Evidence map›Paper›PMID 40252135›Full record

ArticleCancer causes & control : CCC2025

de novo metastases in patients with primary colorectal cancer: a Surveillance, Epidemiology, and End Results analysis.

Nicole C Loroña, Kamya Sankar, Mariana C Stern, Stephanie L Schmit, Jane C Figueiredo

Abstract read
In one paragraph

Article in Cancer causes & control : CCC, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. External validation of a nomogram for de novo bone metastasis in breast cancer: a single-center Mexican cohort.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Nicole C LoroñaDepartment of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars Sinai Medical Center, 700 N. San Vicente Blvd. Suite G599, West Hollywood, Los Angeles, CA, 90069, USA. Nicole.Lorona@cshs.org.
Kamya SankarDepartment of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars Sinai Medical Center, 700 N. San Vicente Blvd. Suite G599, West Hollywood, Los Angeles, CA, 90069, USA.
Mariana C SternDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
Stephanie L SchmitGenomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Jane C FigueiredoDepartment of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars Sinai Medical Center, 700 N. San Vicente Blvd. Suite G599, West Hollywood, Los Angeles, CA, 90069, USA.

Funding

Elucidating the role of transcriptomics in driving ethnicity and ancestry-related disparities in colorectal cancerR01CA284732 · NCI · CEDARS-SINAI MEDICAL CENTER · PI Jane C. Figueiredo, Jennifer Ann Freedman · 2024 to 2026
$2.0M
NCI NIH HHS R01 CA284732NIH HHS R01CA284732
6 · The paper itself

Abstract

purposeNearly one-quarter of colorectal cancer (CRC) cases present with de novo metastatic disease (stage IV) at diagnosis. Some metastatic sites confer poorer prognosis, and emerging data suggests that individuals from certain racial and ethnic populations may be at higher risk for de novo metastases.

methodsWe identified 181,083 CRC cases aged 20-84 between 2010 and 2020 in the Surveillance, Epidemiology, and End Results database. Two outcomes were analyzed: metastatic site (liver, lung, bone, brain) and metastatic pattern (liver only, lung only, liver and lung, other). We used logistic and multinomial logistic regression to calculate odds ratios (OR) and 95% confidence intervals (95% CI) to examine the associations between race and ethnicity and metastatic site and metastatic pattern, respectively, among early-onset (age < 50), screen-eligible (age 50-74), and elderly populations (age 75-84).

results43,054 de novo metastatic CRC cases were identified over the 10-year period. Liver was the most common metastatic site (80%). Non-Hispanic Black patients had higher odds of synchronous lung and liver metastases compared to non-Hispanic White (NHW) patients (early-onset patients: OR: 1.29, 95% CI 1.03-1.61; screen-eligible patients: OR:1.42, 95% CI 1.29-1.55; elderly patients: OR:1.66, 95% CI 1.34-2.05). Early-onset American Indian/Alaska Native patients were over twice as likely to present with lung metastases (OR: 2.10, 95% CI 1.11-3.98) compared to NHW patients.

conclusionsPresentation and patterns of de novo metastatic CRC differed across populations and age groups. Characterizing de novo metastatic CRC provides a unique opportunity to study cancer spread in treatment-naïve individuals and to identify patients at greater risk of metastases associated with poorer prognosis.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsLung NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeoplasm MetastasisPrognosisSEER ProgramUnited StatesYoung AdultColorectal cancerDisparitiesEarly-onsetEthnicityMetastaticRace

Identifiers

PMID40252135
PMCPMC12380965

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.