Extracorporeal photopheresis in Sezary syndrome: hematologic parameters as predictors of response

被引:39
作者
Evans, AV
Wood, BP
Scarisbrick, JJ
Fraser-Andrews, EA
Chinn, S
Dean, A
Watkins, P
Whittaker, SJ
Russell-Jones, R
机构
[1] St Thomas Hosp, St Johns Inst Dermatol, Skin Tumour Unit, London SE1 7EH, England
[2] Kings Coll London, Guys Kings & St Thomas Sch Med, Dept Publ Hlth Sci, London WC2R 2LS, England
关键词
D O I
10.1182/blood.V98.5.1298
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Data were analyzed from 23 patients with Sezary 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 Sezary 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 Sezary 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 Sezary 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 Sezary 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. (C) 2001 by The American Society of Hematology.
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页码:1298 / 1301
页数:4
相关论文
共 24 条
[1]   Mechanisms of HIV-associated lymphocyte apoptosis [J].
Badley, AD ;
Pilon, AA ;
Landay, A ;
Lynch, DH .
BLOOD, 2000, 96 (09) :2951-2964
[2]  
Berger CL, 1998, INT J CANCER, V76, P304, DOI 10.1002/(SICI)1097-0215(19980504)76:3<304::AID-IJC3>3.0.CO
[3]  
2-Z
[4]   Extracorporeal photopheresis induces apoptosis in the lymphocytes of cutaneous T-cell lymphoma and graft-versus-host disease patients [J].
Bladon, J ;
Taylor, PC .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 107 (04) :707-711
[5]   Photopheresis therapy for cutaneous T-cell lymphoma [J].
Duvic, M ;
Hester, JP ;
Lemak, NA .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 35 (04) :573-579
[6]   TREATMENT OF CUTANEOUS T-CELL LYMPHOMA BY EXTRACORPOREAL PHOTOCHEMOTHERAPY - PRELIMINARY-RESULTS [J].
EDELSON, R ;
BERGER, C ;
GASPARRO, F ;
JEGASOTHY, B ;
HEALD, P ;
WINTROUB, B ;
VONDERHEID, E ;
KNOBLER, R ;
WOLFF, K ;
PLEWIG, G ;
MCKIERNAN, G ;
CHRISTIANSEN, I ;
OSTER, M ;
HONIGSMANN, H ;
WILFORD, H ;
KOKOSCHKA, E ;
REHLE, T ;
PEREZ, M ;
STINGL, G ;
LAROCHE, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (06) :297-303
[7]  
EDELSON RL, 1994, BIOL THER CANC UPDAT, V4, P1
[8]   Extracorporeal photopheresis in Sezary syndrome - No significant effect in the survival of 44 patients with a peripheral blood T-cell clone [J].
Fraser-Andrews, E ;
Seed, P ;
Whittaker, S ;
Russell-Jones, R .
ARCHIVES OF DERMATOLOGY, 1998, 134 (08) :1001-1005
[9]   Detection of a peripheral blood T cell clone is an independent prognostic marker in mycosis fungoides [J].
Fraser-Andrews, EA ;
Woolford, AJ ;
Russell-Jones, R ;
Seed, PT ;
Whittaker, SJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (01) :117-121
[10]   Treatment of cutaneous T-cell lymphoma with extracorporeal photopheresis monotherapy and in combination with recombinant interferon alfa: A 10-year experience at a single institution [J].
Gottlieb, SL ;
Wolfe, JT ;
Fox, FE ;
DeNardo, BJ ;
Macey, WH ;
Bromley, PG ;
Lessin, SR ;
Rook, AH .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 35 (06) :946-957