National Oesophago-Gastric Cancer Audit: 2018 Patient Report

The National Oesophago-Gastric Cancer Audit (NOGCA) evaluates the quality of NHS hospital care in England and Wales for people diagnosed with oesophageal or gastric (OG) cancer.

NOGCA has recently published its annual Patient Report which highlights key findings from the 2018 Annual Report and describes the care that most patients can expect to receive in NHS hospitals.  The report is designed to provide patients and their family members with information about the various treatments that patients can receive after being diagnosed with OG cancer.

The Patient Report is available as a pdf via this link: www.nogca.org.uk/reports/2018-patient-report/

Each year, NOGCA publishes an Annual Report to help hospitals to find out what they are doing well and to identify aspects of care that could be improved.  For example, the report describes the typical length of hospital stay and short-term survival after surgery, both of which have improved over the last decade.  The 2018 Annual Report also showed regional variation in the use of non-curative treatments such as palliative chemotherapy and radiotherapy.

The audit team welcome your feedback on the 2018 Patient Report and your suggestions for future reports. If you have any comments, ideas or suggestions, please email: og.cancer@nhs.net

The OPA is represented on the Audit Steering Group by an OPA Trustee, John Taylor (OPA Leeds co-ordinator).

We produce many thousands of our booklets as a valuable reference to patients, carers and their families, all booklets are supplied free of charge and paid for by the OPA. We would be grateful for any donations you could make so we can continue to help those who need it. 

Click here to view our ways to donate page.

In our online shop you can order a range of different products including OPA Scarves and T-shirts, as well as all of the OPA booklets and leaflets.

Click here to have a browse.

Find out about how you have an oesophageal stent put into your food pipe and how you’ll feel afterwards.

An oesophageal stent is a small metal or plastic tube put into the food pipe (oesophagus). It keeps the food pipe open.

A cancer in the food pipe can partly or completely block it and make it difficult to swallow. Putting a stent into the blocked area opens up the food pipe again. This allows you to swallow food and drink more easily.

You have the stent fitted in hospital in the endoscopy department or x-ray department. It usually takes about 30 minutes.

Before your treatment

Your doctor or specialist nurse explains what happens and how they fit the stent. They ask you to sign a form saying that you agree to have the procedure. You can ask them any questions that you have. Tell them about any medicines you are taking.

You shouldn’t eat or drink for at least 6 hours beforehand.

A nurse puts a small tube called a cannula into a vein in the back of your hand. They go with you to the endoscopy or x-ray department.

You have a medicine to make you sleepy injected into the tube in your hand. Or you might have a general anaesthetic.

Having treatment

There are 2 ways of fitting the stent. Your doctor can use a:

  • long, flexible tube called an endoscope put down your throat
  • thin wire to fit the tube during an x-ray

Stent using endoscopy

While you are very sleepy or asleep your doctor puts a long flexible tube called an endoscope into your food pipe. It has a light and a small camera on the end so the doctor can see the blockage. They then put the small mesh tube (stent) into the narrowed area.

Stent using x-ray

Your doctor passes a fine wire down into your food pipe until it reaches the blockage. You then have an x-ray so the doctor can see the blocked area on a screen. They pass the stent down the wire until it is in the right place.

After treatment

You stay in the endoscopy department or x-ray department until the sedation or anaesthetic wears off. You wear an oxygen mask for a short time. A nurse then takes you back to your ward. You need to stay in hospital overnight or for a few days.

The stent expands over a couple of days. This opens up the food pipe so food and drink can pass through again.

Eating and drinking with a stent

You can’t eat or drink for the first 2 to 4 hours after having the stent. Your nurse tells you when you can start drinking. Then you can build up to eating soft foods.

You need to have a soft diet because solid food won’t pass through the stent.

Your dietitian tells you which foods you can eat.

