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Oesophageal cancer
Cancer of the oesophagus takes the
form of either squamous cell carcinoma
or adenocarcinoma of the oesophageal
mucosa
Etiology and risk factors
• The cause is unknown but it is probably
multifaceted
• The major risk factors include:-
Cigarette smoking
Alcohol consumption
HPV has been found in 70% of clients with SCC
of the oesophagus
The greatest risk in AC is Barrett’s oesophagus
Etiology and risk factors cont’d
• Other risk factors for AC include:-
Obesity
Ingestion of smoked meats
Poor nutritional intake of vitamin A, C and
minerals such as magnesium, selenium and
zinc
Diagnosis
• There are no procedures for screening to
detect the conditionearly
• Once Barrett’s oesophagus are detected, it is
recommend that endoscopic surveillance
every 1 to 3 years be initiated
• Health promotion and maintenance behaviour
involve:-
Limiting or stopping smoking, alcohol,
ingestion of hot food and beverages
Pathophysiology
• The oesophagus is lined with squamous
epithelium which is continuous until it reaches
the gastroesophageal junction
• At the junction, columnar tissue lines the
oesophagus
• Most cancers of the oesophagus begin as
slow-growing tissue changes or dysplasia
Squamous Cell Carcinoma
• This is frequently found in the proximal or mid
oesophagus
• Cellular changes are usually seen before the
development
• Changes are found more often in smokers
than non smokers
• SCC can be classified as polypoid, ulcerative,
or infilltrative
Squamous Cell Carcinoma cont’d
• Infiltrative tumours of the oesophagus expand
locally and rapidly causing thickening and
narrowing of the lumen
• A polypoid mass projects into the lumen
obstructing the lumen if undetected
• Ulcerative lesions are raised and may expand
into the mucosa elevating until obstructive
Adenocarcinoma
• Arise from columnar epithelium of the
oesophagus
• The columnar epithelial changes are usually
attributed to Barrett’s oesophagus
• Because the oesophagus has no serosal layer,
tumours are allowed to spread to adjacent
tissue and lymphatic nodes early.
Adenocarcinoma cont’d
• The rich lymphatic supply to the mucosa
provides an excellent means for the cancer to
metastasize widely and quickly causing the
tumour to be unresectable
• Common distant metastatic sites are liver,
lung, pleura and kidneys
• Other areas include bone, peritoneum and
brain
Clinical manifestation
• Dysphagia- which is progressive
• Odynophagia
• Pain in the epigastric region or sternal area
• Loss of appetite
• Malaise
• Increase in salivation and mucus in the throat
• Nocturnal aspiration
• Regurgitation
Manifestations are usually not apparent until the cancer
involves the circumference of the oesophagus
Diagnosis
• Endoscopy with biopsy and cytology
examination is the only definite method of
diagnosing oesopahgeal cancer
• Ultra sound
• CT scan exploratory laparatomy may be used
to visualise and biopsy possible for metastasis
Management
• Inhibit tumour growth
Treatment depends on tumour’s location, size,
metastases, and performance status of the client
If it is found in the early stage, treatment is directed
toward cure; unfortunately, it is directed in late
stages when treatment becomes palliative, aimed
specifically at allowing the client to continue to
live longer with good quality of life
Radiation therapy
• This can be used alone as a single therapy or
before surgery (neoadjuvant), after surgery
(adjuvant), or concurrently with 5-fluorouracil (5-
FU) by continuous infusion (chemoradiation)
• It reduces tumour size and slows tumour growth
• Because radiation can cause stenosis of the
oesophagus, treatments are ussually
administered over a 6 to 8 weeks to minimise this
effect
Chemotherapy
• This may be single or a combination of agents
• The goal is to relieve manifestations and
reduction of tumour size
• Neoadjuvant chemotherapy can facilitate surgical
resection by reducing tumour size and
invasiveness
• Commonly used drugs include:- cisplatin
(Platinol) and 5-fluorouracil (5-FU) docetaxel
(Taxotere), irinotecan (Camptosar)and oxaliplatin
(Eloxatin)
Chemotherapy cont’d
• Newer agents used in conjuction with
chemotherapy are the antiangiogenic
(bevacizumab, {Avastin} and the anti-EGFR
immunoglobulin cetuximab (Erbituxl) in the
treatment of oesophageal cancer
Photodynamic therapy
• This is a relatively new therapy for treatment
of oesophageal cancer in clients who are not
candidates for surgery
• The client receives an injection of a light
sensitive drug (Photofrin), which is followed 2
days later with a special fiberoptic probe with
a light-bearing tip placed in the oesophagus
• The light activates the Photofrin and kills only
cancer cells
Photodynamic therapy cont’d
• This is an outpatient procedure and uses
conscious sedation, takes about 13 minutes to
perform and enables about 1 inch of tumour
to be removed
• Clients return home the same day and resume
their usual activities the same day
Maintain nutrition
• This is a major goal for the client
• Not only does the cancer cause the client to
be at risk for malnutrition, but also the
treatments (both radiation therapy and
chemotherapy) carry a risk of mucositis,
nausea, vomiting and dehydration
• Side effects of must be anticipated and
management swift
Maintain nutrition
cont’d
• Early in the disease the client may be able to
tolerate small, frequent feedings of soft or
semisoft goods
• As the disease progresses, a feeding tube may be
needed
• If necessary, feeding gastrostomy or jejunostomy
may be created
• Proper positioning after meals is necessary for
those experiencing frequent regurgaitation
• Keep the head of the bed always elevated at 30
defrees

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Oesophageal cancer-1.pptx

