Lung Flashcards

1
Q

What are the risk factors for lung cancer?

A

Smoking x10

Asbestos x5

TB

COPD

RT

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2
Q

Outline the histology of lung cancer

A

SCLC

NSCLC

  • adenocarcinoma
  • squamous cell carcinoma
  • large cell carcinoma
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3
Q

What is the 2WW referral criteria for suspected lung cancer?

A

> 40 with 2+ unexplained symptoms

OR

Smoker with 1 symptom

  • Seen within 14 days
  • 31 days from referral to diagnosis
  • 62 days from referral to treatment
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4
Q

How should lung Ca be investigated?

A

Bloods = FBC, U+E, LFT, CRP, bone (hyperCa in SCLC)

CXR –> staging CT NTAP –> PET scan

Biopsy

Radionuclide bone scan (?mets)

Lung function testing - suitability for lobectomy

Tumour markers = CEA, Ca 19.9, Ca 125, PSA

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5
Q

How should lung Ca be managed?

A

NSCLC =
- Curative: surgery, if unfit = radical RT (CHART Continuous hyperfractionated accelerated RT)/chemo (platinum-based), targeted therapy (EGFR TKIs), immunotherapy (pembrolizumab)

SCLC =
- Chemo (cisplatin) + RT (if limited disease), surgery

Palliative: stents, brachytherapy, palliative chemo/DXT

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6
Q

Outline the complications of lung Ca

A

Lung collapse

Effusion

SVCO

RLN palsy

Horner’s syndrome

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7
Q

What are the possible symptoms and signs of lung Ca?

A

Symptoms =

  • dyspnoea (60%)
  • cough (50%)
  • chest pain (33%)
  • haemoptysis (25%)
  • anorexia, weight loss

Signs =

  • consolidation
  • collapse
  • pleural effusion
  • cachexia
  • SVCO
  • horners syndrome
  • hypertrophic pulmonary osteoarthropathy (HPOA) wrist, ankles, knees (common in adenocarcinoma)
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8
Q

What is the prognosis for a pt with lung Ca?

A

NSCLC =

  • without spread: 50% 2y survival
  • spread: 10%

SCLC =

  • treated: 1-1 1/2y
  • untreated: 3m
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9
Q

Outline the features of SCLC

A

Most commonly associated with low Na and LN mass

Kulchitsky Cells (sometimes called neuroendocrine cancer)

Rapidly growing highly malignant

Almost always inoperable at presentation

Responsive to chemotherapy

Poor prognosis

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10
Q

Outline the features of NSCLC

A

Squamous (SCC)

  • Grows slowly, spreads late
  • Obstructive lesion of bronchus leading to infection
  • Common local spread but late widespread mets
  • Can present as cavitating lesion with hyperCa

Adenoacarcinoma

  • Arise from mucous cell in bronchial epithelium
  • Invasion of pleural + LN common.
  • Mets to brain/bones
  • More common in non-smokers vs. other types.
  • Associated with asbestos
  • Bronchoalveolar
  • Peripeheral solitary nodule of diffuse nodular lesion

Large-cell

  • Less differentiated froms of SCC and adenocarcinoma
  • Early mets
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11
Q

What are the classical CXR changes seen for each type of lung Ca?

A

Hilar mass = squamous and SCLC

Peripheral = adenocarcinoma

Cavitation = squamous

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12
Q

How can tissue be obtained for biopsy with regards to lung Ca?

A
  • Diagnostic pleural tap
  • Bronchoscopy
  • CT-guided biopsy
  • Pleural biopsy
  • Thoracoscopy (pleural effusion or peripheral lesion)
  • Excision biopsy
  • EBUS (central lesions)
  • Mediastinoscopy

Mediastinal node involvement = EBUS guided transbronchial needle aspiration is the optimal initial strategy for nodal sampling

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13
Q

How is a pleural tap tested?

A

3 samples – microbiology, biochemistry, cytology

pH, albumin, protein, LDH, glucose (need grey bottle), acid-fast bacteria culture

If necessary can also check cholesterol, triglyceride, haematocrit, amylase

LIGHTS criteria
- If normal serum protein, pleural fluid protein >30g/l is an exudate

Otherwise:

  • Pleural fluid protein/serum protein >0.5
  • Pleural fluid LDH/serum LDH ratio >0.6
  • Pleural fluid LDH > two-thirds upper limit of normal serum LDH
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