Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Dec;12(6):533-539.
doi: 10.5114/jcb.2020.101685. Epub 2020 Dec 16.

High-dose-rate brachytherapy as monotherapy for localized prostate cancer using three different doses - 14 years of single-centre experience

Affiliations

High-dose-rate brachytherapy as monotherapy for localized prostate cancer using three different doses - 14 years of single-centre experience

Carlo Pietro Soatti et al. J Contemp Brachytherapy. 2020 Dec.

Abstract

Purpose: To evaluate clinical outcomes in patients with localized prostate cancer (LPC) treated with 3D conformal high-dose-rate (HDR) brachytherapy (BT) as monotherapy.

Material and methods: From March 2004 to November 2017, 277 men with LPC underwent 3D conformal HDR-BT as monotherapy, with a temporary implant. The dose prescription was: 38 Gy in 4 fractions (149 patients), 27 Gy in 2 fractions (41 patients), and 19-20 Gy in a single fraction (87 patients). Biochemical progression-free survival (bPFS), progression-free survival (PFS), and cancer-specific survival (CSS) were calculated. Acute and late genitourinary (GU) and gastrointestinal (GI) toxicity assessment were performed using Common Terminology Criteria for Adverse Events v5.0.

Results: The mean age was 67 (range, 47-81) years. Overall, 145 patients were low-risk, 116 intermediate-risk, and 16 high-risk prostate cancer. After a median follow-up of six years (range, 6-160 months), bPFS, PFS, and CSS were 81%, 96%, and 97%, respectively. Dose prescription, initial prostate specific antigen (iPSA) ≥ 9,5 ng/ml, and high-risk disease resulted in prognostic factors regarding bPFS. Only G2-G3 acute or late GI and GU toxicities were observed.

Conclusions: HDR-BT as monotherapy is a valid and safe treatment modality for localized prostate cancer. After a long follow-up, patients receiving 19-20 Gy in a single fraction had a lower biochemical control rate compared to patients receiving 38 Gy in 4 fractions or 27 Gy in 2 fractions. Randomized prospective trials with a longer follow-up are necessary to confirm our results, and define total doses and dose per fraction for HDR-BT in patients with LPC.

Keywords: PSA; brachytherapy; high-dose-rate; prostate cancer; prostate-specific antigen.

PubMed Disclaimer

Conflict of interest statement

The authors report no conflict of interest.

Figures

Fig. 1
Fig. 1
Kaplan-Meier curves of biochemical progression-free survival A) in all patients and B) in patients treated with 19-20 Gy in single fraction, 27 in two fractions, and 38 Gy in four fractions
Fig. 2
Fig. 2
Kaplan-Meier curves of progression-free survival (A) and cancer-specific survival of all patients analyzed (B)

Similar articles

Cited by

References

    1. Siegel RL, Miller KD, Jemal A. CA Cancer statistics, 2019. Cancer J Clin 2019; 69: 7-34. - PubMed
    1. Pinsky PF, Prorok PC, Yu K et al. . Extended mortality results for prostate cancer screening in the PLCO trial with median follow-up of 15 years. Cancer 2017; 123: 592-599. - PMC - PubMed
    1. Herget KA, Patel DP, Hanson HA et al. . Recent decline in prostate cancer incidence in the United States, by age, stage, and Gleason score. Cancer Med 2016; 5: 136-141. - PMC - PubMed
    1. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®). Prostate cancer version 2. 2019. Available at: https://www.nccn.org/professionals/physician_gls/pdf/prostate.pdf (accessed April 20, 2019).
    1. Martinez A, Gonzalez J, Stromberg J et al. . Conformal prostate brachytherapy: initial experience of a phase I/II dose-escalating trial. Int J Radiat Oncol Biol Phys 1995; 33: 1019-1027. - PubMed