Preventive cancer screening (adult)
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Confirm preventive screening scope: asymptomatic adult, life expectancy ≥10 yr (below which lead-time + overdiagnosis harm > benefit → STOP-screening). Excludes diagnostic workup of known symptoms/lesions and prior-cancer survivorship surveillance (USPSTF 2021; ACS 2018)
Asymptomatic, eligible, ≥10-yr life expectancy confirmed
Patient inputs (19)
Age sets pre-test prevalence (the Bayesian prior) and eligibility window for every modality (USPSTF 2021/2024)
Breast/cervical screening in female; prostate in male; modifies prevalence prior (USPSTF 2024; USPSTF 2018)
Prior colonoscopy/mammogram/Pap/LDCT dates + findings set the next interval and the conditional post-test prior (USPSTF 2021; USMSTF 2020)
Screening benefit requires ≥10-yr life expectancy; below that the lead-time + overdiagnosis harm exceeds benefit → STOP-screening logic (USPSTF 2021; ACS 2018)
Lynch/BRCA1/BRCA2/Li-Fraumeni/FAP set very high prior → earlier + more frequent screening, different modality (NCCN 2024)
≥20 pack-yr + age 50-80 + quit <15 yr = LDCT-eligible; also PLCOm2012 input — drives lung-ca prior (USPSTF 2021 PMID 33687470)
First-degree relative with breast/colon/ovarian/prostate cancer raises pre-test prevalence and shifts age/modality (USPSTF 2024; ACS 2018; NCCN 2024)
Cirrhosis of any etiology = HCC pre-test prevalence high enough that US ± AFP q6mo exceeds the testing threshold (AASLD 2023 PMID 37199193)
Chronic HBV at sufficient risk (PAGE-B / ethnicity / family hx) warrants HCC surveillance even without cirrhosis (AASLD 2023)
Dense breasts lower mammography sensitivity (test-characteristic shift); supplemental MRI if dense + high lifetime risk (USPSTF 2024; ACR 2023)
FIT sens ~74% CRC / spec ~94%; a positive FIT raises post-test prob enough to mandate diagnostic colonoscopy (USPSTF 2021; USMSTF 2017)
Primary hrHPV sens ~90-95% > cytology; 16/18 genotype → immediate colposcopy, other hrHPV+ → reflex cytology triage (USPSTF 2018; ASCCP 2019)
HPV vaccination does NOT change screening interval per USPSTF 2018 / ACS 2020 (lowers prevalence over time but protocol unchanged)
Pregnancy defers/modifies screening (mammography deferred; cervical may continue per ASCCP; LDCT/colonoscopy deferred) — special-population branch
Prior-cancer survivors follow survivorship surveillance, not average-risk screening — different prior + protocol (NCCN survivorship 2024)
Shared-decision PSA in men 55-69; low specificity → MRI/PI-RADS reflex before biopsy (USPSTF 2018 PMID 29801017; AUA 2023)
AFP adjunct to US q6mo for HCC surveillance; GALAD combines AFP/AFP-L3/DCP for higher sens (AASLD 2023)
Liver US q6mo for HCC surveillance in cirrhosis; sensitivity for early HCC ~45-63%, AFP adjunct raises it (AASLD 2023)
Mantle/chest radiation age 10-30 → very high breast prior → annual MRI + mammo from age 25-30 (NCCN 2024; ACS 2022)
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (7)
- informationallife_threateninglirads_5_definite_hcc_on_surveillance — AASLD 2023LI-RADS 5 definite HCC on surveillance imaging in cirrhosis — surveillance has converted to diagnosisTrigger could not be auto-evaluated — needs clinician judgement.
- informationalseverepositive_screen_high_PPV_route_to_diagnostic_workup — Lung-RADS/BI-RADS/LI-RADSLung-RADS 4 (PPV >15%), BI-RADS 5 (PPV >95%), positive FIT/FIT-DNA, hrHPV 16/18+, LI-RADS 4-5 — post-test probability now high enough that the harm of NOT working up exceeds the harm of the diagnostic cascadeTrigger could not be auto-evaluated — needs clinician judgement.
