TY - JOUR
T1 - Real-time functional proteomics enhances therapeutic targeting in precision oncology molecular tumor boards
AU - Hunt, Allison L.
AU - Randall, Jamie
AU - Mansukhani, Mahesh M.
AU - Nyberg, Kara
AU - Nutcharoen, Aratara
AU - Davis, Justin
AU - Corgiat, Brian
AU - Mueller, Claudius
AU - Melvin, Savannah
AU - Sharma, Meenakshi
AU - Johnston, Laura
AU - Swain, Whitney
AU - Abulez, Tamara
AU - Bateman, Nicholas W.
AU - Maxwell, G. Larry
AU - Deeken, John
AU - Benyounes, Amin
AU - Petricoin, Emanuel F.
AU - Cannon, Timothy L.
AU - Conrads, Thomas P.
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Collaborative review of molecular profiling data by multidisciplinary molecular tumor boards (MTB) is increasingly important for improving patient management and outcomes, though currently relies nearly exclusively on nucleic acid next-generation sequencing (NGS) and limited panels of immunohistochemistry-based protein abundance data. We examined the feasibility of incorporating real-time laser microdissection (LMD) enrichment of tumor epithelium and commercial CLIA-based reverse phase protein array (RPPA) protein drug target expression/activation profiling into our cancer center’s MTB to complement standard clinical NGS-based profiling. The LMD-RPPA workflow was performed within a therapeutically permissive timeframe with a median dwell time of nine days, during which specimens were processed outside of standard clinical workflows. The RPPA-generated data supported additional and/or alternative therapeutic considerations for 54% of profiled patients following review by the MTB. These findings suggest that integrating proteomic/phosphoproteomic and NGS-based genomic data creates opportunities to further personalize clinical decision-making for precision oncology.
AB - Collaborative review of molecular profiling data by multidisciplinary molecular tumor boards (MTB) is increasingly important for improving patient management and outcomes, though currently relies nearly exclusively on nucleic acid next-generation sequencing (NGS) and limited panels of immunohistochemistry-based protein abundance data. We examined the feasibility of incorporating real-time laser microdissection (LMD) enrichment of tumor epithelium and commercial CLIA-based reverse phase protein array (RPPA) protein drug target expression/activation profiling into our cancer center’s MTB to complement standard clinical NGS-based profiling. The LMD-RPPA workflow was performed within a therapeutically permissive timeframe with a median dwell time of nine days, during which specimens were processed outside of standard clinical workflows. The RPPA-generated data supported additional and/or alternative therapeutic considerations for 54% of profiled patients following review by the MTB. These findings suggest that integrating proteomic/phosphoproteomic and NGS-based genomic data creates opportunities to further personalize clinical decision-making for precision oncology.
UR - http://www.scopus.com/inward/record.url?scp=105002985958&partnerID=8YFLogxK
U2 - 10.1038/s41698-025-00868-y
DO - 10.1038/s41698-025-00868-y
M3 - Article
AN - SCOPUS:105002985958
SN - 2397-768X
VL - 9
JO - npj Precision Oncology
JF - npj Precision Oncology
IS - 1
M1 - 111
ER -