Lung adenocarcinoma — master index¶
Last curated: 2026-08-29 · condition status: audited · page status: curated · evidence cutoff: 2026-08-29
Audited corpus: 18 canonical wiki pages · 2,961 wiki lines · 270 unique PubMed records in the bibliography · 42 live-verified ClinicalTrials.gov identifiers · 6 landmark notes · 1 guideline registry · 1 statistics ledger · 4 patient-voice files · 30 stable open questions · 12 cross-domain junctions.
The condition in five sentences¶
Lung adenocarcinoma is the dominant lung-cancer histology in most assessed populations and spans preinvasive AIS/MIA through metastatic disease; lung cancer remains the leading cause of cancer death globally (Travis 2011, PMID 21252716; Bray 2024, PMID 38572751; Luo 2025, PMID 39914442). Its defining clinical feature is molecular partition: EGFR, ALK, ROS1, RET, BRAF V600E, MET exon-14, NTRK, KRAS G12C, and HER2 states route patients into distinct treatments, while PD-L1 guides immune therapy only after actionable-driver testing is complete (TCGA 2014, PMID 25079552; Lindeman 2018, PMID 29398453). Low-dose CT reduces lung-cancer mortality in smoking-exposed high-risk populations, but never-smoker adenocarcinoma—molecularly diverse across geography and linked to pollution and other forces—remains outside smoking-based eligibility (NLST PMID 21714641; NELSON PMID 31995683; Díaz-Gay 2025, PMID 40604281). Curative-intent care now combines surgery or definitive radiation with stage- and genotype-aware perioperative therapy, including adjuvant osimertinib and alectinib and neoadjuvant/perioperative chemo-immunotherapy (ADAURA PMID 37272535; ALINA PMID 38598794; CheckMate 816 PMID 35403841). The frontier is no longer only finding targets: it is choosing lifetime sequences, preventing CNS and molecular relapse, using ctDNA without overtreatment, reducing ILD and immune toxicity, and making complete biomarker access and chronic survivorship equitable.
Sibling condition: lung squamous-cell carcinoma is the deliberate contrast. TNM, LDCT, surgery, chemoradiation, checkpoint toxicity, brain-metastasis care, and palliative care are shared NSCLC domains; histology, driver biology, chemotherapy selection, and targeted-therapy sequencing differ.
Start here: overview. Quantitative lookup: statistics. Research frontier: open questions. Provenance: bibliography. Growth history: curation log.
Reading paths¶
New to the condition¶
Diagnosis and testing¶
Driver-positive metastatic disease¶
- Molecular landscape
- EGFR disease
- ALK, ROS1, and fusion drivers
- KRAS, BRAF, MET, and HER2
- Systemic therapy
- Red flags and safety concerns
Driver-negative and immune therapy¶
Curative-intent disease¶
Implementation, lived experience, and safety¶
- Patient experience and advocacy
- Clinical trials landscape
- Red flags and safety concerns
- Patient-voice sources
- Open questions
Canonical wiki pages¶
| File | Scope | Status |
|---|---|---|
| overview.md | Condition map, evidence boundaries, stage-by-biology frame | curated — audited |
| epidemiology-and-risk-factors.md | Burden, smoking, never-smokers, pollution, susceptibility, equity | curated — audited |
| histology-and-classification.md | IASLC/WHO, AIS/MIA, invasive patterns, grade, STAS, mucinous disease | curated — audited |
| screening-and-early-detection.md | NLST/NELSON, eligibility, nodules, harms, never-smokers, blood/AI tests | curated — audited |
| staging.md | TNM-9, work-up, multiple lesions, oligometastatic disease | curated — audited |
| molecular-landscape.md | Drivers, co-mutations, ancestry/exposure, evolution, spatial states | curated — audited |
| molecular-testing.md | Tissue stewardship, broad DNA/RNA, plasma, resistance, quality metrics | curated — audited |
| egfr-disease.md | IPASS, FLAURA/intensification, ADAURA, resistance, exon-20 disease | curated — audited |
| alk-ros1-and-fusion-drivers.md | ALK, ROS1, RET, NTRK; CNS activity, sequencing, resistance | curated — audited |
