Lung Cancer Flashcards

1
Q

Lung cancer is the ____ most common cancer in the UK

It affects _____ (gender) more than _____ (gender) in the UK

Lung cancer is the ______ most common cause of cancer-related death in the world (in 2020)

Lung cancer usually presents affects those aged ____

A
  • 3rd most common in UK
  • Affects slightly more men than women (52% male, 48% female); incidence in men has increased and incidence in women has decreased (due to changes in smoking habits in recent decades)
  • Lung cancer is the MOST common cause of cancer-related death in the world (WHO 2020)
  • 60-80yrs
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2
Q

State some risk factors for lung cancer- highlighting the most common

A
  • Smoking- including passive smoking (due to the hydrocarbon carcinogens which cause metaplasia of bronchial epithelium from columnar to squamous. 80-90% lung cancers attributable to smoking)
  • Air pollution- particularly from diesel engines
  • Asbestos exposure
  • Previous radiotherapy to chest
  • Radon gas exposure
  • Nickel exposure (used in alloys, stainless steel manufacture, pigments for paints etc)
  • Arsenic exposure (used in industrial production as alloying agent and for production of other materials e.g. glass. Also present in ground water in some countries)
  • Silica exposure
  • Previous TB
  • Family history
  • Underlying lung disease e.g. COPD, interstitial lung disease
  • Use of Beta-carotene in those who smoke or have been exposed to asbestos
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3
Q

State the different types of lung cancer; for each state what % of lung cancers they make up

A
  • Small cell lung cancer (SCLC) = 15-20%
  • Non-small cell lung cancer (NSCLC) = 80%
    • Adenocarcinoma = 40%
    • Squamous cell carcinoma = 35%
    • Large cell carcinoma = 10%
    • Other types = 10% (e.g. carcinoid)
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4
Q

What % of pts with lung cancer experience paraneoplastic syndromes?

A

10%

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5
Q

For small cell lung carcinoma, discuss:

  • Central or peripheral
  • What cells they arise from
  • Differentiation
  • Whether it metastasises late or early
  • Whether cavitation is common
  • What neoplastic syndromes are seen
A
  • Central
  • APUD cells
  • Poorly differentiated
  • Metastasises early (usually metastatic at time of diagnosis)
  • Cavitation rare
  • Paraneoplastic syndromes:
    • Ectopic ADH secretion → hyponatraemia
    • Ectopic ACTH secretion → cushing’s syndrome, bilateral adrenal hyperplasia, hypokalaemic alkalosis (due to high cortisol)
    • Lambert-Eaton syndrome
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6
Q

For adenocarcinoma, discuss:

  • Central or peripheral
  • Differentiation
  • Whether it metastasises late or early
  • Who common in
  • What extrapulmonary manifestations common
  • What therapy it responds well to
A
  • Peripheral
  • Glandular differentiation
  • Metastasise early
  • Most common type seen in non-smokers (although most of people with it are smokers)
  • Thrombophlebitis, gynaecomastia
  • Responds well to immunotherapy
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7
Q

For squamous cell carcinoma discuss:

  • Central or peripheral
  • Differentiation
  • Whether it metastasises late or early
  • Whether cavitation is common
  • What neoplastic syndromes & extrapulmonary manifestations are seen
A
  • Central
  • Squamous differentiation
  • Metastasise late
  • Most likely to have cavitation
  • Neoplastic:
    • PTHrP secretion → hypercalcemia
    • Ectopic TSH → hyperthyroidism
  • Extra-pulmonary:
    • Hypertrophic pulmonary osteoarthropathy (triad of periostitis, digital clubbing and painful arthropathy of the large joints. Can also occur in other types e.g. adenocarcinoma)
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8
Q

For large cell carcinoma discuss:

  • Central or peripheral
  • Differentiation
  • Whether it metastasises late or early
  • Whether cavitation is common
  • What neoplastic syndromes & extrapulmonary manifestations are seen
A
  • Peripheral
  • Large, anaplastic, poorly differentiated
  • Metastasises early
  • May secrete B-HCG
  • Extra-pulmonary manifestations:
    • SVC syndromes
    • Hoarseness
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9
Q

Summary table for types of lung cancer

A

Passmed says both squamous and adenocarcinoma can have hypertrophic pulmonary osteoarthropathy

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10
Q

State some common sites for metastases in lung cancer

A
  • Liver
  • Skeleton
  • Brain (especially SCLC)
  • Adrenal glands (may present with Addison’s)
  • Lymph nodes
  • Skin
  • Other areas of lungs (including contralateral lung)
  • Pleura
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11
Q

State some symptoms of lung cancer

A

Some will be asymptomatic and have been diagnosed as CXR for screening or as part of an investigation of another disease. Up to 20% can present with non-respiratory symptoms.

