Objective Young-onset colorectal cancer (YCRC) incidence is rising. Scant data exist on YCRC risk after presentation with concerning symptoms such as iron-deficiency anaemia (IDA) or haematochezia. We examined the association between IDA and YCRC, and haematochezia and YCRC.
Design Cohort study of US Veterans aged 18–49 years receiving Veterans Health Administration (VHA) care 1999–2016. IDA analytic cohort was created matching individuals without incident IDA to those with IDA 4:1 based on sex, birth year and first VHA visit date (n=239 000). We used this approach to also create a distinct haematochezia analytic cohort (n=653 740). Incident YCRC was ascertained via linkage to cancer registry and/or cause-specific mortality data. We computed cumulative incidence, risk difference (RD) and HRs using Cox models in each cohort.
Results Five-year YCRC cumulative incidence was 0.45% among individuals with IDA versus 0.05% without IDA (RD: 0.39%, 95% CI: 0.33%–0.46%), corresponding to an HR of 10.81 (95% CI: 8.15–14.33). Comparing IDA versus no IDA, RD was 0.78% for men (95% CI: 0.64%–0.92%) and 0.08% for women (95% CI: 0.03%–0.13%), and RD increased by age from 0.14% for <30 years to 0.53% for 40–49 years. YCRC cumulative incidence was 0.33% among individuals with haematochezia versus 0.03% without haematochezia (RD: 0.30%, 95% CI: 0.26%–0.33%), corresponding to an HR of 10.66 (95% CI: 8.76–12.97). Comparing haematochezia versus no haematochezia, RD increased by age from 0.04% for <30 years to 0.43% for 40–49 years.
Conclusion Colonoscopy should be strongly considered in adults aged <50 years with IDA or haematochezia without a clinically confirmed alternate source.
- colorectal cancer
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Significance of this study
What is already known on this subject?
Young-onset colorectal cancer (YCRC) incidence is rising, but scant data exist on YCRC risk after presentation with concerning symptoms such as iron-deficiency anaemia (IDA) or haematochezia.
What are the new findings?
Substantially increased YCRC risk was observed after either IDA or haematochezia diagnosis. Notably, risk was higher among men with IDA and among adults aged ≥30 years with IDA or haematochezia. Despite increased risk, there was low uptake of diagnostic colonoscopy among individuals with IDA or haematochezia.
How might it impact on clinical practice in the foreseeable future?
Colonoscopy should be strongly considered in adults aged <50 years with IDA or haematochezia without a clinically confirmed alternate source.
Colorectal cancer (CRC) is the second leading cause of cancer death in the USA.1 Proportion of CRC diagnosed in adults aged <50 years—hereafter called young-onset CRC (YCRC)—has increased over time, with cases often diagnosed at later stages requiring more intense treatment.2–10 Some have advocated for more aggressive work-up of individuals aged <50 years presenting with purported ‘red flag’ signs or symptoms for CRC, iron-deficiency anaemia (IDA) and haematochezia, under the postulate this may enhance timely diagnosis and treatment.4 11 12 However, US and European clinical practice guidelines conflict regarding whether IDA or haematochezia in adults aged <50 years should trigger diagnostic colonoscopy work-up. For IDA, some guidelines recommend colonoscopy for all individuals, regardless of age or sex, while others recommend colonoscopy for those with IDA aged <50 years based on sex, and presence/absence of key clinical characteristics such as lower abdominal symptoms (table 1).13–15 Similar variation exists across guidelines for work-up of haematochezia, with some recommending colonoscopy as first work-up only for those aged ≥40 years, and others stratifying recommendations based on age, CRC risk factors and bleeding characteristics, such as presence of bright red blood per rectum (table 1).15 16
Inconsistency across guidelines reflects insufficient data on YCRC risk among individuals aged <50 years with IDA or haematochezia. Clarifying risk may inform future guidelines, optimise selection of individuals for diagnostic colonoscopy, and ultimately facilitate earlier stage detection and timely YCRC treatment. To address knowledge gaps regarding YCRC risk related to IDA and haematochezia, we conducted a study examining the association between these potential ‘red flag’ diagnoses and YCRC risk in a large cohort of US Veterans (aged <50 years).
