NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Tissue microarrays from renal cell tumors: exclusion criteria and rate of exclusion.

Author(s): Hager M, Kolbitsch C, Tiefenthaler W, Haufe H, Kemmerling R, Lucia Moser P

Publication: Scand J Urol Nephrol, 2007, Vol. 41, Page 485-9

PubMed ID: 17853046 PubMed Review Paper? No

Purpose of Paper

The aims of this paper were to determine the frequency of tissue microarray (TMA) core loss from slides, identify variables that influence core loss, and determine the number of cores required to prevent case loss.

Conclusion of Paper

The number of TMA cores excluded was influenced by section order and tumor type/subtype. The number of excluded cores was nearly three times higher among sections that were cut last (40th TMA section) compared to those cut first. The predominant reason for exclusion was core loss. The number of excluded cores was also higher in sarcomatoid, papillary, and clear cell renal cell carcinoma (RCC) subtypes. The authors then extrapolated the frequency of core exclusion to presumed situations in which 1, 2, or 3 cores per tumor were analyzed, and concluded that punching three cores per case would limit the probability of case loss to less than 5% for the first section cut and 15% for the last section cut for oncocytoma and RCC diagnoses, with the exception of sarcomatoid.

Studies

  1. Study Purpose

    The aims of this study were to determine the frequency of TMA core loss, identify variables that influence core loss, and determine the number of cores required to prevent case loss. In total, 461 cases were analyzed that represented the diagnoses of oncocytoma and clear cell, papillary, sarcomatoid, Bellini type, and Chromophobe renal cell carcinoma (RCC) subtypes. Four TMA cores (0.6 mm diameter) were punched for each case, yielding a total of 1844 TMA cores that were placed into 10 paraffin blocks. Criteria for TMA core exclusion included core loss, less than 25% tumorous tissue within a core, core folding, a core that contained either a hemorrhagic or necrotic area, or the presence of tumor-negative renal tissue.

    Summary of Findings:

    The number of excluded TMA cores based upon the criteria specified above was influenced by section order and tumor type/subtype. The number of excluded cores was nearly three times higher among sections that were cut last (40th TMA section) compared to those cut first (422 versus 158 excluded TMA cores; 9 verse 23%, respectively). The predominant reason for exclusion was core loss, which was responsible for approximately 60% of exclusions. The authors recommend using donor blocks of similar thickness to avoid core loss. The number of excluded cores was also higher in sarcomatoid, papillary, and clear cell RCC subtypes which may be related to the degree of tumor heterogeneity. The authors then extrapolated the frequency of core exclusion to presumed situations in which 1, 2, or 3 cores per tumor were analyzed, and conclude that punching three cores per case would limit the probability of losing all cores for a given case to less than 5% for the first section cut and 15% for the last section cut for oncocytoma and RCC diagnoses, with the exception of sarcomatoid suptypes which had projected losses of 15% and 30%, respectively.

    Biospecimens
    Preservative Types
    • Formalin
    Diagnoses:
    • Neoplastic - Carcinoma
    Platform:
    AnalyteTechnology Platform
    Morphology H-and-E microscopy
    Morphology Macroscopic observation
    Morphology Tissue microarray
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Aliquots and Components Aliquot sequential collection 1st section
    40th section
    Biospecimen Aliquots and Components Aliquot size/volume 1 TMA core
    2 TMA cores
    3 TMA cores
    4 TMA cores
    Preaquisition Diagnosis/ patient condition Oncocytoma
    Clear cell renal cell carcinoma
    Papillary renal cell carcinoma
    Sarcomatoid renal cell carcinoma
    Bellini type renal cell carcinoma
    Chromophobe renal cell carcinoma

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