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Repp86: a new prognostic marker in mantle cell lymphoma
Author(s) -
Schrader Carsten,
Janssen Dirk,
Meusers Peter,
Brittinger Günter,
Siebmann Jens U.,
Parwaresch Reza,
Tiemann Markus
Publication year - 2005
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1111/j.1600-0609.2005.00540.x
Subject(s) - mantle cell lymphoma , medicine , cyclin d1 , cd20 , cd5 , lymphoma , biopsy , ki 67 , immunohistochemistry , proliferation marker , cyclin d3 , pathology , gastroenterology , oncology , cell cycle , cancer
  Objectives : Proliferation indices are important prognostic factors for the clinical outcome of patients with mantle cell lymphoma (MCL). We investigated whether the expression of repp86 (restrictedly expressed proliferation‐associated protein 86 kDa), a new proliferation specific marker expressed in the cell cycle phases G 2 , S and M, but not in G 1 , correlates with the clinical course in patients with MCL. Patients and Methods : Biopsy specimens from 94 untreated patients enrolled in two multicenter trials were investigated immunohistochemically with monoclonal antibodies against CD20, CD5, CD3, CD23, cyclin D1, and repp86 (Ki‐S2). Results : Patients with 0–1% repp86 expression had a median overall survival time of 71.0 months, compared with 38.2 months for patients with 1–5% positive cells and 25.4 months for patients with 5–10% positive tumor cells. Patients with repp86 expression of more than 10% showed the shortest survival (median: 15.0 months). Kaplan–Meier analysis revealed a significant difference in the overall survival time between patients with very high (>10%) and very low (0–1%) repp86 expression ( P  < 0.0001) in the tumor cells. The multivariate analysis revealed repp86 expression to be superior to other clinical characteristics as a prognostic factor ( P  = 0.0016). Conclusion : Based on these findings, repp86 expression is a new important prognostic factor in MCL.

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