Материал: Oxford American Handbook of Urology ( PDFDrive )

Внимание! Если размещение файла нарушает Ваши авторские права, то обязательно сообщите нам

202 CHAPTER 6 Urological neoplasia

Prostate cancer: transrectal ultrasonography and biopsies

The most common diagnostic modality for prostate cancer is currently transrectal ultrasonography (TRUS) with guided biopsies (Fig. 6.1). TRUS provides imaging of the prostate and seminal vesicles using a 7.5 mHz biplane intrarectal probe measuring approximately 1.5 cm in diameter.

While TRUS imaging may be performed for other reasons (e.g., evaluation of infertility, sizing for treatment planning), a TRUS without biopsy is considered an inadequate way to evaluate for prostate cancer. Many advocate use of an enema before the biopsy to enhance visualization.

The ultrasound-guided periprostatic injection of local anesthetic (1% lidocaine) has become the standard in the United States when biopsy is planned. Rarely, general or regional anesthesia may be necessary, especially in the presence of anal stenosis or if saturation (>20) biopsies are planned.

A careful DRE precedes insertion of the probe. Broad-spectrum antimicrobials (e.g., quinolone antibiotic) are given before and after the procedure.

TRUS can image the outline of the prostate, cysts, abscesses, and calcifications within the prostate. Hypoechoic and hyperechoic lesions in the peripheral zone may be due to prostate cancer or inflammatory conditions, although most prostate cancers are in fact isoechoic and are not visualized on ultrasound.

Advanced biopsy techniques that use microbubble contrast agents with and without color Doppler are being actively investigated to improve yield. There are no convincing data that color Doppler alone can improve the yield of prostate biopsy over the standard grayscale biopsy.

Indications for TRUS without biopsy

•Accurate measurement of prostate volume for treatment planning (e.g., microwave, needle ablation, brachytherapy)

•Male infertility with azoospermia, to look for seminal vesicle and ejaculatory duct obstruction due to calculus or Müllerian cyst

•Suspected prostatic abscess (can be drained by needle aspiration)

•Investigation of chronic pelvic pain, looking for prostatic cyst or calculi

Indications for TRUS with biopsies

•An abnormal DRE and/or an elevated PSA (exceptions include very elderly men with massively elevated PSA and abnormal DRE, or those in whom a TURP is indicated for severe LUTS/retention where histology will be obtained). See Table 6.1 (p. 199).

•Previous biopsies showing multifocal high-grade PIN or ASAP

•Previous biopsies normal, but PSA rising or DRE abnormal

•To confirm viable prostate cancer following treatment if further treatment is being considered

PROSTATE CANCER: TRANSRECTAL ULTRASONOGRAPHY & BIOPSIES 203

 

Pubic

Urethra

Bladder

symphysis

 

 

Prostate

Peritoneum

 

gland

 

 

 

 

Biopsy

 

 

needle

 

 

Spring-loaded

 

 

biopsy needle

 

 

‘gun’

Seminal

Rectum

Ultrasound

vesicles

 

probe

Figure 6.1 Transrectal ultrasound scanning (TRUS). An ultrasound probe is inserted into the rectum to guide the biopsy needle into the correct position so that multiple core biopsies can be taken from different areas of the prostate.

Biopsy protocol

Ten to 12 18 French Tru-Cut needle biopsies are taken in a systematic fashion to include any palpable or sonographic target lesion. The traditional sextant protocol (a parasagittal base, mid-gland, and apex from each side) is no longer considered an adequate technique. To the 10–12 biopsy regimen, add samples from the far lateral peripheral zones (Fig. 6.2). Studies have demonstrated that these extra biopsies detect up to 15% more cancers.

Additional biopsies of each transition zone may be taken if a transition zone cancer is suspected or if a patient is undergoing repeat biopsies due to a rising PSA. Seminal vesicles biopsies occasionally add staging information if they appear abnormal on DRE, TRUS, or MRI.

