Lymphoma is the most common blood cancer. It occurs when lymphocytes, a type of white blood cell found in lymph nodes, grow and multiply uncontrollably, causing the lymph nodes to swell.
Click to enlarge the infographic below
• A new training course has been developed by blood cancer support charity Leukaemia CARE, in collaboration with the Royal College of General Practitioners (RCGP), and launched to mark the start of Blood Cancer Awareness Month
• The course set to radically improve GP knowledge of blood cancer symptoms, potentially saving around 1,000 lives a year
• Blood cancer survival from GP referral stands at 83.6% – but falls to 53.1% if diagnosis is delayed until the emergency admissions route.
• However, blood cancer symptoms can be easily confused with the symptoms of other less serious illnesses like the flu, leading to 33% of blood cancers – more than 10,000 patients – only diagnosed via emergency admissions
• Blood cancers such as leukaemia, lymphoma and myeloma are statistically the nation’s fifth largest cancer threat with 34,000 people diagnosed each year, and are the third biggest cancer killer
A new online training course designed to raise awareness of the symptoms of blood cancer among GPs is set to radically improve the rate of early diagnosis, bringing the UK up to EU standards and potentially saving around 1,000 lives a year.
Blood cancer support charity Leukaemia CARE, in collaboration with the Royal College of General Practitioners (RCGP), has developed the course in a bid to deliver better outcomes for the 34,000 people diagnosed with blood cancers in the UK each year.
When combined, blood cancers like leukaemia, lymphoma and myeloma are statistically the nation’s fifth largest cancer threat and third biggest cancer killer. And yet because many of the symptoms of blood cancer experienced by patients, such as persistent fatigue, night sweats, joint pain, bruising and recurrent infections, may also be linked with a wide range of other less serious diseases, 33% of blood cancers – more than 10,000 patients – are only diagnosed via the emergency admissions route, including accident and emergency.
Research shows that early diagnosis has a major impact on survival rates. For instance, the one year survival rate for myeloma patients diagnosed following a GP referral stands at 83.6% – but falls to 53.1% if diagnosis is delayed until the emergency admissions route3.
While online courses for GPs are available for other major cancers, this is the first of its kind for all blood cancers. Free of charge, it combines information on how to recognise the symptoms with case studies and, like all RCGP training courses, carries Continuous Professional Development (CPD) points – which GPs must complete to demonstrate that they are meeting the standards set by the General Medical Council.
The news comes as the UK marks its third Blood Cancer Awareness Month (1-30 September).
We interview Tony Gavin the Director of Campaigning and Advocacy at Leukaemia CARE and Dr Ishani Patel who is a GP and the Royal College of General Practitioners (RCGP) Clinical Lead for Early Diagnosis of Cancer and Quality Improvement
Question – What is blood cancer?
Dr Ishani Patel – Blood cancer is an excessive growth of blood cells. For diseases such as lymphoma and leukaemia, this can be an excessive growth of white blood cells. The white blood cell is responsible for immunity and fighting off infection. However, when there is an overgrowth or an excessive amount of white cells, patients can often present with symptoms such as tiredness, excessive sweating, bone pains, bruising and bleeding. That’s a very brief overview of what a blood cancer is.
Question – How do leukaemia, lymphoma and myeloma differ from each other?
Tony Gavin – That is a huge question because within those disease areas there are also other disease types. There are 90 different leukaemias and 60 different lymphomas. There’s about 5 or 6 main types of myeloma, as well as other types, so we couldn’t really begin to describe the differences between them.
Collectively blood cancers are a huge problem in the UK and they are very poorly understood. At Leukaemia Care we think of them as a Cinderella disease, tucked away in the background with nobody fully aware of them, but blood cancers are the fourth largest notifiable cancer amongst men and women. Indeed if you look at the mortality rates and the people who die from blood cancer, more people die from blood cancer than die from breast cancer, more people die from blood cancer than die from prostate cancer. The sixth largest notifiable cancer in the UK is malignant melanoma (skin cancer). More people die from blood cancer than are actually diagnosed with skin cancer.
That’s how significant the problem is and that’s why we decided we needed to do something to help general practitioners recognise the signs and symptoms of the disease.
Question – What do the stages of different cancers mean?
Dr Ishani Patel – The different stages correspond with how much the disease has progressed.
For example in the context of blood cancers and the subset myeloma, if you present to the GP and are referred onto a specialist, your 1 year survival rate is 84% because you are diagnosed at an early stage, so stage 1.
However if you present as an emergency presentation, which is a third of all blood cancers, your 1 year survival rate drops to 55% so that’s a late stage diagnosis, which could be considered stage 3 or 4.
It’s difficult to drill into the detail of what each stage means because it’s obviously different depending on the type of blood cancer and as Tony’s just mentioned there are over 100 different types of blood cancers just within that terminology.
Question – What are the early signs and symptoms of blood cancers?
Dr Ishani Patel – Signs and symptoms to look out for include tiredness, excessive sweating, bone pain, bruising, bleeding, and recurrent infections. These can all present as individual signs or as a cluster of an early blood cancer. However if patients experience loss of appetite or weight loss, those are obviously signs of perhaps a cancer that has progressed.
Tony Gavin – With the lymphomas for instance you might have lumps in the neck or lumps in the armpit, or lumps in the groin. And the other thing to look out for is that quite a lot of the symptoms can be defined by something else. They could be just a common cold or flu or even menopause for the older patient. It’s when these signs and symptoms are persistent that you really need to take notice of them.
Question – Who treats these cancers and how?
Dr Ishani Patel – If we were to look at a classic patient journey, the GP who thinks there is a collection of symptoms that are causing concern would arrange for blood tests and perhaps a urine test or potentially even x-rays within primary care. They would arrange for what’s called a fast track cancer referral, which is a two-week-wait cancer referral where the patient can then be met by a haematologist. However, not all patients experience the same journey because of the varying ways that they present.
