Infection
Conditions
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
Study design
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
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
| Measure | Time frame | Description |
|---|---|---|
| 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-biopsy | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Patient Reporting Biopsy Pain and Discomfort | Immediately following biopsy, 7 days post-biopsy | Patient reported pain via a yes/no questionnaire |
| Change in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale | Immediately following biopsy | Anxiety 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 ≥ 2 | 7 days post-biopsy | 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). |
| Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | 7 days post-biopsy | 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. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| 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 |
| Total | 687 |
Baseline characteristics
| Characteristic | Transrectal | Transperineal | Total |
|---|---|---|---|
| Age, Customized | 66 years | 66 years | 66 years |
| Race/Ethnicity, Customized Hispanic Hispanic ethnicity | 10 Participants | 11 Participants | 21 Participants |
| Race/Ethnicity, Customized Hispanic Unknown | 332 Participants | 334 Participants | 666 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 16 Participants | 12 Participants | 28 Participants |
| Race (NIH/OMB) Black or African American | 44 Participants | 32 Participants | 76 Participants |
| Race (NIH/OMB) More than one race | 15 Participants | 17 Participants | 32 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 99 Participants | 95 Participants | 194 Participants |
| Race (NIH/OMB) White | 168 Participants | 189 Participants | 357 Participants |
| Region of Enrollment United States | 342 Participants | 345 Participants | 687 Participants |
| Sex: Female, Male Female | 0 Participants | 0 Participants | 0 Participants |
| Sex: Female, Male Male | 342 Participants | 345 Participants | 687 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 280 | 0 / 287 |
| other Total, other adverse events | 8 / 280 | 1 / 287 |
| serious Total, serious adverse events | 0 / 280 | 0 / 287 |
Outcome results
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.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Transrectal | 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) | Infection | 1.4 percentage of participants |
| Transrectal | 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) | Urinary Retention | 1.1 percentage of participants |
| Transrectal | 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) | Bleeding requiring intervention | 0.4 percentage of participants |
| Transperineal | 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) | Infection | 0 percentage of participants |
| Transperineal | 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) | Urinary Retention | 0.3 percentage of participants |
| Transperineal | 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) | Bleeding requiring intervention | 0 percentage of participants |
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.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Transrectal | Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | Infection | 4 Participants |
| Transrectal | Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | Urinary Retention | 3 Participants |
| Transrectal | Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | Bleeding requiring intervention | 1 Participants |
| Transperineal | Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | Infection | 0 Participants |
| Transperineal | Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | Urinary Retention | 1 Participants |
| Transperineal | Change in Adverse Events, as Measured on Transrectal Ultrasound Guided Prostate Biopsy Questionnaire (TRUS-BxQ) | Bleeding requiring intervention | 0 Participants |
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.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Transrectal | Change in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale | 4.2 score on a scale | Standard Deviation 2.9 |
| Transperineal | Change in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale | 3.9 score on a scale | Standard Deviation 3 |
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.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Transrectal | Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2 | Gleason grade group ≥ 2 | 141 Participants |
| Transrectal | Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2 | Gleason grade group 1 | 62 Participants |
| Transrectal | Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2 | No Gleason Score | 77 Participants |
| Transperineal | Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2 | Gleason grade group ≥ 2 | 151 Participants |
| Transperineal | Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2 | Gleason grade group 1 | 49 Participants |
| Transperineal | Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2 | No Gleason Score | 87 Participants |
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.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Transrectal | Percentage of Patient Reporting Biopsy Pain and Discomfort | Immediately following biopsy - pain | 3.0 percentage of participants |
| Transrectal | Percentage of Patient Reporting Biopsy Pain and Discomfort | Immediately following biopsy - discomfort | 3.8 percentage of participants |
| Transrectal | Percentage of Patient Reporting Biopsy Pain and Discomfort | 7-day post biopsy - pain | 3.6 percentage of participants |
| Transrectal | Percentage of Patient Reporting Biopsy Pain and Discomfort | 7-day post biopsy - discomfort | 1.7 percentage of participants |
| Transperineal | Percentage of Patient Reporting Biopsy Pain and Discomfort | 7-day post biopsy - discomfort | 2.0 percentage of participants |
| Transperineal | Percentage of Patient Reporting Biopsy Pain and Discomfort | Immediately following biopsy - pain | 3.7 percentage of participants |
| Transperineal | Percentage of Patient Reporting Biopsy Pain and Discomfort | 7-day post biopsy - pain | 4.5 percentage of participants |
| Transperineal | Percentage of Patient Reporting Biopsy Pain and Discomfort | Immediately following biopsy - discomfort | 4.2 percentage of participants |