Pirarubicin (
THP), a novel
anthracycline derivative of
doxorubicin (ADM), is effective in treating patients with advanced, relapsed or recurrent high-grade
osteosarcoma. But its role in neoadjuvant/
adjuvant chemotherapy of
osteosarcoma is still not defined. We conducted a retrospective evaluation of THP-containing
chemotherapy for
osteosarcoma in comparison with ADM-containing
chemotherapy to determine differences in efficacy and toxicities between THP- and ADM-containing regimens. From January 2008 to May 2011, 112 stage IIB limb high-grade
osteosarcoma patients were treated in our institute. Fifty-four patients received a median 6 cycles of neoadjuvant/
adjuvant chemotherapy consisted of THP (
pirarubicin), DDP (
cisplatin), IFO (
ifosfamide) and MTX (
methotrexate), while 58 patients received a median 6 cycles of neoadjuvant/
adjuvant chemotherapy consisted of ADM (
doxorubicin), DDP (
cisplatin), IFO (
ifosfamide) and MTX (
methotrexate). Efficacy and toxicity of the 2
anthracyclines given as
combination chemotherapy were assessed in these patients. The
limb salvage rate, histologic response rate, 2-year recurrence rate, 2-year
metastasis rate, 2-year disease-free survival rate, 2-year overall survival rate, median disease-free survival time (DFS) and median overall survival time (OS) in THP-containing group were similar to that in ADM-containing group. Toxicities were well balanced in two groups. No death related to
chemotherapy was observed. Left ventricular ejection fraction was unchanged 1 and 2 years after
chemotherapy in two groups. Efficacy and toxicity of THP-containing combination are similar to those of ADM-containing combination in neoadjuvant/
adjuvant chemotherapy for stage IIB limb high-grade
osteosarcoma.