Complications of prostatic biopsy

•Occasional vasovagal reaction (fainting) immediately after procedure

•Small risk of urinary tract infection and rarely urosepsis, which may be life threatening

•Small risk of significant rectal bleeding

•Mild hemospermia or hematuria, for several weeks after the procedure

Prostate cancer may also be diagnosed by transurethral resection of the prostate (TURP) histology or clinically (without histology) in certain circumstances. For example, it could be viewed as unnecessarily invasive to biopsy an elderly and frail symptomatic patient with a rock-hard prostate and a PSA of >100 ng/mL prior to commencing hormone therapy.

204 CHAPTER 6 Urological neoplasia

Box 6.2

It is not safe to biopsy a patient who is anticoagulated on warfarin; biopsying patients on low-dose aspirin remains controversial but is not considered unsafe by many. Other antiplatelet drugs (e.g., clopidogrel) are usually stopped for 7–10 days prior to biopsy.

It is important that the patient appreciates that negative biopsies do not exclude the possibility of prostate cancer, and that a positive result will not necessarily result in the recommendation of immediate treatment.

 

Seminal vesicles

(a)

 

 

Base

Posterior

Traditional

surface of

sextant

prostate

 

 

Apex

(b)

8-core

(c)

12-core

Figure 6.2 Biopsy protocols. A 10to 12-core biopsy regimen is considered the standard of care today. Obtaining 4 apical cores can often be difficult.

This page intentionally left blank

206 CHAPTER 6 Urological neoplasia

Prostate cancer staging

Tumor staging uses the most current 2002 TNM (tumor, nodes, malignancy) classification (see Table 6.2 and Fig. 6.3). As with all cancer, prostate cancer staging may be considered clinical (prefixed with c) or pathological (prefixed with p), dependent on available data. (Note: In 2010 the American Joint Committee on Cancer (AJCC) will begin to incorporate PSA and Gleason Score into the staging system for prostate cancer.)

Tstage

Tstage is assessed primarily by digital rectal examination (see Fig. 6.3). Current imaging resolution limits reliability in detection of focal and microscopic extraprostatic extension of disease by means of MRI or TRUS. Recent prostatic biopsy may also confuse the interpretation of MRI images, particularly regarding the seminal vesicles.

Table 6.2 TNM (2002) staging of adenocarcinoma of the prostate

 

 

T0

No tumor (pT0 if no cancer found by histological examination)

 

 

Tx

T stage uncertain

 

 

 

 

T1a

Cancer nonpalpable on digital rectal examination (DRE), present

 

 

 

in <5% of TURP specimens (in up to 18% of TURPs)

 

 

T1b

Cancer nonpalpable on DRE, present in >5% of TURP specimens

 

 

T1c

Cancer nonpalpable on DRE, present in needle biopsy taken

 

 

 

because of elevated PSA

 

 

T2a

Palpable tumor, feels confined, in <half of one lobe on DRE

 

 

T2b

Palpable tumor, feels confined, in >half of one lobe on DRE

 

 

T2c

Palpable tumor, feels confined, in both lobes on DRE

 

 

T3a

Palpable tumor, locally advanced into periprostatic fat, unior

 

 

 

bilateral and mobile on DRE

 

 

T3b

Palpable tumor, locally advanced into seminal vesicle(s) on DRE

 

 

T4a

Palpable tumor, locally advanced into adjacent structures, feels

 

 

 

fixed on DRE

 

 

T4b

Palpable tumor, locally advanced into pelvic side-wall, feels fixed

 

 

 

on DRE

 

 

Nx

Regional lymph not assessed

 

 

N0

No regional lymph node metastasis

 

 

N1

Tumor involves regional (pelvic) lymph nodes

 

 

Mx

Distant metastases not assessed

 

 

M0

No distant metastasis

 

 

M1a

Nonregional lymph node metastasis

 

 

M1b

Tumor metastasis in bone

 

 

M1c

Tumor metastasis in other sites

 

 

 

 

Источник: https://studfile.net/preview/16690383/