BACKGROUND. The authors hypothesized that the outcomes for young patie
nts who present with primary osteosarcoma of flat bones or secondary o
steosarcoma after other primary malignancies are similar because the s
ites of these tumors rarely makes them amenable to complete surgical r
esection. METHODS, The authors reviewed their experience with 27 patie
nts with primary osteosarcomas involving flat bones and 18 patients wi
th secondary osteosarcomas of any site, evaluating treatment, metastat
ic patterns, and outcome. RESULTS, Eleven of the 27 primary osteosarco
mas and 10 of the 18 secondary osteosarcomas were at least partially r
esectable at the time of initial diagnosis. At last follow-up, 10 of t
he 27 patients with primary flat bone osteosarcoma were alive, eight o
f whom were disease free. Three of 18 with the secondary osteosarcoma
patients were alive, including one with locally recurrent disease afte
r recent disease resections. Chemotherapy with single or combinations
of agents rarely yielded responses for primary flat bone or secondary
osteosarcomas. CONCLUSIONS, Outcome for both groups of patients was po
or due to metastases and failure of local control. Sixteen of the 27 p
atients with primary osteosarcoma of flat bones died of their tumor; a
n additional patient died of doxorubicin-related cardiomyopathy and ha
d microscopic disease in the primary site at autopsy. Thirteen of the
18 patients with secondary osteosarcoma died of their second metastati
c cancer, 2 additional patients died of doxorubicin-related cardiomyop
athy/coccidioidomycosis, and another of acute renal toxicity. (C) 1997
American Cancer Society.