Tips

  • Take your time when eating and sit upright.
  • Chew food well and remove any lumps or gristle.
  • If you have dentures, wear them to make chewing easier.
  • Sip nourishing fluids while eating to help food pass down through the stent.
  • Avoid tough lumps of meat, white bread and stringy fruits and vegetables.

Side effects

Sore throat

You might feel some soreness as the stent expands. Taking painkillers for a few days helps.

After a few days, the soreness usually goes away but you might still have some soreness at times.

Tell your nurse or doctor if you still have pain.

Feeling sick

Let your nurse or doctor know if you feel sick. They can give you medicines to reduce sickness.

Heartburn or acid reflux

Tell your nurse or doctor if you have heartburn or acid reflux. They can give you anti acid medicine.

Sleeping upright in bed helps to prevent heartburn. You can use pillows or cushions to support yourself.

Bleeding

You might have some slight bleeding in the food pipe. It might give you a metallic taste in your mouth. This usually gets better over a few days.

Your nurse will give you mouthwashes. Tell them if you cough up blood.

A hole in the food pipe

Damage to the food pipe can tear it or make a hole (perforation). This is very rare. You might need to have surgery to mend the hole if this happens.

In the first 3 days after having treatment, tell your doctor or nurse straight away if you

  • have difficulty breathing
  • get severe chest pain
  • vomit blood
  • can’t keep food or drinks down

If food blocks the stent

Your swallowing might change or eating and drinking gets difficult or uncomfortable. Or you may find that you suddenly can’t swallow.

If this happens

  • try not to panic
  • drink plenty of fizzy or warm drinks to try and clear the blockage
  • walk around as this sometimes helps

Call your doctor or nurse for advice if you still can’t swallow

If the stent moves

After a time, the stent might move and food may not be able to pass through. If this happens you won’t be able to swallow and food or drink will come back up. Your doctor will remove or replace the stent.

At home with a stent

You have support from community nurses or your local symptom control team. You also have regular appointments at the hospital to check the stent.

The hospital or your GP give you any medicines that you need.

This article is from Cancer Research UK – https://www.cancerresearchuk.org/about-cancer/oesophageal-cancer/treatment/advanced-treatment/making-swallowing-easier/oesophageal-stent

A great way to raise funds for us – and one of the easiest ways – is to shop online.

You can shop from almost 3,000 retailers who will give a donation every time you buy something at no extra cost.

If all our supporters remembered to do their online shopping through Easy Fundraising, then we could set up more support groups for patients across the UK.

How it works:

For a step to step guide on how to use Easy Fundraising, click here.

Start at easyfundraising.org.uk

If you want to buy a pair of shoes, an item of clothing, your groceries in fact anything you need, instead of going direct to the retailer website you go to the easyfundraising.org.uk website first – or you can use the Easy Fundraising Donation Reminder widget.

Making a purchase

Click from the Easy Fundraising site through to your chosen retailer to make your purchase.

Then get your donation

When you have made your purchase the retailer will make a donation to our cause as a thank you for shopping with them. There will be no extra charge for your purchase and Easy Fundraising will collect these donations for us. Brilliant! It really is easy.

Click here to view the Easy Fundraising Booklet.

A great way to raise funds for us – and one of the easiest ways – is to shop online.

You can shop from almost 3,000 retailers who will give a donation every time you buy something at no extra cost.

If all our supporters remembered to do their online shopping through Easy Fundraising, then we could set up more support groups for patients across the UK.

How it works:

For a step to step guide on how to use Easy Fundraising, click here.

Start at easyfundraising.org.uk

If you want to buy a pair of shoes, an item of clothing, your groceries in fact anything you need, instead of going direct to the retailer website you go to the easyfundraising.org.uk website first – or you can use the Easy Fundraising Donation Reminder widget.

Making a purchase

Click from the Easy Fundraising site through to your chosen retailer to make your purchase.

Then get your donation

When you have made your purchase the retailer will make a donation to our cause as a thank you for shopping with them. There will be no extra charge for your purchase and Easy Fundraising will collect these donations for us. Brilliant! It really is easy.

