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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Non-small-cell lung cancer

Oncology and palliative care · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Acute complication of thoracic malignancy

Major haemoptysis, central airway obstruction, superior vena cava obstruction, spinal or brain compression, severe hypercalcaemia, pulmonary embolism or treatment-related pneumonitis can be the immediate NSCLC presentation.

Action: Use the relevant emergency pathway and acute oncology, respiratory, surgical, interventional or critical-care support first, obtaining tissue and stage in parallel only where this does not delay airway, bleeding, neurological or metabolic rescue.

Synopsis

Integrate pathology, TNM stage, invasive nodal assessment, molecular drivers, PD-L1, cardiopulmonary reserve and patient priorities to select curative local, multimodality or advanced systemic treatment.

  • NSCLC includes adenocarcinoma, squamous carcinoma and less common subtypes; subtype determines tissue handling, predictive testing and systemic options.
  • Diagnosis requires adequate tissue with morphology and immunohistochemistry while preserving material for genomic and PD-L1 testing.
  • First-line anatomical staging uses contrast CT chest and upper abdomen, followed by PET-CT when curative treatment is possible; suspicious nodes often need EBUS or EUS tissue confirmation.
  • Gold-standard pathological stage comes from systematically sampled or dissected nodes and resection tissue when surgery occurs; PET uptake alone is neither cancer proof nor complete nodal exclusion.
  • Early resectable disease is considered for anatomical resection with systematic nodal evaluation; stereotactic ablative radiotherapy is a preferred curative alternative for selected medically inoperable early disease.
  • Stage III disease requires a thoracic MDT because resectable and unresectable subgroups need different sequences of surgery, systemic treatment and radiotherapy.
  • Before non-emergency advanced treatment, obtain the current NHS genomic panel and PD-L1 result; an actionable driver usually changes the preferred first systemic sequence.
  • Supportive and palliative care, smoking treatment, nutrition, exercise and symptom control run alongside curative or systemic therapy rather than after anticancer options end.

Key red flags

Large-volume haemoptysis, stridor, monophonic wheeze, severe hypoxaemia or inability to clear secretions suggests central airway or bleeding threat.

Facial and arm swelling with chest-wall collaterals suggests superior vena cava obstruction and needs severity-based urgent imaging and decompression review.

New focal neurological deficit, seizure, spinal pain with weakness or sphincter change indicates possible metastatic neural compression.

A solitary distant lesion that alone removes curative intent should be confirmed with high diagnostic confidence or tissue where feasible.

New breathlessness during immunotherapy or thoracic radiotherapy requires assessment for pneumonitis, infection, embolism, effusion and progression.

Metastatic presentation

Seizure, bone pain, fracture, jaundice, hypercalcaemia, adrenal lesion or weight loss may reveal distant disease.

Investigation priorities

01
Tissue diagnosis with subtypeFirst step

Confirm malignancy and distinguish adenocarcinoma, squamous and other NSCLC while preserving predictive material.

02
First-line contrast CT chest and upper abdomenFirst line

Define primary anatomy, nodes, pleura, liver and adrenal disease and identify biopsy targets.

Management branches

DiagnoseObtain tissue that also stages

Imaging suggests a primary lung cancer.

  1. Review CT with respiratory and radiology teams and choose bronchoscopy, EBUS, CT-guided core or metastatic-site biopsy that offers adequate tissue with lowest harm.
  2. Confirm NSCLC subtype and preserve material for the national genomic panel and PD-L1 rather than exhausting it on broad non-decision-changing stains.
  3. Complete PET-CT and brain or other imaging appropriate to intended treatment and verify any solitary finding that alone removes curative intent.

Key medicines

Osimertinib for qualifying EGFR-mutated NSCLCGive osimertinib 80 mg orally once daily under the current licensed and NICE-funded early, locally advanced or metastatic indication, continuing until the protocol stop point or unacceptable toxicity.Confirm the qualifying alteration and indication. Monitor ECG and QT, electrolytes, ventricular function when indicated, eye symptoms and blood count and investigate new breathlessness urgently for interstitial lung disease.
PembrolizumabGive pembrolizumab 200 mg intravenously every 3 weeks or 400 mg every 6 weeks within the licensed NSCLC regimen and current NICE biomarker and combination criteria.Immune toxicity can affect any organ and occur after stopping; review autoimmune disease, transplant, infection and immunosuppression and hold treatment for clinically significant suspected toxicity.
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Sources and review status5 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE NG122 lung cancer diagnosis and stagingTissue, PET-CT, mediastinal staging, distant-site confirmation and fitness.
  • NICE NG122 lung cancer managementSurgery, radiotherapy, multimodality and systemic-treatment principles.
  • NHS England National Genomic Test DirectoryCurrent genomic eligibility and national testing pathway.
  • Tagrisso Summary of Product CharacteristicsOsimertinib dose, indications, interactions and safety monitoring.
  • Pembrolizumab Summary of Product CharacteristicsLicensed schedules and immune-mediated safety.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom