Skip to main content
Erschienen in: Virchows Archiv 2/2021

03.04.2021 | Original Article

Performance comparison of anti-p504s (SP116) Rabbit Monoclonal Primary Antibody vs. Monoclonal Rabbit Anti-Human AMACR clone 13H4 when duplexed with VENTANA Basal Cell Cocktail (34βE12+p63) as a diagnostic aid for prostatic adenocarcinoma using immunohistochemistry

verfasst von: Veronique Lindner, Anne Waydelich, Chen Chun Chen, Carol Jones, Steven P. Stratton

Erschienen in: Virchows Archiv | Ausgabe 2/2021

Einloggen, um Zugang zu erhalten

Abstract

Alpha-methylacyl-coenzyme A-racemase (AMACR), also known as p504s, is overexpressed in prostatic adenocarcinoma and is frequently used in combination with basal cell markers to aid in diagnosing difficult prostate adenocarcinoma cases. In this retrospective method comparison study, we examined the sensitivity and specificity of the ready-to-use anti-p504s (SP116) Rabbit Monoclonal Primary Antibody compared to the monoclonal rabbit anti-human AMACR clone 13H4 in prostatic adenocarcinoma samples. De-identified prostatic adenocarcinoma tissue samples were stained with either the SP116 or 13H4 antibody clone in combination with the VENTANA Basal Cell Cocktail (34βE12+p63) and scored as positive or negative for prostatic adenocarcinoma. The scoring pathologist was blinded to the known historical diagnosis of each sample. The scoring pathologist correctly diagnosed each sample regardless of which p504s clone was used. Both assays using either clone were 100% concordant in their sensitivity and specificity. This study demonstrates that the ready-to-use anti-p504s (SP116) Rabbit Monoclonal Primary Antibody is equivalent to clone 13H4 concentrate when used according to package insert instructions in combination with the VENTANA Basal Cell Cocktail (34βE12+p63) to aid pathologists in the diagnosis of prostatic adenocarcinoma.
Literatur
1.
Zurück zum Zitat Howlader N, Noone A, Krapcho M, Neyman N, Aminou R, Waldron W, Altekruse S, Kosary C, Ruhl J, Tatalovich Z (2011) SEER cancer statistics review, 1975-2008. National Cancer Institute, Bethesda Howlader N, Noone A, Krapcho M, Neyman N, Aminou R, Waldron W, Altekruse S, Kosary C, Ruhl J, Tatalovich Z (2011) SEER cancer statistics review, 1975-2008. National Cancer Institute, Bethesda
2.
Zurück zum Zitat Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A (2018) Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68(6):394–424CrossRef Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A (2018) Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68(6):394–424CrossRef
3.
Zurück zum Zitat Siegel RL, Miller KD, Goding Sauer A, Fedewa SA, Butterly LF, Anderson JC, Cercek A, Smith RA, Jemal A (2020) Colorectal cancer statistics, 2020. CA Cancer J Clin 70(3):145–164 Siegel RL, Miller KD, Goding Sauer A, Fedewa SA, Butterly LF, Anderson JC, Cercek A, Smith RA, Jemal A (2020) Colorectal cancer statistics, 2020. CA Cancer J Clin 70(3):145–164
4.
Zurück zum Zitat Howlader N, Noone A, Krapcho M, Miller D, Brest A, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis D (2019) SEER Cancer Statistics Review, 1975-2016. National Cancer Institute Howlader N, Noone A, Krapcho M, Miller D, Brest A, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis D (2019) SEER Cancer Statistics Review, 1975-2016. National Cancer Institute
5.
Zurück zum Zitat Catalona WJ, Richie JP, Ahmann FR, Hudson MLA, Scardino PT, Flanigan RC, DeKernion JB, Ratliff TL, Kavoussi LR, Dalkin BL (1994) Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter clinical trial of 6,630 men. J Urol 151(5):1283–1290CrossRef Catalona WJ, Richie JP, Ahmann FR, Hudson MLA, Scardino PT, Flanigan RC, DeKernion JB, Ratliff TL, Kavoussi LR, Dalkin BL (1994) Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter clinical trial of 6,630 men. J Urol 151(5):1283–1290CrossRef
7.
Zurück zum Zitat Zhou M, Aydin H, Kanane H, Epstein JI (2004) How often does alpha-methylacyl-CoA-racemase contribute to resolving an atypical diagnosis on prostate needle biopsy beyond that provided by basal cell markers? Am J Surg Pathol 28(2):239–243CrossRef Zhou M, Aydin H, Kanane H, Epstein JI (2004) How often does alpha-methylacyl-CoA-racemase contribute to resolving an atypical diagnosis on prostate needle biopsy beyond that provided by basal cell markers? Am J Surg Pathol 28(2):239–243CrossRef
8.
Zurück zum Zitat Yang XJ, Wu C-L, Woda BA, Dresser K, Tretiakova M, Fanger GR, Jiang Z (2002) Expression of α-methylacyl-CoA racemase (P504S) in atypical adenomatous hyperplasia of the prostate. Am J Surg Pathol 26(7):921–925CrossRef Yang XJ, Wu C-L, Woda BA, Dresser K, Tretiakova M, Fanger GR, Jiang Z (2002) Expression of α-methylacyl-CoA racemase (P504S) in atypical adenomatous hyperplasia of the prostate. Am J Surg Pathol 26(7):921–925CrossRef
9.
Zurück zum Zitat Zhou M, Jiang Z, Epstein JI (2003) Expression and diagnostic utility of alpha-methylacyl-CoA-racemase (P504S) in foamy gland and pseudohyperplastic prostate cancer. Am J Surg Pathol 27(6):772–778CrossRef Zhou M, Jiang Z, Epstein JI (2003) Expression and diagnostic utility of alpha-methylacyl-CoA-racemase (P504S) in foamy gland and pseudohyperplastic prostate cancer. Am J Surg Pathol 27(6):772–778CrossRef
10.
Zurück zum Zitat Hameed O, Humphrey PA (2005) Immunohistochemistry in diagnostic surgical pathology of the prostate. In: Seminars in diagnostic pathology, vol 1. Elsevier, pp 88–104 Hameed O, Humphrey PA (2005) Immunohistochemistry in diagnostic surgical pathology of the prostate. In: Seminars in diagnostic pathology, vol 1. Elsevier, pp 88–104
