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DETECTION
Early
detection of bowel cancer can lead to a greater chance of
long-term cure. Patients who report with bowel symptoms should
have a history taken, including a detailed account of the
type of symptoms, the severity and the length of time since
onset. They should also undergo an appropriate clinical examination
taking into account any jaundice or pallor, an abdominal examination
and a
digital rectal examination. Although bowel cancer commonly
affects people of a slightly older age group, alarm symptoms
in the younger patient should also be dealt with urgently
particularly if there is family history of the disease.
RECTAL
BLEEDING AND HAEMORRHOIDS
GPs
will be well aware that it is important not to rule out the
possibility of bowel cancer when considering a
haemorrhoids diagnosis. This is especially true if the patient
is presenting other high-risk symptoms. However, if piles
are confirmed and a surgical treatment is considered, GPs
should look at whether Procedure for Prolapse and Haemorrhoids
(PPH) would be suitable. PPH (also known as a stapled
haemorrhoidectomy or a stapled anopexy) is a minimally invasive
surgical treatment. It uses a circular stapling device to
cut out the prolapsed tissue and reposition the haemorrhoids
to their normal anatomical position, rather than the traditional
surgical method of cutting the haemorrhoids away. As a result,
people who have undergone PPH report little post-operative
pain, a shorter and more comfortable recovering period 1 and
a quicker return to normal activities compared to a Milligan-Morgan
haemorrhoidectomy procedure.3 The surgery can be performed
under a local, general or regional anaesthetic.1 As with any
surgical procedure, there are risks accompanying PPH and patients
should be encouraged to discuss them with their GP.
For
more information please call the PPH InfoLine on 0800 028
2231 or visit www.allaboutpph.co.uk
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Patients who present with alarm symptoms can be urgently referred
via the two-week rule which will ensure that a hospital appointment
is booked within two-weeks of the referral being received.
Each Cancer Network has developed an urgent suspected colorectal
cancer proforma.
This is usually available in each practice and can be faxed
through to a designated line in the hospital. The appointment
is then made and the date/time faxed back to the G.P. If it
is not already known it is worth finding out from the local
hospital the number of the designated telephone
fax line. This proforma should only be used for patients where
there is a high grade of suspicion of colorectal cancer and
not as a method of 'fast-tracking’ routine patients.
In order
to make an appropriate referral the following guidelines can
be used to help determine the urgency at which the referral
needs to be made.
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Click
here to download the referral guidelines
for suspected cancer. |
NHS Bowel Cancer Screening Programme (England: 60-69 years)
As promised, April 2006 finally saw the Government's official
commitment to a national screening programme for bowel cancer,
with the news that funding (£10m) has been released
for the first phase of the three year initiative.
A programme
of this scale will take time to be effectively implemented
across the whole country. The Government initially set out
a three year phased roll out which will see the whole of the
eligible population (people aged between 60 and above) covered
by the end of 2009.
Screening
centres currently open are listed on the Cancer
Screening Website.
Patients
living in these areas, and aged between 60-69 and registered
with a GP, will receive an invitation for screening via the
post.
Read more
in the Information
for Primary Care Booklet. and the Information
for Primary Care Leaflet.
We will
update our website regularly as and when new centres open,
and all information is also available on the NHS Screening
Programmes website at www.cancerscreening.nhs.uk
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Scottish
Bowel Cancer Screening Programme (Scotland: 50-74 years)
A Scottish
Bowel Cancer Screening Programme commenced in March 2007.
The programme will offer men and women aged 50 to 74 years
a FOB test every two years.
The screening
programme will be phased in gradually over a three year period
giving Health Boards time to prepare and allocate resources.
The programme will cost £19.5 million in its first three
years of roll-out from 2007-08 to 2009-10. This funding will
be met from existing NHS Board allocation increases.
Following
the successful pilot in NHS Tayside, Grampian and Fife, testing
kits will be posted to 650,000 people in the target age range
every year. These tests are completed at home and are then
returned for screening. Patients will receive results within
two weeks.