Click here to view the Easy Fundraising Booklet.

My Donate

We wanted to let you know that My Donate is closing down on 30th June 2019. For all of our Fundraisers on My Donate, we have added the frequently added questions below with some more information.

FAQ

1) When is the last date that donations can be made?
Sunday 30 June 2019 is the last date you can make donations on MyDonate.

2) We’re a charity and take donations through MyDonate, what will happen after 30 June 2019? 
Donations made up to midnight on 30 June 2019 will reach charities within 30 days and we’re working with HMRC to make sure all Gift Aid is paid as quickly as possible. You can find out more about how to access your data in our Privacy Policy here.

3) What if my fundraiser ends after 30 June 2019?
You’ll still be able to accept donations up to midnight on 30 June 2019, after this date donations will no longer be accepted. Any funds raised up to 30 June 2019 will be sent to your chosen charity.

4) What happens if I make regular donations through MyDonate?
We’ll process any donations you make before midnight on 30 June 2019 as usual. But after this date you’ll no longer be able to donate.

5) Can I transfer my raised funds to another donation site?
No but you can continue to collect donations through MyDonate until midnight on 30 June 2019 when raised funds will be processed. If you’d like to continue to fundraise after 30 June 2019 you’ll need to use another service.

More FAQs here.

We are now using Virgin Money Giving.

Venue:     Porritt Room, 10th floor, St Mary’s Hospital Praed Street, London W2 1NY
Date:        Friday 8th February 2019
Time:       1pm – 4pm

We have been contacted by the Principle Researcher James Butterworth who is based at Imperial College London.

You are being invited to take part in a research study. Before you decide whether or not to take part it is important for you to understand why the research is being done and what it will involve. Please take time to read the following information.

Please find below the relevant documents:

Participant Information Sheet

Patient Perspective Focus Group Plan

Informed consent Pt Perspective Focus Group

If you or someone you know has been diagnosed with cancer, chances are you’ve been told that they’re at a certain stage of the disease.

“The main purpose for staging is to evaluate the extent of cancer spread,” and determine a patient’s prognosis, says Ali Mahdavi, MD, a gynecologic oncologist and the Medical Director, Specialty Care Ascension Medical Group, OB/GYN Clinic at Ascension Columbia St. Mary’s Hospital in Milwaukee, Wisconsin. In other words, it gives the doctor information on how the disease is likely to progress over time, what symptoms to expect, what the survival rate is, and what some of the potential complications could be. Generally speaking, the earlier the stage of the cancer, the better the prognosis.

Staging also dictates treatment options. For instance, if an early-stage cancer is located in one particular area, it may be easier to remove surgically or treat with radiation as opposed to a late-stage cancer that has spread to other areas of the body and may require chemotherapy.


The most common cancer staging system: TNM

The most widely used cancer staging system is called the TNM classification system. This system assigns letters and numbers to the cancer to describe the tumor (T), the lymph nodes (N), and how much the cancer has metastasized (M). These individual evaluations help determine the overall stage of the cancer.

Tumor

The T category in TNM provides information about the tumor, like its size, how much it has grown into the organ it originated from, and whether it has spread to other tissues.

  • TX means the tumor can’t be measured.
  • T0 means the tumor can’t be found.
  • Tis means the cancer is growing only in the most superficial layer of tissue (this is usually true with Stage 0 or in situ cancer).
  • T1-T4 describes the size of the tumor and the extent to which it has spread to nearby tissues. The higher the number after the T, the larger the tumor.

Lymph nodes

The N category describes whether the cancer has spread to the lymph nodes.

  • NX means the nearby lymph nodes can’t be evaluated.
  • N0 means nearby lymph nodes don’t contain cancer.
  • N1-N3 describes the size, location, and/or the number of nearby lymph nodes affected by the cancer.

