TY - JOUR
T1 - NCI SEER-Linked Virtual Tissue Repository Pilot
AU - Sanchez, Pamela
AU - Van Dyke, Alison L.
AU - Petkov, Valentina I.
AU - Yuan, Yao
AU - Bonds, Sarah
AU - Valenzuela, Connor
AU - Tuan, Alyssa W.
AU - Moravec, Radim
AU - Altekruse, Sean F.
AU - Singhi, Aatur D.
AU - Serdy, Kate M.
AU - Wu, Yun
AU - Cress, Rosemary D.
AU - Doherty, Jennifer A.
AU - Mueller, Lloyd
AU - Hernandez, Brenda Y.
AU - Lynch, Charles F.
AU - Tucker, Thomas C.
AU - Wu, Xiao Cheng
AU - Matrisian, Lynn
AU - Penberthy, Lynne
N1 - Publisher Copyright:
© 2024 Published by Oxford University Press.
PY - 2024/8/1
Y1 - 2024/8/1
N2 - Background: The Surveillance, Epidemiology, and End Results (SEER) Program with the National Cancer Institute tested whether population-based cancer registries can serve as honest brokers to acquire tissue and data in the SEER-Linked Virtual Tissue Repository (VTR) Pilot. Methods: We collected formalin-fixed, paraffin-embedded tissue and clinical data from patients with pancreatic ductal adenocarcinoma (PDAC) and breast cancer (BC) for two studies comparing cancer cases with highly unusual survival (≥5 years for PDAC and ≤30 months for BC) to pair-matched controls with usual survival (≤2 years for PDAC and ≥5 years for BC). Success was defined as the ability for registries to acquire tissue and data on cancer cases with highly unusual outcomes. Results: Of 98 PDAC and 103 BC matched cases eligible for tissue collection, sources of attrition for tissue collection were tissue being unavailable, control paired with failed case, second control that was not requested, tumor necrosis ≥20%, and low tumor cellularity. In total, tissue meeting the study criteria was obtained for 70 (71%) PDAC and 74 (72%) BC matched cases. For patients with tissue received, clinical data completeness ranged from 59% for CA-19-9 after treatment to >95% for margin status, whether radiation therapy and chemotherapy were administered, and comorbidities. Conclusions: The VTR Pilot demonstrated the feasibility of using SEER cancer registries as honest brokers to provide tissue and clinical data for secondary use in research. Studies using this program should oversample by 45% to 50% to obtain sufficient sample size and targeted population representation and involve subspecialty matter expert pathologists for tissue selection.
AB - Background: The Surveillance, Epidemiology, and End Results (SEER) Program with the National Cancer Institute tested whether population-based cancer registries can serve as honest brokers to acquire tissue and data in the SEER-Linked Virtual Tissue Repository (VTR) Pilot. Methods: We collected formalin-fixed, paraffin-embedded tissue and clinical data from patients with pancreatic ductal adenocarcinoma (PDAC) and breast cancer (BC) for two studies comparing cancer cases with highly unusual survival (≥5 years for PDAC and ≤30 months for BC) to pair-matched controls with usual survival (≤2 years for PDAC and ≥5 years for BC). Success was defined as the ability for registries to acquire tissue and data on cancer cases with highly unusual outcomes. Results: Of 98 PDAC and 103 BC matched cases eligible for tissue collection, sources of attrition for tissue collection were tissue being unavailable, control paired with failed case, second control that was not requested, tumor necrosis ≥20%, and low tumor cellularity. In total, tissue meeting the study criteria was obtained for 70 (71%) PDAC and 74 (72%) BC matched cases. For patients with tissue received, clinical data completeness ranged from 59% for CA-19-9 after treatment to >95% for margin status, whether radiation therapy and chemotherapy were administered, and comorbidities. Conclusions: The VTR Pilot demonstrated the feasibility of using SEER cancer registries as honest brokers to provide tissue and clinical data for secondary use in research. Studies using this program should oversample by 45% to 50% to obtain sufficient sample size and targeted population representation and involve subspecialty matter expert pathologists for tissue selection.
UR - http://www.scopus.com/inward/record.url?scp=85200712047&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85200712047&partnerID=8YFLogxK
U2 - 10.1093/jncimonographs/lgae034
DO - 10.1093/jncimonographs/lgae034
M3 - Article
C2 - 39102878
AN - SCOPUS:85200712047
SN - 1052-6773
VL - 2024
SP - 180
EP - 190
JO - Journal of the National Cancer Institute - Monographs
JF - Journal of the National Cancer Institute - Monographs
IS - 65
ER -