TY - JOUR
T1 - Keratin 17 is a prognostic and predictive biomarker in pancreatic ductal adenocarcinoma
AU - Delgado-Coka, Lyanne A.
AU - Roa-Peña, Lucia
AU - Babu, Sruthi
AU - Horowitz, Michael
AU - Petricoin, Emanuel F.
AU - Matrisian, Lynn M.
AU - Blais, Edik M.
AU - Marchenko, Natalia
AU - Allard, Felicia D.
AU - Akalin, Ali
AU - Jiang, Wei
AU - Larson, Brent K.
AU - Hendifar, Andrew E.
AU - Picozzi, Vincent J.
AU - Choi, Minsig
AU - Shroyer, Kenneth R.
AU - Escobar-Hoyos, Luisa F.
N1 - Publisher Copyright:
© 2024 American Society for Clinical Pathology,.
PY - 2024/9/1
Y1 - 2024/9/1
N2 - Objectives: To determine the role of keratin 17 (K17) as a predictive biomarker for response to chemotherapy by defining thresholds of K17 expression based on immunohistochemical tests that could be used to optimize therapeutic intervention for patients with pancreatic ductal adenocarcinoma (PDAC). Methods: We profiled K17 expression, a hallmark of the basal molecular subtype of PDAC, by immunohistochemistry in 2 cohorts of formalin-fixed, paraffin-embedded PDACs (n = 305). We determined a K17 threshold of expression to optimize prognostic stratification according to the lowest Akaike information criterion and explored the potential relationship between K17 and chemoresistance by multivariate predictive analyses. Results: Patients with advanced-stage, low K17 PDACs treated using 5-fluorouracil (5-FU)-based chemotherapeutic regimens had 3-fold longer survival than corresponding cases treated with gemcitabine-based chemotherapy. By contrast, PDACs with high K17 did not respond to either regimen. The predictive value of K17 was independent of tumor mutation status and other clinicopathologic variables. Conclusions: The detection of K17 in 10% or greater of PDAC cells identified patients with shortest survival. Among patients with low K17 PDACs, 5-FU-based treatment was more likely than gemcitabine-based therapies to extend survival.
AB - Objectives: To determine the role of keratin 17 (K17) as a predictive biomarker for response to chemotherapy by defining thresholds of K17 expression based on immunohistochemical tests that could be used to optimize therapeutic intervention for patients with pancreatic ductal adenocarcinoma (PDAC). Methods: We profiled K17 expression, a hallmark of the basal molecular subtype of PDAC, by immunohistochemistry in 2 cohorts of formalin-fixed, paraffin-embedded PDACs (n = 305). We determined a K17 threshold of expression to optimize prognostic stratification according to the lowest Akaike information criterion and explored the potential relationship between K17 and chemoresistance by multivariate predictive analyses. Results: Patients with advanced-stage, low K17 PDACs treated using 5-fluorouracil (5-FU)-based chemotherapeutic regimens had 3-fold longer survival than corresponding cases treated with gemcitabine-based chemotherapy. By contrast, PDACs with high K17 did not respond to either regimen. The predictive value of K17 was independent of tumor mutation status and other clinicopathologic variables. Conclusions: The detection of K17 in 10% or greater of PDAC cells identified patients with shortest survival. Among patients with low K17 PDACs, 5-FU-based treatment was more likely than gemcitabine-based therapies to extend survival.
KW - chemotherapies
KW - immunohistochemistry
KW - pancreatic ductal adenocarcinoma
KW - predictive biomarkers
UR - http://www.scopus.com/inward/record.url?scp=85203149683&partnerID=8YFLogxK
U2 - 10.1093/ajcp/aqae038
DO - 10.1093/ajcp/aqae038
M3 - Article
C2 - 38642081
AN - SCOPUS:85203149683
SN - 0002-9173
VL - 162
SP - 314
EP - 326
JO - American Journal of Clinical Pathology
JF - American Journal of Clinical Pathology
IS - 3
ER -