Evaluation of DD23 as a marker for detection of recurrent transitional cell carcinoma of the bladder in patients with a history of bladder cancer

To determine whether DD23 increases the sensitivity of urinary-based detection of transitional cell carcinoma (TCC) recurrence. The murine monoclonal antibody DD23 recognizes a 185-kDa tumor-associated antigen that is expressed in human bladder cancer cells in vitro and in vivo but is not detected i...

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Veröffentlicht in:Urology (Ridgewood, N.J.) N.J.), 2003-03, Vol.61 (3), p.539-543
Hauptverfasser: Gilbert, Scott M, Veltri, Robert W, Sawczuk, Alex, Shabsigh, Ahmad, Knowles, David R, Bright, Steven, O’Dowd, Gerald J, Olsson, Carl A, Benson, Mitchell C, Sawczuk, Ihor S
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container_end_page 543
container_issue 3
container_start_page 539
container_title Urology (Ridgewood, N.J.)
container_volume 61
creator Gilbert, Scott M
Veltri, Robert W
Sawczuk, Alex
Shabsigh, Ahmad
Knowles, David R
Bright, Steven
O’Dowd, Gerald J
Olsson, Carl A
Benson, Mitchell C
Sawczuk, Ihor S
description To determine whether DD23 increases the sensitivity of urinary-based detection of transitional cell carcinoma (TCC) recurrence. The murine monoclonal antibody DD23 recognizes a 185-kDa tumor-associated antigen that is expressed in human bladder cancer cells in vitro and in vivo but is not detected in normal urothelium. Using alcohol-fixed urinary cytology, matched voided urine and bladder wash specimens were evaluated for the contribution of DD23 antigen expression in the detection of recurrent TCC. The selected patient population had a history of bladder cancer, and urine cytology analysis was performed in a single commercial reference laboratory. DD23 antigen expression in a cohort of 81 patients was compared with urine cytology findings, and the sensitivity and specificity for each urine-based test was determined. The presence of recurrent disease was determined by positive pathologic biopsy. The 81-patient cohort produced 151 urine specimens for which both biopsy and cytology information were obtained. Of these specimens, 64 were confirmed by a tissue diagnosis for TCC recurrence. These biopsy-proven recurrences were used as the dependent variable to assess the accuracy of cytology testing. For the detection of TCC, the DD23 antigen had a sensitivity of 70.3% and a specificity of 59.8%. Combined with cytopathologic findings, DD23 enhanced the sensitivity for the detection of TCC from 43.8% (cytology alone) to 78.1%. For low-grade TCC (n = 20) DD23 enhanced the sensitivity from 20.0% (cytology alone) to 55.0%. For high-grade TCC (n = 25), DD23 enhanced the sensitivity from 64.0% (cytology alone) to 76.0%. In patients with a prior history of intravesical treatment, DD23 had a sensitivity of 94.7% and a specificity of 33.3% compared with a sensitivity of 52.6% and a specificity of 83.3% for cytology. DD23 antigen expression can be used as an adjunct to cytopathologic evaluation to enhance the sensitivity of urinary cytology detection of TCC. In addition, DD23 does not appear to lose sensitivity in patients with a prior history of bladder cancer treated with intravesical agents.
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The murine monoclonal antibody DD23 recognizes a 185-kDa tumor-associated antigen that is expressed in human bladder cancer cells in vitro and in vivo but is not detected in normal urothelium. Using alcohol-fixed urinary cytology, matched voided urine and bladder wash specimens were evaluated for the contribution of DD23 antigen expression in the detection of recurrent TCC. The selected patient population had a history of bladder cancer, and urine cytology analysis was performed in a single commercial reference laboratory. DD23 antigen expression in a cohort of 81 patients was compared with urine cytology findings, and the sensitivity and specificity for each urine-based test was determined. The presence of recurrent disease was determined by positive pathologic biopsy. The 81-patient cohort produced 151 urine specimens for which both biopsy and cytology information were obtained. Of these specimens, 64 were confirmed by a tissue diagnosis for TCC recurrence. These biopsy-proven recurrences were used as the dependent variable to assess the accuracy of cytology testing. For the detection of TCC, the DD23 antigen had a sensitivity of 70.3% and a specificity of 59.8%. Combined with cytopathologic findings, DD23 enhanced the sensitivity for the detection of TCC from 43.8% (cytology alone) to 78.1%. For low-grade TCC (n = 20) DD23 enhanced the sensitivity from 20.0% (cytology alone) to 55.0%. For high-grade TCC (n = 25), DD23 enhanced the sensitivity from 64.0% (cytology alone) to 76.0%. In patients with a prior history of intravesical treatment, DD23 had a sensitivity of 94.7% and a specificity of 33.3% compared with a sensitivity of 52.6% and a specificity of 83.3% for cytology. DD23 antigen expression can be used as an adjunct to cytopathologic evaluation to enhance the sensitivity of urinary cytology detection of TCC. 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Urinary tract diseases ; Prospective Studies ; Sensitivity and Specificity ; Therapeutic Irrigation ; Tumors of the urinary system ; Urinalysis - methods ; Urinary Bladder - cytology ; Urinary Bladder - pathology ; Urinary Bladder Neoplasms - diagnosis ; Urinary Bladder Neoplasms - immunology ; Urinary Bladder Neoplasms - urine ; Urinary tract. 