Pyridinoline (PYD), deoxypyridinoline (DPD), and N-telopeptide (NTX) are ma
rkers of bone resorption. In cancer patients with bone metastases, NTX is m
ore often elevated than either of the pyridinolines. Bisphosphonates inhibi
t osteoclasts and their treatment decreases skeletal complications of malig
nancy. The aim of this study was to correlate urinary PYD, DPD, and NTX lev
els with clinical events in patients receiving pamidronate. 25 cancer patie
nts with lytic bone disease were treated with monthly pamidronate combined
with endocrine or chemotherapy; 27 others were on placebo. Twenty-four hour
urines were collected at baseline, 1, 3 and 6 months. NTX values were dete
rmined by enzyme-linked immunosorbent assay (ELISA); PYD and DPD values wer
e determined by reverse phase high performance liquid chromatography (HPLC)
. Two hour urines were also collected weekly for 21 patients. The greatest
difference as a result of pamidronate treatment was observed in NTX values.
Maximum suppression was achieved 2 weeks after treatment. Of the 25 patien
ts who received pamidronate, 21 had initially elevated NTX values. 12 of th
e 21 finished with normal NTX values, whilst 9/21 had NTX values which rema
ined abnormally elevated. The proportions of patients with fractures betwee
n these two subgroups approached statistical significance (P= 0.07) while t
he proportions with bony disease progression were significant (P= 0.03, Fis
her's exact test). Measuring NTX levels appears useful in monitoring bispho
sphonate therapy of bone metastases. The goal of treatment should be to nor
malise NTX excretion. (C) 1998 Elsevier Science Ltd. All rights reserved.