Clinical significance of IDC-P as predictive factor after intensity-modulated radiation therapy.


Journal

Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776

Informations de publication

Date de publication:
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

2425-2433

Informations de copyright

© 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

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Auteurs

Rihito Aizawa (R)

Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Toyonori Tsuzuki (T)

Department of Surgical Pathology, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Japan.

Hironori Haga (H)

Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.

Kiyonao Nakamura (K)

Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Takashi Ogata (T)

Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Takahiro Inoue (T)

Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Department of Nephro-Urologic Surgery and Andrology, Mie University Graduate School of Medicine, Tsu-shi, Japan.

Takashi Kobayashi (T)

Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Shusuke Akamatsu (S)

Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Takayuki Goto (T)

Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Osamu Ogawa (O)

Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Division of Urology, Otsu Redcross Hospital, Otsu-shi, Japan.

Takashi Mizowaki (T)

Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

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Classifications MeSH