Lung Cancer Flashcards

1
Q

What is the epidemiology of lung cancer?

A

Decreasing over time but still c.350,000/yr

More common in men than women

Biggest killing cancer, 3rd largest cause of death
- Often presents really late

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2
Q

What is the aetiology of lung cancer?

A

Smoking predominantly - 80-90%

Occupational remainder

  • Asbestos (+smoking = 90% risk)
  • Radon
  • Coal related
  • Petroleum production
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3
Q

What are the types of lung cancer?

including pleural cancers, metastases, important genetic mutations and non-cancerous tumours

A

Non small cell - 85%:

  • Squamous - 42% = bronchial carcinomas that obstruct and lead to infection; local spread common, mets late
  • Adenocarcinoma -39% = from the mucous cells in the bronchi; more common in non-smokers; often mets to brain/bones
  • Large cell 8% - less differentiated, met early
  • Carcinoid tumours (7%)
  • Pancoast tumour - a type of NSCLC defined by its location in the right or left apex of the lung - can cause a specific set of symptoms

Small cell - 15%
- Rapidly growing, met early - almost always inoperable at presentation

Epithelial growth factor R mutation

  • Means can be treated with a specific type of chemo
  • 15-30% of adenocarcinoma
  • 6-11% of all cancers

Other

  • Malignant mesothelioma**
  • Lymphomas = BALTOMA – bronchus associated tissue lymphoma
  • Hamartomas = non carcinoma, benign proliferation of cartilage, glandular, fat and blood vessels
  • Pleural fibroma (soft tissue, mostly benign neoplasm of pleura) vs

Metastases:

Common sites for lung metastases:

  • Lymph nodes
  • Bone
  • Brain
  • Liver
  • Adrenal glands

Sites where cancers metastasise from (to the lungs):

  • Kidney
  • Prostate
  • Breast
  • Bone
  • Colorectal
  • Cervix, ovary
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4
Q

How does lung cancer present?

A

Systemic:

  • Weight loss
  • Anorexia
  • Night sweats, fever
  • Bone pain (mets)
  • Finger clubbing

General features:

  • Cough - 40% patients +/- haemoptysis (7%)
  • SOB
  • Chest pain
  • (Recurrent) chest infection

Other features depending on tumour location:

  • Wheeze - Monophonic = may indicate a single blockage of a large airway (i.e. by the tumour) as opposed to polyphonic wheezes of COPD/Asthma (though most patients will also have COPD)
  • Dysphagia

Pancoast tumour

  • Horner’s syndrome (miosis, ptosis, anhidrosis) - as invasion of sympathetic chain e.g. at T1
  • Pain + weakness in hand /arm muscles - brachial plexus involvement
  • Hoarse voice + bovine cough - recurrent laryngeal nerve involvement
  • Facial swelling, cyanosis and dilatation of neck veins - superior vena cava obstruction

Paraneoplastic symptoms:

  • c.10% of people with lung Ca, commonly
  • Humoral hypercalcaemia of malignancy - secretion of PTH-related peptide (squamous cell)
  • SIADH - secretion of ADH (small cell)
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5
Q

Who should I refer for a 2 week wait in lung cancer?

A

SEE ONCOLOGY DECK

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6
Q

How do you investigate lung cancer?

A

CXR:

  • Symptomatic tumours will usually be visible; lateral views can help
  • ‘coin lesion’ = solitary, round, circumscribed shadow in lung field (but not a specific sign)
  • Hilar enlargement
  • Pleural effusion

CT + contrast:

  • For better detail +/- staging
  • Can also be used to guide biopsy of peripheral lesions

Bronchoscopy:

  • With biopsy for cytology
  • Only useful if tumours near the hilum

PET-CT:
- For all potentially curable patients before treatment

Biopsies:

  • Neck USS + biopsy of visible lymph nodes
  • Non-USS guided transbronchial needle aspiration (TNBA)
  • Percutaneous transthoracic needle biopsy
  • Surgical biopsy

Lung function tests

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7
Q

How do you stage NSCLC?

A

TNM(7) classification:

  • TX - +ve cytology, no lesion seen
  • T0 = no evidence of primary
  • T1 = tumour <3cm
  • T2 = 3-7cm +/- involving main bronchus +/- invading visceral pleura
  • T3 = >7cm that directly invades chest wall +/- diaphragm +/- phrenic nerve +/- mediastinal pleura +/- parietal pericardium
  • T4 = invasion of mediastinal organs e.g. oesophagus, trachea. great vessels, malignant pleural effusion etc

N

  • N0 = no lymph nodes
  • N1 = ipsilateral bronchopulmonary or hilar nodes
  • N2 = ipsilateral mediastinal or subcarinal nodes
  • N3 = contralateral mediastinal, hilar or supraclavicular nodes

M

  • M0 = no mets
  • M1 = mets
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8
Q

How do you mange lung cancer?

A

Smoking cessation - especially those with good prognosis

Lung function tests + cardiovascular risk calculated pre-surgery for those eligible

Surgical resection:

  • Treatment of choice for early stage Ca
  • What is removed depends on extent and location of disease

Radiotherapy:

  • For all patients not suitable for surgery
  • Can be used in palliative settings for symptom control

Chemotherapy:

  • Wide variety of drugs e.g. vinblastine, carboplatin, docetaxel etc in a variety of regimens
  • Some specific agents better for specific types of cancers e.g. Erlotinib for EGFR-TK mutation
  • Mutlidrug regimens are standard for SCLC which is usually inoperable

Palliative care = commonly used as 5.5% 10yr survival rates even with treatment…

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9
Q

What are the key features of mesothelioma?

A

Predominantly caused by asbestos exposure:

  • Often those who manufactured it
  • Blue fibres** - lodge in lungs, aren’t removed, cause inflammation, effects exacerbated by smoking
  • Takes 20-50yrs to present - >75yrs = most common

Presents in a similar way to lung Ca:

  • Dyspnoea
  • Chest pain
  • Weight loss, anorexia
  • Fever, night sweats
  • Finger clubbing
  • Pleural effusion, ascites

CXR + CT:

  • Pleural thickening or mass
  • Rib destruction
  • Pleural effusions (drain + cytology)
  • CT guided biopsy

Treated with:

  • Limited role for surgery
  • Platinum based chemo
  • Possible radiotherapy

Needs referring to HM coroner; patients may be entitled to compensation
- People generally live 1-2yrs post Dx

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