  • 1. Oesophageal cancer Cancer of the oesophagus takes the form of either squamous cell carcinoma or adenocarcinoma of the oesophageal mucosa
  • 2. Etiology and risk factors • The cause is unknown but it is probably multifaceted • The major risk factors include:- Cigarette smoking Alcohol consumption HPV has been found in 70% of clients with SCC of the oesophagus The greatest risk in AC is Barrett’s oesophagus
  • 3. Etiology and risk factors cont’d • Other risk factors for AC include:- Obesity Ingestion of smoked meats Poor nutritional intake of vitamin A, C and minerals such as magnesium, selenium and zinc
  • 4. Diagnosis • There are no procedures for screening to detect the conditionearly • Once Barrett’s oesophagus are detected, it is recommend that endoscopic surveillance every 1 to 3 years be initiated • Health promotion and maintenance behaviour involve:- Limiting or stopping smoking, alcohol, ingestion of hot food and beverages
  • 5. Pathophysiology • The oesophagus is lined with squamous epithelium which is continuous until it reaches the gastroesophageal junction • At the junction, columnar tissue lines the oesophagus • Most cancers of the oesophagus begin as slow-growing tissue changes or dysplasia
  • 6. Squamous Cell Carcinoma • This is frequently found in the proximal or mid oesophagus • Cellular changes are usually seen before the development • Changes are found more often in smokers than non smokers • SCC can be classified as polypoid, ulcerative, or infilltrative
  • 7. Squamous Cell Carcinoma cont’d • Infiltrative tumours of the oesophagus expand locally and rapidly causing thickening and narrowing of the lumen • A polypoid mass projects into the lumen obstructing the lumen if undetected • Ulcerative lesions are raised and may expand into the mucosa elevating until obstructive
  • 8. Adenocarcinoma • Arise from columnar epithelium of the oesophagus • The columnar epithelial changes are usually attributed to Barrett’s oesophagus • Because the oesophagus has no serosal layer, tumours are allowed to spread to adjacent tissue and lymphatic nodes early.
  • 9. Adenocarcinoma cont’d • The rich lymphatic supply to the mucosa provides an excellent means for the cancer to metastasize widely and quickly causing the tumour to be unresectable • Common distant metastatic sites are liver, lung, pleura and kidneys • Other areas include bone, peritoneum and brain
  • 10. Clinical manifestation • Dysphagia- which is progressive • Odynophagia • Pain in the epigastric region or sternal area • Loss of appetite • Malaise • Increase in salivation and mucus in the throat • Nocturnal aspiration • Regurgitation Manifestations are usually not apparent until the cancer involves the circumference of the oesophagus
  • 11. Diagnosis • Endoscopy with biopsy and cytology examination is the only definite method of diagnosing oesopahgeal cancer • Ultra sound • CT scan exploratory laparatomy may be used to visualise and biopsy possible for metastasis
  • 12. Management • Inhibit tumour growth Treatment depends on tumour’s location, size, metastases, and performance status of the client If it is found in the early stage, treatment is directed toward cure; unfortunately, it is directed in late stages when treatment becomes palliative, aimed specifically at allowing the client to continue to live longer with good quality of life
  • 13. Radiation therapy • This can be used alone as a single therapy or before surgery (neoadjuvant), after surgery (adjuvant), or concurrently with 5-fluorouracil (5- FU) by continuous infusion (chemoradiation) • It reduces tumour size and slows tumour growth • Because radiation can cause stenosis of the oesophagus, treatments are ussually administered over a 6 to 8 weeks to minimise this effect
  • 14. Chemotherapy • This may be single or a combination of agents • The goal is to relieve manifestations and reduction of tumour size • Neoadjuvant chemotherapy can facilitate surgical resection by reducing tumour size and invasiveness • Commonly used drugs include:- cisplatin (Platinol) and 5-fluorouracil (5-FU) docetaxel (Taxotere), irinotecan (Camptosar)and oxaliplatin (Eloxatin)
  • 15. Chemotherapy cont’d • Newer agents used in conjuction with chemotherapy are the antiangiogenic (bevacizumab, {Avastin} and the anti-EGFR immunoglobulin cetuximab (Erbituxl) in the treatment of oesophageal cancer
  • 16. Photodynamic therapy • This is a relatively new therapy for treatment of oesophageal cancer in clients who are not candidates for surgery • The client receives an injection of a light sensitive drug (Photofrin), which is followed 2 days later with a special fiberoptic probe with a light-bearing tip placed in the oesophagus • The light activates the Photofrin and kills only cancer cells
  • 17. Photodynamic therapy cont’d • This is an outpatient procedure and uses conscious sedation, takes about 13 minutes to perform and enables about 1 inch of tumour to be removed • Clients return home the same day and resume their usual activities the same day
  • 18. Maintain nutrition • This is a major goal for the client • Not only does the cancer cause the client to be at risk for malnutrition, but also the treatments (both radiation therapy and chemotherapy) carry a risk of mucositis, nausea, vomiting and dehydration • Side effects of must be anticipated and management swift
  • 19. Maintain nutrition cont’d • Early in the disease the client may be able to tolerate small, frequent feedings of soft or semisoft goods • As the disease progresses, a feeding tube may be needed • If necessary, feeding gastrostomy or jejunostomy may be created • Proper positioning after meals is necessary for those experiencing frequent regurgaitation • Keep the head of the bed always elevated at 30 defrees