Bronchogenic Carcinoma
Epidemiology
• Bronchial carcinoma is the most common malignant tumour
worldwide
• The most common cause of cancer-related death
• It is the fifth most frequent cause of death in the UK
• 90% of cases are related to tobacco smoking
• Risk factors- other than smoking
- Environmental: radon exposure, asbestos, polycyclic aromatic
hydrocarbons and ionizing radiation; occupational exposure to
arsenic, chromium, nickel, petroleum products and oils.
- Host factors : underling lung disease IPF, genetic factors
Pathology
• Histology of lung cancer
1- small cell lung cancer (SCLC)
2- non small cell lung cancer(NSCLC)
a. Squamous cell carcinoma
b. Adenocarcinoma
c. Large cell carcinoma
3- other primary lung cancers
1. Small cell lung cancer (SCLC) 20%
arises from neuroendocrine cells (APUD cells)
can secrete polypeptide hormone
metastasizes early, poorer prognosis
often arise centrally
2.a. squamous cell carcinoma 35%
arises from epithelial cells
often arise centrally
cavitation with central necrosis is common
can causes bronchial compression with post obstructive infection
local spread is common, often metastasize late
2.b. adenocarcinoma 30% and increasing
arises from mucus secreting glandular cells
the most common lung cancer in non-smokers
often arise peripherally
2.c. large cell lung cancer 10-15%
poorly differentiated cells
often arises peripherally
metastasizes early
3. Other types of primary lung cancer less than 3%
carcinoid tumours, bronchoalveolar carcinoma, sarcomatoid carcinomas and others
Clinical features
• Symptoms caused by local effects
cough ✓ recurrent infections
breathlessness ✓ invasion of the phrenic nerve
hemoptysis ✓ superior vena cava
obstruction
chest pain ✓ stridor (tracheal tumor)
wheeze
hoarseness of voice
nerve compression
Pancoast’s tumor
- Tumor of the pulmonary apex
- It can invades the roots of the brachial plexus causing C8/T1 palsy
- Present with hand weakness and muscle wasting, with pain radiating
down the arm
- If the sympathetic ganglia are invaded by the tumor, Horner’s
syndrome occurs (myosis, ptosis, anhidrosis)
- Pancoast’s syndrome: apical tumor with arm pain, muscle wasting
and Horner's syndrome
superior vena cava obstruction
- swelling of the neck and face, conjunctival oedema, headache and
dilated veins on the chest wall
- Severity of swelling varies over the daytime
- Most commonly caused by lymphoma
Clinical features
• Metastatic spread
lymph nodes (mediastinal, cervical and axillary)
skin
liver
bone
adrenal gland
brain
malignant pleural effusion
Clinical features
• Non metastatic extrapulmonary manifestations
(paraneoplastic syndromes)
caused by the tumor production of signaling molecules (hormones or
cytokines) or immune response (antibodies) to the tumor cells that
cross-react with other normal cells
unlike the mass effect of tumor itself or the effect of the metastasis
sometimes the symptoms of paraneoplastic syndrome show before
the diagnosis of malignancy
metabolic:
anorexia, lethargy, weight loss
endocrine:
syndrome of inappropriate ADH secretion (SIADH): SCLC
ectopic ACTH secretion: SCLC
hypercalcemia:
- due to either osteolysis of metastasis or due to release of PTH-like peptide
- PTH-like peptide secretion is associated with squamous cell lung cancer
gynecomastia
neurological manifestations
Lambert- Eaton syndrome:
- associated with SCLC
- Antibodies against the tumor cells are cross-reactive against acetylcholine
receptors at neuromuscular junctions
- Present with proximal muscle weakness of the limbs
Myelopathies
Encephalopathies
Neuropathies (sensory or motor)
vascular and hematological:
thrombophlebitis migrans
microcytic/normocytic anemia
musculoskeletal:
hypertrophic pulmonary osteoarthropathy: associated with
adenocarcinoma
finger clubbing : common with all types of lung cancer
dermatological:
dermatomyositis
acanthosis nigricans
herpes zoster
Investigations
• Goals of investigations
1. Obtain a tissue diagnosis
2. Stage the extent of disease
3. Assess fitness to undergo treatment
• Chest Xray
- Can be normal if the lesion is small or if it is confined to a central
structure like the trachea, but it can show:
- Mass lesion
- Pleural effusion
- Unresolving consolidation
- Collapse
- Hilar lymphadenopathy
- Reticular shadowing
Cxr lung ca
• Computed tomography
Chest CT and CT of other site that are common for metastasis, i.e. liver,
adrenals and brain
• PET-CT
• Bone scan: for bone metastasis
Ct lung ca
• obtain cytology and histology
flexible bronchoscopy
endobronchial ultrasound with transbronchial biopsy
CT/US guided transthoracic lung biopsy
ultrasound guided biopsy of liver metastasis, lymph node or skin
lesion
mediastinoscopy
thoracoscopy
thoracentesis
Flex brscpy ca
Staging of the disease
• To evaluate the extent of the disease and then guide the treatment
• Staging is normally based on PET-CT
• Further evaluation with biopsies may be needed
• In non-small cell lung cancer TNM system is used for staging
• In small cell lung cancer is classified into limited and extensive stage
disease
Treatment
• Surgery
- Surgery with curative intent is limited to early stages (stage I and II)
non-small cell lung cancer and limited extent small cell lung cancer
• Radiation
- Radiation with curative intent in early stages of non-small cell lung
cancer if the patient has contraindication for surgery
- Palliative radiation therapy help relieve the symptoms, e.g. bronchial
obstruction, bone metastasis, chest wall metastasis
• Chemotherapy, targeted therapy and immunotherapy
- Adjuvant chemotherapy with radiotherapy in advanced non-small cell
lung cancer prolongs survival
- In late stages of NSLC particularly adenocarcinoma, Targeted agents
against EGFR (Epidermal growth factor receptor), tyrosine kinases and
anaplastic lymphoma kinase (ALK) can be used as second line to
chemotherapy
- Immunotherapy (monoclonal antibodies)
• Cryotherapy, laser therapy and tracheobronchial stents
- Can be used as palliative treatment if a large bronchus is obstructed
causing dyspnea or cough
• Palliative treatment
- Goal is to relieve of symptoms and improve the patient’s wellbeing
- Involves emotional support to the patient and family
Prognosis
• Very poor prognosis, because it is usually diagnosed at a late
inoperable stage (75% of patients)
• 70% die within a year of diagnosis
• Overall 5-year survival is less than 10%
• Best results seen in operable squamous cell carcinoma