Study design, setting and data sources
We conducted a retrospective cohort study among US Veterans aged 18–49 years receiving care within Veterans Health Administration (VHA), one of the largest US healthcare providers.17 We used a matched cohort design, matching individuals with IDA or haematochezia diagnosis to individuals without a diagnosis (online supplemental appendix figure 1). Matched cohort designs ensure balance of covariate distributions across exposure groups and comparable follow-up between exposed and unexposed individuals using a matched follow-up start date.18–20 Matching characteristics included birth year, sex and first VHA visit date (±180 days). The ‘Matching’ package in R, version 3.5.1 was used to conduct matching.21
To identify study population data, we used several Department of Veterans Affairs (VA) data resources, including the VA Corporate Data Warehouse (CDW), VHA Vital Status file and National Death Index (NDI). The VA CDW provided discrete data, including demographic characteristics, administrative claims-based diagnosis and procedure codes, prescriptions, anthropometric measures, and free-text data including procedure notes and pathology reports. The VHA Vital Status file was used to ascertain follow-up time through date of last visit, represented as the date and time the last vital record was taken by the healthcare provider.22 NDI cause-specific mortality data were used to assess vital status and cause of death, and offer the advantage of capturing cause of death within and outside VHA. Person-level linkage between VHA data and the NDI cause-specific mortality data was derived through collaboration between VA and Department of Defense partners, with matching based on social security number (SSN) or VA-scrambled SSN.23
IDA analytic cohort
Participants: IDA analytic cohort
The IDA analytic cohort included individuals aged 18–49 years receiving VHA care between 1999 and 2016. All Veterans in the IDA analytic cohort had at least one blood test measuring haemoglobin conducted within the VHA; this blood test date was defined as date of cohort entry. For each individual with IDA diagnosis, we sampled (with replacement) four matched undiagnosed individuals among those alive on the index date (date of IDA diagnosis of exposed individual). Follow-up of each 4:1 unexposed to exposed matched group—hereafter referred to as matched clusters—started on index date and continued until YCRC diagnosis, death from non-CRC causes, turning age 50, 5 years of follow-up or end of study (31 December 2016). We excluded individuals with YCRC or IBD diagnoses prior to start of follow-up. Additionally, we excluded Veterans based on any International Classification of Diseases, Ninth and Tenth Revision (ICD-9, ICD-10) diagnosis codes for IDA prior to the date of cohort entry (date of haemoglobin blood test). Only full 4:1 clusters were included.
IDA exposure variable
IDA was identified by lab diagnosis using the WHO criteria: a haemoglobin test identifying anaemia (haemoglobin <130 g/L in men, < 120 g/L in women) with a follow-up iron test within 3 months indicating iron deficiency (ferritin levels ≤15 ng/mL or transferrin saturation levels ≤16%).24 Exposed individuals were required to have an iron test to confirm presence of iron deficiency. To account for potential variations in sensitivity and specificity of IDA diagnostic criteria, we conducted a sensitivity analysis where iron deficiency was defined by ferritin levels ≤45 ng/mL (per 2020 American Gastroenterological Association guidelines)25 and transferrin saturation levels ≤16%.
Haematochezia analytic cohort
Participants: haematochezia analytic cohort
The haematochezia analytic cohort included individuals aged 18–49 years receiving VHA care between 1999 and 2016. For the haematochezia analytic cohort, date of cohort entry was defined by the first Current Procedural Terminology (CPT) code for an office visit initiating care within the VHA (online supplemental appendix table 1). Similar to the IDA analytic cohort, for each individual with haematochezia diagnosis, we sampled (with replacement) four matched undiagnosed individuals among those alive on the index date (date of haematochezia diagnosis of exposed individual). Follow-up of each 4:1 matched cluster started on index date and continued until YCRC diagnosis, death from non-CRC causes, turning age 50, 5 years of follow-up or end of study (31 December 2016). We excluded individuals with YCRC or IBD diagnoses prior to start of follow-up. Additionally, we excluded Veterans based on ICD-9/ICD-10 diagnosis codes for haematochezia prior to the date of cohort entry. Only full 4:1 clusters were included.
