Evidence map›Paper›PMID 42835580›Full record

ArticleBMJ oncology2026

Incidence of new-onset depression after colorectal cancer diagnosis and associated mortality: a population-based cohort study.

Vicki Cheng, Eric C Sayre, Jonathan M Loree, Sharlene Gill, Rachel A Murphy, Mary A De Vera

Abstract read
In one paragraph

Article in BMJ oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Vicki ChengFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Eric C SayreBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Jonathan M LoreeBC Cancer - Vancouver, Vancouver, British Columbia, Canada.
Sharlene GillBC Cancer - Vancouver, Vancouver, British Columbia, Canada.
Rachel A MurphyBC Cancer - Vancouver, Vancouver, British Columbia, Canada.
Mary A De VeraFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-2205-2683

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To examine the incidence of and factors associated with new-onset depression following colorectal cancer (CRC) diagnosis and its association with all-cause and CRC-specific mortality. Design: Population-based retrospective cohort study using linked administrative health databases. Setting: British Columbia, Canada. Participants: Individuals diagnosed with CRC from 2010 to 2017 without a history of physician-recorded depression diagnoses in the 5 years preceding the CRC diagnosis. Main outcome measures: New-onset depression following CRC diagnosis was identified using International Classification of Diseases (ICD)-9 and ICD-10 diagnostic codes. Cumulative incidence and incidence rates of new-onset depression were estimated, and factors associated with new-onset depression were examined using Cox proportional hazards models. Depression was modelled as a time-varying exposure in mortality analyses, with Cox proportional hazards models used to estimate hazard ratios (HR) and 95% confidence intervals (CI) for all-cause and CRC-specific mortality. Results: Among 13 986 patients with CRC (55.2% males, mean age 66.0), the 5-year cumulative incidence of new-onset depression among those without a history of depression was 6.63% following CRC diagnosis. Incidence rates were highest in the first year post-CRC diagnosis (3.54 per 100 person-years), indicating that new-onset depression was most common early after diagnosis. Factors associated with new-onset depression included female sex (HR 1.40 (95% CI 1.22 to 1.61)) and stage 4 disease (HR 1.77 (95% CI 1.34 to 2.33)). New-onset depression after CRC diagnosis was associated with 97% higher all-cause mortality (HR 1.97 (95% CI 1.74 to 2.23)) and 73% higher CRC-specific mortality (HR 1.73 (95% CI 1.48 to 2.03)). Conclusions: The cumulative incidence of new-onset depression increased over time, with incidence rates highest in the first year following CRC diagnosis. New-onset depression after CRC diagnosis was associated with higher all-cause and CRC-specific mortality. Findings highlight the importance of early identification of patients at high risk for depression and consideration of longitudinal mental healthcare in CRC care.

Indexed as

Colorectal cancerEpidemiologyMortality

Identifiers

PMID42835580
PMCPMC13636315

What OpenQuestion holds

Textmetadata
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.