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PReclude Infection EVEnts With No Prophylaxis Transperineal Biopsy

Evaluation of Transperineal Biopsy Under Local Anesthesia, a Novel Approach to Decrease Post-Biopsy Infections and Improve Cancer Detection

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04843566
Acronym
PREVENT
Enrollment
687
Registered
2021-04-13
Start date
2021-03-22
Completion date
2024-04-19
Last updated
2025-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infection

Keywords

prostate cancer, prostate biopsy, biopsy infection, fusion biopsy, MRI-targeted biopsy, transperineal, transrectal

Brief summary

Approximately one million transrectal prostate biopsies are performed annually in the U.S., and the risk of post- biopsy infection is increasing due to greater antibiotic resistance of rectal flora. Preliminary data demonstrates that a transperineal MRI-targeted biopsy approach under local anesthesia compared to the standard practice transrectal MRI-targeted prostate biopsy has a much lower risk of infection, comparable pain/discomfort and may improve detection of prostate cancer. This randomized controlled trial will be the first prospective study to evaluate in-office transperineal MRI targeted prostate biopsy. The investigators hypothesize that a transperineal MRI-targeted biopsy approach under local anesthesia compared to the standard practice transrectal MRI-targeted prostate biopsy has a much lower risk of infection, comparable pain/discomfort and may improve detection of prostate cancer.

Detailed description

Prostate cancer is the most commonly diagnosed malignancy in U.S. men. There are approximately 1 million prostate biopsy performed annually in the U.S. Almost all biopsies are performed as an office based procedure in under 15 minutes. The precision of biopsy has improved over the last decade with the introduction of MRI guidance/targeting of suspicious lesions within the prostate. However, significant limitations remain with this approach, including a significantly increasing risk of post-biopsy infection. This arises because more than 97% of all prostate biopsy are performed via a transrectal approach that introduces rectal bacteria with each pass of the biopsy needle into the sterile urinary tract. The current risk of post-transrectal biopsy infection, even with antimicrobial prophylaxis, is high at approximately 7% overall with 3% (30,000 men) requiring hospitalization annually. Transperineal biopsy is an alternate approach that eliminates the direct introduction of bacteria from the rectum to the prostate. This approach, which is performed without antimicrobial prophylaxis, instead passes the biopsy needle through the perineal skin and pelvic floor. Transperineal biopsy has not been widely adopted for several reasons. Historically, it has been considered too painful for patients in the clinic and thus was traditionally performed under general anesthesia. The added time, inconvenience and cost has limited its national adoptance. Second, when transrectal biopsy was initially adopted over 40 years ago, antibiotic resistance of rectal flora was not a challenge. Beyond the potential for in-office transperineal biopsy to significantly reduce or eliminate biopsy infections, transperineal biopsy may also improve cancer detection: studies of transperineal biopsy (performed under general anesthesia) demonstrate higher detection rates for prostate cancer, particularly for anterior zone tumors, compared to transrectal biopsy. This is notable, as anterior tumors are difficult to sample with transrectal. Anterior tumors are also twice as likely to occur in African American men. In fact, our research demonstrates that some of the outcomes disparities in African American men may stem from an underdiagnosis of anterior prostate cancers. Although transrectal biopsy is used widely, it is associated with a significant and increasing risk of biopsy infections due to growing antibiotic resistance, highlighting the urgent need for a safer alternative approach to prostate biopsy. The study investigators have refined a transperineal approach under local anesthesia with MRI-targeting/guidance without the need for antibiotic prophylaxis. The investigators hypothesize that transperineal MRI targeted biopsy will: (1) largely eliminate post-biopsy infections and costly hospitalizations for urosepsis; (2) be performed in the office with similar discomfort and non-infectious complications compared to transrectal MRI targeted biopsy; and (3) have significantly better detection of prostate cancer. This multi-center randomized controlled trial will be conducted to evaluate in-office transperineal MRI targeted vs. transrectal MRI targeted biopsy, the current gold standard. This has transformative impact to change current standard of practice.

Interventions

Transperineal prostate biopsy will be performed under local anesthesia in the office. This approach avoids transrectal needle tracking.

Transrectal prostate biopsy is currently the most popular approach to evaluate a positive screening test for prostate cancer.

For men undergoing transrectal biopsy, antibiotic prophylaxis will be administered in accordance with guidelines from the American Urological Association (AUA). No antibiotic prophylaxis will be administered for men undergoing transperineal biopsy.

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Masking description

Radiologists assessing MRI results are blinded to treatment assignment. Pathologists assessing biopsy results are blinded to treatment assignment.

Intervention model description

Men enrolled in this prospective, randomized trial will be randomized in a 1:1 ratio to receive either transperineal MRI-targeted or transrectal MRI-targeted prostate biopsy.