Haematochezia exposure variable
Haematochezia was identified by ICD-9 (569.3, 578.1) or ICD-10 (K62.5, K92.1) codes determined by the research team. To account for potential variations in administrative claims codes used to indicate haematochezia, we conducted a sensitivity analysis where the haematochezia exposure included ICD-9 (578.9) and ICD-10 (K92.2) codes corresponding to unspecified GI haemorrhage.
Primary outcome was YCRC within 5 years of start of follow-up, defined by primary and secondary diagnoses identified in VA Central Cancer Registry and Oncology Raw, which can accurately identify 90% of CRC cases,26 or NDI-identified YCRC. YCRC cases were divided into three anatomical sites based on methodology from prior studies.27–29 American Joint Committee on Cancer stage was also derived from Oncology Raw. The 5-year time window is based on an a priori assumption that IDA or haematochezia diagnoses would be either resolved or otherwise unrelated to YCRC outcome outside this time period.
Covariates were identified through a priori examination of the literature for potential common causes of IDA or haematochezia and YCRC. Covariates included race/ethnicity, body mass index (BMI), diabetes, aspirin use and smoking status (current, former, never). We defined race/ethnicity in six mutually exclusive categories: non-Hispanic White (White); non-Hispanic Black (Black); Hispanic; Asian or Native Hawaiian/Pacific Islander; American Indian or Alaska Native; and other (multiracial and those designating ‘other’ race) using race and ethnicity data within CDW. BMI and diabetes were characterised based on previously derived algorithms.30 31 Aspirin exposure was defined as at least two prescriptions or mentions of aspirin in free-text notes up to 1 year prior to start of follow-up, an approach found to have a positive predictive value and negative predictive value of 99.2% and 97.5%, respectively.32 Smoking status was determined from the VHA Health Factors structured data domain, classifying individuals based on terminology including ‘current smoker’, ‘former smoker’ or ‘never smoker’.33
The IDA and haematochezia analytic cohorts were analysed separately. We used univariable analyses to compare Veterans with IDA or haematochezia versus without IDA or haematochezia diagnosis using Wilcoxon rank-sum tests or Χ2 tests for continuous and categorical variables, respectively. Five-year cumulative YCRC incidence was derived using Kaplan-Meier estimation to account for censoring.34 Cumulative incidence was used to calculate risk differences. Number needed to scope (NNS) to identify one YCRC case was estimated by postulating that cumulative incidence over 5 years represented baseline prevalence of CRC, and computing the inverse of YCRC prevalence among exposed individuals.35 Corresponding 95% CIs for cumulative incidence, risk difference and NNS estimates were derived through bootstrapping with 1000 replications.36 We used Cox proportional hazard models to estimate YCRC hazard ratios (HRs). Follow-up of each matched cluster started on index date and continued until YCRC diagnosis or first censoring date. We estimated HRs and corresponding 95% CIs using mixed Cox regression models adjusted for race/ethnicity, BMI (categorical), prevalent diabetes, smoking status and aspirin use, and accounting for similar covariate distributions of matched clusters using cluster-specific random intercepts.37 Missingness in covariates was treated as an additional category to avoid data loss. An additional sensitivity analysis was performed adjusting for diagnosis of change in bowel habit (ICD-9: 787.99; ICD-10: R19.4) and unexplained weight loss (ICD-9: 783.21; ICD-10: R63.4) within ±60 days of follow-up start date in adjusted Cox regression models. Additional sex-stratified and age-stratified analyses were also performed, including analyses stratified by both age and sex. We also considered joint exposure of IDA and haematochezia on YCRC risk and sensitivity analyses excluding persons with joint exposures of IDA and haematochezia.
Additionally, we descriptively examined proportion of individuals receiving colonoscopy after IDA or haematochezia diagnosis. Colonoscopy was ascertained using CPT codes (online supplemental appendix table 2) summarised as proportion receiving colonoscopy (1) within 5 years and (2) within 60 days. Additional sensitivity analyses were performed to examine whether shorter first VHA visit date matching window (±90 days), excluding YCRC cases only ascertained from NDI records, excluding women in the IDA cohort with prior diagnoses of menorrhagia (ICD-9: 627.0, 626.2; ICD-10: N92.0) or prior hysterectomy (ICD-9: V88.01; ICD-10: Z90.71, Z90.710) impacted results qualitatively. Online supplemental appendix table 3 includes a description of algorithm and codes used to derive study variables. Analyses were performed using R, version 126.96.36.199
Investigators JD, LL and SG had full access to databases used for this study and used to develop the study population. This research was done without patient involvement. Patients were not invited to comment on the study design, develop patient relevant outcomes, interpret the results, or contribute to the writing or editing of this document for readability or accuracy.
