Prognostic Value of Lymphoma-specific S-Phase Fraction Compared with that of Other Cell Proliferation Markers

Authors

  • Harald Holte From the Departments of Oncology, Oslo, Norway
  • Zhenhe Suo Pathology, Oslo, Norway
  • Erlend B. Smeland Immunology, Oslo, Norway
  • Stein Kvaløy From the Departments of Oncology, Oslo, Norway
  • Ruth Langholm Pathology, Oslo, Norway
  • Trond Stokke Biophysics, The Norwegian Radium Hospital and Institute for Cancer Research, University of Oslo, Montebello, Oslo, Norway

DOI:

https://doi.org/10.1080/028418699432040

Abstract

The proliferation-associated antigens Ki67 (immunohistochemistry) and proliferative cell nuclear antigen (PCNA) (immunohistochemistry and immunoblotting) were analysed together with DNA synthesis (3H-thymidine incorporation) and cell-cycle distribution (tumour-specific S-phase fraction determined by flow cytometry) in lymph node suspensions from 63 patients with newly diagnosed B-Cell non-Hodgkin's lymphomas. Details of clinical parameters, treatment and patient outcome were available for all patients, and retrospectively analysed. Of the proliferation-associated parameters, only high S-phase fraction (p<0.00001) and high PCNA expression by immunoblotting (p=0.012) were predictive of a poor prognosis. Of the conventional parameters, high-grade malignancy, high International Prognostic Index (IPI) score, bulky disease and presence of B symptoms predicted a patient for poor survival. High S-phase fraction was predictive of a short survival for the low-grade lymphomas analysed separately (p<0.00001), as well as for patients treated with an Adriamycin- and a non-Adriamycin-containing regimen (p<0.005 for both groups). In a multivariate analysis, S-phase fraction (p=0.00006), IPI score (p=0.015) and B symptoms (p=0.017) had independent prognostic values, but not histological grade.

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Published

1999-01-01

How to Cite

Holte, H., Suo, Z., Smeland, E. B., Kvaløy, S., Langholm, R., & Stokke, T. (1999). Prognostic Value of Lymphoma-specific S-Phase Fraction Compared with that of Other Cell Proliferation Markers. Acta Oncologica, 38(4), 495–503. https://doi.org/10.1080/028418699432040