Tissue microarrays are reliable tools for the clinicopathological characterization of lung cancer tissue.

Schmidt LH, Biesterfeld S, Kümmel A, Faldum A, Sebastian M, Taube C, Buhll R, Wiewrodt R

Forschungsartikel (Zeitschrift)

Zusammenfassung

The advantage of tissue microarray (TMA) is its ability to efficiently analyze large numbers of tissue specimens in a methodologically uniform way. The reliability of TMAs, especially with regard to clinicopathological characterizations, when compared to conventional immunohistochemistry (IHC) was evaluated.Seventy-two embedded tissue sections from lung cancer specimens were stained with monoclonal antibodies against the tumor-associated markers TA-MUC1 and Lewis Y. Three representative cores of every tumor were embedded in a paraffin array multiblock. The IHC was evaluated by the immunoreactive score (IRS).The data for the TMA IHC and the conventional IHC were concordant (kappa > or = 80%) for both markers. Likewise, discordance (McNemar's test) was low, and sensitivity and specificity were above 80% for both markers. In the samples with high positive expression, the concordance increased (kappa > or = 90%), discordance disappeared (McNemar p = 1.0), and sensitivity and specificity increased above 90% for both markers. Using Cox regression models, all the clinicopathological dependencies were equivalent for both techniques and both markers.Immunohistochemistry with tissue microarrays is valid and provides results equivalent to conventional immunohistochemistry with respect to expression patterns and clinicopathological characterizations.

Details zur Publikation

FachzeitschriftAnticancer Research (Anticancer Res)
Jahrgang / Bandnr. / Volume29
Ausgabe / Heftnr. / Issue1
Seitenbereich201-209
StatusVeröffentlicht
Veröffentlichungsjahr2009
Sprache, in der die Publikation verfasst istEnglisch
StichwörterHumans; Middle Aged; Carcinoma Non-Small-Cell Lung; Immunohistochemistry; Lung Neoplasms; Mucin-1. Antibodies Monoclonal; Tissue Array Analysis; Staining and Labeling; Lewis Blood-Group System; Aged; Carcinoma Small Cell; Prognosis; Male; Female; Humans; Middle Aged; Carcinoma Non-Small-Cell Lung; Immunohistochemistry; Lung Neoplasms; Mucin-1. Antibodies Monoclonal; Tissue Array Analysis; Staining and Labeling; Lewis Blood-Group System; Aged; Carcinoma Small Cell; Prognosis; Male; Female

Autor*innen der Universität Münster

Faldum, Andreas
Institut für Biometrie und Klinische Forschung (IBKF)
Schmidt, Lars Henning
Medizinische Klinik A (Med A)
Wiewrodt, Rainer Gerhard
Medizinische Klinik A (Med A)