Of 2 934 140 Veterans aged 18–49 years, 2 493 861 were eligible for the IDA analytic cohort, and 2 930 957 Veterans were eligible for the haematochezia analytic cohort. After applying predefined exclusion criteria and matching, there were 239 000 Veterans in the IDA analytic cohort and 653 740 Veterans in the haematochezia analytic cohort (online supplemental appendix figure 2).
IDA and YCRC risk
In the IDA analytic cohort, there were 0.8 million person-years of follow-up time and 257 YCRC diagnoses. Median age at index date was 42 (quartile 1–quartile 3 (Q1–Q3): 36–46) with a median 3.8 years of follow-up time (Q1–Q3: 1.7–5.0; table 2). Most were aged 40–49 years (63%), 49% were White and 55% were overweight or obese. There were more Veterans with IDA who were Black (43% vs 27%), obese (37% vs 29%) and aspirin users (13% vs 6%), compared with Veterans without IDA. YCRC anatomic site distribution was 38% proximal, 40% distal, 20% rectal and 2% unknown, with 39% of cancers diagnosed at stage III or stage IV (online supplemental appendix table 4).
Among 47 800 Veterans with IDA, there were 184 YCRCs (cumulative incidence: 0.45%) versus 73 YCRCs in 191 200 Veterans without IDA (cumulative incidence: 0.05%; table 3), corresponding to a risk difference (RD) of 0.39% (95% CI: 0.33%–0.46%). YCRC risk was higher among those with IDA versus without IDA (HR: 10.81, 95% CI: 8.15–14.33). There were 8482 Veterans (17%; 8482/47 800) who received a colonoscopy within 5 years of IDA diagnosis, with 2409 (28%; 2409/8482) receiving colonoscopies within 60 days.
Five-year cumulative incidence among men with IDA versus without IDA was 0.85% (95% CI: 0.72%–1.00%) compared with 0.08% (95% CI: 0.06%–0.11%; RD: 0.78%, 95% CI: 0.64%–0.92%). Five-year cumulative incidence among women with IDA versus without IDA was 0.11% (95% CI: 0.07%–0.17%) compared with 0.03% (95% CI: 0.02%–0.05%; RD: 0.08%; 95% CI: 0.03%–0.13%; table 3). Sensitivity analyses excluding women with prior menorrhagia or hysterectomy yielded similar results. In age-stratified analyses, 5-year cumulative incidence increased with increasing age for those with IDA: 0.14% (95% CI: 0.04%–0.27%) for ages <30 years, 0.20% (95% CI: 0.12%–0.28%) for ages 30–39 years and 0.61% (95% CI: 0.51%−0.72%) for ages 40–49 years (table 3). Age-stratified RDs similarly increased among those with IDA: 0.14% for ages <30 years (95% CI: 0.04%−0.26%), 0.18% for ages 30–39 years (95% CI: 0.10%–0.26%) and 0.53% for ages 40–49 years (95% CI: 0.41%–0.63%). In analyses stratified by age and sex, men aged 40–49 years with IDA had a 5-year cumulative incidence of 1.02% (95% CI: 0.84%–1.19%) compared with 0.10% (95% CI: 0.07%–0.14%) without IDA, yielding an RD of 0.91% (95% CI: 0.74%–1.09%). Age-stratified results among women were qualitatively similar.
Haematochezia diagnosis and YCRC risk
In the haematochezia analytic cohort, there were 2.62 million person-years of follow-up time and 556 YCRC cases. Median age at index date was 42 (Q1–Q3: 34–46) with median follow-up 5 years (Q1–Q3: 3.1–5.0), with 60% ages 40–49 years, 87% men, and 53% White. More Veterans with haematochezia were overweight or obese (72% vs 49%) and aspirin users (10% vs 6%) compared with Veterans without haematochezia (table 2). YCRC anatomic site distribution was 15% proximal, 45% distal, 38% rectal and 1% unknown, with 40% of cancers diagnosed at stage III or stage IV (online supplemental appendix table 4).