- informationalseverehereditary_cancer_syndrome_confirmed — NCCN 2024Confirmed Lynch (MLH1/MSH2/MSH6/PMS2 — CRC lifetime up to ~50-80%), BRCA1/2 (breast ~55-72% lifetime), Li-Fraumeni (TP53), or FAP (APC, near-100% CRC) — very high prior requiring earlier + more frequent multi-organ surveillanceTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderaterisk_model_crosses_action_threshold_expand_or_intensify — Tammemägi/ACR/USPSTF2019PLCOm2012 6-yr ≥1.3-1.7% (→ LDCT eligible despite categorical miss), Tyrer-Cuzick lifetime ≥20% (→ add annual MRI), Gail/BCRAT 5-yr ≥1.67% (→ chemoprevention), or GALAD-elevated in cirrhosis — the calculated prior crosses the action thresholdTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatefalse_positive_cascade_and_overdiagnosis_harm — NLST/ERSPCA positive screen in a low-prior context is much more likely false-positive (LDCT 96.4% of positives FP over 3 rounds — NLST) or overdiagnosed (prostate ERSPC incidence RR 1.57 vs mortality RR 0.79; mammography ~10-20% overdiagnosis) — the harm side of the Bayesian ledgerTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmildpretest_prevalence_below_testing_threshold_do_not_screen — USPSTF/AASLDAge below modality lower bound, life expectancy <10 yr, or risk tier too low (e.g., HCC without cirrhosis/high-risk-HBV; cervical <21; CRC <45 average-risk; PSA ≥70) — pre-test prevalence × harm of false-positive cascade + overdiagnosis exceeds expected benefitTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmildstop_screening_life_expectancy_or_age_bound — USPSTF/ACSLife expectancy <10 yr OR age exceeds modality upper bound (mammo >74, CRC >85, cervical >65 with adequate prior negatives, PSA ≥70, LDCT quit >15 yr or curative-surgery-ineligible, HCC if not transplant/treatment candidate) — the deprescribing-equivalentTrigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
Lung — LDCT (USPSTF 2021 Grade B PMID 33687470; NLST PMID 21714641; NELSON PMID 31995683)- low_dose_chest_ct_annualfirst lineimaging_screenLDCT annually, age 50-80, ≥20 pack-yr, current or quit <15 yr • imaging • annualNLST (Aberle NEJM 2011 PMID 21714641): 20% lung-ca mortality RR + 6.7% all-cause RR vs CXR; 96.4% of positives false-positive over 3 rounds. NELSON (de Koning NEJM 2020 PMID 31995683): cumulative lung-ca death RR 0.76 men / 0.67 women at 10 yr with only 2.1% referral rate (volumetric Lung-RADS reduces FP).
- plco_m2012_risk_model_eligibilityadd onrisk_modelPLCOm2012 6-yr risk ≥1.3-1.7% threshold • n/a • at eligibility assessmenttriggers: borderline_pack_year_or_quit_interval, risk_model_expansionExpands LDCT to higher-yield candidates missed by categorical pack-year criteria (Tammemägi NEJM 2013).
- smoking_cessation_pharmacotherapy_vareniclineadd oncessationVarenicline 1 mg BID × 12 wk (or NRT/bupropion) at every screen visit • PO • per cessation protocoltriggers: active_smoker_in_lung_screening_programLDCT mortality benefit is conditional on cessation; integrate at each screen (USPSTF 2021).
outpatient playbook — drug actions (2)
- 1. tamoxifen 20 mg or raloxifene 60 mg daily × 5 yr20 mg (tamoxifen) / 60 mg (raloxifene) • PO • dailytrigger: Gail/BCRAT 5-yr risk ≥1.67% and shared decision (USPSTF 2019)Breast cancer risk-reducing therapy; weigh VTE/endometrial harm (USPSTF 2019)
- 2. smoking cessation pharmacotherapy (varenicline preferred)1 mg BID • PO • BID × 12 wktrigger: Active smoker in lung-screening program (USPSTF 2021)LDCT benefit conditional on cessation — integrate at each screen
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Routine preventive/wellness visit — age/sex-appropriate cancer screening due (USPSTF 2021/2024); Known hereditary cancer syndrome (Lynch/BRCA/Li-Fraumeni/FAP) requiring intensified surveillance (NCCN 2024); Overdue or never-screened patient identified at any encounter (USPSTF 2021).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Preventive cancer screening (adult)** (prev.cancer-screening.core.v1). Phenotype framing: Average-risk vs high-risk pathway, AND true-positive (early cancer) vs false-positive (benign nodule, inflammatory polyp, dense-tissue artifact, BPH-driven PSA) — the false-positive cascade and overdiagnosis are encoded as harm data, not prose. Screen-detected positive routes to the dx engine; screen-negative returns to interval (USPSTF 2021; NLST FP 96.4%) Scope: Confirm preventive screening scope: asymptomatic adult, life expectancy ≥10 yr (below which lead-time + overdiagnosis harm > benefit → STOP-screening). Excludes diagnostic workup of known symptoms/lesions and prior-cancer survivorship surveillance (USPSTF 2021; ACS 2018) No severity triggers fired against current inputs.