Welsh
Bowel Cancer Screening Programme (Wales: 50-74 years)
This programme
will commence in March 2008, as per the Scotland programme.
Screening for high-risk patients
There
are however screening programmes in place for families with
certain hereditary conditions or those with a family history
of colorectal cancer. In around 30% of colorectal cancer cases
there is a family history of the
disease. 5% of these cases have an inherited condition, which
makes them genetically predisposed to colorectal cancer such
as Familial Adenomatous Polyposis (FAP) and Hereditary Non-Polyposis
Colorectal Cancer(HNPCC).The remaining 25% of cases are patients
who have a
strong family history of the disease, which occurs too frequently
to be considered coincidental but is not consistent with the
previously mentioned hereditary forms of the disease (Information
from Public Health Genetics
Unit at www.phgu.org.uk
last updated November 2004).
Genetic Risk
Familial Adenomatous Polyposis (FAP) – this condition
where numerous polyps are formed in the bowel is an autosomal
dominant hereditary condition. Once diagnosed in an individual,
the family are referred to a regional genetics centre and
screened for the condition. If diagnosed with FAP, the treatment
is a prophylactic colectomy as the mean age for cancer onset
is 39 years. In some cases, due to personal reasons, surgery
is deferred. In these cases (for patients who have the documented
APC gene mutation) screening should take the form of 6 monthly
flexible sigmoidoscopy and annual colonoscopy but surgery
should be strongly recommended before the age of 25.
Hereditary Non-Polyposis Colorectal Cancer (HNPCC) –
this condition is diagnosed either through the fulfilment
of certain criteria (Amsterdam Bethedsa Criteria) or by the
pathogenic mutation in one of the DNA mismatch repair genes.
(Information from Clinical Molecular Genetics Society at www.cmgs.org).
Again patients and their families with HNPCC are referred
to regional genetics centres for counselling and screening.
HNPCC families are screened via total colonic surveillance
every 2 years starting at the age of 25 or 5 years below the
age of the first cancer
case in the family and should continue until the age of 75.
Family History
In this group of patients colorectal cancer occurs too frequently
to be considered coincidental but does not accurately fulfil
the criteria for an hereditary condition. In this group of
patients current guidelines are a screening colonoscopy 10
years below the age at which the youngest
family member was diagnosed.
Patients presenting with a family history of bowel cancer
should be referred to the local colorectal specialist for
a full assessment of risk and referral for appropriate screening.
Clinical Examination
Low rectal cancers can be diagnosed on clinical examination.
Either they are digitally palpable and can be felt on rectal
examination, or some are within reach of a rigid sigmoidoscope.
In both cases the cancer can be provisionally diagnosed in the
outpatient clinic, biopsies
taken (unless there is any contraindication to do so) and appropriate
staging investigations requested i.e. CT, MRI and Colonoscopy.
Flexible Sigmoidoscopy
Left-sided colorectal cancers can be diagnosed on flexible
sigmoidscopy. This investigation involves endoscopic visualisation
of the left colon (up to the splenic flexure). If a cancer is
found biopsies can be taken and appropriate staging investigations
requested i.e. CT, MRI (for rectal cancers only) and completion
colonoscopy.If polyp(s) are seen which are not considered malignant
a full
colonoscopy +/-polypectomy should be requested.
Colonoscopy
This is complete endoscopic visualisation of the colon and at
present is the gold standardfor examination of the large bowel.
Again, if a cancer is found biopsies are taken for tissue diagnosis
and the relevant staging investigations requested.
Barium Enema
This examination can be used when there is a slightly lower
clinical suspicion of malignancy or if the patient has any other
conditions which increase the risks of colonoscopy i.e. severe
heart/lung disease. With good bowel preparation a barium enema
examination is able to detect colonic lesions as small as 5mm.