Among 130 748 Veterans with haematochezia, there were 406 YCRCs (5-year cumulative incidence: 0.33%, 95% CI: 0.30%–0.36%) compared with 150 YCRCs in 522 992 Veterans without haematochezia (5-year cumulative incidence: 0.03%, 95% CI: 0.03%–0.04%), corresponding to an RD of 0.30% (95% CI: 0.26%–0.33%; table 4). YCRC risk among Veterans with haematochezia was 10.66-fold higher (adjusted HR: 10.66, 95% CI: 8.76–12.97). Among those with haematochezia, 59 936 (46%) received a colonoscopy within 5 years follow-up, with 59% (35 298/59 936) of colonoscopies within 60 days of haematochezia diagnosis.
Five-year cumulative incidence among men with haematochezia versus without haematochezia was 0.35% (95% CI: 0.31%–0.38%) compared with 0.04% (95% CI: 0.03%–0.04%; RD: 0.31%; 95% CI: 0.27%–0.35%; table 4). Five-year cumulative incidence among women with haematochezia versus without haematochezia was 0.22% (95% CI: 0.15%–0.30%) compared with 0.01% (95% CI: 0.00%–0.02; RD: 0.21%; 95% CI: 0.14%–0.29%). Five-year cumulative incidence among Veterans with haematochezia increased with increasing age: 0.05% (95% CI: 0.02%–0.08%) for age <30 years, 0.16% (95% CI: 0.12%–0.20%) for ages 30–39 years and 0.50% (95% CI: 0.44%−0.55%) for ages 40–49 years. Age-stratified RDs similarly increased with increasing age: 0.04% for ages <30 years (95% CI: 0.01%−0.08%), 0.15% for ages 30–39 years (95% CI: 0.11%–0.19%) and 0.43% for ages 40–49 years (95% CI: 0.38%–0.49%).
In analyses stratified by age and sex, men aged 40–49 years with haematochezia had a 5-year cumulative incidence of 0.52% (95% CI: 0.47%–0.58%) compared with 0.07% (95% CI: 0.06%–0.08%) without haematochezia, yielding an RD of 0.46% (95% CI: 0.39%–0.52%). Among women, age-stratified RDs increased with increasing age: 0.22% for ages 30–39 years (95% CI: 0.09%–0.38%) and 0.25% for ages 40–49 years (95% CI: 0.14%–0.37%).
NNS to detect one YCRC
NNS was 259.8 (95% CI: 226.8–301.6) in the IDA analytic cohort and 322 (95% CI: 293.4–359.1) in the haematochezia analytic cohort. NNS was 140.3 (95% CI: 121.5–165.6) for men and 1056.5 (95% CI: 741–1692) for women in the IDA analytic cohort and 308 (95% CI: 280.3–342.9) for men and 471.1 (95% CI: 350.2–686.1) for women in the haematochezia analytic cohort. NNS decreased with increasing age. In the IDA analytic cohort, NNS was 703.6 (95% CI: 377.2–2422) for ages <30 years, 583.6 (95% CI: 399.2–943.8) for ages 30–39 years and 196.3 (95% CI: 171.1–235.9) for ages 40–49 years. The NNS was lowest among men aged 40–49 years at 124.3 (95% CI: 106.4 –149.3).
In the haematochezia analytic cohort, NNS was 2188.9 (95% CI: 1312–4985) for ages <30 years, 637.4 (95% CI: 497.4–865.6) for ages 30–39 years and 227 (95% CI: 206.3–253.3) for ages 40–49 years. Among men, NNS decreased with increasing age: 2727.8 for ages <30 years (95% CI: 1428.6–10 000), 694 for ages 30–39 years (95% CI: 526.3–1000) and 215.8 for ages 40–49 years (95% CI: 196.1–243.9). Among women, NNS was lowest among those aged 40–49 years (NNS: 400.5, 95% CI: 263.2–666.7).
Among 1320 Veterans with concurrent IDA and haematochezia, there were 31 YCRCs (5-year cumulative incidence: 2.50%, 95% CI: 1.65%–3.36%), compared with 226 YCRCs among 237 680 Veterans with only either or neither IDA or haematochezia diagnosis (5-year cumulative incidence: 0.12%, 95% CI: 0.10%–0.14%), corresponding to an RD of 2.39% (online supplemental appendix table 5).