Plan
Regimen axis: **Lung — LDCT (USPSTF 2021 Grade B PMID 33687470; NLST PMID 21714641; NELSON PMID 31995683)**. 1. low_dose_chest_ct_annual LDCT annually, age 50-80, ≥20 pack-yr, current or quit <15 yr imaging annual (imaging_screen, first line) — NLST (Aberle NEJM 2011 PMID 21714641): 20% lung-ca mortality RR + 6.7% all-cause RR vs CXR; 96.4% of positives false-positive over 3 rounds. NELSON (de Koning NEJM 2020 PMID 31995683): cumulative lung-ca death RR 0.76 men / 0.67 women at 10 yr with only 2.1% referral rate (volumetric Lung-RADS reduces FP). 2. plco_m2012_risk_model_eligibility PLCOm2012 6-yr risk ≥1.3-1.7% threshold n/a at eligibility assessment (risk_model, add on) — Expands LDCT to higher-yield candidates missed by categorical pack-year criteria (Tammemägi NEJM 2013). 3. smoking_cessation_pharmacotherapy_varenicline Varenicline 1 mg BID × 12 wk (or NRT/bupropion) at every screen visit PO per cessation protocol (cessation, add on) — LDCT mortality benefit is conditional on cessation; integrate at each screen (USPSTF 2021). Setting playbook (outpatient) — Set the pre-test prevalence prior (age/sex/risk-model), order the age/sex/risk-appropriate screen, apply PPV reasoning to positives, route follow-up, document shared decisions + harms, schedule recall, and apply STOP-screening logic when harm exceeds benefit (USPSTF 2021/2024/2018; AASLD 2023) 4. tamoxifen 20 mg or raloxifene 60 mg daily × 5 yr 20 mg (tamoxifen) / 60 mg (raloxifene) PO daily — Gail/BCRAT 5-yr risk ≥1.67% and shared decision (USPSTF 2019) (Breast cancer risk-reducing therapy; weigh VTE/endometrial harm (USPSTF 2019)) 5. smoking cessation pharmacotherapy (varenicline preferred) 1 mg BID PO BID × 12 wk — Active smoker in lung-screening program (USPSTF 2021) (LDCT benefit conditional on cessation — integrate at each screen) Non-pharmacologic actions: - Order LDCT if eligible (or PLCOm2012-expanded) — document 96.4% false-positive + overdiagnosis (USPSTF 2021; NLST PMID 21714641) - Order biennial mammography 40-74; add MRI if Tyrer-Cuzick ≥20% (USPSTF 2024; ACR 2023) - Order hrHPV-primary q5yr (30-65, 2025 WPSI preferred) or cytology q3yr (21-29) (USPSTF 2018) - Order colonoscopy q10yr / FIT annual / FIT-DNA q1-3yr / CTC q5yr (USPSTF 2021; ACS 2018) - Shared-decision PSA 55-69; MRI/PI-RADS reflex before biopsy (USPSTF 2018; AUA 2023) - Order US ± AFP q6mo in cirrhosis / high-risk HBV; GALAD adjunct (AASLD 2023) - Refer to genetics if hereditary syndrome criteria met (NCCN 2024) - HPV vaccination catch-up through age 26 if unvaccinated (ACIP 2019) - Patient education: test sensitivity/specificity, PPV, false-positive cascade, overdiagnosis, value of stopping when harm dominates (USPSTF 2021) AVOID / contraindication checks: - No_ldct_if_life_expectancy_lt_10yr_or_unable_unwilling_curative_surgery (USPSTF 2021 PMID 33687470) - Stop_ldct_once_quit_gt_15yr (USPSTF 2021 — prevalence falls below benefit threshold) - Shared_decision_required_document_false_positive_96pct_and_overdiagnosis (USPSTF 2021; NLST PMID 21714641) - Special_pop:pregnancy_defer_ldct_unless_compelling (radiation; defer to postpartum) - Special_pop:prior_lung_cancer_survivor_use_survivorship_surveillance_not_screening (NCCN 2024)
Monitoring
Regimen monitoring: - annual ldct while eligible age 50 to 80 (USPSTF 2021) - lung rads structured reporting PPV by category (ACR Lung-RADS 2022) - stop screening review each visit life expectancy and quit interval (USPSTF 2021) Setting (outpatient) monitoring: - LDCT annually 50-80 while eligible (USPSTF 2021) - Mammography biennially 40-74 (USPSTF 2024) - hrHPV q5yr / cytology q3yr per age band (USPSTF 2018; 2025 WPSI) - Colonoscopy q10yr or FIT annual or FIT-DNA q1-3yr (USPSTF 2021) - PSA q1-2yr 55-69 if shared decision to screen (USPSTF 2018) - US + AFP q6mo in cirrhosis (AASLD 2023) - Post-polypectomy surveillance per USMSTF 2020 risk strata Follow-up plan: