Publication: Grade and stage misclassification in intermediate unfavorable-risk prostate cancer radiotherapy candidates
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Sorce, Gabriele
Flammia, Rocco Simone
Hoeh, Benedikt
Chierigo, Francesco
Hohenhorst, Lukas
Panunzio, Andrea
Stabile, Armando
Gandaglia, Giorgio
Tian, Zhe
Tilki, Derya
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NO
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Abstract
Background: we tested for upgrading (Gleason grade group [GGG] >= 4) and/or upstaging to non-organ-confined stage ([NOC] >= pT3/pN1) in intermediate unfavorable-risk (IU) prostate cancer (PCa) patients treated with radical prostatectomy, since both change the considerations for dose and/or type of radiotherapy (RT) and duration of androgen deprivation therapy (ADT). Methods: we relied on Surveillance, Epidemiology, and End Results (2010-2015). Proportions of (a) upgrading, (b) upstaging, or (c) upgrading and/or upstaging were tabulated and tested in multivariable logistic regression models. Results We identified 7269 IU PCa patients. Upgrading was recorded in 479 (6.6%) and upstaging in 2398 (33.0%), for a total of 2616 (36.0%) upgraded and/or upstaged patients, who no longer fulfilled the IU grade and stage definition. Prostate-specific antigen, clinical stage, biopsy GGG, and percentage of positive cores, neither individually nor in multivariable logistic regression models, discriminated between upgraded and/or upstaged patients versus others. Conclusions: IU PCa patients showed very high (36%) upgrading and/or upstaging proportion. Interestingly, the overwhelming majority of those were upstaged to NOC. Conversely, very few were upgraded to GGG >= 4. In consequence, more than one-third of IU PCa patients treated with RT may be exposed to suboptimal dose and/or type of RT and to insufficient duration of ADT, since their true grade and stage corresponded to high-risk PCa definition, instead of IU PCa. Data about magnetic resonance imaging were not available but may potentially help with better stage discrimination.
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Publisher
Wiley
Subject
Endocrinology and metabolism, Urology and nephrology
Citation
Has Part
Source
The Prostate
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Edition
DOI
10.1002/pros.24349