Journal of Clinical Oncology, Vol 4, 74-79, Copyright © 1986 by American Society of Clinical Oncology
Phase I and II study of fludarabine phosphate in leukemia: therapeutic efficacy with delayed central nervous system toxicity
RP Warrell Jr and E Berman
Fludarabine phosphate (9-beta-D-arabinofuranosyl-2-fluoroadenine), a novel
purine nucleoside, has demonstrated excellent preclinical antitumor
activity and little toxicity in phase I clinical trials. We evaluated the
clinical use of fludarabine given as a continuous intravenous (IV) infusion
for remission induction in patients with relapsed or refractory leukemia.
Thirty infusions were administered to 25 patients. At doses less than or
equal to 125 mg/m2/d for five days, only three of 17 patients cleared their
bone marrow of leukemic cells, and none achieved complete remission (CR).
Nine patients received doses of 150 mg/m2/d for five days or 125 mg/m2/d
for seven days. Four of these patients achieved CR (three patients with
acute nonlymphoblastic leukemia (ANLL), one patient with acute
lymphoblastic leukemia (ALL]. However, severe CNS toxicity was encountered
in five patients at the two highest dose levels. Initial symptoms of
neurotoxicity were delayed from 21 to 43 days after starting treatment and
consisted of optic neuritis, cortical blindness, altered mental status, and
generalized seizure. Only one patient regained visual and neurologic
function; four other patients experienced progressive neurologic
deterioration and died. Clinicopathologic evaluation suggested widespread,
severe demyelination as the etiology of these reactions. We conclude that
fludarabine is an effective drug for remission induction in acute leukemia.
However, doses required to achieve CR are associated with unacceptable CNS
toxicity. In view of its potent antileukemic activity, further evaluation
of fludarabine at lower doses (less than or equal to 75 mg/m2/d for five
days) may be warranted in combination with other chemotherapeutic agents
for the treatment of patients with acute leukemia.

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