TY - JOUR
T1 - Concurrent sunitinib and stereotactic body radiotherapy for patients with oligometastases
T2 - Final report of a prospective clinical trial
AU - Kao, Johnny
AU - Chen, Chien Ting
AU - Tong, Charles C.L.
AU - Packer, Stuart H.
AU - Schwartz, Myron
AU - Chen, Shu Hsia
AU - Sung, Max W.
N1 - Funding Information:
Conflict of interest This study was partly supported by Pfizer investigator initiated award #2005-1082 and the Ellen Katz Foundation Award to J.K. Sunitinib was provided by Pfizer.
PY - 2014/6
Y1 - 2014/6
N2 - Preliminary results demonstrated that concurrent sunitinib and stereotactic body radiation therapy (SBRT) is an active regimen for metastases limited in number and extent. This analysis was conducted to determine the long-term survival and cancer control outcomes for this novel regimen. Forty-six patients with oligometastases, defined as five or fewer clinical detectable metastases from any primary site, were treated on a phase I/II trial from February 2007 to September 2010. The majority of patients were treated with 37.5 mg sunitinib (days 1-28) and SBRT 50 Gy (days 8-12 and 15-19) and maintenance sunitinib was used in 39 % of patients. Median follow up for surviving patients is 3.6 years. The 4-year estimates for local control, distant control, progression-free and overall survival were 75 %, 40 %, 34 % and 29 %, respectively. At last follow-up, 26 % of patients were alive without evidence of disease, 7 % were alive with distant metastases, 48 % died from distant metastases, 2 % died from local progression, 13 % died from comorbid illness, and 4 % died from treatment-related toxicities. Patients with kidney and prostate primary tumors were associated with a significantly improved overall survival (hazard ratio=0.25, p=0.04). Concurrent sunitinib and SBRT is a promising approach for the treatment of oligometastases and further study of this novel combination is warranted.
AB - Preliminary results demonstrated that concurrent sunitinib and stereotactic body radiation therapy (SBRT) is an active regimen for metastases limited in number and extent. This analysis was conducted to determine the long-term survival and cancer control outcomes for this novel regimen. Forty-six patients with oligometastases, defined as five or fewer clinical detectable metastases from any primary site, were treated on a phase I/II trial from February 2007 to September 2010. The majority of patients were treated with 37.5 mg sunitinib (days 1-28) and SBRT 50 Gy (days 8-12 and 15-19) and maintenance sunitinib was used in 39 % of patients. Median follow up for surviving patients is 3.6 years. The 4-year estimates for local control, distant control, progression-free and overall survival were 75 %, 40 %, 34 % and 29 %, respectively. At last follow-up, 26 % of patients were alive without evidence of disease, 7 % were alive with distant metastases, 48 % died from distant metastases, 2 % died from local progression, 13 % died from comorbid illness, and 4 % died from treatment-related toxicities. Patients with kidney and prostate primary tumors were associated with a significantly improved overall survival (hazard ratio=0.25, p=0.04). Concurrent sunitinib and SBRT is a promising approach for the treatment of oligometastases and further study of this novel combination is warranted.
KW - Image-guided radiation therapy
KW - Metastases
KW - Oligometastases
KW - Stereotactic body radiation therapy (SBRT)
KW - Sunitinib
UR - https://www.scopus.com/pages/publications/84902550806
U2 - 10.1007/s11523-013-0280-y
DO - 10.1007/s11523-013-0280-y
M3 - Article
C2 - 23660867
AN - SCOPUS:84902550806
SN - 1776-2596
VL - 9
SP - 145
EP - 153
JO - Targeted Oncology
JF - Targeted Oncology
IS - 2
ER -