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The murine monoclonal antibody DD23 recognizes a 185-kDa tumor-associated antigen that is expressed in human bladder cancer cells in vitro and in vivo but is not detected in normal urothelium. Using alcohol-fixed urinary cytology, matched voided urine and bladder wash specimens were evaluated for the contribution of DD23 antigen expression in the detection of recurrent TCC. The selected patient population had a history of bladder cancer, and urine cytology analysis was performed in a single commercial reference laboratory. DD23 antigen expression in a cohort of 81 patients was compared with urine cytology findings, and the sensitivity and specificity for each urine-based test was determined. The presence of recurrent disease was determined by positive pathologic biopsy. The 81-patient cohort produced 151 urine specimens for which both biopsy and cytology information were obtained. Of these specimens, 64 were confirmed by a tissue diagnosis for TCC recurrence. 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Urinary tract diseases</subject><subject>Prospective Studies</subject><subject>Sensitivity and Specificity</subject><subject>Therapeutic Irrigation</subject><subject>Tumors of the urinary system</subject><subject>Urinalysis - methods</subject><subject>Urinary Bladder - cytology</subject><subject>Urinary Bladder - pathology</subject><subject>Urinary Bladder Neoplasms - diagnosis</subject><subject>Urinary Bladder Neoplasms - immunology</subject><subject>Urinary Bladder Neoplasms - urine</subject><subject>Urinary tract. 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Prostate gland</topic><topic>Urine - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gilbert, Scott M</creatorcontrib><creatorcontrib>Veltri, Robert W</creatorcontrib><creatorcontrib>Sawczuk, Alex</creatorcontrib><creatorcontrib>Shabsigh, Ahmad</creatorcontrib><creatorcontrib>Knowles, David R</creatorcontrib><creatorcontrib>Bright, Steven</creatorcontrib><creatorcontrib>O’Dowd, Gerald J</creatorcontrib><creatorcontrib>Olsson, Carl A</creatorcontrib><creatorcontrib>Benson, Mitchell C</creatorcontrib><creatorcontrib>Sawczuk, Ihor S</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gilbert, Scott M</au><au>Veltri, Robert W</au><au>Sawczuk, Alex</au><au>Shabsigh, Ahmad</au><au>Knowles, David R</au><au>Bright, Steven</au><au>O’Dowd, Gerald J</au><au>Olsson, Carl A</au><au>Benson, Mitchell C</au><au>Sawczuk, Ihor S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of DD23 as a marker for detection of recurrent transitional cell carcinoma of the bladder in patients with a history of bladder cancer</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>61</volume><issue>3</issue><spage>539</spage><epage>543</epage><pages>539-543</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><coden>URGYAZ</coden><abstract>To determine whether DD23 increases the sensitivity of urinary-based detection of transitional cell carcinoma (TCC) recurrence. The murine monoclonal antibody DD23 recognizes a 185-kDa tumor-associated antigen that is expressed in human bladder cancer cells in vitro and in vivo but is not detected in normal urothelium. Using alcohol-fixed urinary cytology, matched voided urine and bladder wash specimens were evaluated for the contribution of DD23 antigen expression in the detection of recurrent TCC. The selected patient population had a history of bladder cancer, and urine cytology analysis was performed in a single commercial reference laboratory. DD23 antigen expression in a cohort of 81 patients was compared with urine cytology findings, and the sensitivity and specificity for each urine-based test was determined. The presence of recurrent disease was determined by positive pathologic biopsy. The 81-patient cohort produced 151 urine specimens for which both biopsy and cytology information were obtained. Of these specimens, 64 were confirmed by a tissue diagnosis for TCC recurrence. These biopsy-proven recurrences were used as the dependent variable to assess the accuracy of cytology testing. For the detection of TCC, the DD23 antigen had a sensitivity of 70.3% and a specificity of 59.8%. Combined with cytopathologic findings, DD23 enhanced the sensitivity for the detection of TCC from 43.8% (cytology alone) to 78.1%. For low-grade TCC (n = 20) DD23 enhanced the sensitivity from 20.0% (cytology alone) to 55.0%. For high-grade TCC (n = 25), DD23 enhanced the sensitivity from 64.0% (cytology alone) to 76.0%. In patients with a prior history of intravesical treatment, DD23 had a sensitivity of 94.7% and a specificity of 33.3% compared with a sensitivity of 52.6% and a specificity of 83.3% for cytology. DD23 antigen expression can be used as an adjunct to cytopathologic evaluation to enhance the sensitivity of urinary cytology detection of TCC. In addition, DD23 does not appear to lose sensitivity in patients with a prior history of bladder cancer treated with intravesical agents.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12639642</pmid><doi>10.1016/S0090-4295(02)02400-7</doi><tpages>5</tpages></addata></record>
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ispartof Urology (Ridgewood, N.J.), 2003-03, Vol.61 (3), p.539-543
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Administration, Intravesical
Animals
Antibodies, Monoclonal
Antigens, Neoplasm - immunology
Antigens, Neoplasm - urine
Antineoplastic Agents - administration & dosage
Biological and medical sciences
Biomarkers, Tumor - urine
Carcinoma, Transitional Cell - diagnosis
Carcinoma, Transitional Cell - immunology
Carcinoma, Transitional Cell - urine
Cystoscopy
Female
Humans
Male
Medical sciences
Mice
Mice, Inbred BALB C
Neoplasm Recurrence, Local - diagnosis
Neoplasm Recurrence, Local - urine
Nephrology. Urinary tract diseases
Prospective Studies
Sensitivity and Specificity
Therapeutic Irrigation
Tumors of the urinary system
Urinalysis - methods
Urinary Bladder - cytology
Urinary Bladder - pathology
Urinary Bladder Neoplasms - diagnosis
Urinary Bladder Neoplasms - immunology
Urinary Bladder Neoplasms - urine
Urinary tract. Prostate gland
Urine - cytology
title Evaluation of DD23 as a marker for detection of recurrent transitional cell carcinoma of the bladder in patients with a history of bladder cancer
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