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Annals of Hematology

, Volume 83, Issue 7, pp 414–419 | Cite as

Assessment of biological prognostic factors provides clinically relevant information in patients with diffuse large B-cell lymphoma—a Nordic Lymphoma Group study

  • M. JerkemanEmail author
  • H. Anderson
  • M. Dictor
  • S. Kvaløy
  • M. Åkerman
  • E. Cavallin-Ståhl
Original Article

Abstract

The purpose of this study was to investigate the prognostic effects of four biological markers, BCL2, TP53, Ki-67, and P-glycoprotein, and their possible clinical relevance in addition to the international prognostic index (IPI) in diffuse large B-cell lymphoma (DLBCL). A total of 405 patients with aggressive lymphoma, stage II-IV, between 18 and 67 years, were randomized in a trial comparing CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) with MACOP-B (methotrexate, doxorubicin, cyclophosphamide, vincristine, prednisone, and bleomycin). Of these, 267 cases were classified as DLBCL, with adequate paraffin blocks available in 207 cases, enabling immunohistochemical assessment of the expression of BCL2, TP53, P-glycoprotein, and Ki-67. In a multivariate analysis, stratified for IPI, high BCL2 expression (>10%) low (<60%) expression of Ki-67, and high TP53 protein expression (>75%) were shown to provide additional prognostic information with regard to overall or failure-free survival. We found no association between expression of P-glycoprotein and outcome. Assessment of BCL2 positivity might be introduced as part of the routine investigation in patients with DLBCL, but further studies are necessary to confirm the clinical relevance of Ki-67 and TP53 expression.

Keywords

BCL2 Diffuse large B-cell lymphoma P-glycoprotein Proliferation TP53 

Notes

Acknowledgements

This study was supported by grants from the Swedish Cancer Society, the foundations of the University Hospital of Lund, the Gunnar, Arvid, and Elisabeth Nilsson Foundation, and the Mrs Berta Kamprad Foundation. We also thank Carina Strand, Research Laboratory, Department of Oncology, Lund, and Christina Andersson, Immunohistochemistry Laboratory, Department of Pathology, Lund, for expert technical assistance.

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Copyright information

© Springer-Verlag 2004

Authors and Affiliations

  • M. Jerkeman
    • 1
    Email author
  • H. Anderson
    • 2
  • M. Dictor
    • 3
  • S. Kvaløy
    • 4
  • M. Åkerman
    • 3
  • E. Cavallin-Ståhl
    • 1
  1. 1.Department of Oncology, Jubileum InstituteLund University HospitalLundSweden
  2. 2.Department of Cancer Epidemiology, Jubileum InstituteLund University HospitalLundSweden
  3. 3.Department of Pathology, Jubileum InstituteLund University HospitalLundSweden
  4. 4.Department of OncologyNorwegian Radium Hospital, MontebelloOsloNorway

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