Lung cancer Flashcards

1
Q

Symptoms suspicious of lung cancer

A
  • • Cough - that doesn’t go away or a long standing cough gets worse
  • • Recurrent infections
  • Breathlessness – lobar/lung collapse (co-existing COPD)
  • Haemoptysis
  • Unexplained weight loss
  • Chest and/or shoulder pains
  • Hoarse voice
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2
Q

Risk factors

A

Smoking in 85% Passive smoking, occupational asbestos, silica and nickel exposure, pulmonary fibrosis

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3
Q

Investigations

A

Aims of Investigation

  • To make a diagnosis – NSCLC or SCLC
  • Stage the disease
  • Assess fitness to undergo treatment

Most Common Investigations

  • Routine bloods – FBC, U+E, LFTs, serum calcium, CRP
  • Imaging
    • • CXR
    • CT chest and upper abdomen – look for lymph nodes, evidence of liver or adrenal metastases
    • CT / Positron emission tomography (CT-PET) - combined imaging to look for metastases
  • Tissue diagnosis
    • Bronchoscopy – will detect more central lesions
    • Percutaneous needle aspiration and biopsy – CT guided – for peripheral lesions
  • Other techniques
    • Endobronchial ultrasound – to visualize and guide needle biopsy of mediastinal lymph nodes
    • Ultra-sound guided aspiration of supraclavicular lymph nodes
    • VATS (video-assisted thoracoscopic surgery) – to diagnose and treat pleural effusions
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4
Q

Assessing fitness for treatment

A

Lung function tests – need full PFTs if considering surgery (for surgery generally need an FEV1 > 1.5 litres)

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5
Q

CXR changes in lung cancer

A

• Mass lesion • Pleural effusion • Lobar or lung collapse • Slowly resolving consolidation • Mediastinal widening or hilar lymph nodes • Normal

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6
Q

Histological classification

A

Non small cell carcinoma - better prognosis Small cell carcinoma

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7
Q

Non small cell carcinoma subtypes

A

• Squamous cell (40-60%) - closely linked to smoking history, keratinization and/or intercellular bridges on histology, central airways, high frequency of p53 mutations • Adenocarcinoma (10 -20%) - arises from mucus producing cells within bronchial epithelium,, most common form in women and non-smokers, more peripherally located, TTF-1 positive, if EGFR mutations present may benefit from treatment with EGFR inhibitors • Large cell (5-15%) - undifferentiated epithelial tumour

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8
Q

Staging of non small cell carcinoma

A

• T – tumour size • N – regional lymph node involvement • M – presence or absence of distant metastases TNM used together to give stage of disease

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9
Q

histology of small cell carcinoma

A
  • usually central -Arise from APUD cells (amine - high amine content, Precursor uptake- high uptake of amine precursors, decarboxylase - high content of enzyme decarboxylase) - associated with ectopic ADH, ACTH secretion
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10
Q

Staging of SCC

A

Staged as Limited or Extensive disease Limited disease – confined to one hemithorax and the ipsilateral supraclavicular fossa (30%) Extensive disease – all other patients (70%)

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11
Q

prognosis of SCC

A

Without treatment: survival 2-3 months in limited disease, 4 weeks in extensive disease With treatment: Limited disease survival 15 – 20 months, 10 -13 % 5 year survival Extensive disease – 8 -13 months median survival, 1-2% survive 5 years

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12
Q

Treatment of non small cell carcinoma

A

Surgery - early stages (Stage I or II)

Radiotherapy

  • Curative intent (radical radiotherapy) in some with early stages if not thought to be fit for surgery
    • Side effects – radiation pneumonitis in 10 – 15 %, radiation fibrosis around oneyear after
  • symptom control (palliative radio) - good for bone chest and chest wall pain, haemoptysis, occluded bronchi and SVCO

Chemotherapy

  • platinum based chemo (cisplastin/carboplastin) in combination with pacilatxel
  • can be used to down stage tumours for surgery or to palliate symptoms
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13
Q

Small cell carcinoma treatment

A

Limited Stage – chemotherapy (cisplatin and etoposide/irinotecan) and radiotherapy

Extensive disease - chemotherapy (carboplatin and etoposide or irinotecan) 4-6 cycles of etopside + ciplatin or carboplatin

