Hydroxyurea
Hydroxyurea is used most commonly for patients with
chronicmyelogenous leukemia.
Hydroxyurea is also used for solid tumors and head
and neck cancer.
Hydroxyurea is readily absorbed and well
distributed into CSF af-ter oral administration. It reaches a peak serum level
2 hours after administration.
About one-half of the dose is metabolized by
the liver to carbon dioxide, which is excreted by the lungs, or to urea, which
is ex-creted by the kidneys. The remaining one-half is excreted un-changed in urine.
Hydroxyurea exerts its effect by inhibiting
the enzyme ribonu-cleotide reductase, which is necessary for DNA synthesis.
Hydroxyurea kills cells in the S phase of the cell
cycle and holds other cells in the G1 phase, where they’re most susceptible to
irra-diation.
Hydroxyurea is used to treat selected
myeloproliferative disor-ders. It may produce temporary remissions in some
patients with metastatic malignant melanomas as well.
Hydroxyurea is also used in combination therapy
with radiation to treat cancers of the head, neck, and lungs.
Cytotoxic drugs and radiation therapy enhance
the toxicity of hy-droxyurea. (See Adverse
reactions to hydroxyurea.)
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