AI Article Synopsis

  • Data from 23 patients with Sézary syndrome showed significant improvement in skin scores after extracorporeal photopheresis, with 57% achieving over 25% reduction in skin scores within a year (P = .001).
  • A correlation was found between reduction in skin score and Sézary cell count percentage (P = .03), but no significant differences were noted when comparing responders and nonresponders.
  • Higher baseline lymphocyte counts and Sézary cell percentages were linked to better outcomes, suggesting that minimal tumor burden may be essential for effective treatment response, warranting further investigation into tumor-specific cytotoxic T cells.

Article Abstract

Data were analyzed from 23 patients with Sézary syndrome (defined by erythroderma, more than 10% circulating atypical mononuclear cells, and peripheral blood T-cell clone) undergoing monthly extracorporeal photopheresis as the sole therapy for up to 1 year. The cohort showed a significant reduction of skin scores during treatment (P =.001). Thirteen patients (57%) achieved a reduction in skin score greater than 25% from baseline at 3, 6, 9, or 12 months (responders). Reduction in skin score correlated with reduction in the Sézary cell count as a percentage of total white cell count (P =.03). Responders and nonresponders were compared. None of the measured parameters was significantly different between the 2 groups. It was assessed whether any of the baseline parameters predicted outcome. A higher baseline lymphocyte count was significantly associated with a decrease in skin score at 6 months (P <.05). A higher baseline Sézary cell count as a percentage of total white cell count predicted a subject was more likely to be a responder after 6 months of treatment (P =.021). No other parameters predicted responder status. These data show that the modest falls in CD4, CD8, and Sézary cell counts were seen in all patients and might have resulted from lymphocyte apoptosis. This mechanism could explain the more favorable response seen in patients with higher percentages of Sézary cells in the peripheral blood. Alternatively, minimum tumor burden might be required for the induction of a cytotoxic response. Analysis of tumor-specific cytotoxic T cells is needed to investigate these possibilities further.

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http://dx.doi.org/10.1182/blood.v98.5.1298DOI Listing

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