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Early outcomes of high-dose-rate brachytherapy combined with ultra-hypofractionated radiation in higher-risk prostate cancer.
Gorovets, Daniel; Hopkins, Margaret; Kollmeier, Marisa; Moore, Assaf; Goel, Arun; Shasha, Daniel; Brennan, Victoria; McBride, Sean; Cohen, Gilad; Damato, Antonio L; Zelefsky, Michael J.
Affiliation
  • Gorovets D; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY. Electronic address: gorovetd@mskcc.org.
  • Hopkins M; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kollmeier M; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Moore A; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Goel A; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Shasha D; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Brennan V; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • McBride S; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Cohen G; Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Damato AL; Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Zelefsky MJ; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
Brachytherapy ; 20(6): 1099-1106, 2021.
Article in En | MEDLINE | ID: mdl-34588146
ABSTRACT

PURPOSE:

This study evaluated outcomes associated with a high-dose-rate (HDR) brachytherapy boost combined with stereotactic body radiation therapy (SBRT) for patients with higher-risk localized prostate cancer. MATERIALS AND

METHODS:

We identified 101 patients with National Comprehensive Cancer Network high-risk, unfavorable intermediate-risk, or favorable intermediate-risk with probable extra-prostatic extension treated with HDR brachytherapy (15 Gy x 1 fraction) followed by SBRT (5 Gy x 5 daily fractions to the prostate and/or seminal vesicles and/or pelvic lymph nodes). Androgen deprivation therapy was used in 55.4% of all patients (90% of high-risk, 33% of intermediate-risk). Toxicities according to Common Terminology Criteria for Adverse Events (CTCAE) v4.0 and International Prostate Symptom Scores were prospectively documented at each followup visit. Biochemical relapse was defined as PSA nadir +2ng/mL.

RESULTS:

The median follow-up time after SBRT was 24.1 months. No grade ≥3 toxicities were observed. The incidence of acute and late grade 2 gastrointestinal toxicities was both 0.99%. Acute and late grade 2 genitourinary (GU) toxicities were observed in 5.9% and 9.9%, respectively. Median time to a grade 2 GU toxicity was 6 months with a 14% 2-year actuarial rate of grade 2 GU toxicity. Median International Prostate Symptom Scores at 24 months was not significantly different than baseline (6 vs. 5; p = 0.24). Inclusion of pelvic lymph nodes and absence of a rectal spacer were significantly associated with more frequent grade ≥1 GU toxicity, but not grade ≥2 GU or gastrointestinal toxicity. The 2-year biochemical relapse free survival was 97%.

CONCLUSIONS:

HDR brachytherapy combined with SBRT was associated with a favorable early toxicity profile and encouraging cancer control outcomes.
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Full text: 1 Database: MEDLINE Main subject: Prostatic Neoplasms / Brachytherapy Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Brachytherapy Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Prostatic Neoplasms / Brachytherapy Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Brachytherapy Year: 2021 Type: Article