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Clinical Trial
. 2011 Apr 15;117(8):1736-44.
doi: 10.1002/cncr.25744. Epub 2010 Nov 8.

Addition of pamidronate to chemotherapy for the treatment of osteosarcoma

Affiliations
Clinical Trial

Addition of pamidronate to chemotherapy for the treatment of osteosarcoma

Paul A Meyers et al. Cancer. .

Abstract

Background: This study evaluated the safety and feasibility of the addition of pamidronate to chemotherapy for treatment of osteosarcoma.

Methods: The authors treated 40 patients with osteosarcoma with cisplatin, doxorubicin, and methotrexate with the addition of pamidronate 2 mg/kg/dose (max dose 90 mg) monthly for 12 doses. Survival, event-free survival (EFS), and durability of orthopedic reconstruction were evaluated.

Results: For patients with localized disease, event-free survival (EFS) at 5 years was 72% and overall survival 93%. For patients with metastatic disease, EFS at 5 years was 45% and overall survival 64%. Toxicity was similar to patients treated with chemotherapy alone. Thirteen of 14 uncemented implants demonstrated successful osteointegration. Among allograft reconstructions, there were 2 graft failures, 4 delayed unions, and 6 successful grafts. Overall, 5 of 33 reconstructions failed. There were no stress fractures or growth disturbances.

Conclusions: Pamidronate can be safely incorporated with chemotherapy for the treatment of osteosarcoma. It does not impair the efficacy of chemotherapy. Pamidronate may improve the durability of limb reconstruction.

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Figures

Figure 1
Figure 1
Event free survival for patients who presented with localized or metastatic osteosarcoma at initial presentation.
Figure 2
Figure 2
Overall survival for patients who presented with localized or metastatic osteosarcoma at initial presentation.

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