Immunohistochemical expression and clinical significance of P-glycoprotein in previously untreated extranodal NK/T-cell lymphoma, nasal type

Am J Hematol. 2008 Oct;83(10):795-9. doi: 10.1002/ajh.21256.

Abstract

Overexpression of P-glycoprotein (P-gp) has been identified by a variety of methods in NK cells and NK malignancies. The aim of this study was to determine the clinical significance of P-gp in previously untreated extranodal NK/T-cell lymphoma, nasal type. Tumor specimens from 30 patients initially treated with CHOP or CHOP-based chemotherapy were examined by immunohistochemistry using JSB-1, a monoclonal antibody recognizing the intracellular epitope of P-gp molecule. Twenty cases (67%) were positive for P-gp expression. The complete response rate achieved in P-gp positive patients was significantly lower than in P-gp negative ones (20% vs. 60%, P = 0.045). With a median follow-up of 25 months, the 2-year progression-free survival (PFS) and overall survival (OS) rates for all patients were 66 and 69%, respectively. Compared with both PFS and OS rates of P-gp positive patients, those of P-gp negative patients showed a trend of benefit that did not reach statistical significance for borderline P values (PFS: 90% vs. 54%, P = 0.1057; OS: 90% vs. 61%, P = 0.2028). Our results suggest that P-gp expression is related with poor treatment outcomes of extranodal NK/T-cell lymphoma, nasal type.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cyclophosphamide / therapeutic use
  • Disease-Free Survival
  • Doxorubicin / therapeutic use
  • Female
  • Follow-Up Studies
  • Humans
  • Immunohistochemistry
  • Killer Cells, Natural / metabolism*
  • Lymphoma, T-Cell / drug therapy
  • Lymphoma, T-Cell / genetics
  • Lymphoma, T-Cell / pathology*
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Nasal Mucosa* / metabolism
  • Neoplasm Staging
  • Nose Neoplasms / drug therapy
  • Nose Neoplasms / genetics
  • Nose Neoplasms / pathology*
  • Nose* / pathology
  • Prednisone / therapeutic use
  • Time Factors
  • Treatment Outcome
  • Vincristine / therapeutic use

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Vincristine
  • Doxorubicin
  • Cyclophosphamide
  • Prednisone

Supplementary concepts

  • CHOP protocol