In a sensitivity analysis excluding cases ascertained only from NDI records, 5-year cumulative incidence estimates slightly decreased, but were similar to the main analyses (online supplemental appendix tables 6 and 7). In sensitivity analysis modifying exposure definitions of IDA to include individuals with ferritin levels ≤45 ng/mL and haematochezia to include those with unspecified GI haemorrhage, the findings were similar to those of the primary analyses (online supplemental appendix table 8). In sensitivity analyses excluding individuals with joint exposures to IDA and haematochezia from each analytic cohort to examine independent effects of each exposure, the findings remained robust (online supplemental appendix table 9). In sensitivity analyses additionally adjusting for change in bowel habit and abnormal weight loss in Cox models, there was no meaningful difference in the effect of IDA or haematochezia on YCRC risk (online supplemental appendix table 10).
In two distinct analytic cohorts derived from a sample of 2.9 million Veterans aged 18–49 years, we found both IDA and haematochezia diagnosis were associated with 10-fold increased YCRC risk. YCRC risk was particularly elevated for men with IDA or haematochezia, and risk increased with increasing age in both cohorts. Given current evidence gaps in YCRC risk and burden, our findings could inform clinical guidelines and improve timely YCRC detection and treatment.
NNS was 140.3 for men and 1056.5 for women in the IDA analytic cohort, and 308 for men and 471.1 for women in the haematochezia analytic cohort. Prior work estimated the NNS to detect CRC among asymptomatic individuals undergoing screening colonoscopy is 333 among adults aged 50–75 years.39 The estimated NNS results for men in both cohorts were lower than these thresholds, suggesting these groups should be strongly considered for colonoscopy to rule out CRC. Notably, when adjusting for both age and sex, men aged 40–49 years had the lowest NNS at 124.3 in the IDA analytic cohort and 215.8 in the haematochezia analytic cohort. While NNS for women in the IDA and haematochezia analytic cohorts were markedly higher (1056.5 and 471.1, respectively), women aged 40–49 years in the IDA analytic cohort (NNS: 826.4) and the haematochezia analytic cohort (NNS: 400.5) had lower NNS values. In age-stratified analyses, risk difference increased by age, such that Veterans aged 40–49 years in both IDA (NNS: 196.3) and haematochezia (NNS: 227) cohorts had NNS below the 333 threshold.
YCRC risk among individuals exposed versus unexposed to IDA has not been widely studied. Hung et al found a positive association between IDA diagnosis and CRC, aligning with our findings.40 Perhaps because of the paucity of prior evidence on YCRC risk associated with IDA versus without IDA, practice guidelines regarding work-up including colonoscopy vary widely (table 1). While our study findings strengthen evidence to support guidelines recommending colonoscopy for men aged <50 years with IDA, they also raise questions concerning recommendations by some to restrict colonoscopy to postmenopausal women aged <50 years rather than all younger women. Women in our IDA analytic cohort had markedly lower YCRC risk compared with men but still had increased risk among those with IDA, even after excluding those with prior menorrhagia or hysterectomy. As such, YCRC risk findings among women aged <50 years with IDA diagnosis suggest harms and benefits of colonoscopy uptake should be carefully considered and studied further. The findings also clarify YCRC risk by age of IDA diagnosis, as the risk difference increases sharply with age, justifying discussion about age-specific colonoscopy referral to rule out YCRC.
YCRC risk among individuals with haematochezia versus without haematochezia has also not been widely studied. Prior studies retrospectively assessed symptoms in patients with YCRC at time of diagnosis, finding between 37% and 59% of symptomatic individuals had rectal bleeding at diagnosis; these symptoms sometimes led to delays in diagnosis because they were attributed to haemorrhoids.41–45 Our findings suggest clinicians should recommend patients aged <50 years with haematochezia for complete diagnostic colonoscopy work-up, particularly those between ages 40 and 49 years, or if symptoms persist. If these results are replicated by other population-based studies, practice guidelines may need to be updated to recommend colonoscopy as the primary test to evaluate haematochezia.
