Journal of Clinical Oncology, Vol 15, 2667-2672, Copyright © 1997 by American Society of Clinical Oncology
Treatment of T-cell prolymphocytic leukemia with human CD52 antibody
R Pawson, MJ Dyer, R Barge, E Matutes, PD Thornton, E Emmett, JC Kluin-Nelemans, WE Fibbe, R Willemze and D Catovsky
Academic Department of Hematology and Cytogenetics, Royal Marsden Hospital, London, United Kingdom.
PURPOSE: T-prolymphocytic leukemia (T-PLL) is an aggressive malignancy of
mature T cells refractory to conventional chemotherapy, with a median
survival duration of 7.5 months. We report here promising results with the
use of a genetically reshaped human CD52 antibody, CAMPATH-1H. PATIENTS AND
METHODS: Fifteen patients with T-PLL, most of whom had received the purine
analog deoxycoformycin (DCF), were treated with CAMPATH-1H. Results were
compared with those of 25 patients treated with DCF. RESULTS: Major
responses occurred in 11 patients (73%) treated with CAMPATH-1H compared
with 40% with DCF. Complete remissions (CRs) were documented in nine (60%)
of the CAMPATH-1H cases and only three (12%) were obtained with DCF. CRs
with CAMPATH-1H were durable, and re-treatment with the antibody resulted
in second CRs in three relapsed patients. Two of them were successfully
autografted with peripheral-blood and bone marrow stem cells collected
during the first CR. Apart from first-dose reactions, infusions of
CAMPATH-1H were well tolerated. However, two responding patients developed
severe bone marrow aplasia that was fatal in one; the second remained
moderately pancytopenic 21 weeks after stopping CAMPATH-1H therapy. The
cause of this adverse effect is unknown. CONCLUSION: CAMPATH-1H is an
effective agent in T-PLL and represents a significant improvement over
other types of therapy. However, CAMPATH-1H alone is not sufficient for
long- term remissions, and the role of autologous stem-cell transplantation
needs further investigation.
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