Showing posts with label week 2 - patient 6 - lung carcinoma. Show all posts
Showing posts with label week 2 - patient 6 - lung carcinoma. Show all posts

Respiratory system review
Cough?
Phlegm?
Blood in phlegm?
Wheeze?
Sob?
Chest pain on breathing?
Sinus
Hoarse voice?
Fevers/night sweats?
Primary tumours of lung
SYMPTOMS
Cough (worsening gradually)
Haemoptysis (invasion of cancer into vessel wall)
Breathlessness( caused by occlusion of bronchus causing collapse [atelactasis] or development of pleural effusion)
Wheezing(narrowing the bronchus in or around which it is growing )
Stridor ( narrowing of lower trachea, carina or main bronchi)
Pleural pain (malignant invasion of of pleura)
Weight loss and lack of appetite(metastatic spread)
Hoarse voice( left apex of lung compressing on left recurrent laryngeal nerve)

Signs
General: cachexic, palor( anaemia)
Hands and wrists: clubbing, hypertrophic pulmonary osteoarthropathy(periostits of long bones such as radius and ulna, periosteum is a connective tissue covering bones and have bone forming potentialities), fine muscle wasting
Nodes: supraclavicular or axillary lymphadenopathy
Chest: consolidation, collapse, pleural effusion
Metastases: bone tenderness, hepatomegaly, proximal myopathy
Endocrine sx
Cushings syndrome

 

Clinical Presentation
-Cough, dyspnoea, chest pain, heamoptysis, and hoarseness of voice.

If Invasion or obstruction of vital thoracic organs occur
-Superior vena cavae obstruction
-Pleural/ pericardial effusion
-Pancoast syndrome
-Paralysis of the recurrent laryngeal nervehoarseness of voice
-Phrenic nerve palsy paralysis of ipsilateral hemidiaphragm
-Horner’s syndrome
-Dysphagia oesophageal compression
-Intense and radiating neuropathic pain in the ipsilateral upper extremity due to superior sulcus tumour compression of the brachial plexus roots.

Metastatic Disease
-metastasize to liver, adrenal glands, bone, brain and regional lymph nodes.
-Bone pain, seizures, hemiplegia and hepatomegaly.

General Presentation
-Drastic/ significant weight loss, malaise, fatigue and anorexic.

Para-neoplastic Syndrome
-syndrome of Inappropriate Anti-diuretic Hormone (SIADH)
-Hypercalcaemia
-Gynecomastia and galactorrhea large cell carcinoma
-Cushing Syndrome small cell carcinoma
-Neurological Syndrome
- Eaton- Lambert Syndrome manifestation of small cell carcinoma due to defective acetycholine release at neuromuscular junction proximal muscle weakness and reduction of tendon reflexes. Can be accompanied by xerostomia (mouth dryness), sexual impotence and peripheral neuropathy.



Superior Vena Cava Syndrome
-characterized by gradual, insidious compression of the superior vena cava, can be life-threatening
-thin wall coupled with low intravascular pressurerelative easy to be compress possible thrombus formation and increase venous pressure interstitial oedema and retrograde collateral flow.
-Causes early morning headache, facial congestion, dusky skin colouration and oedema in upper limbs, and distended jugular veins.
-90% associated with malignancy (bronchogenic carcinoma)

Horner’s Syndrome
-Interruption of the sympathetic ganglion chain causing miosis (constricted pupil), partial ptosis and loss of hemifacial sweating.
-Pancoast tumour in apical of lungs compressing on the sympathetic chain

