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The Journal of Bone and Joint Surgery, Vol 66, Issue 4 602-607, Copyright © 1984 by Journal of Bone and Joint Surgery, Inc
Effects of chemotherapeutic agents on bone. I. Short-term methotrexate and doxorubicin (adriamycin) treatment in a rat model
GE Friedlaender, RB Tross, AC Doganis, JM Kirkwood and R Baron
Wistar-Lewis rats received therapeutic doses of doxorubicin or methotrexate
daily for five days, were pulse-labeled with a fluorescent compound
(calcein) on the seventh and thirteenth days, and were killed fourteen days
after initiation of the protocol. Proximal tail vertebrae were then
evaluated histomorphometrically, and the effects of the chemotherapeutic
agents on trabecular bone were quantitated with respect to changes in total
bone mass, new-bone formation, and resorption. Short-term administration of
methotrexate caused a 26.9 per cent reduction in net trabecular bone volume
and doxorubicin, an 11.5 per cent decrease. Both drugs significantly and
profoundly diminished bone-formation rates by nearly 60 per cent. The toxic
effect on osteoblasts was also reflected in reduced volume and thickness of
osteoid, but the total numbers of osteoblasts and the per cent of
trabecular surface covered by bone-forming cells were not affected. The
numbers of osteoclasts and the extent of their activity were not clearly
different from those in untreated rats, but rates of resorption were not
determined. The effects of chronic treatment with these chemotherapeutic
agents on intact, fractured, and transplanted bone and the biomechanical
significance of these changes has not yet been evaluated. Clinical
Relevance: Chemotherapeutic agents have an adverse effect on normal
physiological bone turnover, especially osteoblastic activity, and would
also be expected to alter fracture-healing and bone-allograft incorporation
by these same mechanisms. Knowledge of these changes and efforts to
favorably affect the remodeling cycle must address these specific defects
before bone allografts can be reliably used and fracture-healing can be
improved concomitant with chemotherapy.

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