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male sex * Age ≥18 years * Men without previous prostate biopsy (first time prostate biopsy) * Willingness to sign informed consent and adhere to the study protocol

Exclusion criteria

* Acute prostatitis within the last 6 months * PSA \> 20 ng/mL in men who have previously undergone prostate biopsy * Current non-urologic bacterial infection requiring active treatment with antibiotics * Unfit to undergo prostate biopsy under local anesthesia * Prior definitive therapy for prostate cancer, such as radiation therapy or partial gland ablation * Men who have previously undergone prostate biopsy in whom artifact would reduce quality of prostate MRI (extensive orthopedic pelvic metal) * Contraindication to prostate MRI (claustrophobia, pacemaker, chronic kidney disease) in men who have previously undergone prostate biopsy

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)7 days post-biopsyOutcome measure Description Now says: Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) is a validated biopsy questionnaire that measures adverse events that have occurred due to infection. Patient questionnaires that reported infection complications and duration of symptoms, had their electronic medical records verified to confirm if an infection occurred or not.

Secondary

MeasureTime frameDescription
Percentage of Patient Reporting Biopsy Pain and DiscomfortImmediately following biopsy, 7 days post-biopsyPatient reported pain via a yes/no questionnaire
Change in Patient-reported Anxiety, as Measured on a 0-10 Likert ScaleImmediately following biopsyAnxiety will be scored on a 0-10 Likert scale. 0 indicates no anxiety and high scores indicate greater anxiety.
Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 27 days post-biopsyGleason Grade Group is a prostate cancer grading system released by the International Society of Urological Pathology (ISUP). Grade Group 1 indicates Low/Very Low Risk, Grade Group 2 indicates Intermediate (Favorable) Risk, Grade Group 3 indicates Intermediate (Unfavorable) Risk, and Grade Groups 4 and 5 indicate High/Very High Risk. Prostate cancer grade will be categorized into insignificant (Gleason Grade Group 1) and clinically significant (Grade Group ≥ 2).
Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)7 days post-biopsyTransrectal Ultrasound Guided prostate Biopsy Questionnaire (TRUS-BxQ) is a validated biopsy questionnaire that measures adverse events that have occurred, such as hospital re-admissions, aborted procedures due to discomfort, hematuria, urinary retention, hematospermia, and/or hematochezia. Patient questionnaire consists of Yes/No questions about general complications and duration of adverse events.

Countries

United States

Participant flow

Participants by arm

ArmCount
Transrectal
Patients will receive a transrectal MRI-guided prostate biopsy. Transrectal MRI-guided prostate biopsy: Transrectal prostate biopsy is currently the most popular approach to evaluate a positive screening test for prostate cancer. Antibiotic (prophylaxis): For men undergoing transrectal biopsy, antibiotic prophylaxis will be administered in accordance with guidelines from the American Urological Association (AUA). No antibiotic prophylaxis will be administered for men undergoing transperineal biopsy.
342
Transperineal
Patients will receive a transperineal MRI-guided prostate biopsy. Transperineal MRI-guided prostate biopsy: Transperineal prostate biopsy will be performed under local anesthesia in the office. This approach avoids transrectal needle tracking.
345
Total687

Baseline characteristics

CharacteristicTransrectalTransperinealTotal
Age, Customized66 years66 years66 years
Race/Ethnicity, Customized
Hispanic
Hispanic ethnicity
10 Participants11 Participants21 Participants
Race/Ethnicity, Customized
Hispanic
Unknown
332 Participants334 Participants666 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
16 Participants12 Participants28 Participants
Race (NIH/OMB)
Black or African American
44 Participants32 Participants76 Participants
Race (NIH/OMB)
More than one race
15 Participants17 Participants32 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
99 Participants95 Participants194 Participants
Race (NIH/OMB)
White
168 Participants189 Participants357 Participants
Region of Enrollment
United States
342 Participants345 Participants687 Participants
Sex: Female, Male
Female
0 Participants0 Participants0 Participants
Sex: Female, Male
Male
342 Participants345 Participants687 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 2800 / 287
other
Total, other adverse events
8 / 2801 / 287
serious
Total, serious adverse events
0 / 2800 / 287

Outcome results

Primary

Percentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)

Outcome measure Description Now says: Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) is a validated biopsy questionnaire that measures adverse events that have occurred due to infection. Patient questionnaires that reported infection complications and duration of symptoms, had their electronic medical records verified to confirm if an infection occurred or not.

Time frame: 7 days post-biopsy

Population: Subjects in the transrectal arm that underwent a transperineal biopsy or withdrew were excluded from analysis. Subjects in the transperineal arm that underwent a transrectal biopsy or withdrew were excluded from analysis.

ArmMeasureGroupValue (NUMBER)
TransrectalPercentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Infection1.4 percentage of participants
TransrectalPercentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Urinary Retention1.1 percentage of participants
TransrectalPercentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Bleeding requiring intervention0.4 percentage of participants
TransperinealPercentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Infection0 percentage of participants
TransperinealPercentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Urinary Retention0.3 percentage of participants
TransperinealPercentage of Subjects That Experienced Infection, Urinary Retention or Bleeding Requiring Intervention Within 7 Days of Biopsy Based on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Bleeding requiring intervention0 percentage of participants
Comparison: Infectionp-value: 0.04Fisher Exact
Comparison: Urinary retentionp-value: 0.3Fisher Exact
Comparison: Bleeding requiring interventionp-value: 0.31Fisher Exact
Secondary

Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)

Transrectal Ultrasound Guided prostate Biopsy Questionnaire (TRUS-BxQ) is a validated biopsy questionnaire that measures adverse events that have occurred, such as hospital re-admissions, aborted procedures due to discomfort, hematuria, urinary retention, hematospermia, and/or hematochezia. Patient questionnaire consists of Yes/No questions about general complications and duration of adverse events.

