TY - JOUR
T1 - Building research infrastructure to advance precision medicine in colorectal cancer
AU - Schmit, Stephanie L.
AU - Loroña, Nicole C.
AU - Sobieski, Daniel
AU - Matejcic, Marco
AU - Nguyen, Nathalie T.
AU - Hoehn, Hannah J.
AU - Diaz, Diana B.
AU - Shankar, Kritika
AU - Cockman, Eric M.
AU - Jean-Baptiste, Esther
AU - Tsai, Ya Yu
AU - Buchalter, R. Blake
AU - Brito, Karina
AU - Wilson, Rusche
AU - Coppola, Domenico
AU - Fulmer, Clifton
AU - Saglam, Ozlen
AU - Tassielli, Alexandra F.
AU - Beato, Francisca
AU - Dai, Ruifan
AU - Freedman, Jennifer A.
AU - Purrington, Kristen
AU - Hu, Bo
AU - McGrail, Daniel
AU - Gibson, Heather
AU - Jiang, Kun
AU - Muñoz-Antonia, Teresita
AU - Flores, Idhaliz
AU - Gordian, Edna
AU - Oliveras Torres, José A.
AU - Cheng, Iona
AU - Van Blarigan, Erin L.
AU - Felder, Seth I.
AU - Sanchez, Julian A.
AU - Fleming, Jason B.
AU - Siegel, Erin M.
AU - Cress, Douglas
AU - Thompson, Patricia
AU - Stern, Mariana C.
AU - Teer, Jamie K.
AU - Figueiredo, Jane C.
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/6/1
Y1 - 2025/6/1
N2 - Background: Addressing critical gaps in precision medicine initiatives in colorectal cancer (CRC) requires building larger collaborative studies. Methods: The Latino Colorectal Cancer Consortium (LC3) is a resource that harmonizes data collected in observational studies with data from individuals who identify as Hispanic/Latino with a diagnosis of primary colorectal adenocarcinoma. Data collected includes demographics, medical history, family history, and lifestyle risk factors from patient-completed surveys. Vital status, cause of death, treatment, and clinicopathological characteristics were obtained through medical chart abstraction, pathology reports, and/or linkage to state cancer registries. Blood, saliva, or normal colonic tissues were used to extract and genotype germline DNA. Tumor tissue (snap frozen or formalin-fixed paraffin-embedded) was evaluated by pathologists for diagnosis, tissue content, tumor cellularity, necrosis, immune infiltration, and additional histopathological characteristics. A centralized database with a virtual tumor repository was created to facilitate collaborative research. Results: As of April 2024, LC3 assembled data from 2210 patients (diagnosed 1994 to 2023). The mean age at diagnosis was 57 (range: 19–93) years; 54.3% of participants were male, and 62.0% had been diagnosed with colon cancer. Surveys were completed by 1722 (77.8%) participants. Ongoing multi-omics profiling on up to 600 patients include: genome-wide germline genotyping, paired tumor/ normal whole exome sequencing, bulk RNA-seq, T cell receptor immunosequencing, and multiplex immunofluorescence. Conclusions: This consortium fills an important gap in research infrastructure in CRC as well as improving precision medicine initiatives for all individuals.
AB - Background: Addressing critical gaps in precision medicine initiatives in colorectal cancer (CRC) requires building larger collaborative studies. Methods: The Latino Colorectal Cancer Consortium (LC3) is a resource that harmonizes data collected in observational studies with data from individuals who identify as Hispanic/Latino with a diagnosis of primary colorectal adenocarcinoma. Data collected includes demographics, medical history, family history, and lifestyle risk factors from patient-completed surveys. Vital status, cause of death, treatment, and clinicopathological characteristics were obtained through medical chart abstraction, pathology reports, and/or linkage to state cancer registries. Blood, saliva, or normal colonic tissues were used to extract and genotype germline DNA. Tumor tissue (snap frozen or formalin-fixed paraffin-embedded) was evaluated by pathologists for diagnosis, tissue content, tumor cellularity, necrosis, immune infiltration, and additional histopathological characteristics. A centralized database with a virtual tumor repository was created to facilitate collaborative research. Results: As of April 2024, LC3 assembled data from 2210 patients (diagnosed 1994 to 2023). The mean age at diagnosis was 57 (range: 19–93) years; 54.3% of participants were male, and 62.0% had been diagnosed with colon cancer. Surveys were completed by 1722 (77.8%) participants. Ongoing multi-omics profiling on up to 600 patients include: genome-wide germline genotyping, paired tumor/ normal whole exome sequencing, bulk RNA-seq, T cell receptor immunosequencing, and multiplex immunofluorescence. Conclusions: This consortium fills an important gap in research infrastructure in CRC as well as improving precision medicine initiatives for all individuals.
UR - https://www.scopus.com/pages/publications/105008102354
UR - https://www.scopus.com/pages/publications/105008102354#tab=citedBy
U2 - 10.1093/jncics/pkaf027
DO - 10.1093/jncics/pkaf027
M3 - Article
C2 - 40111849
AN - SCOPUS:105008102354
SN - 2515-5091
VL - 9
JO - JNCI Cancer Spectrum
JF - JNCI Cancer Spectrum
IS - 3
M1 - pkaf027
ER -