This article may have showed up before.  Perhaps related to these
observations and perhaps not but the authors did postulate that Gleevec
inhibited bone remodeling.  This could lead to impaired bone growth in
a develping child or teen.  I copied abstract:

Altered bone and mineral metabolism in patients receiving imatinib
mesylate.
Berman E, Nicolaides M, Maki RG, Fleisher M, Chanel S, Scheu K, Wilson
BA, Heller G, Sauter NP.
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New
York, NY 10021, USA. [EMAIL PROTECTED]

BACKGROUND: Imatinib mesylate inhibits several tyrosine kinases,
including BCR-ABL, the C-KIT receptor, and the platelet-derived growth
factor receptors alpha and beta, all of which are associated with
disease. We observed that hypophosphatemia developed in some patients
with either chronic myelogenous leukemia or gastrointestinal stromal
tumors who were receiving imatinib. METHODS: We identified 16 patients
who had low serum phosphate levels and 8 patients who had normal serum
phosphate levels, all of whom were receiving imatinib. We performed the
following biochemical measurements: whole-blood levels of ionized
calcium, plasma levels of intact parathyroid hormone, and serum levels
of total calcium, phosphate, 25-hydroxyvitamin D, 1,25-dihydroxyvitamin
D, magnesium, and markers of bone formation (bone alkaline phosphatase
and osteocalcin) and bone resorption (N-telopeptide of collagen
cross-links); urinalysis; and phosphate, calcium, and creatinine levels
in "spot" urine specimens. RESULTS: Patients in the low-phosphate group
(median serum phosphate level, 2.0 mg per deciliter [0.6 mmol per
liter]; normal level, >2.5 mg per deciliter [0.8 mmol per liter]) had
elevated parathyroid hormone levels and low-to-normal serum calcium
levels, were younger, and were receiving a higher dose of imatinib than
patients in the normal-phosphate group (median level, 3.2 mg per
deciliter [1.0 mmol per liter]). Both groups had high levels of
phosphate excreted in the urine and markedly decreased serum levels of
osteocalcin and N-telopeptide of collagen cross-links. CONCLUSIONS:
Hypophosphatemia, with associated changes in bone and mineral
metabolism, develops in a proportion of patients taking imatinib for
either chronic myelogenous leukemia or gastrointestinal stromal tumors.
The drug may inhibit bone remodeling (formation and resorption), even
in patients with normal serum phosphate levels.


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