Time frame: 7 days post-biopsy

Population: Subjects in the transrectal arm that underwent a transperineal biopsy or withdrew were excluded from analysis. Subjects in the transperineal arm that underwent a transrectal biopsy or withdrew were excluded from analysis.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
TransrectalChange in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Infection4 Participants
TransrectalChange in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Urinary Retention3 Participants
TransrectalChange in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Bleeding requiring intervention1 Participants
TransperinealChange in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Infection0 Participants
TransperinealChange in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Urinary Retention1 Participants
TransperinealChange in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ)Bleeding requiring intervention0 Participants
Comparison: Infectionp-value: 0.04Fisher Exact
Comparison: Urinary retentionp-value: 0.3Fisher Exact
Comparison: Bleeding requiring interventionp-value: 0.31Fisher Exact
Secondary

Change in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale

Anxiety will be scored on a 0-10 Likert scale. 0 indicates no anxiety and high scores indicate greater anxiety.

Time frame: Immediately following biopsy

Population: Subjects in the transrectal arm that underwent a transperineal biopsy or withdrew were excluded from analysis. Subjects in the transperineal arm that underwent a transrectal biopsy or withdrew were excluded from analysis. Any subject that didn't complete a questionnaire was excluded from analysis.

ArmMeasureValue (MEAN)Dispersion
TransrectalChange in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale4.2 score on a scaleStandard Deviation 2.9
TransperinealChange in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale3.9 score on a scaleStandard Deviation 3
p-value: 0.23t-test, 2 sided
Secondary

Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2

Gleason Grade Group is a prostate cancer grading system released by the International Society of Urological Pathology (ISUP). Grade Group 1 indicates Low/Very Low Risk, Grade Group 2 indicates Intermediate (Favorable) Risk, Grade Group 3 indicates Intermediate (Unfavorable) Risk, and Grade Groups 4 and 5 indicate High/Very High Risk. Prostate cancer grade will be categorized into insignificant (Gleason Grade Group 1) and clinically significant (Grade Group ≥ 2).

Time frame: 7 days post-biopsy

Population: Subjects in the transrectal arm that underwent a transperineal biopsy or withdrew were excluded from analysis. Subjects in the transperineal arm that underwent a transrectal biopsy or withdrew were excluded from analysis.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
TransrectalDetection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2Gleason grade group ≥ 2141 Participants
TransrectalDetection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2Gleason grade group 162 Participants
TransrectalDetection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2No Gleason Score77 Participants
TransperinealDetection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2Gleason grade group ≥ 2151 Participants
TransperinealDetection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2Gleason grade group 149 Participants
TransperinealDetection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2No Gleason Score87 Participants
Comparison: Gleason grade \>=2p-value: 0.59Chi-squared
Secondary

Percentage of Patient Reporting Biopsy Pain and Discomfort

Patient reported pain via a yes/no questionnaire

Time frame: Immediately following biopsy, 7 days post-biopsy

Population: Subjects in the transrectal arm that underwent a transperineal biopsy or withdrew were excluded from analysis. Subjects in the transperineal arm that underwent a transrectal biopsy or withdrew were excluded from analysis. Any subject that didn't complete a questionnaire was excluded from analysis.

ArmMeasureGroupValue (NUMBER)
TransrectalPercentage of Patient Reporting Biopsy Pain and DiscomfortImmediately following biopsy - pain3.0 percentage of participants
TransrectalPercentage of Patient Reporting Biopsy Pain and DiscomfortImmediately following biopsy - discomfort3.8 percentage of participants
TransrectalPercentage of Patient Reporting Biopsy Pain and Discomfort7-day post biopsy - pain3.6 percentage of participants
TransrectalPercentage of Patient Reporting Biopsy Pain and Discomfort7-day post biopsy - discomfort1.7 percentage of participants
TransperinealPercentage of Patient Reporting Biopsy Pain and Discomfort7-day post biopsy - discomfort2.0 percentage of participants
TransperinealPercentage of Patient Reporting Biopsy Pain and DiscomfortImmediately following biopsy - pain3.7 percentage of participants
TransperinealPercentage of Patient Reporting Biopsy Pain and Discomfort7-day post biopsy - pain4.5 percentage of participants
TransperinealPercentage of Patient Reporting Biopsy Pain and DiscomfortImmediately following biopsy - discomfort4.2 percentage of participants
Comparison: Immediately following biopsy - Painp-value: 0.002t-test, 2 sided
Comparison: Immediately following biopsy - Discomfortp-value: 0.05t-test, 2 sided
Comparison: 7-day post biopsy - Painp-value: <0.0001t-test, 2 sided
Comparison: 7-day post biopsy - Discomfortp-value: 0.07t-test, 2 sided

Source: ClinicalTrials.gov · Data processed: Apr 28, 2026