Author
Listed:
- Cheryl A London
- Heather L Gardner
- Tamra Mathie
- Nicole Stingle
- Roberta Portela
- Michael L Pennell
- Craig A Clifford
- Mona P Rosenberg
- David M Vail
- Laurel E Williams
- Kim L Cronin
- Heather Wilson-Robles
- Antonella Borgatti
- Carolyn J Henry
- Dennis B Bailey
- Jennifer Locke
- Nicole C Northrup
- Martin Crawford-Jakubiak
- Virginia L Gill
- Mary K Klein
- David M Ruslander
- Doug H Thamm
- Brenda Phillips
- Gerald Post
Abstract
Background: We hypothesized that the addition of toceranib to metronomic cyclophosphamide/piroxicam therapy would significantly improve disease-free interval (DFI) and overall survival (OS) in dogs with appendicular osteosarcoma (OSA) following amputation and carboplatin chemotherapy. Methods and Findings: This was a randomized, prospective clinical trial in which dogs with OSA free of gross metastatic disease (n = 126) received carboplatin chemotherapy (4 doses) following amputation. On study entry, dogs were randomized to receive piroxicam/cyclophosphamide with or without toceranib (n = 63 each) after completing chemotherapy. Patient demographics were not significantly different between both groups. During or immediately following carboplatin chemotherapy, 32 dogs (n = 13 toceranib; n = 19 control) developed metastatic disease, and 13 dogs left the study due to other medical conditions or owner preference. Following carboplatin chemotherapy, 81 dogs (n = 46 toceranib; n = 35 control) received the metronomic treatment; 35 dogs (n = 20 toceranib; n = 15 control) developed metastatic disease during the maintenance therapy, and 26 dogs left the study due to other medical conditions or owner preference. Nine toceranib-treated and 11 control dogs completed the study without evidence of metastatic disease 1-year following amputation. Toceranib-treated dogs experienced more episodes of diarrhea, neutropenia and weight loss than control dogs, although these toxicities were low-grade and typically resolved with supportive care. More toceranib-treated dogs (n = 8) were removed from the study for therapy-associated adverse events compared to control dogs (n = 1). The median DFI for control and toceranib treated dogs was 215 and 233 days, respectively (p = 0.274); the median OS for control and toceranib treated dogs was 242 and 318 days, respectively (p = 0.08). The one year survival rate for control dogs was 35% compared to 38% for dogs receiving toceranib. Conclusions: The addition of toceranib to metronomic piroxicam/cyclophosphamide therapy following amputation and carboplatin chemotherapy did not improve median DFI, OS or the 1-year survival rate in dogs with OSA.
Suggested Citation
Cheryl A London & Heather L Gardner & Tamra Mathie & Nicole Stingle & Roberta Portela & Michael L Pennell & Craig A Clifford & Mona P Rosenberg & David M Vail & Laurel E Williams & Kim L Cronin & Heat, 2015.
"Impact of Toceranib/Piroxicam/Cyclophosphamide Maintenance Therapy on Outcome of Dogs with Appendicular Osteosarcoma following Amputation and Carboplatin Chemotherapy: A Multi-Institutional Study,"
PLOS ONE, Public Library of Science, vol. 10(4), pages 1-17, April.
Handle:
RePEc:plo:pone00:0124889
DOI: 10.1371/journal.pone.0124889
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