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Optimal Androgen Deprivation Therapy Combined with Proton Beam Therapy for Prostate Cancer: Results from a Multi-Institutional Study of the Japanese Radiation Oncology Study Group.

Authors :
Murakami M
Ishikawa H
Shimizu S
Iwata H
Okimoto T
Takagi M
Murayama S
Akimoto T
Wada H
Arimura T
Sato Y
Gosho M
Nakamura K
Sakurai H
Source :
Cancers [Cancers (Basel)] 2020 Jun 25; Vol. 12 (6). Date of Electronic Publication: 2020 Jun 25.
Publication Year :
2020

Abstract

Background: Androgen deprivation therapy (ADT) combined with radiation therapy benefits intermediate- and high-risk prostate cancer (PC) patients. The optimal ADT duration in combination with high-dose proton beam therapy (PBT) remains unknown.<br />Methods: Intermediate- and high-risk PC patients treated with PBT combined with ADT for various durations were analyzed retrospectively. To assess the relationship between ADT and biochemical relapse-free (bRF) rate, Cox proportional hazards models including T stage, prostate specific antigen (PSA) level, Gleason score (GS), and total radiation dose were used.<br />Results: In the intermediate-risk PC patients ( n = 520), ADT use improved bRF (HR 0.49, 95% CI 0.26-0.93; p = 0.029), especially in those with multiple intermediate-risk factors (T2b-2c, PSA 10-20 ng/mL, and GS 7). In the high-risk PC patients ( n = 555), a longer ADT duration (>6 months) conferred a benefit for bRF (HR 0.54, 95% CI 0.32-0.90; p = 0.018), which was most apparent in patients with multiple high-risk factors (T3a-4, PSA > 20 ng/mL, and GS ≥ 8) treated with ADT for ≥21 months.<br />Conclusions: Short-term (≤6 months) ADT is beneficial for intermediate-risk PC patients, but likely unnecessary for those with a single risk factor, whereas ADT for >6 months is necessary for high-risk PC patients and ADT for ≥21 months might be optimal for those with multiple risk factors in combination of high-dose PBT.

Details

Language :
English
ISSN :
2072-6694
Volume :
12
Issue :
6
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
32630494
Full Text :
https://doi.org/10.3390/cancers12061690