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  Vol. 135 No. 5, May 1999 TABLE OF CONTENTS
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Sézary Syndrome, Cutaneous T-Cell Lymphoma, and Extracorporeal Photopheresis

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

The report by Fraser-Andrews et al1 of their experience with extracorporeal photopheresis (ECP) treatment of patients with leukemic cutaneous T-cell lymphoma (CTCL) who had previously failed treatment with systemic chemotherapy provides valuable information. Since most of the previously reported patients received ECP as an initial systemic therapy, the study patients of Fraser-Andrews et al differ in this quite important way from those whom we and other investigators have treated with this type of active immunotherapy. The median survival of 39 months for the patients in the study of Fraser-Andrews et al did not differ in a statistically significant manner from the median survival of 22 months for their historical control group, and was shorter than the 60 to 100 months in prior reports in which many of the best responders also had clear evidence of clonal malignant cells. The relatively poorer survival data of Fraser-Andrews and colleagues may result from . . . [Full Text of this Article]



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