  • Persistent cough >3 weeks
  • Haemoptysis
  • Dyspnoea
  • Chest pain
  • Recurrent infections
  • Hoarseness of voice (compression of recurrent laryngeal nerve)
  • Neck/arm pain (invasion of T1 nerve root)
  • Bone pain
  • Weight loss
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12
Q

State some signs of lung cancer

A
  • Finger clubbing
  • Nicotine staining
  • Lymphadenopathy (often supraclavicular)
  • Dullness to percussion over tumour
  • Wheeze
  • SVC obstruction/swelling of face/neck/arms
  • Horner’s syndrome (**partial ptosis, anhidrosis and miosis)
  • Cachexia
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13
Q

State some differential diagnoses for lung cancer and how you would differentiate these from lung cancer

A
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14
Q

Discuss the 2WW referral for lung cancer

A
  • Refer for 2WW appointment if:
    • CXR findings suggestive of lung cancer
    • >/=40yrs with unexplained haemoptysis
  • Refer for urgent CXR (within 2 weeks) if >/=40yrs and have 2 or more of the following or if they have ever smoked and have 1 or more of the following:
    • Cough.
    • Fatigue.
    • Shortness of breath.
    • Chest pain.
    • Weight loss.
    • Appetite loss
  • Consider urgent CXR (within 2 weeks) to assess for lung cancer in people >/=40yrs with any of the following:
    • Persistent or recurrent chest infection.
    • Finger clubbing.
    • Supraclavicular lymphadenopathy or persistent cervical lymphadenopathy.
    • Chest signs consistent with lung cancer.
    • Thrombocytosis.
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15
Q

What are the government/department of health targets relation to the lung cancer screening/diagnostic pathways

A
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16
Q

What investigations are done in suspected lung cancer?

A
  • First line= CXR (both AP and lateral)
  • CT Thorax & upper abdomen (using contrast): for staging
  • PET scans: look for metastases
  • Biopsy:
    • Bronchoscopy +/- endobronchial ultrasound (EBUS): if have bronchial lesion and/or mediastinal lymph nodes (central lesion)
    • CT guided biopsy (for peripheral tumours)
    • Thoracoscopy (if pleural effusion)
    • US guided neck node fine needle aspiration (for cytology)
  • MRI (thorax or brain): to get more detailed view of invasion into e.g. blood vessels, nerves. MRI brain if suspect brain mets in SCLC
  • Bloods: look for signs that may suggest cancer (see separate FC)
17
Q

What bloods would you order in someone with suspected lung cancer? What might you find?

A
  • FBC: anaemia. thrombocytosis, leukocytosis
  • LFTs: deranged LFTs due to liver mets e.g. raised ALP
  • Calcium profile/bone profile: hypercalaemia, hyperphosphatemia, raised ALP
  • U&Es: baseline renal function, SIADH may lead to hyponatraemia
  • INR

*likely do full set baseline bloods so include U&Es

18
Q

What might you see on a CXR of a pt with lung cancer?

A
  • Discrete opacity (may be cavitating)
  • Hilar lymphadenopathy
  • Pulmonary collapse
  • Pleural effusion
19
Q

What further investigations will someone need prior to surgery?

A
  • Mediastinoscopy (as CT scan doesn’t show mediastinal lymph node involvement)
  • Lung function testing e.g. spirometry (as FEV1 helps guide what kind of surgery they are suitable for e.g. wedge resection, lobectomy, pneumonectomy)
  • Other usual pre-op investigations e.g. ECG, bloods
20
Q

What staging is used for lung cancer?

*Be sure to be specific about how this staging is interpreted in terms of lung cancer

A

TNM

21
Q

In SCLC, a two category staging system is also used alongside TNM staging; describe this two category staging system

A
  • Limited (30% pts): confined to ipsilateral hemithorax and fits in/can be treated in one radiation field (may include ipsilateral supraclavicular nodes)
  • Extensive (70%): disease other than limited
22
Q

Discuss the management of SCLC

A

SCLC is usually metastatic disease at time of diagnosis. Management depends on extent of disease. All pts should be advised to stop smoking. Chemotherapy is the mainstay of treatment.

  • Very early stage disease (T1-2a, N0, M0): considered for surgery and then adjuvant chemotherapy- RARE AS OFTEN PRESENT METASTASES
  • Limited disease: combination of chemotherapy (with platinum based chemotherapy agents) and radiotherapy to the chest. Prophylactic cranial irradiation to prevent brain metastases if show good response to initial treatment.
  • More extensive disease: chemotherapy + immunotherapy (Immunotherapy offered to those with extensive disease and performance status 0-1). Prophylactic cranial irradiation to prevent brain metastases if show good response to initial treatment. (May give radiotherapy if show complete extra thoracic and partial intrathoracic response to chemo or may use to palliate symptoms)

*Immunotherapy treatments targeting PDL-1 (check Dr Chauhan’s slide when available)

*SCLC very chemo sensitive however there is a high relapse rate. Immunotherapy can help extend overall survival by ~2months

23
Q

Discuss the treatment of NSCLC

A

Management depends on extent of disease. NSCL has poorer response to chemotherapy than SCLC. All should be advised to stop smoking. Options include:

