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Analysis of separate training and validation radical prostatectomy cohorts identifies 0.25 mm diameter as an optimal definition for "large" cribriform prostatic adenocarcinoma.
Chan, Emily; McKenney, Jesse K; Hawley, Sarah; Corrigan, Dillon; Auman, Heidi; Newcomb, Lisa F; Boyer, Hilary D; Carroll, Peter R; Cooperberg, Matthew R; Klein, Eric; Fazli, Ladan; Gleave, Martin E; Hurtado-Coll, Antonio; Simko, Jeffry P; Nelson, Peter S; Thompson, Ian M; Tretiakova, Maria S; Troyer, Dean; True, Lawrence D; Vakar-Lopez, Funda; Lin, Daniel W; Brooks, James D; Feng, Ziding; Nguyen, Jane K.
Afiliação
  • Chan E; Department of Pathology, University of California San Francisco (UCSF), San Francisco, CA, USA. Emily.Chan@ucsf.edu.
  • McKenney JK; Robert J. Tomsich Institute of Pathology and Laboratory Medicine, Cleveland Clinic, Cleveland, OH, USA.
  • Hawley S; Canary Foundation, Palo Alto, CA, USA.
  • Corrigan D; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Auman H; Canary Foundation, Palo Alto, CA, USA.
  • Newcomb LF; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Boyer HD; University of Washington Medical Center, Seattle, WA, USA.
  • Carroll PR; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Cooperberg MR; Department of Urology, University of California San Francisco (UCSF), San Francisco, CA, USA.
  • Klein E; Department of Urology, University of California San Francisco (UCSF), San Francisco, CA, USA.
  • Fazli L; Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Gleave ME; University of British Columbia, Vancouver, BC, Canada.
  • Hurtado-Coll A; University of British Columbia, Vancouver, BC, Canada.
  • Simko JP; University of British Columbia, Vancouver, BC, Canada.
  • Nelson PS; Department of Pathology, University of California San Francisco (UCSF), San Francisco, CA, USA.
  • Thompson IM; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Tretiakova MS; University of Washington Medical Center, Seattle, WA, USA.
  • Troyer D; CHRISTUS Medical Center Hospital, San Antonio, TX, USA.
  • True LD; University of Washington Medical Center, Seattle, WA, USA.
  • Vakar-Lopez F; Eastern Virginia Medical School, Norfolk, VA, USA.
  • Lin DW; Department of Pathology, UT Health, San Antonio, TX, USA.
  • Brooks JD; University of Washington Medical Center, Seattle, WA, USA.
  • Feng Z; University of Washington Medical Center, Seattle, WA, USA.
  • Nguyen JK; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Mod Pathol ; 35(8): 1092-1100, 2022 08.
Article em En | MEDLINE | ID: mdl-35145197
ABSTRACT
Cribriform growth pattern is well-established as an adverse pathologic feature in prostate cancer. The literature suggests "large" cribriform glands associate with aggressive behavior; however, published studies use varying definitions for "large". We aimed to identify an outcome-based quantitative cut-off for "large" vs "small" cribriform glands. We conducted an initial training phase using the tissue microarray based Canary retrospective radical prostatectomy cohort. Of 1287 patients analyzed, cribriform growth was observed in 307 (24%). Using Kaplan-Meier estimates of recurrence-free survival curves (RFS) that were stratified by cribriform gland size, we identified 0.25 mm as the optimal cutoff to identify more aggressive disease. In univariable and multivariable Cox proportional hazard analyses, size >0.25 mm was a significant predictor of worse RFS compared to patients with cribriform glands ≤0.25 mm, independent of pre-operative PSA, grade, stage and margin status (p < 0.001). In addition, two different subset analyses of low-intermediate risk cases (cases with Gleason score ≤ 3 + 4 = 7; and cases with Gleason score = 3 + 4 = 7/4 + 3 = 7) likewise demonstrated patients with largest cribriform diameter >0.25 mm had a significantly lower RFS relative to patients with cribriform glands ≤0.25 mm (each subset p = 0.004). Furthermore, there was no significant difference in outcomes between patients with cribriform glands ≤ 0.25 mm and patients without cribriform glands. The >0.25 mm cut-off was validated as statistically significant in a separate 419 patient, completely embedded whole-section radical prostatectomy cohort by biochemical recurrence, metastasis-free survival, and disease specific death, even when cases with admixed Gleason pattern 5 carcinoma were excluded. In summary, our findings support reporting cribriform gland size and identify 0.25 mm as an optimal outcome-based quantitative measure for defining "large" cribriform glands. Moreover, cribriform glands >0.25 mm are associated with potential for metastatic disease independent of Gleason pattern 5 adenocarcinoma.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Adenocarcinoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Mod Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Adenocarcinoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Mod Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos