Results of a Randomized, Double-Blinded, Placebo-Controlled, Phase 2.5 Study of Saracatinib (AZD0530), in Patients with Recurrent Osteosarcoma Localized to the Lung
Kristin Baird,
John Glod,
Seth M. Steinberg,
Denise Reinke,
Joseph G. Pressey,
Leo Mascarenhas,
Noah Federman,
Neyssa Marina,
Sant Chawla,
Joanne P. Lagmay,
John Goldberg,
Mohammed Milhem,
David M. Loeb,
James E. Butrynski,
Brian Turpin,
Arthur Staddon,
Sheri L. Spunt,
Robin L. Jones,
Eve T. Rodler,
Scott M. Schuetze,
Scott H. Okuno,
Lee Helman
Affiliations
Kristin Baird
Center for Cancer Research, NCI, NIH, Building 10 CRC, Room 1W-3750, MSC 110410 Center Drive, Bethesda, MD 20892-1104, USA
John Glod
Center for Cancer Research, NCI, NIH, Building 10-CRC, Room 1-5750, Bethesda, MD 20892-1100, USA
Seth M. Steinberg
Center for Cancer Research, NCI, NIH, 9609 Medical Center Drive, Room 2W334, MSC 9716, Bethesda, MD 20892, USA
Denise Reinke
SARC, 24 Frank Lloyd Wright Drive, Ann Arbor, MI 48106, USA
Joseph G. Pressey
Cincinnati Children’s Hospital Medical Center, 3333 Burnet Ave., MLC 7015, Cincinnati, OH 45229, USA
Leo Mascarenhas
Children’s Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Boulevard Mail Stop # 54, Los Angeles, CA 90027, USA
Noah Federman
Mattel Children’s Hospital, David Geffen School of Medicine, University of California, 10833 Le Conte Avenue, Los Angeles, CA 90095-6901, USA
Neyssa Marina
Stanford University School of Medicine, Palo Alto, CA 94305, USA
Sant Chawla
Sarcoma Oncology Research Center, 2811 Wilshire Boulevard, Suite 411, Santa Monica, CA 90403, USA
Joanne P. Lagmay
University of Florida Health Shands Children’s Hospital, 1600 SW Archer HD 204, Gainesville, FL 32610, USA
John Goldberg
Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA 02215, USA
Mohammed Milhem
University of Iowa Hospitals and Clinics, 200 Hawkins Drive C32 GH, Iowa City, IA 52242, USA
David M. Loeb
Children’s Hospital at Montefiore, Albert Einstein College of Medicine, 3411 Wayne Ave., Room 910, Bronx, New York, NY 10467, USA
James E. Butrynski
Willamette Valley Cancer Institute and Research Center, 520 Country Club Road, Eugene, OR 97401, USA
Brian Turpin
Cincinnati Children’s Hospital Medical Center, 3333 Burnett Avenue, Cincinnati, OH 45229, USA
Arthur Staddon
Abramson Cancer Center, University of Pennsylvania Health System, 230 W. Washington Square, Philadelphia, PA 19106, USA
Sheri L. Spunt
Stanford University School of Medicine, 1000 Welch Road Suite 300, MC 5798, Palo Alto, CA 94304, USA
Robin L. Jones
The Royal Marsden Hospital and Institute of Cancer Research, Fulham Road, London SW3 6JJ, UK
Eve T. Rodler
Comprehensive Cancer Center University of California, Davis, 2279 45th Street, Sacramento, CA 95717, USA
Scott M. Schuetze
University of Michigan, 1500 East Medical Center Dr. Ann Arbor, Ann Arbor, MI 48109, USA
Scott H. Okuno
Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA
Lee Helman
Children’s Hospital Los Angeles, Keck School of Medicine, University of Southern California Children’s Hospital Los Angeles, 4650 Sunset Blvd Mail Stop 57, Los Angeles, CA 90027, USA
Purpose. Osteosarcoma is a rare cancer and a third of patients who have completed primary treatment will develop osteosarcoma recurrence. The Src pathway has been implicated in the metastatic behavior of osteosarcoma; about 95% of samples examined express Src or have evidence of downstream activation of this pathway. Saracatinib (AZD0530) is a potent and selective Src kinase inhibitor that was evaluated in adults in Phase 1 studies. The primary goal of this study was to determine if treatment with saracatinib could increase progression-free survival (PFS) for patients who have undergone complete resection of osteosarcoma lung metastases in a double-blinded, placebo-controlled trial. Patients and Methods. Subjects with recurrent osteosarcoma localized to lung and who had complete surgical removal of all lung nodules were randomized within six weeks after complete surgical resection. Saracatinib, or placebo, was administered at a dose of 175 mg orally, once daily, for up to thirteen 28-day cycles. Results. Thirty-seven subjects were included in the analyses; 18 subjects were randomized to receive saracatinib and 19 to receive placebo. Intent-to-treat analysis demonstrated a median PFS of 19.4 months in the saracatinib treatment group and 8.6 months in the placebo treatment group (p=0.47). Median OS was not reached in either arm. Conclusions. Although saracatinib was well tolerated in this patient population, there was no apparent impact of the drug in this double-blinded, placebo-controlled trial on OS, and Src inhibition alone may not be sufficient to suppress metastatic progression in osteosarcoma. There is a suggestion of potential clinical benefit as evidenced by longer PFS in patients randomized to saracatinib based on limited numbers of patients treated.