Phase II Trial of Trastuzumab in Combination With Cytotoxic Chemotherapy for Treatment of Metastatic Osteosarcoma With Human Epidermal Growth Factor Receptor 2 Overexpression: A Report From the Children's Oncology Group

Author:

Ebb David1,Meyers Paul1,Grier Holcombe1,Bernstein Mark1,Gorlick Richard1,Lipshultz Steven E.1,Krailo Mark1,Devidas Meenakshi1,Barkauskas Donald A.1,Siegal Gene P.1,Ferguson William Shay1,Letson George Douglas1,Marcus Karen1,Goorin Allen1,Beardsley Peter,Marina Neyssa

Affiliation:

1. David Ebb, Massachusetts General Hospital; Holcombe Grier, Karen Marcus, Allen Goorin, Dana-Farber Cancer Institute, Boston, MA; Paul Meyers, Memorial Sloan-Kettering Cancer Center; Richard Gorlick, Montefiore Medical Center, New York, NY; Steven E. Lipshultz, University of Miami Miller School of Medicine, Miami; Meenakshi Devidas, Children's Oncology Group, Gainesville; George Douglas Letson,, H. Lee Moffitt Cancer Center, Tampa, FL; Mark Krailo, Donald A. Barkauskas, Keck School of Medicine at the...

Abstract

PurposeDespite efforts to intensify chemotherapy, survival for patients with metastatic osteosarcoma remains poor. Overexpression of human epidermal growth factor receptor 2 (HER2) in osteosarcoma has been shown to predict poor therapeutic response and decreased survival. This study tests the safety and feasibility of delivering biologically targeted therapy by combining trastuzumab with standard chemotherapy in patients with metastatic osteosarcoma and HER2 overexpression.Patients and MethodsAmong 96 evaluable patients with newly diagnosed metastatic osteosarcoma, 41 had tumors that were HER2-positive by immunohistochemistry. All patients received chemotherapy with cisplatin, doxorubicin, methotrexate, ifosfamide, and etoposide. Dexrazoxane was administered with doxorubicin to minimize the risk of cardiotoxicity from treatment with trastuzumab and anthracycline. Only patients with HER2 overexpression received concurrent therapy with trastuzumab given for 34 consecutive weeks.ResultsThe 30-month event-free and overall survival rates for patients with HER2 overexpression treated with chemotherapy and trastuzumab were 32% and 59%, respectively. For patients without HER2 overexpression, treated with chemotherapy alone, the 30-month event-free and overall survival rates were 32% and 50%, respectively. There was no clinically significant short-term cardiotoxicity in patients treated with trastuzumab and doxorubicin.ConclusionDespite intensive chemotherapy plus trastuzumab for patients with HER2-positive disease, the outcome for all patients was poor, with no significant difference between the HER2-positive and HER2-negative groups. Although our findings suggest that trastuzumab can be safely delivered in combination with anthracycline-based chemotherapy and dexrazoxane, its therapeutic benefit remains uncertain. Definitive assessment of trastuzumab's potential role in treating osteosarcoma would require a randomized study of patients with HER2-positive disease.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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