Pleural/ Pericardial Effusion
- infiltration into parietal pleura/ pericardial sac.
Metabolic (universal at some stage)
Loss of weight
Lassitude
Anorexia
Endocrine (10%) (usually small-cell carcinoma)
Ectopic adrenocorticotrophin syndrome
Syndrome of inappropriate secretion of antidiuretic hormone (SIADH)
Hypercalcaemia (usually squamous cell carcinoma)
Rarer: hypoglycaemia, thyrotoxicosis, gynaecomastia
Neurological (2-16%)
Encephalopathies - including subacute cerebellar degeneration
Myelopathies - motor neurone disease
Neuropathies - peripheral sensorimotor neuropathy
Muscular disorders - polymyopathy, myasthenic syndrome (Eaton-Lambert syndrome)
Vascular and haematological (rare)
Thrombophlebitis migrans
Non-bacterial thrombotic endocarditis
Microcytic and normocytic anaemia
Disseminated intravascular coagulopathy
Thrombotic thrombocytopenic purpura
Haemolytic anaemia
Skeletal
Clubbing (30%)
Hypertrophic osteoarthropathy (± gynaecomastia) (3%)
Cutaneous (rare)
Dermatomyositis
Acanthosis nigricans
Herpes zoster

 

1. History
a. Onset?
b. Associated symptoms suggestive of infection?
c. Wheeze?
d. Associated symptoms suggestive of:
i. Post nasal drip syndrome (PNDS)
ii. GERD
e. Associated with fever and sputum?
f. Risk factor?
i. Smoking
ii. Environment
iii. HIV
g. Medication = ACE inhibitor


Cough Ix
1. CXR
2. ENT Ex
3. Lung Function Test
4. Barium Esophagography
5. CT scan
6. V/Q scans
7. fibreoptic bronchoscopy
8. ECG
9. Psychiatric appraisal



Evaluating Chronic Cough


Lung CA Ix
1. Chest radiograph
• Non-diagnostic
• Just to screen possibilities of infection, tumour, pleural effusion.
• If a mass is observed than send for CT.

2. Sputum cytology
a. By fibreopticbronchoscopy (or transtracheal aspiration)
• the reason to do a transtracheal aspiration is to collect sputum arising from deep regions of the lung (inc alveolus). In doing so, the bronchials are stimulated to produce a cough reflex. Sputum will be cough out from the deep region and can be collected. The procedure is done after doing at CT scan showing that there are abnormalities of the peripheral region. A fibreoptic bronchoscopy will not be able to collect sputum within the alveoli.
• Transtracheal aspiration brings extra advantage when required to investigate on lower respiratory infection. Normal sputum collection (by patient coughing it out) will be contaminated with other organism at URT.


3. High Resolution CT Scan

• Look for local spread of tumour
• Can have a 3D view so that we know the amount of lung area affected
• But cannot see nodes involvement


4. Positron Emission Tomography (PET)

• Fluorodeoxyglucose
• detect abnormalities not demonstrated on CT scans.
• Differentiate between benign and malignant
• Not usually done (limited to certain places e.g. Putrajaya
• Risky because the whole body is radiated
• But the procedure allows us to see any distant metastasis
o Bone marrow scan is usually done instead of PET to investigate marrow involvement.

5. Biopsy
• Fibreoptic bronchoscopy
i. Used to define bronchial anatomy and take biopsy
1. viewing possibility of resection
2. if more than 2cm of tumour (from carina), than cannot undergo surgery
**. concept = avascular area will not heal and leads to fibrous tissue. Thus brings more complication

• Mediastinoscopy and scalene node biopsy
i. Carcinoma of bronchus
ii. Involves inspection of the mediastinal structures using a mediastinoscope inserted by blunt dissection downwards from behind the proximal end of the clavicle
iii. Biopsy of enlarge lymph node taken

• Fine Needle Aspiration
i. Biopsy of peripheral lung
ii. Under appropriate CT guidance

 

Choices:
1) surgery
2) chemotherapy
3) radiation as appropriate, depending on tumor type and stage

Eligibility of treatment may be affected by:
1) poor cardiopulmonary reserve
2) malnutrition
3) frailty/ poor physical performance status
4) co-morbidities inc. cytopenias
5) psychiatric or cognitive illness

* all may lead to a decision for palliative over curative treatment or for no treatment at all, even though cure might technically be possible.


