CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Bcl-2 protein expression is the strongest independent prognostic factor of survival in primary cutaneous large B-cell lymphomas

نویسندگان

  • Florent Grange
  • Tony Petrella
  • Marie Beylot-Barry
  • Pascal Joly
  • Michel D’Incan
  • Michele Delaunay
  • Laurent Machet
  • Marie-Francoise Avril
  • Sophie Dalac
  • Philippe Bernard
  • Agnes Carlotti
  • Eric Esteve
  • Beatrice Vergier
  • Pierre Dechelotte
  • Elisabeth Cassagnau
  • Philippe Courville
  • Philippe Saiag
  • Liliane Laroche
  • Martine Bagot
چکیده

Bcl-2 protein expression has been associated with poor prognosis in patients with noncutaneous diffuse large B-cell lymphomas. In primary cutaneous large B-cell lymphomas, the location on the leg, the round-cell morphology defined as the predominance of centroblasts and immunoblasts over large centrocytes, and multiple skin lesions were identified as adverse prognostic factors. The prognostic value of bcl-2 protein expression has not been studied in large series of patients. We evaluated 80 primary cutaneous large B-cell lymphomas collected by the French Study Group on Cutaneous Lymphomas. The prognostic value of age, sex, number of lesions, cutaneous extent, location, serum lactate dehydrogenase (LDH) level, B symptoms, morphology, and bcl-2 protein expression was studied. The overall 5-year specific survival rate was 65%. In univariate analysis, advanced age, multiple skin lesions (n 48), location on the leg (n 25), round-cell morphology (n 32), and bcl-2 expression (n 39) were significantly related to death from lymphoma. In multivariate analysis, bcl-2 expression (P .0003), multiple skin lesions (P .004), and age remained independent prognostic factors. The 5-year specific survival rates in bcl-2–positive and bcl-2–negative patients were 41% and 89%, respectively (P < .0001). A new prognostic classification of primary cutaneous B-cell lymphoma should be based primarily on bcl-2 protein expression rather than the location of skin lesions. (Blood. 2004;103: 3662-3668)

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تاریخ انتشار 2004