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The prognostic role of tertiary Gleason pattern 5 in a contemporary grading system for prostate cancer.
Jang, W S; Yoon, C Y; Kim, M S; Kang, D H; Kang, Y J; Jeong, W S; Abalajon, M J; Ham, W S; Choi, Y D.
Afiliación
  • Jang WS; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Yoon CY; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Kim MS; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Kang DH; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Kang YJ; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Jeong WS; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Abalajon MJ; Department of Urology, Santo Tomas University Hospital, Manila, Philippines.
  • Ham WS; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Choi YD; Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.
Prostate Cancer Prostatic Dis ; 20(1): 93-98, 2017 03.
Article en En | MEDLINE | ID: mdl-27845330
ABSTRACT

BACKGROUND:

Recently, a new prostate cancer (PC) grading system has been introduced, where Gleason score (GS) 7 (3+4) and GS 7 (4+3) are categorized into two separate groups. However, GS 7 with tertiary Gleason pattern 5 (TGP5) was not incorporated in the new grading system. In the present study, we validated the prognostic role of TGP5 in the new classification.

METHODS:

We retrospectively reviewed the records of 1396 patients with localized GS 6-8 PC (pT2-3N0M0) who underwent radical prostatectomy at our institution between 2005 and 2014. After excluding patients who received neoadjuvant or adjuvant therapy, or had incomplete pathological or follow-up data, 1229 patients were included in the final analysis. The Kaplan-Meier method was used to estimate and compare the probabilities of biochemical recurrence (BCR). Cox regression models were used to investigate associations between variables and the risk of BCR.

RESULTS:

Of 732 GS 7 patients, 75 (10.2%) had a TGP5. The BCR-free survival rate for men with TGP5 was significantly worse than for those without TGP5 (P<0.001). In multivariate Cox regression analyses for GS 7 PC, TGP5 was a significant predictor of BCR (hazard ratio 1.750, P=0.027). When the total cohort was stratified into four grade groups according to the new classification, group 2 with TGP5 had a BCR risk comparable to group 3, and group 3 with TGP5 behaved like group 4.

CONCLUSIONS:

Our study shows that TGP5 increased the BCR risk after RP in GS 7 PC. Moreover, we demonstrated that the presence of a TGP5 in GS 7 upgraded the BCR risk to one comparable with the next higher category under the new classification. These findings support incorporating TGP5 into GS 7 to aid with future risk assessment and follow-up scheduling for PC.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans / Male / Middle aged Idioma: En Revista: Prostate Cancer Prostatic Dis Asunto de la revista: ENDOCRINOLOGIA / NEOPLASIAS / UROLOGIA Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans / Male / Middle aged Idioma: En Revista: Prostate Cancer Prostatic Dis Asunto de la revista: ENDOCRINOLOGIA / NEOPLASIAS / UROLOGIA Año: 2017 Tipo del documento: Article