Surgery
• performed only on patient who will have adequate pulm. reserve once a lobe or lung is resected
• pneumonectomy- can be tolerated by patients with FEV1 > 2 L
• FEV1 < 2 L – undergo a quantitative radionuclide perfusion scan to determine the proportion of function the patient can expect to lose from resection.

Chemotherapy
• multiple chemo regimens exist- no one regimen is proven superior
• choice of regimen- depends on local practice, contraindications and toxicities
• for disease that recurs after treatment, treatment options vary by location and include:
• repeat chemo for local recurrence
• radiation therapy for metastases
• brachytherapy* for endobronchial disease (disease of the lining of bronchi) when additional external radiation can’t be tolerated
*a type of radiation therapy, also called internal radiation therapy. Allows physician to use a higher total dose of radiation to treat smaller areas and in shorter time than is possible with external radiation therapy

Radiation treatment
• Carries risk of radiation pneumonitis (inflammation of lung tissue)- when large areas of lung are exposed to high doses of radiation over time.
• can occur up to 3 mo after treatment.
• Clinical presentation: Cough, dyspnoea, low-grade fever, pleuritic chest pain, pleural friction rub.
• Chest x-rays- may be nonspecific
• CTs may show nonspecific infiltration without discrete mass.
• Treated with 60 mg for 2 to 4 wk followed by a gradual decrease of dosage.

End-of-life care
• should be anticipated since many patients with lung CA die
• common symptoms- breathlessness, pain, anxiety, nausea, anorexia
• can be treated with:
• parenteral morphine,
• oral, transdermal / parenteral opioids
• antiemetics

SMALL CELL LUNG CARCINOMA (SCLC)
• typically initially responsive to treatment, but responses are usually short-lived.
• Surgery generally plays no role in treatment of SCLC- but it may be curative in the rare patient who has a small focal tumor without spread (e.g. a solitary pulmonary nodule).

Limited-stage disease- 30%, confined to one hemithorax and regional lymph nodes inc mediastinal, contralateral hilar, and ipsilateral supraclavicular nodes- whther tumor can be encompassed within a tolerable radiation therapy port
- etoposide + a platinum compound (either cisplatin/ carboplatin) in 4-6 cycles  Thought to be most effective
- Other commonly used drugs: vinca alkaloids (vinblastine, vincristine
, vinorelbine), alkylating drugs (cyclophosphamide, ifosfamide), doxorubicin, taxanes (docetaxel, paclitaxel), and gemcitabine
• Cranial radiation- to prevent brain metastases since micrometastases are common in SCLC and chemotherapy doesn’t cross BBB

Extensive-stage disease-70%exceeding those boundaries
• treatment - the same as with limited-stage disease but without concurrent radiation
• Replacing etoposide with topoisomerase inhibitors (irinotecan/topotecan) may improve survival.
• Radiation is often used as palliative treatment for metastases to bone or brain.
**In general, recurrent SCLC carries a poor prognosis- but patients who maintain good performance status should be offered a clinical trial.


NON-SMALL CELL LUNG CARCINOMA (NSCLC)
• Treatment depends on the stage.

Stage I and II disease
• surgical resection with lobectomy (removal of a lobe) / pneumonectomy (removal of entire lung) combined with mediastinal lymph node sampling or complete dissection.
• Patients with poor pulm reserve- lesser resections, inc segmentectomy and wedge resection (removal of a small wedge-shaped piece of lung that contains the lung cancer and a margin of healthy tissue around the cancer) - likely to be done when lung function would be decreased too much by lobectomy
• Surgery - curative in about 55-75% of patients with stage I ;35-55% of patients with stage II
• Adjuvant chemotherapy- probably helpful in early-stage disease (stages Ib and II).
• An ↑ in 5-yr overall survival (69% vs 54%) and disease-free survival (61% vs 49%) occurs with cisplatin + vinorelbine. Because the improvement is small, the decision for adjuvant chemotherapy should be made on an individual basis.
• role of neoadjuvant chemotherapy (treatment given prior to surgery to ↓ the tumor size eg chemotherapy/radiation therapy) in early-stage NSCLC = under investigation.

