The National Cancer Institute’s Comparative Oncology Trials Consortium (NCI-COTC)

AL Amy K. LeBlanc
CM Christina Mazcko
AC Aswini Cherukuri
EB Erika P. Berger
WK William C. Kisseberth
MB Megan E. Brown
SL Susan Lana
KW Kristen Weishaar
BF Brian K. Flesner
JB Jeffrey N. Bryan
DV David M. Vail
JB Jenna H. Burton
JW Jennifer L. Willcox
AM Anthony J. Mutsaers
JW J. Paul Woods
NN Nicole C. Northrup
CS Corey Saba
KC Kaitlin M. Curran
HL Haley Leeper
HW Heather Wilson-Robles
BW Brandan G. Wustefeld-Janssens
SL Stephanie Lindley
AS Annette N. Smith
ND Nikolaos Dervisis
SK Shawna Klahn
MH Mary Lynn Higginbotham
RW Raelene M. Wouda
EK Erika Krick
JM Jennifer A. Mahoney
CL Cheryl A. London
LB Lisa G. Barber
CB Cheryl E. Balkman
AM Angela L. McCleary-Wheeler
SS Steven E. Suter
OM Olya Martin
AB Antonella Borgatti
KB Kristine Burgess
MC Michael O. Childress
JF Janean L. Fidel
SA Sara Allstadt
DG Daniel L. Gustafson
LS Laura E. Selmic
CK Chand Khanna
TF Timothy M. Fan
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The COTC infrastructure provides a facile means of conducting multi-center clinical trials in pet dogs to advance anti-cancer drug development and cancer biology questions that are not sufficiently asked or answered in other animal models.23,24 Eighteen COTC member institutions participated in this randomized 2-arm parallel superiority trial following CONSORT guidelines. The study period included the entirety of the dogs’ disease-free interval (DFI) after diagnosis, amputation of the affected limb, and administration of adjuvant carboplatin therapy with or without adjuvant sirolimus administration. Dogs were considered off-study at the time metastatic disease progression was detected and confirmed through standard clinical radiographic imaging methods and/or tissue analysis.

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