The Big 4 - Lung Flashcards

1
Q

How common is lung cancer?

A

-Lifetime prevalence of 1 in 13 men / 1 in 15 women
10% 5YSR
-13% of all cancers
-21% of all cancer deaths
-Majority present with advanced disease

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2
Q

What are the risk factors for lung cancer?

A

-Genetic predisposition
-Cigarette smoking
-Increasing age
-Hx of COPD
-Industrial exposure to asbestos, chromium, arsenic and iron oxide
-Radiation exposure

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3
Q

What are the different histological types of lung cancer?

A

-Differentiated between small cell and non-small cell cancers

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4
Q

What are the features of small cell lung cancer?

A

SMALL CELL (15%)
–highly aggressive, rapid growth, often metastasised and inoperable at point of diagnosis
–can respond to chemo at first but often relapse
–often associated with paraneoplastic syndromes eg SIADH, Cushing’s

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5
Q

What are the features of non-small cell lung cancer?

A

3 main types of NSCLC (85%)
SQUAMOUS CELL CARCINOMA (30%)
–often found centrally, close to bronchi, can present with bronchial obstruction
–close link to cig smoking
–often causes clubbing
–secrete PTHrp –> hyperCa2+
ADENOCARCINOMA (50%)
–often peripheral
–more common in women, non-smokers and asbestos exposure
—EGFR and ALK mutations
LARGE CELL CARCINOMA (5%)
–less differentiated, metastasise early
Other types: carcinoid, mesothelioma, sarcoma, lymphoma

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6
Q

How to patients present with lung cancer?

A

-Cough, dyspnoea, haemoptysis, chest pain, recurrent chest infections
-Specific site of tumour may produce more specific syndromes eg:
–apical tumour –> Horner’s syndrome / pain in nerve roots
–mediastinal invasion –> recurrent laryngeal nerve palsy, SVCO

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7
Q

What investigations would someone with suspected lung cancer have?

A

-CXR
-CT chest + upper abdo – assess disease extent
-PET scan – if disease is operable to check for distant mets
-Bronchoscopy + biopsy (EBUS used to biopsy mediastinal lymph nodes)
-Tumour markers – LDH and NSE
-Lung Function – important for deciding fitness for treatment
-Cardiopulmonary exercise testing – important for deciding fitness for surgery

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8
Q

How is SCLC managed?

A

CHEMOTHERAPY
-Considered a systemic disease so most given palliative chemo
-Very chemo-sensitive, so is the mainstay of management
-Can treat complications of disease eg SVCO
-Most will respond but also most will relapse (mets to brain is most common form of relapse)
RADIOTHERAPY
-Highly radio-sensitive
-Used to treat the primary tumour, prophylactically to prevent brain mets, palliatively
SURGERY
-Mostly inappropriate

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9
Q

What is the prognosis of SCLC?

A

-Median survival = 2-4 months
-For those receiving chemo = 6-12 months
-10-15% survival in patients with good performance status, favourable biochemistry and limited disease

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10
Q

How is NSCLC managed?

A

CHEMOTHERAPY
-Mostly used for those with metastatic / locally advanced disease
-Targeted therapy for those positive for mutations (EGFR+ALK)
-Immunotherapy eg pembrolizumab can be used also for those expression PDL1
RADIOTHERAPY
-Radical RT given to those with early stage disease and are unsuitable for surgery
-CHART used and given 3x a day for 12 days
-Also concurrent chemo-RT (later stage) and palliative RT given
SURGERY
-30% of NSCLC patients are suitable for surgery
-Resection has a good prognosis in early stage disease
-Adjuvant chemo given to those fit enough / with larger tumours

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11
Q

What is the prognosis of NSCLC?

A

-3-6 months without treatment
-Increases to 1-2 years with chemo / immunotherapies

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