Pm. Patel et al., PHARMACOKINETICS OF HIGH-DOSE METHYLPREDNISOLONE AND USE IN HEMATOLOGICAL MALIGNANCIES, Hematological oncology, 11(2), 1993, pp. 89-96
The pharmacokinetics of oral and intravenous high dose methylprednisol
one (Solu-medrone, Upjohn) were compared in patients with hematologica
l malignancies. The aim of the study was to determine the oral bioavai
lability of high dose methylprednisolone and to establish whether this
is a feasible and more convenient route of administration. The plasma
pharmacokinetics were described by a one-compartment open model with
peak plasma levels of 6.9 +/- 2.5 mug/ml. Total area under the plasma
concentration versus time curve was similar by either route. Mean rela
tive oral bioavailability was generally high (91 +/- 27 per cent). Ret
rospective analysis of 34 patients with chronic lymphocytic leukemia (
CLL), non-Hodgkin's and Hodgkin's lymphoma treated with high dose meth
ylprednisolone showed 11 responses including two complete remissions a
mong nine patients with CLL. There was significant improvement in plat
elet counts in thrombocytopenic patients and treatment was well tolera
ted and toxicity was relatively low. High dose methylprednisolone may
therefore be a useful palliative treatment for hematological malignanc
ies, particularly where marrow suppression is a problem.