| kras-braf-met-her2.md | Allele-specific targeting, co-mutations, resistance, ADC/TKI strategy | curated — audited |
| immunotherapy.md | PD-L1, mono/chemo-IO, driver interaction, resistance, toxicity | curated — audited |
| early-stage-and-perioperative-therapy.md | Surgery, SABR, chemotherapy, adjuvant targeted therapy, perioperative IO, MRD | curated — audited |
| systemic-therapy.md | Integrated first-/later-line routing and progression classification | curated — audited |
| biomarkers.md | Genomic selectors, PD-L1, TMB, ctDNA/MRD, histology, multi-omics | curated — audited |
| guidelines.md | Cross-guideline synthesis, disagreements, version and jurisdiction hazards | curated — audited |
| clinical-trials-landscape.md | Live registry snapshot, active driver/MRD portfolios, design failure modes | curated — audited |
| patient-experience-and-advocacy.md | Stigma, testing wait, chronic TKI life, caregivers, access, survivorship | curated — audited |
| red-flags-and-safety-concerns.md | Emergencies, missed testing, TKI/ADC/IO toxicity, CNS vigilance | curated — audited |
The Pages table is the canonical filename list for link discipline. All 18 pages passed the 2026-08-29 claim-to-citation, currency, structure, and link audit and therefore carry status: curated.
Literature layer¶
| Asset | Purpose | Status |
|---|---|---|
| BIBLIOGRAPHY.md | 270 unique PubMed records, topic-grouped with every citing page | audited |
| Mok 2009 — IPASS | Predictive-genotype turning point | audited |
| TCGA 2014 | Multiplatform molecular atlas | audited |
| Soria 2018 — FLAURA | First-line CNS-active EGFR backbone | audited |
| Wu 2020 — ADAURA | Adjuvant EGFR paradigm and OS | audited |
| Forde 2022 — CheckMate 816 | Neoadjuvant chemo-immunotherapy | audited |
| Díaz-Gay 2025 — Sherlock-Lung | Never-smoker genomic epidemiology | audited |
| Guideline registry | Worldwide/current sources, supersession, disagreements, watch list | audited |
| Statistics ledger | Effect sizes, denominators, methods, conflicts, reuse rules | audited |
| Patient-voice README | Method, ethics, coverage and update protocol | audited |
| Organizations | 12 live-fetched public organizations | audited |
| Themes | Aggregate themes with ≥2 sources each | audited |
| Sources | Annotated research and public-source ledger | audited |
Evidence architecture¶
- Adenocarcinoma-direct evidence: histology-specific molecular cohorts, driver-restricted trials, pathology studies.
- Mixed NSCLC evidence: screening, TNM, surgery, perioperative IO, stage III, brain metastases, supportive care.
- Mechanistic evidence: mutational signatures, organoids, spatial/single-cell atlases, resistance models.
- Guidance and registry state: living recommendations, authorizations, reimbursement, and trial status that require date-specific rechecking.
Highest-priority unresolved questions¶
- Who needs first-line EGFR intensification?
- Can ctDNA safely individualize adjuvant targeted or immune therapy?
- Which lifetime ALK/ROS1/RET/HER2 sequence best prevents CNS failure?
- Are STK11 and KEAP1 predictive or primarily prognostic?
- Can never-smoker screening show mortality benefit without unacceptable overdiagnosis?
- Is postoperative checkpoint therapy necessary after neoadjuvant response?
- What improves survival after chemo-immunotherapy resistance?
- How should chronic targeted-therapy survivorship and access be measured?
See OPEN-QUESTIONS.md for 30 study-shaped questions and the “Dots not yet connected” map.
Curation state¶
Full audit completed 2026-08-29. All 270 PMIDs used anywhere in the condition were re-queried live through PubMed E-utilities, all 42 NCT identifiers were re-fetched through ClinicalTrials.gov API v2, every page passed claim-to-citation and structural checks, and all 18 canonical pages are curated. See LOG.md for audit counts, corrections, limitations, and remaining dated evidence gaps.