Prognostic Impact of Different Gleason Patterns on Biopsy Within Grade Group 4 Prostate Cancer

  • Keiichiro Mori
  • Vidit Sharma
  • Eva M Comperat
  • Shun Sato
  • Ekaterina Laukhtina
  • Victor M Schuettfort
  • Benjamin Pradere
  • Reza Sari Motlagh
  • Hadi Mostafaei
  • Fahad Quhal
  • Mehdi Kardoust Parizi
  • Mohammad Abufaraj
  • Pierre I Karakiewicz
  • Shin Egawa
  • Derya Tilki
  • Stephen A Boorjian
  • Shahrokh F Shariat

Beteiligte Einrichtungen

Abstract

BACKGROUND: Grade group (GG) 4 prostate cancer (PC) is considered a single entity; however, there are questions regarding prognostic heterogeneity. This study assessed the prognostic differences among various Gleason scores (GSs) classified as GG 4 PC on biopsy before radical prostatectomy (RP).

METHODS: We conducted a multicenter retrospective study, and a total of 1791 patients (GS 3 + 5: 190; GS 4 + 4: 1557; and GS 5 + 3: 44) with biopsy GG 4 were included for analysis. Biochemical recurrence (BCR)-free survival, cancer-specific survival, and overall survival were analyzed using the Kaplan-Meier method and the log-rank test. Logistic regression analysis was performed to identify factors associated with high-risk surgical pathologic features. Cox regression models were used to analyze time-dependent oncologic endpoints.

RESULTS: Over a median follow-up of 75 months, 750 patients (41.9%) experienced BCR, 146 (8.2%) died of any causes, and 57 (3.2%) died of PC. Biopsy GS 5 + 3 was associated with significantly higher rates of GS upgrading in RP specimens than GS 3 + 5 and GS 4 + 4. On multivariable analysis adjusted for clinicopathologic features, different GSs within GG 4 were significantly associated with BCR (p = 0.03) but not PC-specific or all-cause mortality. Study limitations include the lack of central pathological specimen evaluation.

CONCLUSIONS: Patients with GG 4 at biopsy exhibited some limited biological and clinical heterogeneity. Specifically, GS 5 + 3 had an increased risk of GS upgrading. This can help individualize patients' counseling and encourage further study to refine biopsy specimen-based GG classification.

Bibliografische Daten

OriginalspracheEnglisch
ISSN1068-9265
DOIs
StatusVeröffentlicht - 12.2021

Anmerkungen des Dekanats

© 2021. The Author(s).

PubMed 34117577