyperplasia among urologists.

Authors:  Kalyan Gudaru; Daniel A Gonzalez Padilla; Daniele Castellani; Leonardo Tortolero Blanco; Yiloren Tanidir; Lo Ka Lun; Marcelo Langer Wroclawski; Pankaj N Maheshwari; Felipe Carvalho A De Figueiredo; Jeremy Yuen-Chun Teoh
Journal:  Andrologia       Date:  2020-06-28       Impact factor: 2.775

Review 3.  The contemporary concept of significant versus insignificant prostate cancer.

Authors:  Guillaume Ploussard; Jonathan I Epstein; Rodolfo Montironi; Peter R Carroll; Manfred Wirth; Marc-Oliver Grimm; Anders S Bjartell; Francesco Montorsi; Stephen J Freedland; Andreas Erbersdobler; Theodorus H van der Kwast
Journal:  Eur Urol       Date:  2011-05-17       Impact factor: 20.096

4.  Contemporary Management of Incident Prostate Cancer in Large Community Urology Practices in the United States.

Authors:  Jeremy B Shelton; Phil Buffington; Richard Augspurger; Franklin Gaylis; Todd Cohen; Bryan Mehlhaff; Ronald Suh; Timothy J Bradford; Lorna Kwan; Alec S Koo; Neal Shore
Journal:  Urology       Date:  2019-04-05       Impact factor: 2.649

5.  Careful selection and close monitoring of low-risk prostate cancer patients on active surveillance minimizes the need for treatment.

Authors:  Mark S Soloway; Cynthia T Soloway; Ahmed Eldefrawy; Kristell Acosta; Bruce Kava; Murugesan Manoharan
Journal:  Eur Urol       Date:  2010-08-20       Impact factor: 20.096

6.  Long-term follow-up of a large active surveillance cohort of patients with prostate cancer.

Authors:  Laurence Klotz; Danny Vesprini; Perakaa Sethukavalan; Vibhuti Jethava; Liying Zhang; Suneil Jain; Toshihiro Yamamoto; Alexandre Mamedov; Andrew Loblaw
Journal:  J Clin Oncol       Date:  2014-12-15       Impact factor: 44.544

7.  Active Surveillance for Intermediate Risk Prostate Cancer: Survival Outcomes in the Sunnybrook Experience.

Authors:  Hima Bindu Musunuru; Toshihiro Yamamoto; Laurence Klotz; Gabriella Ghanem; Alexandre Mamedov; Peraka Sethukavalan; Vibhuti Jethava; Suneil Jain; Liying Zhang; Danny Vesprini; Andrew Loblaw
Journal:  J Urol       Date:  2016-08-26       Impact factor: 7.450

8.  Medium-term outcomes of active surveillance for localised prostate cancer.

Authors:  Elizabeth D Selvadurai; Mausam Singhera; Karen Thomas; Kabir Mohammed; Ruth Woode-Amissah; Alan Horwich; Robert A Huddart; David P Dearnaley; Chris C Parker
Journal:  Eur Urol       Date:  2013-02-18       Impact factor: 20.096

9.  Clinically Localized Prostate Cancer: AUA/ASTRO/SUO Guideline. Part II: Recommended Approaches and Details of Specific Care Options.

Authors:  Martin G Sanda; Jeffrey A Cadeddu; Erin Kirkby; Ronald C Chen; Tony Crispino; Joann Fontanarosa; Stephen J Freedland; Kirsten Greene; Laurence H Klotz; Danil V Makarov; Joel B Nelson; George Rodrigues; Howard M Sandler; Mary Ellen Taplin; Jonathan R Treadwell
Journal:  J Urol       Date:  2018-01-10       Impact factor: 7.450

10.  Impact of COVID-19 on clinical practice, income, health and lifestyle behavior of Brazilian urologists.

Authors:  Cristiano M Gomes; Luciano A Favorito; João Victor T Henriques; Alfredo F Canalini; Karin M J Anzolch; Roni de Carvalho Fernandes; Carlos H S Bellucci; Caroline S Silva; Marcelo L Wroclawski; Antonio Carlos L Pompeo; José de Bessa
Journal:  Int Braz J Urol       Date:  2020 Nov-Dec       Impact factor: 1.541

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