11.
Zurück zum Zitat Kumaresan K, Kakkar N, Verma A, Mandal AK, Singh SK, Joshi K (2010) Diagnostic utility of α-methylacyl CoA racemase (P504S) & HMWCK in morphologically difficult prostate cancer. Diagn Pathol 5(1):83CrossRef Kumaresan K, Kakkar N, Verma A, Mandal AK, Singh SK, Joshi K (2010) Diagnostic utility of α-methylacyl CoA racemase (P504S) & HMWCK in morphologically difficult prostate cancer. Diagn Pathol 5(1):83CrossRef
12.
Zurück zum Zitat Sanderson SO, Sebo TJ, Murphy LM, Neumann R, Slezak J, Cheville JC (2004) An analysis of the p63/α-methylacyl coenzyme A racemase immunohistochemical cocktail stain in prostate needle biopsy specimens and tissue microarrays. Am J Clin Pathol 121(2):220–225CrossRef Sanderson SO, Sebo TJ, Murphy LM, Neumann R, Slezak J, Cheville JC (2004) An analysis of the p63/α-methylacyl coenzyme A racemase immunohistochemical cocktail stain in prostate needle biopsy specimens and tissue microarrays. Am J Clin Pathol 121(2):220–225CrossRef
13.
Zurück zum Zitat Molinié V, Fromont G, Sibony M, Vieillefond A, Vassiliu V, Cochand-Priollet B, Hervé JM, Lebret T, Baglin AC (2004) Diagnostic utility of a p63/α-methyl-CoA-racemase (p504s) cocktail in atypical foci in the prostate. Mod Pathol 17(10):1180–1190CrossRef Molinié V, Fromont G, Sibony M, Vieillefond A, Vassiliu V, Cochand-Priollet B, Hervé JM, Lebret T, Baglin AC (2004) Diagnostic utility of a p63/α-methyl-CoA-racemase (p504s) cocktail in atypical foci in the prostate. Mod Pathol 17(10):1180–1190CrossRef
14.
Zurück zum Zitat Hameed O, Sublett J, Humphrey PA (2005) Immunohistochemical stains for p63 and α-methylacyl-CoA racemase, versus a cocktail comprising both, in the diagnosis of prostatic carcinoma: a comparison of the immunohistochemical staining of 430 foci in radical prostatectomy and needle biopsy tissues. Am J Surg Pathol 29(5):579–587CrossRef Hameed O, Sublett J, Humphrey PA (2005) Immunohistochemical stains for p63 and α-methylacyl-CoA racemase, versus a cocktail comprising both, in the diagnosis of prostatic carcinoma: a comparison of the immunohistochemical staining of 430 foci in radical prostatectomy and needle biopsy tissues. Am J Surg Pathol 29(5):579–587CrossRef
15.
Zurück zum Zitat Hameed O, Humphrey PA (2005) p63/AMACR antibody cocktail restaining of prostate needle biopsy tissues after transfer to charged slides: a viable approach in the diagnosis of small atypical foci that are lost on block sectioning. Am J Clin Pathol 124(5):708–715CrossRef Hameed O, Humphrey PA (2005) p63/AMACR antibody cocktail restaining of prostate needle biopsy tissues after transfer to charged slides: a viable approach in the diagnosis of small atypical foci that are lost on block sectioning. Am J Clin Pathol 124(5):708–715CrossRef
16.
Zurück zum Zitat Jiang Z, Li C, Fischer A, Dresser K, Woda BA (2005) Using an AMACR (P504S)/34βE12/p63 cocktail for the detection of small focal prostate carcinoma in needle biopsy specimens. Am J Clin Pathol 123(2):231–236CrossRef Jiang Z, Li C, Fischer A, Dresser K, Woda BA (2005) Using an AMACR (P504S)/34βE12/p63 cocktail for the detection of small focal prostate carcinoma in needle biopsy specimens. Am J Clin Pathol 123(2):231–236CrossRef
17.
Zurück zum Zitat Ventana (2010) VENTANA Basal Cell Cocktail [package insert]. vol 1009140EN Rev E. USA Ventana (2010) VENTANA Basal Cell Cocktail [package insert]. vol 1009140EN Rev E. USA
18.
Zurück zum Zitat Dako (2017) Monoclonal Rabbit Anti-Human AMACR [package insert]. USA Dako (2017) Monoclonal Rabbit Anti-Human AMACR [package insert]. USA
19.
Zurück zum Zitat Newcombe RG (1998) Improved confidence intervals for the difference between binomial proportions based on paired data. Stat Med 17(22):2635–2650CrossRef Newcombe RG (1998) Improved confidence intervals for the difference between binomial proportions based on paired data. Stat Med 17(22):2635–2650CrossRef
20.
Zurück zum Zitat Newcombe RG (1998) Two-sided confidence intervals for the single proportion: comparison of seven methods. Stat Med 17(8):857–872CrossRef Newcombe RG (1998) Two-sided confidence intervals for the single proportion: comparison of seven methods. Stat Med 17(8):857–872CrossRef
21.
Zurück zum Zitat Epstein JI, Egevad L, Humphrey PA, Montironi R, Group IIiDUP (2014) Best practices recommendations in the application of immunohistochemistry in the prostate: report from the International Society of Urologic Pathology consensus conference. Am J Surg Pathol 38(8):e6–e19CrossRef Epstein JI, Egevad L, Humphrey PA, Montironi R, Group IIiDUP (2014) Best practices recommendations in the application of immunohistochemistry in the prostate: report from the International Society of Urologic Pathology consensus conference. Am J Surg Pathol 38(8):e6–e19CrossRef
Metadaten
Titel
Performance comparison of anti-p504s (SP116) Rabbit Monoclonal Primary Antibody vs. Monoclonal Rabbit Anti-Human AMACR clone 13H4 when duplexed with VENTANA Basal Cell Cocktail (34βE12+p63) as a diagnostic aid for prostatic adenocarcinoma using immunohistochemistry
verfasst von
Veronique Lindner
Anne Waydelich
Chen Chun Chen
Carol Jones
Steven P. Stratton
Publikationsdatum
03.04.2021
Verlag
Springer Berlin Heidelberg
Erschienen in
Virchows Archiv / Ausgabe 2/2021
Print ISSN: 0945-6317
Elektronische ISSN: 1432-2307
DOI
https://doi.org/10.1007/s00428-021-03088-4