Metastasis

Metastasis shows whether the cancer has spread to other parts of the body.

  • MX means that the metastasis can’t be measured.
  • M0 means that the cancer hasn’t spread widely.
  • M1 means that the cancer has spread to distant organs or tissues.

Cancer stages 0 to IV

Once T, N, and M are determined, a doctor will assign the cancer a stage from zero to four. Staging differs a bit from cancer to cancer—sometimes stages are subdivided into A and B categories, for instance—but here’s a ballpark overview of how each stage is diagnosed.

Stage 0 cancer

Truth be told, whether or not stage 0 is the first and earliest stage of cancer or a precancerous stage is up for debate. (And not all cancers have a stage 0.) But once you get past the semantic argument, this is the gist:

“If we think of precancerous as a spectrum, from slightly abnormal cells on one end to very abnormal precancerous cells on the other end, stage 0 is the severest form of precancer on the extreme end of that spectrum,” says June Hou, MD, a gynecologic oncologist and assistant professor of obstetrics and gynecology at Columbia University Irving Medical Center.

For most cancers, stage 0 is called carcinoma in situ (CIS). “Stage 0 typically means that there are cancer cells that haven’t penetrated through the lining or the initial wall,” says David N. Oubre, MD, an oncologist and the founder of the Pontchartrain Cancer Center, which has two offices in Louisiana. “For instance, if it’s breast cancer, you can get something called DCIS: ductal carcinoma in situ. In that situation, the cancer hasn’t spread from the milk duct into the regular breast tissue.”

But the in situ phase is still dangerous. “In time, they’ll eventually become invasive. So there’s nothing about them that’s not cancer. It just hasn’t developed fully,” Dr. Oubre explains.

Stage I and II cancer

In these stages, the cancer is generally in only one area of the body. Stage I cancer is usually smaller in size and stage II is usually larger in size.

Stage III

During this stage, it often means that the cancer has spread to the lymph nodes.

Stage IV

This stage typically indicates that the cancer has spread widely throughout the body or has metastasized.


3 common questions about cancer staging

Does TNM coincide with cancer stage?

It’s important to note that the combination of TNM categories you have doesn’t necessarily coincide with the stage of cancer you have.

“You might have a T3, N0, M0 colon cancer, and that would be stage II. But a T3, N0, M0 of cancer of a different type might be stage I,” says Dr. Oubre.

There are other factors that affect the stage of cancer. For example, the grade of your cancer measures how abnormal the cancer cells look. Low-grade cancers look similar to cells in normal tissue and grow slowly while high-grade cancers grow rapidly. Cell type also helps determine the stage of cancer because your treatment will depend on the type of cancer cell.

Do cancer stages change over time?

Interestingly, the stage of cancer that you have never changes over time, even if it metastasizes. It remains whatever it was called at the time of diagnosis.

So, if you were diagnosed with stage II breast cancer and went into remission, but it came back and spread to your bones, it wouldn’t be called stage IV. It would be called stage II breast cancer with recurrent disease in the bones.

Is one person’s stage III cancer the same as another person’s stage III cancer?

With all of this said, keep in mind that all cancers at different stages have different prognosis and treatment options. So someone with stage III for one type of cancer doesn’t necessarily have the same treatment or prognosis as another type of cancer at the same stage.

“Patients often come with memories or accounts of how their friend/family coped with their cancer treatments. I always remind patients that not all cancers behave the same way,” says Dr. Hou. “And advancements in cancer treatments differ across different cancer types.”

That’s why you should always discuss your diagnosis in depth with your doctor to make sure that you understand what it means for you and your treatment.


Article from Prevention – https://www.prevention.com/health/a23415937/cancer-stages/

1. The Oesophageal Patients Association

2. The Reality of Oesophageal Cancer

3. A Message from our Patron Fiona Wade

4. A Personal Introduction to the Oesophageal Patients Association

5. A Lifeline to Patients, Families & Carers