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Diagnostic and prognostic implications of a three-antibody molecular subtyping algorithm for non-muscle invasive bladder cancer.
Jackson, Chelsea L; Chen, Lina; Hardy, Céline Sc; Ren, Kevin Ym; Visram, Kash; Bratti, Vanessa F; Johnstone, Jeannette; Sjödahl, Gottfrid; Siemens, David Robert; Gooding, Robert J; Berman, David M.
Afiliação
  • Jackson CL; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Chen L; Division of Cancer Biology and Genetics, Queen's Cancer Research Institute, Queen's University, Kingston, ON, Canada.
  • Hardy CS; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Ren KY; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Visram K; Division of Cancer Biology and Genetics, Queen's Cancer Research Institute, Queen's University, Kingston, ON, Canada.
  • Bratti VF; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Johnstone J; Department of Urology, Queen's Cancer Research Institute, Queen's University, Kingston, ON, Canada.
  • Sjödahl G; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Siemens DR; Division of Cancer Biology and Genetics, Queen's Cancer Research Institute, Queen's University, Kingston, ON, Canada.
  • Gooding RJ; Department of Urology, Queen's Cancer Research Institute, Queen's University, Kingston, ON, Canada.
  • Berman DM; Division of Urologic Research, Department of Translational Medicine, Lund University, Lund, Sweden.
J Pathol Clin Res ; 8(2): 143-154, 2022 03.
Article em En | MEDLINE | ID: mdl-34697907
ABSTRACT
Intrinsic molecular subtypes may explain marked variation between bladder cancer patients in prognosis and response to therapy. Complex testing algorithms and little attention to more prevalent, early-stage (non-muscle invasive) bladder cancers (NMIBCs) have hindered implementation of subtyping in clinical practice. Here, using a three-antibody immunohistochemistry (IHC) algorithm, we identify the diagnostic and prognostic associations of well-validated proteomic features of basal and luminal subtypes in NMIBC. By IHC, we divided 481 NMIBCs into basal (GATA3- /KRT5+ ) and luminal (GATA3+ /KRT5 variable) subtypes. We further divided the luminal subtype into URO (p16 low), URO-KRT5+ (KRT5+ ), and genomically unstable (GU) (p16 high) subtypes. Expression thresholds were confirmed using unsupervised hierarchical clustering. Subtypes were correlated with pathology and outcomes. All NMIBC cases clustered into the basal/squamous (basal) or one of the three luminal (URO, URO-KRT5+ , and GU) subtypes. Although uncommon in this NMIBC cohort, basal tumors (3%, n = 16) had dramatically higher grade (100%, n = 16, odds ratio [OR] = 13, relative risk = 3.25) and stage, and rapid progression to muscle invasion (median progression-free survival = 35.4 months, p = 0.0001). URO, the most common subtype (46%, n = 220), showed rapid recurrence (median recurrence-free survival [RFS] = 11.5 months, p = 0.039) compared to its GU counterpart (29%, n = 137, median RFS = 16.9 months), even in patients who received intravesical immunotherapy (p = 0.049). URO-KRT5+ tumors (22%, n = 108) were typically low grade (66%, n = 71, OR = 3.7) and recurred slowly (median RFS = 38.7 months). Therefore, a simple immunohistochemical algorithm can identify clinically relevant molecular subtypes of NMIBC. In routine clinical practice, this three-antibody algorithm may help clarify diagnostic dilemmas and optimize surveillance and treatment strategies for patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Pathol Clin Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Pathol Clin Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá