Published January 1, 2012 | Version v1
Journal article

Stereotactic Body Radiotherapy as Monotherapy or Post–External Beam Radiotherapy Boost for Prostate Cancer: Technique, Early Toxicity, and PSA Response

  • 1. Department of Radiation Oncology, University of California San Francisco, San Francisco, California (United States)
  • 2. Biostatistics and Computational Biology Core, Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California (United States)
  • 3. Department of Urology, University of California San Francisco, San Francisco, California (United States)

Description

Purpose: High dose rate (HDR) brachytherapy has been established as an excellent monotherapy or after external-beam radiotherapy (EBRT) boost treatment for prostate cancer (PCa). Recently, dosimetric studies have demonstrated the potential for achieving similar dosimetry with stereotactic body radiotherapy (SBRT) compared with HDR brachytherapy. Here, we report our technique, PSA nadir, and acute and late toxicity with SBRT as monotherapy and post-EBRT boost for PCa using HDR brachytherapy fractionation. Patients and Methods: To date, 38 patients have been treated with SBRT at University of California—San Francisco with a minimum follow-up of 12 months. Twenty of 38 patients were treated with SBRT monotherapy (9.5 Gy × 4 fractions), and 18 were treated with SBRT boost (9.5 Gy × 2 fractions) post-EBRT and androgen deprivation therapy. PSA nadir to date for 44 HDR brachytherapy boost patients with disease characteristics similar to the SBRT boost cohort was also analyzed as a descriptive comparison. Results: SBRT was well tolerated. With a median follow-up of 18.3 months (range, 12.6–43.5), 42% and 11% of patients had acute Grade 2 gastrourinary and gastrointestinal toxicity, respectively, with no Grade 3 or higher acute toxicity to date. Two patients experienced late Grade 3 GU toxicity. All patients are without evidence of biochemical or clinical progression to date, and favorably low PSA nadirs have been observed with a current median PSA nadir of 0.35 ng/mL (range, <0.01–2.1) for all patients (0.47 ng/mL, range, 0.2–2.1 for the monotherapy cohort; 0.10 ng/mL, range, 0.01–0.5 for the boost cohort). With a median follow-up of 48.6 months (range, 16.4–87.8), the comparable HDR brachytherapy boost cohort has achieved a median PSA nadir of 0.09 ng/mL (range, 0.0–3.3). Conclusions: Early results with SBRT monotherapy and post-EBRT boost for PCa demonstrate acceptable PSA response and minimal toxicity. PSA nadir with SBRT boost appears comparable to those achieved with HDR brachytherapy boost.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2010.10.026

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2010.10.026;
PII
S0360-3016(10)03447-4;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
82
Journal Issue
1
Journal Page Range
p. 228-234
ISSN
0360-3016
CODEN
IOBPD3

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
44016319
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANDROGENS; BEAMS; BRACHYTHERAPY; DOSE RATES; DOSIMETRY; FRACTIONATION; NEOPLASMS; PATIENTS; PROSTATE; TOXICITY
Descriptors DEC
ANDROSTANES; BODY; DISEASES; GLANDS; HORMONES; MALE GENITALS; MEDICINE; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANS; RADIOLOGY; RADIOTHERAPY; SEPARATION PROCESSES; STEROID HORMONES; STEROIDS; THERAPY

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.