SBRT in patients with oligometastatic renal cell carcinoma: A multi-institutional analysis
PO-1425
Abstract
SBRT in patients with oligometastatic renal cell carcinoma: A multi-institutional analysis
Authors: Ozan Cem Guler1, Pervin Hurmuz2, Gokhan Ozyigit2, Cem Onal1
1Baskent University, Radiation Oncology, Adana, Turkey; 2Hacettepe University, Radiation Oncology, Ankara, Turkey
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Purpose or Objective
To investigate the effects of stereotactic body radiotherapy (SBRT) on local control or survival in
oligometastatic renal cell cancer (RCC) patients in the era of immunotherapy.
Material and Methods
A total of 33 patients and 63 lesions treated between March 2013 and October
2020. Twenty patients (60.6%) had de novo
oligometastasis and 11 patients (33.4%) had oligoprogression during treatment
or follow-up. Only patients with bone metastasis included this retrospective study
with the aim of homogenous group. The diagnosis of metastasis was based on
imaging studies. Histopathological verification was not mandatory. The local
control (LC), overall survival (OS), and progression-free survival (PFS) rates
were calculated using Kaplan-Meier analyses.
Results
Median follow-up was 20 months. Fourteen patients (42.4%) were alive at
last visit. Estimated median OS and PFS were 27.5 months (range, 14.6-40.4
months) and 19.4 months (range, 7.7-31 months), respectively. When we
stratified patients by changing or keeping same systemic treatment there was no
significant difference between two groups for OS (p=0.381) or PFS (p= 0.201). 1-year OS, PFS and local control (LC) rates
were 69%, 38% and 82%, respectively. Clinical or radiological progression was
observed in 8 irradiated lesions at first year. There was no grade 3 or more
acute or late toxicity in the study cohort.
Conclusion
By providing excellent local control and low toxicity profile, SBRT is
an effective treatment in oligometastatic RCC patients. The clinical outcomes seems
similar for patients who continues to the same systemic chemotherapeutic or
immunotherapy agent after local treatment of progressed lesion.