Clinical significance of IDC-P as predictive factor after intensity-modulated radiation therapy.
high-risk
intensity-modulated radiation therapy
intraductal carcinoma of the prostate
prostate cancer
very high-risk
Journal
Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776
Informations de publication
Date de publication:
Jul 2022
Jul 2022
Historique:
revised:
20
04
2022
received:
17
01
2022
accepted:
30
04
2022
pubmed:
7
5
2022
medline:
15
7
2022
entrez:
6
5
2022
Statut:
ppublish
Résumé
The clinical significance of intraductal carcinoma of the prostate (IDC-P) in men with nonmetastatic prostate cancer (PCa) treated with high-dose external-beam radiation therapy remains unclear. The aim of this study was to evaluate the impact of IDC-P in men who received intensity-modulated radiation therapy (IMRT) for nonmetastatic PCa. All patients with high-risk (H-R) and very high-risk (VH-R) PCa who received IMRT between September 2000 and December 2013 at our institution were analyzed retrospectively. We re-reviewed biopsy cores for the presence of IDC-P. Treatment consisted of IMRT (median: 78 Gy at 2 Gy per fraction) plus 6-month neoadjuvant hormonal therapy (HT). In total, 154 consecutive patients with H-R and VH-R PCa were analyzed. Intraductal carcinoma of the prostate was present in 27.9% (n = 43). The median follow-up period was 8.4 years. The 10-year PCa-specific survival, biochemical failure (BF), clinical failure, and castration-resistant PCa rates were 90.0%, 47.8%, 27.5%, and 24.5% in patients with IDC-P, and 96.6%, 32.6%, 10.8%, and 7.0% in those without IDC-P, respectively (p = 0.12, 0.04, 0.0031, and 0.012, respectively). In multivariable analysis, IDC-P was not identified as an independent predictive factor for BF (p = 0.26). The presence of IDC-P was correlated with a significantly higher incidence of disease progression in men with H-R and VH-R PCa who received IMRT, although it was not identified as an independent predictive factor for BF. Further investigations are needed to determine the significance of IDC-P as an independent predictive factor for survival outcomes.
Identifiants
pubmed: 35514196
doi: 10.1111/cas.15392
pmc: PMC9277254
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2425-2433Informations de copyright
© 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
Références
Am J Surg Pathol. 1996 Jul;20(7):802-14
pubmed: 8669528
J Urol. 2019 Oct;202(4):710-716
pubmed: 31059665
Am J Surg Pathol. 2020 Aug;44(8):e87-e99
pubmed: 32459716
Mod Pathol. 2016 Feb;29(2):166-73
pubmed: 26743470
Int J Clin Oncol. 2019 Oct;24(10):1247-1255
pubmed: 31152322
Int J Radiat Oncol Biol Phys. 2006 Jul 15;65(4):965-74
pubmed: 16798415
J Clin Oncol. 2009 May 20;27(15):2450-6
pubmed: 19380444
Bone Marrow Transplant. 2013 Mar;48(3):452-8
pubmed: 23208313
Eur Urol. 2018 Jun;73(6):834-844
pubmed: 29037513
Cancer Sci. 2022 Jul;113(7):2425-2433
pubmed: 35514196
Am J Surg Pathol. 2016 Feb;40(2):244-52
pubmed: 26492179
Eur Urol. 2020 Feb;77(2):191-198
pubmed: 31439369
Eur J Cancer. 2012 Jun;48(9):1318-25
pubmed: 22405699
J Urol. 2020 Nov;204(5):909-917
pubmed: 32698712
Int J Clin Oncol. 2018 Jun;23(3):584-590
pubmed: 29397469
Prostate. 2018 Jan;78(1):11-16
pubmed: 29094384
Urol Oncol. 2021 Feb;39(2):131.e9-131.e15
pubmed: 33127301
Cancer. 2020 Sep 1;126(17):3961-3971
pubmed: 32573779
Urol Oncol. 2017 Dec;35(12):673.e9-673.e14
pubmed: 28919182
Int J Urol. 2015 Feb;22(2):140-5
pubmed: 25358604
Prostate. 2017 Jun;77(8):859-865
pubmed: 28240424
Prostate. 2014 May;74(6):680-7
pubmed: 24481730
Mod Pathol. 2016 Jun;29(6):630-6
pubmed: 26939875
Eur J Cancer. 2014 Jun;50(9):1610-6
pubmed: 24703897
J Urol. 2020 Feb;203(2):311-319
pubmed: 31483693
Int J Clin Oncol. 2021 Nov;26(11):2113-2122
pubmed: 34338920
Prostate. 2015 Feb 15;75(3):225-32
pubmed: 25307858