This is only a diagnostic procedure and in the event of any
abnormality a colonoscopy would
normally be performed to visualise the lesion and obtain a tissue
diagnosis.
CT Scan
In suspected cases of colorectal cancer, a CT scan is not the
first line investigation used to gain a diagnosis. However some
patients with unknown colorectal cancer who have been referred
for a CT scan for other reasons are then diagnosed on CT.
Blood Tests
Blood tests done for a variety of reasons can pick up abnormalities
such as anaemia, which will then lead to further investigations
and a diagnosis of colorectal cancer.
Staging
Once colorectal cancer has been diagnosed pre-operative staging
of the tumour must take place prior to any treatment. Pre-operative
imaging such as CT and MRI scans can, as accurately as possible,
determine the exact site of the tumour as well as identify
any local infiltration of the disease or distant metastases.
Staging can help determine if it is appropriate to administer
radiotherapy (in the case of rectal cancers) prior to surgery
or just to proceed directly to an operation. If the cancer
was not diagnosed at colonoscopy wherever possible a completion
colonoscopy should be performed to exclude any synchronous
tumours or adenomatous polyps. If this is not possible pre-operatively
then a full colonoscopy should be performed within
6 months from the time of surgery.
Surgery
The first line treatment for many cases of colorectal cancer
is surgery. Even in cases where metastases are present it
is now widely considered that, if the patient is fit enough,
surgery to remove the primary tumour should be carried out
as response to palliative chemotherapy for secondary disease
is generally improved.
Surgery involves resection of the segment of the bowel containing
the tumour as well as some surrounding tissue and lymph nodes.
Where possible the bowel is rejoined providing continuity
of the colon and a stoma is avoided. In the case of low rectal
tumours or in some emergency procedures a temporary or permanent
stoma is unavoidable.
Along with open surgery, The National Institute of Health
and
Clinical Excellence has recently issued new guidance that
laparoscopic, or keyhole surgery, (including laparoscopically
assisted resection) is a recommended alternative. Laparoscopic
colorectal surgery should be performed only by surgeons who
have completed appropriate training in the technique and who
perform the procedure frequently enough to maintain competence.
The decision about which of the procedures (open or laparoscopic)
is undertaken should be made after an informed discussion
between patient and surgeon. In particular, the suitability
of the lesion for laparoscopic resection should be considered,
along with the
risks and benefits, and the experience of the surgeon, for
either procedure. Whilst patients will discuss this with their
surgeons, they may also require advice and guidance from their
GPs.
Click
here to download the list of recommended colorectal centres
offering laparoscopic surgery.
TEMS procedure (transanal endoscopic microsurgery)
This is a minimally invasive procedure for rectal tumours
in which the surgeon removes the tumour through a scope placed
in the anal canal.This procedure has the advantage of a quicker
recovery time and potentially fewer complications. It is potentially
suitable for those
patients with very early stage tumours although the possibility
of nodal invasion needs to be discussed. It is also suitable
for some non-malignant polyps. Patients with advanced rectal
cancers may undergo this procedure to improve quality of life.
Radiotherapy
Radiotherapy is only administered in the case of rectal cancers.
It can either be given neo-adjuvantly i.e. prior to the operation
in an attempt to ‘downstage’ the tumour before
resection or post-operatively (if final histological grading
shows a T4 tumour or there is circumferential margin involvement)
to try to reduce the chance of recurrence in the
future.
Chemotherapy
Chemotherapy is generally given after surgery, particularly
if the histology report confirms the presence of involvement
of any of the lymph nodes removed in the specimen. Chemotherapy
can be given in combination with radiotherapy post-operatively
in the case of rectal
cancers.Chemotherapy can also be given, in smaller doses,
with radiotherapy in the pre-operative setting as it helps
enhance the action of the radiotherapy.