Stage III disease
Stage IIIA tumors- with occult mediastinal nodal metastases discovered during surgery - resection results in 20 to 25% 5-yr survival.
• Radiation therapy with/without concurrent chemo = standard for unresectable clinically staged IIIA disease- survival is poor (median survival, 10 to 14 mo). Recent trials suggest slightly better results with preoperative chemo +radiation followed by surgery and subsequent chemotherapy remains an area of investigation.
Stage IIIB tumors- with contralateral mediastinal nodal disease, supraclavicular nodal disease/ malignant pleural effusions – radiation/chemo/both.
• addition of radiation-sensitizing chemotherapeutic drugs, eg cisplatin, paclitaxel, vincristine, and cyclophosphamide↑ survival slightly.
• Patients with locally advanced tumors invading the heart, great vessels, mediastinum, or spine usually receive radiation.
• T4N0M0 tumors,surgical resection with either neoadjuvant or adjuvant chemoradiation
• 5-yr survival rate for treated stage IIIB patients is 5%.

Stage IV disease goal = palliation of symptoms.
• Chemo and radiation may be used to reduce tumor burden, treat symptoms, and improve quality of life.
• median survival is only 9 mo; < 25% of patients survive 1 yr.

 

Types of Lung Ca

There are 2 main types of lung carcinoma, categorized by the size and appearance of the malignant cells seen by a histopathologist under a microscope: non-small cell (80.4%) and small-cell (16.8%) lung carcinoma. This classification, based on histological criteria, has important implications for clinical management and prognosis of the disease.

Non-Small Cell Lung Carcinoma (NSCLC)

Non-small cell lung cancer includes three different subtypes:

Squamous cell carcinoma
This type of cancer is usually the by product of smoking
Adenocarcinoma
This type of non small cell lung cancer is usually found on the outer edge of the lung
Large-cell undifferentiated carcinoma
Appears in any area of the lung and spreads very quickly

Small Cell Lung Carcinoma (SC
LS)

Small cell lung carcinoma (SCLC, also called "oat cell carcinoma") is less common. It tends to arise in the larger airways (primary and secondary bronchi) and grows rapidly, becoming quite large.The "oat" cell contains dense neurosecretory granules which give this an endocrine syndrome association. While initially more sensitive to chemotherapy, it ultimately carries a worse prognosis and is often metastatic at presentation.

Mixed small cell/large cell cancer
When lung cancer has characteristics of both small cell lung cancer and non small cell lung cancer, it is then called mixed small cell/large cell cancer.



Staging of Lung Ca

It is an important factor affecting the prognosis and potential treatment of lung cancer. Non-small cell lung carcinoma is staged from IA ("one A", best prognosis) to IV ("four", worst prognosis). Small cell lung carcinoma is classified as limited stage if it is confined to one half of the chest and within the scope of a single radiotherapy field. Otherwise it is extensive stage.

Relevance of Staging for Surgery

Staging for surgery is usually done for Non-small Cell Lung Carcinoma. Small cell Ca is usually treated with chemotherapy and/or radiotherapy. The TNM system is used for staging. (T-primary tumor, N-lymph nodes, M-distant metastasis) Mountain Classification further categorizes the cancer into stages. In patients with stages I and II non-small cell lung cancer the treatment of choice is surgery. Radiation is often prescribed to patients with stage III disease or those with stages I or II for whom surgery is not performed.

chris

 

Saree- Aetiology & risk factors for lung carcinoma, Mechanism of cough
Yazid- Investigations (chronic cough, Lung CA)
Maz- Treatment of Lung CA
Christine- Signs & symptoms of Lung CA (Clinical presentation)
Chris- Types of Lung CA + Staging, candidates for surgery
Alvin- Complications of Lung CA (Clinical presentation-horner's etc)