Lung cancer Flashcards

1
Q

Most common type of lung cancer?

A

Squamous cell (NSCLC) - typically central, can secrete PTHrP (–> hypercalcaemia)

NSCLC = 82% of which squamous cell is 32%

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2
Q

1st line management of NSLCL for stage 1/2 without chest wall invasion?

A

Surgery + adjuvant chemo

80% 5 year survival

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3
Q

Management of NSLCL if surgery is not possible?

A

Radiotherapy + concurrent chemo

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4
Q

What metastases would palliative radiotherapy be indicated for?

A

Brain mets, SVCO, SCC

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5
Q

Chemotherapy options for NSCLC

A

Carboplatin + gemcitabine/paclitaxel

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6
Q

Targeted therapy option for NSCLC

A

TKI - erlotimab

Often used in a palliative setting

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7
Q

5 year survival of different stages of NSCLC

A
1 = 50%
2 = 40%
3a = 25%
3b = <5%

(4 = 6 months to live)

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8
Q

Proportion of lung cancers that are small cell in origin?

A

20%

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9
Q

What treatment options are SCLC particularly responsive to?

A

Radio and chemotherapy

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10
Q

Paraneoplastic syndromes of SCLC?

A

ADH –> hyponatremia

ACTH –> cushings –> muscle weakness, hypokalemia, HTN, oedema

Lambert-eaton syndrome - antibodies for voltage gated calcium channel –> myasthenia like syndrome

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11
Q

Usual presentation of SCLC? (i.e. local or disseminated)

A

Usually metastasised at presentation (poor prognosis)

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12
Q

Management of limited SCLC (i.e. fairly localised)

A

If tumour is at very ealry stages (12a, N0, M0) then can do surgery

Most patients = Chemo + concurrent radial radiotherapy

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13
Q

Management of extensive SCLC?

A

Chemo (palliative)

90% responsive but high relapse rates

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14
Q

Risk factors for LC?

A

Age>40
Smoking
occupation (asbestos, uranium mining, ship building etc)

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15
Q

Causes of lung cancer?

A
TSG inactivation via chromosomal deletions
Oncogene overexpression - RAS, myc
EGFR activation (common in adenocarcinoma)
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16
Q

Clinical presentation?

A
Non-specific:
Persistent cough +/- haemoptysis 
Dyspnoea
Recurrent chest infections
Chest pain

Syndromal (dependent on tumour location):

  • Apical tumours –> horner’s, pancout’s syndrome
  • Paraneoplastic
  • Mediastinal –> SVCO, recurrent laryngeal nerve palsy (voiceless)
17
Q

Investigations?

A
  1. CXR - 95% tumours visible at presentation
  2. Sputum cytology - can detect and analyse malignant cells
  3. Bronchoscopy - take biopsy
  4. Trans-thoracic biopsy if peripheral tumour
  5. CT chest + upper abdomen + head - metastases/staging
  6. PET scan - for patients with operable disease to check for distant mets
    (7. tumour markers - NSE and LDH, not routinely used)

Also: Function test e.g. spirometry

18
Q

T, N and M

A
T1 = <3cm (surrounded by pleura)
T2 = <7cm (invades main bronchus)
T3 = >7cm (Local invasion e.g. chest wall)
T4 = organ invasion (inoperable)
N1 = I/L Bronchopulmonary and hilar LN
N2 = I/L mediastinal or subcarinal LN
N3 = Supraclavicular or contralateral LN

M1a - C/L lung
M1b - distant metastases

19
Q

Staging

A
Stage 1 = T1/T2, N0, M0
Stage 2 = T1/T2, N1, M0 or T3, N0, M0
Stage 3a = T1/T2/T3, N2, N0 or T3/T4, N1, M0
Stage 3b = T4, N2, M0 or any N + M0
Stage 4 = M1 (any)
20
Q

At what stage does lung cancer become inoperable?

A

Stage 3b

21
Q

Definition of limited disease?

A

one hemithorax (I/L mediastinal and supraclavicular LN)