The latest NICE guidelines relating to bowel cancer, and information
on current appraisals, can be found in our research
and reports section on this website. Alternatively, you
can contact NICE direct:
National Institute for Health and Clinical Excellence (NICE) MidCity Place 71 High Holborn London WC1V 6NA Telephone: 020 7067 5800 Fax: 020 7067 5801 Website: www.nice.org.uk
The purpose
of follow-up for patients who have undergone surgery for colorectal
cancer is to detect recurrent disease, either locally within
the field of surgery or distant recurrence particularly in the
liver or lungs. If detected early enough, in some cases, there
may be the opportunity to undergo further treatment, which aims
to either cure the cancer or slow the progression of the disease.
In addition follow-up also enables the detection of new or metachronous
cancers
in the bowel.
Methods of follow-up include:
Clinical
Examination: the patient is seen in clinic and questioned
about any recent symptoms. A clinical examination is performed
including observing for signs of jaundice or anaemia, abdominal
examination and in the case of rectal cancers a rigid sigmoidoscopy
to check the anastomosis can also be performed.
Blood
Tests: Tumour markers in the blood can rise in the
presence of active tumour and two indicators if possible recurrent
cancer are Carcinoembryonic Antigen(CEA) and CA19-9. Generally
a rising CEA or CA19 –9 can be indicative of recurrent
cancer and so if one or
other is raised on blood testing further investigations may
be requested to determine if there is recurrent disease.
CT
Imaging or Ultrasound: These can be done as part
of the hospitals’ follow-up protocol for patients who
have had surgery for bowel cancer or may be requested in the
presence of abnormal symptoms or elevated tumour markers.
Scans may initially concentrate on the area of surgery as
well as common areas for metastases such as the liver and
lungs.
Colonoscopy:
Current guidelines recommend that all patients with colorectal
cancer undergo a complete colonoscopy at the time of diagnosis.
If this is not possible due to the presence of an obstructing
lesion a completion colonoscopy should be carried out within
6 months
of surgery. After that repeat colonoscopy should be performed
every 5 years until the age of 75 (providing no polyps are
found – refer to BSG guidelines on polyp follow-up).
For all guidelines refer to the British Society of Gastroenterology at www.bsg.org.uk
The current
debate surrounding the most appropriate method of follow-up
has been brought about by the lack of hard evidence to support
one method of surveillance over another. In addition the cost
of follow-up per life year gained is uncertain and therefore
a case for intensive follow-up cannot be adequately argued.
At present follow-up practices
vary widely between Trusts and is
very often dictated by each individual consultant’s personal
preference.
In attempt
to answer the question of the benefit of follow-up there is
currently running in the UK a multi-centre randomised controlled
trial looking at the cost-effectiveness of intensive versus
no scheduled follow-up in patients who have undergone resection
for colorectal cancer
with curative intent (FACS Trial). Details of this can be
found on the National Cancer Research Network Website www.ncrn.org.uk
Other articles addressing this issue are;
Renehan AG, Egger M, Saunders MP, O’Dwyer ST. Impact
on survival of intensive follow-up after curative resection
for colorectal cancer: systemic review and meta-analysis of
randomised trials. BMJ 2002;324: 813
Renehan AG,
O’Dwyer
ST, Whynes DK. Cost effectiveness analysis of intensive versus
conventional follow-up after curative
resection for
colorectal cancer. BMJ 2004; 328: 81
If it
is not known what the current follow-up practice is in your
local hospital it may be worth contacting either the Consultant
Colorectal Surgeon or the Colorectal Nurse Specialist so that
you are aware of
what regime is followed.
How common is bowel cancer?
35,500 people are diagnosed every year with bowel cancer. Nearly half,
16,265 will die of the disease.
What is the main treatment?
In most cases
surgery is the first line treatment for bowel cancer and aims to remove
the effected portion of the bowel. Other treatments such as chemotherapy
and radiotherapy can be given alongside.
What are monoclonal antibodies?
Monoclonal antibodies are a new breed of drugs that when combined with certain
chemotherapy agents have shown to improve the length of survival in patients
with advanced disease.
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