Our findings highlight some of the decision-making challenges clinicians face in determining the threshold for colonoscopy follow-up for individuals with IDA or haematochezia but provide a range of data for decision-making. While there may not yet be consensus on whether to base decision-making on relative risk increases, absolute risk increases or cumulative 5-year YCRC incidence, our data provide all of these parameters. As such, clinicians and guideline makers may use these data based on the parameters they feel are most important for clinical decisions, including for shared decision-making with patients.
Despite observed increased YCRC risk after IDA or haematochezia diagnosis, few patients received follow-up colonoscopy. Only 17% with IDA diagnosis and 46% with haematochezia diagnosis received colonoscopy, despite being at a higher YCRC risk than individuals without these clinical findings. No published studies, to our knowledge, have measured colonoscopy uptake among adults aged <50 years with IDA or haematochezia. The disconnect between increased risk and low uptake may herald an opportunity for health services interventions to promote colonoscopy uptake, particularly for individuals at highest risk for YCRC, such as men with IDA, and individuals with IDA or haematochezia aged 40–49 years.
Several limitations may be considered in interpreting our results. First, findings of association between IDA or haematochezia diagnosis and YCRC risk are not causal, but instead identify potential YCRC warning signs, and whether colonoscopy is indicated in these scenarios. As Veterans may receive healthcare services outside of VHA, the results potentially underestimate burden of IDA and haematochezia in the Veteran population and resultant colonoscopy uptake. Despite the sizeable proportion of YCRC cases that arise as a result of a family history of CRC,46 we were unable to account for family history of CRC due to inadequate documentation within the data source. We relied on commonly used diagnostic codes and prior laboratory criteria to inform ascertainment of haematochezia and IDA exposures, respectively. While we did not validate our IDA or haematochezia definitions, which could impact measurement precision, we conducted multiple sensitivity analyses using different exposure definitions, none of which meaningfully impacted our primary results. We also could not distinguish severity of haematochezia among patients; cancer risks might be markedly different among individuals with minor bleeding (blood on toilet paper) versus more obvious, persistent blood in stool. VHA disproportionately cares for a higher number of men versus women, which can over-represent an effect more prevalent among men. However, our IDA and haematochezia study cohorts included significant absolute numbers of women compared with other VHA-based studies.
Our study also has several strengths. To our knowledge, it is one of the largest studies to examine association between clinically suspicious CRC signs and YCRC risk. We identified IDA diagnosis using lab reports, which is a more robust methodology than relying on diagnosis codes. Cohort matching enabled adjustment for potential factors that might induce bias, specifically birth year, sex, first VHA visit and time of follow-up initiation. Further, sensitivity analyses to account for possible variations in clinical care and sampling methodology helped ensure robustness of our findings.
We found YCRC risk is elevated among Veterans aged 18–49 years after IDA or haematochezia diagnosis. Among Veterans with IDA, risk is highest among men and individuals aged ≥30 years. Among Veterans with haematochezia, YCRC risk is similar among men and women and highest among individuals aged ≥30 years. Despite increased observed risk, colonoscopy uptake after either IDA or haematochezia diagnosis was low. Our results offer the opportunity to inform clinical decision-making and practice guidelines that may facilitate earlier detection and treatment of the rising number of adults aged <50 years at risk for incident and fatal YCRC.
The study was approved by the VA San Diego Healthcare System: H130441 and the University of California San Diego Institutional Review Boards: 191787.
We acknowledge the Joint Veterans Administration/Department of Defense Mortality Data Repository and the Center for Disease Prevention Control for providing access to National Data Index data.
Twitter @dembj13, @samirguptaGI
Contributors JD, LL, CM, CAD, MEM and SG—concept and design. JD, LL, CM, CAD, MEM and SG—analysis and Interpretation of data. JD and SG—drafting of the manuscript. JD, LL, CM, CAD, MEM and SG—critical revision of the manuscript for Important intellectual content. JD, LL, CM, CAD, MEM and SG—statistical analysis.
Funding This research was supported by Grant #: 5F32CA239360-02 (PI: JD) from National Cancer Institute/National Institutes of Health; Grant # 5I01HX001574-05 (PI: SG) from VA Health Services Research and Development; and Grant #: 5R37CA222866-02 (PI: SG) from National Cancer Institute/National Institutes of Health.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.
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