Literature DB >> 22261455

Histologic tumor necrosis is an independent prognostic indicator for clear cell and papillary renal cell carcinoma.

Martin Pichler1, Georg C Hutterer, Thomas F Chromecki, Johanna Jesche, Karin Kampel-Kettner, Peter Rehak, Karl Pummer, Richard Zigeuner.   

Abstract

Histologic tumor necrosis (TN) has been reported to indicate a poor prognosis for different human cancers. In papillary renal cell carcinoma (RCC), data regarding the prognostic impact of TN are conflicting. We retrospectively studied the pathology records of 2,333 consecutive patients who underwent nephrectomy from 1984 to 2006 at a single tertiary academic center. In multivariate analyses regarding clear cell RCC, the presence of histologic TN was an independent negative prognostic factor for metastasis-free (hazard ratio [HR], 2.32; confidence interval [CI], 1.86-2.9; P < .001) and overall (HR, 1.52; CI, 1.31-1.76; P < .001) survival. Regarding papillary RCC, the presence of histologic TN represented an independent predictor of metastasis-free (HR, 5.22; CI, 2.2-12.5; P < .001) and overall (HR, 1.69; CI, 1.11-2.58; P = .015) survival. Our findings suggest that the presence of TN is an independent predictor of clinical outcome in clear cell and papillary RCC. Thus, histologic TN might be a reliable prognostic indicator and should, therefore, routinely be examined during pathologic analysis of RCC specimens.

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Year:  2012        PMID: 22261455     DOI: 10.1309/AJCPLBK9L9KDYQZP

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  31 in total

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5.  Nonenhancing Component of Clear Cell Renal Cell Carcinoma on Computed Tomography Correlates With Tumor Necrosis and Stage and Serves as a Size-Independent Prognostic Biomarker.

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7.  Factors affecting the time to recurrence after radical nephrectomy for localized renal cell carcinoma.

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Review 8.  [Ablative therapy of small renal masses].

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9.  Papillary renal cell carcinoma with abscess formation: A report of three cases.

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10.  Sensitizing acute myeloid leukemia cells to induced differentiation by inhibiting the RIP1/RIP3 pathway.

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