SBRT for clinically localized prostate cancer in men with hip replacements: a cautionary note
PO-1424
Abstract
SBRT for clinically localized prostate cancer in men with hip replacements: a cautionary note
Authors: Dylan Conroy1, Abigail Pepin2, Harry Tsou1, Harriss Rashid1, Marilyn Ayoob1, Malika Danner1, Thomas Yung1, Brian Collins1, Pranay Krishnan3, Siyuan Lei1, Simeng Suy1, Shaan Kataria4, Nima Aghdam5, Sean Collins1
1MedStar Georgetown University Hospital, Radiation Medicine, Washington, DC, USA; 2University of Pennsylvania, Radiation Medicine, Philadelphia, PA, USA; 3MedStar Georgetown University Hospital, Radiology, Washington, DC, USA; 4Virginia Hospital Center, Radiation Medicine, Arlington, VA, USA; 5Beth Israel Deaconess Medical Center, Radiation Medicine, Boston, MA, USA
Show Affiliations
Hide Affiliations
Purpose or Objective
SBRT has been established as a safe and effective
treatment for prostate cancer. SBRT
requires high accuracy to reduce treatment margins. Metal hip prostheses create image artifacts, distorting pelvic imaging and potentially decreasing the accuracy of target/organ
at risk identification and radiation dose calculations. Data on the safety and efficacy of
SBRT after hip replacement is limited. This single-institution study sought to
evaluate the safety and local control following SBRT for prostate cancer in men
with hip replacements.
Material and Methods
Twenty-four patients with localized prostate cancer and a
history of pre-treatment hip replacement, treated with SBRT from 2007-2017
at MedStar Georgetown University Hospital, were included in this retrospective
analysis. Minimum follow-up was three years.
Treatment was delivered
using the CyberKnife with
doses of 35-36.25 Gy in 5 fractions. The target and OARs were identified and
contoured by a single experienced Radiation Oncologist. In treatment
planning, care was taken to avoid
treatment beams that directly traversed the hip replacement(s). Toxicities
were recorded and scored using the Common Terminology Criteria for Adverse
Events version 4.0. Local recurrence was confirmed by magnetic
resonance imaging and/or prostate biopsy.
Results
The median follow-up was 8 years. The patients were elderly (Median age = 71.5 years) with a high rate of
comorbidities (Carlson Comorbidity Index > 2 in 25%). Four patients had bilateral hip replacements. The
majority were low to intermediate risk (91.7%) according to the D’Amico classification. Median pre-treatment PSA was 6.3 ng/mL. 12.5% received upfront ADT. Ten
were treated with 35 Gy and 14 were treated with 36.25 Gy. The rates of late > Grade 3
GU toxicity and late > Grade 2 GI toxicity were 8.3% and 4.2%, respectively, with no Grade 4 or 5 toxicities. Six patients (25%) developed a local
recurrence at a median time of 7.5 years. Of these six patients, four had
unilateral hip replacements and two had bilateral. Three underwent salvage
cryotherapy and three received salvage ADT.
Conclusion
Local recurrence and
high-grade late toxicity are uncommon following prostate SBRT in the general
population. However, in this cohort of patients with prior hip replacements,
prostate SBRT had higher than expected rates of both.
In the opinion of the authors, such patients should be counseled
on these elevated risks and treatment alternatives. Brachytherapy, with its ultrasound guidance, circumvents CT image artifact interference, while moderately-hypofractionated/conventionally-fractionated IMRT utilizes larger treatment margins and is therefore less susceptible to target miss. Both represent preferable
radiation options in this patient population. If these patients are treated
with SBRT, they should be monitored for local recurrence so early
salvage can be performed. It is hoped that recent advances in metal artifact
reduction techniques and dose-calculation algorithms will improve future
outcomes.