Other Treatments

  • Endobronchial treatments – laser, stents to deal with tumour obstructing large airways
  • Palliative care – opiates to treat pain and breathlessness (important as lung cancer often diagnosed at an advanced stage in patients with other health problems e.g. COPD, IHD
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14
Q

Metastatic lung cancer common sites

A
  • Lymph nodes – mediastinal (causing superior vena caval obstruction),cervical, axillary
  • Pleural effusion
  • Liver
  • Bone - bone pain, may cause spinal cord compression
  • Brain
  • Adrenals
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15
Q

Common non-metstatic manifestations of lung cancer (paraneoplastic syndromes)

A

Disease or symptoms cause by cancer but not due to local presence of cancer cells.

Mediated by the hromones or cytokines produced by cancer cells or by an immune response against the tumour.

  • Metabolic – weight loss, anorexia, lassitude
  • Endocrine -
    • SIADH -small cell - concentrated urine, no hypovolaemia, oedema or diuretics
    • ACTH (cushings) - small celll -PTH- squamous cell - Hypercalcaemia - parathyroid-related peptide, bony metastases
  • Neurological - Eaton Lambert syndrome-affects proximal limbs and trunk with autonmic involvement (dry mouth, constipation) (pre-synaptic calcium channel absence)
  • -Neuropathy (antibodies against the myelin sheath)
  • Dermatological dermatomyositis (heliotrope rash on eye lids, purple papules on knuckles)
  • Cutaneous -Finger clubbing -Hypertrophic osteoarthropathy
  • Gynaecomastia -acanthosis nigricans -Erythema gyratum repens
  • Rarely – vascular, haematological and cutaneous effects
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16
Q

Emergencys associated with lung cancer

A

Superior vena cava obstruction

17
Q

Superior vena cav obstruction

A

Superior vena cava obstruction – due mediastinal nodes compressing SVC • Symptoms - breathless, dysphagia, stridor, swollen oedematous face and right arm • Signs – venous congestion in the neck, dilated veins in the arm • Treatment – high dose steroids, vascular stents, anti-coagulation, radiotherapy or chemotherapy

18
Q

Spinal cord compression

A

Spinal cord compression • Symptoms – leg weakness and numbness, reduce bladder and bowel control • Signs – upper motor neurone signs in legs, sensory level • Treatment – high dose steroids, urgent oncology input (radiotherapy) and/or neurosurgical input

19
Q

prognosis of NCLC

A

Surgery:

20
Q

Local tumour effects/ complications

A

-Recurrent larygneal nerve palsy -phrenic nerve palsy -brachial plexus invasion -horners syndrome

21
Q

Distant tumour effects

A
  • Mets (Brain, Bone. Liver) -adrenal symptoms (addisons)
22
Q

Clinical presentations of lung cancer

A

Chest symptoms -haemoptysis -cough -wheeze -stridor -Pain -hoarse voice General symptoms -weight loss, anorexia, lethargy, anaemia Chest X-ray -lobar collapse, peripheral nodule, cavitating mass, enlarged hilar nodes, pleural effusion Metastases -Bone: pain -Brain: Hemiparesis, fits -Liver: jaunice -Skin: Nodules Paraneoplastic syndromes -peripheral neuropathy -cerebellar degerenation - Lambort-Eaton myasthenic syndrome -dermatomyositis Neuroendocrine syndromes - hypercalcaemia -SIADH -gynaecomastia

23
Q

Hypertrophic pulmonary oesteoarthropathy

A

characterised by: -suberiosteal new bone formation at the distal ends of long bones, metatarsals, metacarpals and proximal phalanges -symmetrical arthropathy of adjacent joints -clubbing of the fingers -gynaecomastia

24
Q

Pancoast tumour

A

Apical lung tumour - most NSCL Can cause -compression of brachiocephallic vein, subclavia artery, phernic nerve and recurrent laryngeal nerve or Horners syndrome - compression of sympathetic ganglions -muscle wasting of small muscles of the hand (T1) -brachial plexopathy - pain and weakness, thoracic outlet syndrome

25
Q

Horners syndrome

A

Miosis - constriction of the pupil Ptosis - dropping of the eyelid Anhydrosis (decreased sweating) =/- enopthlamus - (apparent sunken eye)