  • Early stage (I-IIIa):
    • Surgical resection (wedge resection, lobectomy, pneumonectomy)
    • May have neoadjuvant or adjuvant chemotherapy if higher stage (platinum based- may be adjuvant or neoadjuvant dependent on tumour)
    • If not suitable for surgery, either radiotherapy alone or combination chemoradiotherapy with curative intent
  • Later stage (IIIb-IV):
    • Concurrent chemoRT
    • Chemo followed by RT
    • Radical RT alone
    • Palliative chemo
    • Palliative RT
    • Targeted therapy (targets mutations that drive cancer)
    • Immunotherapy: targets immune checkpoints
  • **Will often tell pts we can offer then SACT (systemic anticancer treatment) which includes chemotherapy, targeted therapy & immunotherapy*
  • **Examples of targeted therapies:*
  • EGFR → gefitinib
  • ALK → alectinib
  • ROS1 → crizotinib
  • **Examples of immunotherapy:*
  • PDL-1 inhibitors → pembrolizumab, Nivolumab
24
Q

Some pts with NSCLC can be offered surgery; state some contraindications to surgery

A
  • poor general health
  • stage IIIb or IV (i.e. metastases present)
  • FEV1 < 1.5 litres is considered a general cut-off point for lobectomy
  • FEV1 <2 is considered a general cut-off point for pneumonectomy
  • malignant pleural effusion
  • tumour near hilum
  • vocal cord paralysis
  • SVC obstruction
25
Q

Management is by MDT; who is involved in MDT

A
  • Oncologist
  • Specialist Nurse
  • Radiologist
  • Pathologist
  • Thoracic Surgeon
  • Palliative Care Team
  • MDT Co-ordinator
26
Q

What is the 5yr survival for SCLC?

What is the 5 year survival for NSCLC?

What are some prognostic factors?

A
  • SCLC: 5yr survival is 5% (untreated SCLC median survival is 4-12 weeks)
  • NSCL: 5yr survival is 10-20%
  • Prognostic factors:
    • Stage at presentation
    • Performance status
    • Small cell histology has poorer prognosis
27
Q

State some potential complications of radiotherapy to the thorax

A
  • Pneumonitis
  • Oesophagitis
  • Mucositis
28
Q

State some potential complications of surgery for lung cancer

A
  • Empyema
  • Decrease in respiratory reserve
  • Seeding of tumour into thoracotomy scars & sc tissue
  • Persistent bronchopleural fistula
29
Q

State some potential tumour related complications of lung cancer

A
  • Pneumonia
  • Pleural effusion
  • Lung abscess
  • Empyema
  • Pneumothorax
  • Massive pulmonary or pleural haemorrhage
  • AF
  • Pericardial effusion
  • Dysphage
  • Broncho-oesphageal fistula
  • Horner’s syndrome
  • Spinal cord compression
  • SVC obstruction
  • Sudden death from rupture of one of great vessels
30
Q

What investigations would you do if you suspect pleural mesothelioma?

A
  • CXR: pleural mass, may be associated pleural effusion
  • Pleural fluid cytology: blood stained & high in protein
  • Pleural biopsy: may be US or CT guided or via thoracoscopy or thoracotomy
  • CT scan thorax & abdomen: assess extent and look for involvement of other structures e.g. peritoneum
31
Q

For mesothelioma, discuss:

  • Whether it is common
  • Most common age presentation
  • Which gender more common in and why
  • Main risk factor
  • Latent period between risk factor exposure & presentation
A
  • Rare (accounts for 0.8% all cancer cases)
  • 50-70yrs
  • Male:female is 5:1 reflecting occupational exposure to asbestos
  • Asbestos exposure- crocidolite (blue) asbestos is most dangerous (note: those who live with people exposed to asbestos also at risk as fibres are carried home on clothing. Those who lived near asbestos mines or processing factories also at risk)
  • Latent period of ~30-40yrs
32
Q

Discuss the pathophysiology of pleural mesothelioma

A
  • Arises from mesothelial cells of pleura (mesotheliomas can arise from mesothelial cells in other parts of body e.g. peritoneum, pericardium etc…)
  • Slightly more common on R side (probably because there is a greater SA of pleura on the R)
  • Tumour nodules are present, on both parietal and visceral pleura, and then coalesce to form plaques
  • These plaques encase the lungs and infiltrate into fissures & interlobular septa
  • Eventually pleural space is obliterated
  • May be associated pleural effusion which is blood-stained & rich in protein
33
Q

Describe symptoms and signs of pleural mesothelioma

A

Symptoms

  • Increasing dyspnoea on exertion
  • Chest pain on affected side
  • Persistent dry cough
  • Systemic symptoms e.g. anorexia, weight loss, fever
  • Haemoptysis is uncommon unlike in lung cancer

Signs

  • Finger clubbing
  • Reduced chest expansion on affected side
  • Dullness to percussion
  • Reduced breath sounds
34
Q

Discuss the treatment of pleural mesothelioma

A
  • Managing recurrent pleural effusions:
    • Talc pleurodesis
    • Indwelling catheter
    • Pleurectomy (other two seem to be recommended)
  • Chemotherapy: if have good performance status of 0 or 1
  • Radiotherapy for palliating chest pain
35
Q

Discuss the prognosis of mesothelioma

A
  • 30% survival at 1yr
  • 5yr survival (sources vary but between 5-10%)