Premium
Stereotactic body radiotherapy for primary prostate cancer: A systematic review
Author(s) -
Tan TzeJian,
Siva Shankar,
Foroudi Farshad,
Gill Suki
Publication year - 2014
Publication title -
journal of medical imaging and radiation oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.31
H-Index - 43
eISSN - 1754-9485
pISSN - 1754-9477
DOI - 10.1111/1754-9485.12213
Subject(s) - medicine , prostate cancer , toxicity , cyberknife , prostate , urinary system , radiation therapy , urology , dose fractionation , colorectal cancer , cancer , oncology , radiosurgery
Summary Stereotactic body radiotherapy ( SBRT ) for prostate cancer allows overall treatment times to be reduced to as little as 1 week while maintaining a non‐invasive approach. This study provides a comprehensive summary of the literature relating to SBRT in prostate cancer. A systematic review of the relevant literature was performed using structured search terms. Fourteen phase I – II trials and retrospective studies using SBRT for the treatment of prostate cancer were used. Three studies were identified which addressed cost. Dose fractionation, radiotherapy procedures, biochemical progression‐free survival, toxicity, cost and quality of life were critically appraised. A total of 1472 patients were examined across studies. Median follow‐up ranged from 11 to 60 months. The most common dose fractionation was 35–36.25 Gy in five fractions, used in nine out of 14 studies. Ten of 14 studies used C yber K nife. The overall biochemical progression‐free survival ranged 81–100%. Acute grade 2 urinary and rectal toxicities were reported in 5–42% and 0–27% of patients, respectively. Acute grade 3 or more urinary and rectal toxicity were 0.5% and 0%, respectively. Late grade 2 urinary toxicity was reported in 0–29% of patients, while 1.3% had a late grade 3 urinary toxicity. There were no late grade 4 urinary toxicities seen. Late grade 2 rectal toxicity was reported in 0–11%, while 0.5% had a late grade 3 rectal toxicity. Late grade 4 rectal toxicity was reported in 0.2% of patients.