STOP-screening / survivorship logic (the deprescribing-equivalent): discontinue when life expectancy <10 yr, age exceeds the upper bound (mammo >74, CRC >85, cervical >65 with adequate prior negatives, PSA ≥70, LDCT after 15 yr quit or curative-surgery-ineligible, HCC if not transplant/treatment candidate). Patient education on false-positive rate (LDCT 96.4% over 3 rounds — NLST), overdiagnosis (mammography ~10-20%, prostate substantial), and the value of NOT screening when harm dominates (USPSTF 2021; ACS 2018) - Close-out criterion: Stop-screening decision OR continued-interval education delivered and documented Monitoring phase: Interval + recall: LDCT annually while eligible 50-80 (USPSTF 2021); mammography biennially 40-74 (USPSTF 2024); cytology q3yr 21-29, hrHPV q5yr or co-test q5yr 30-65 (USPSTF 2018; 2025 WPSI hrHPV-primary preferred 30-65); colonoscopy q10yr / FIT annual / FIT-DNA q1-3yr / CTC q5yr (USPSTF 2021); PSA q1-2yr 55-69 if shared decision to screen (USPSTF 2018); AFP + US q6mo in cirrhosis (AASLD 2023); post-polypectomy surveillance per USMSTF 2020 risk strata
Disposition
Current setting: outpatient — Set the pre-test prevalence prior (age/sex/risk-model), order the age/sex/risk-appropriate screen, apply PPV reasoning to positives, route follow-up, document shared decisions + harms, schedule recall, and apply STOP-screening logic when harm exceeds benefit (USPSTF 2021/2024/2018; AASLD 2023) Disposition criteria: - Continue per interval if results negative and still eligible (USPSTF 2021; ACS 2018) - Refer to specialist diagnostic engine for positive screen (USPSTF 2021) - STOP screening when life expectancy <10 yr or age exceeds modality upper bound — deprescribing-equivalent (USPSTF 2021; ACS 2018) Escalation triggers (move to higher acuity): - Lung-RADS 4 → pulmonology/thoracic surgery; route onc.lung-cancer.core.v1 (ACR Lung-RADS 2022) - BI-RADS 4-5 → breast surgery/biopsy (ACR BI-RADS; USPSTF 2024) - Advanced adenoma or CRC on colonoscopy → GI/oncology (USMSTF 2020) - PSA elevated/rising → urology mpMRI/PI-RADS ± biopsy (AUA 2023) - LI-RADS 4-5 → hepatology/transplant oncology; route gi.hcc.core.v1 (AASLD 2023) - Hereditary syndrome confirmed → NCCN high-risk protocol + cascade testing (NCCN 2024)
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] LI-RADS 5 definite HCC on surveillance imaging in cirrhosis — surveillance has converted to diagnosis - [SEVERE] Lung-RADS 4 (PPV >15%), BI-RADS 5 (PPV >95%), positive FIT/FIT-DNA, hrHPV 16/18+, LI-RADS 4-5 — post-test probability now high enough that the harm of NOT working up exceeds the harm of the diagnostic cascade - [SEVERE] Confirmed Lynch (MLH1/MSH2/MSH6/PMS2 — CRC lifetime up to ~50-80%), BRCA1/2 (breast ~55-72% lifetime), Li-Fraumeni (TP53), or FAP (APC, near-100% CRC) — very high prior requiring earlier + more frequent multi-organ surveillance
Citations
- USPSTF 2018-2024 cancer screening recommendation statements + ACS 2018 colorectal + AASLD 2023 HCC + NCCN 2024 hereditary high-risk; 2025 WPSI cervical hrHPV-primary [PMID:33687470](https://pubmed.ncbi.nlm.nih.gov/33687470/) - Cited evidence (PMID 21714641) [PMID:21714641](https://pubmed.ncbi.nlm.nih.gov/21714641/) - Cited evidence (PMID 31995683) [PMID:31995683](https://pubmed.ncbi.nlm.nih.gov/31995683/) - Cited evidence (PMID 38687503) [PMID:38687503](https://pubmed.ncbi.nlm.nih.gov/38687503/) - Cited evidence (PMID 30140884) [PMID:30140884](https://pubmed.ncbi.nlm.nih.gov/30140884/) Last reconciled with current guidelines: 2026-05-16.
- USPSTF 2018-2024 cancer screening recommendation statements + ACS 2018 colorectal + AASLD 2023 HCC + NCCN 2024 hereditary high-risk; 2025 WPSI cervical hrHPV-primary — PMID:33687470
- Cited evidence (PMID 21714641) — PMID:21714641
- Cited evidence (PMID 31995683) — PMID:31995683
- Cited evidence (PMID 38687503) — PMID:38687503
- Cited evidence (PMID 30140884) — PMID:30140884