Weitere Artikel der Ausgabe 2/2021

Virchows Archiv 2/2021 Zur Ausgabe

Neu im Fachgebiet Pathologie

Molekularpathologische Untersuchungen im Wandel der Zeit

Open Access Biomarker Leitthema

Um auch an kleinen Gewebeproben zuverlässige und reproduzierbare Ergebnisse zu gewährleisten ist eine strenge Qualitätskontrolle in jedem Schritt des Arbeitsablaufs erforderlich. Eine nicht ordnungsgemäße Prüfung oder Behandlung des …

Vergleichende Pathologie in der onkologischen Forschung

Pathologie Leitthema

Die vergleichende experimentelle Pathologie („comparative experimental pathology“) ist ein Fachbereich an der Schnittstelle von Human- und Veterinärmedizin. Sie widmet sich der vergleichenden Erforschung von Gemeinsamkeiten und Unterschieden von …

Gastrointestinale Stromatumoren

Open Access GIST CME-Artikel

Gastrointestinale Stromatumoren (GIST) stellen seit über 20 Jahren ein Paradigma für die zielgerichtete Therapie mit Tyrosinkinaseinhibitoren dar. Eine elementare Voraussetzung für eine mögliche neoadjuvante oder adjuvante Behandlung bei …

Personalisierte Medizin in der Onkologie

Aufgrund des erheblichen technologischen Fortschritts in der molekularen und genetischen Diagnostik sowie zunehmender Erkenntnisse über die molekulare Pathogenese von Krankheiten hat in den letzten zwei Jahrzehnten ein grundlegender …