If a patient presents with, for example, a neck lump or a lump in their armpit or groin, they may go straight to a surgeon because they need to get a tissue sample or a biopsy to get a diagnosis.
However if a patient that presents with these symptoms then has a blood test and the blood test itself is abnormal, then they may be routed to a haematologist. Not everybody sees a haematologist straight away because it does very much depend on how they present in the first place.
Tony Gavin – The problem with bone pain is you would probably be referred to an orthopaedic surgeon before they realize it could be myeloma for instance. Within the blood cancer specialist community, within the haematology community, there are people that will specialise in leukaemias, lymphomas, and myelomas, and indeed within the leukaemias you may get people that specialise with chronic myeloid leukaemia, and those that specialize with acute myeloid leukaemia, so it varies. There are generalists and there are very, very specific specialists.
Question – How effective are the treatments?
Tony Gavin – That’s a really good question but a very difficult one to answer because you will find different treatments for the whole range of different disease areas. I can quote one disease area where there is really, really good news. About 12 years ago survival rates for chronic myeloid leukaemia (CML) were poor. If you were diagnosed with CML in 2000 for instance then your survival prospects would be 3 – 5 years. In 2001 a new drug called Imatanib was developed – a tyrosine-kinase inhibitor. This class of drug has completely and utterly revolutionised the treatment of CML. Patients that respond to these drugs will not die from CML, they will not die from the leukaemia. This particular class of drugs is amazing, it’s one of the best good luck stories going around. It is a huge step change in the treatment of that particular disease.
Question – Please tell us about this new online tool, what it does and what its value will be.
Dr Ishani Patel – Leukaemia Care and the Royal College of General Practitioners have come together to develop a one hour learning course for not only GPs but all primary care health professionals. GPs are legally and professionally required to commit and evidence their own professional development i.e. the time they contribute to their own education. What Leukaemia Care has recognised is that the other cancers have a lot of attention both in the media and within GP education and we didn’t want blood cancers to be overlooked. So what this course does is provide case based scenarios almost like it is in real life. As a GP you’re sitting in your consultation room and a patient presents with a cluster of symptoms and it challenges the GP to think about what their next steps would be. For example if a patient presents with tiredness and with a lump in the neck what would they do next? And then once they have submitted their answers and evidenced their own reflection, it then takes them through to the gold standard and through the NICE guidelines on what they should do next, how to ensure rapid investigation and how to ensure that the patient’s route to diagnosis is as quick as possible.
Question – What one piece of advice would you give to someone who has just been diagnosed with a blood cancer?
Dr Ishani Patel – That’s a very tough question because there are different types of blood cancers. What I would say is that something that does get overlooked with all cancer treatments is nutrition. I would advise any patient going through or preparing to go through cancer treatments that could include steroids, chemotherapy, stem cell transplants and as Tony was saying tyrosine-kinase inhibitors that having a high protein diet and ensuring their nutrition is adequate will support them through their journey especially with managing the adverse effects of treatments. That would be my input from a GP perspective.
Tony Gavin – From my perspective, I would echo what Dr Patel has said but also say that they are not alone. They need to get in touch with a specialist organisation like Leukaemia Care, which can support them through their treatment. They can go online to leukaemiacare.org.uk and they can talk to our specialist nurse or talk to our care line experts. We have a care line that operates 24/7 so they can phone us at any time for help and advice and we can also put them in touch with patients who have been diagnosed with a similar disease so they can share their concerns and their worries. The other thing I have to say is there are breakthrough drugs coming through all the time in all the different disease areas and some of the new treatments coming through are superb. So first of all, don’t lose hope, get in touch with an organisation like Leukaemia Care and we’ll put you in touch with other groups too if you need to speak to somebody else.
We have a wealth of information online too and there’s lots that they can do to educate themselves on the disease.
Question – Where can people go for more information?
Dr Ishani Patel – Leukaemia Care provides robust information that is easy for patients to understand. From a GP perspective, I would encourage GPs to go to the Royal College of GPs website and do the online learning exercises to then be able to communicate that back to patients.
Tony Gavin – If patients do need more information once they have been in touch with Leukaemia Care, we can signpost them onto other areas.
This month is National Blood Cancer Awareness Month promoted by the Leukemia and Lymphoma Society.
The have produced a brilliant infographic below. Please do share to help us raise awareness of blood cancers such as Leukemia and Lymphoma.
In particular we have looked at the area of stem cells in particular as a treatment for multiple sclerosis. You can check out our recent blog here.
Interestingly cord blood ( ie from the newly born’s umbilical cord). I would strongly recommend you pop round to the Parent’s Guide to Cord Blood Foundation which gives , for my money, the best overview , of cord blood and cord blood banking. They say “The term “cord blood” is used to describe the blood that remains in the umbilical cord and the placenta after the birth of a baby. Up until recently this blood was discarded as medical waste. Cord blood contains stem cells that may be cryopreserved for later use in medical therapies, such as stem cell transplantation or new emerging therapies.”
The site useful gives a list of cord blood banks not just in America.
Indeed they mention that over 80 different medical conditions could be treated with stem cells from cord blood. These include types of Leukemia , some anemias, Lymphoma, Thrombocytopenia, Bone Marrow Cancers and some solid tumours. That being said it is currently under going clinical trials for such diverse conditions as autism, rheumatoid arthritis, Cerebral Palsy and some types of motor neurone disease.
So it all looks very promising.
As well as raising awareness of Cord Blood Awareness Month we are also interested in your views ion the subject. It would be great if you could share your responses to the following questions using the comment box below:-
a) Have you “banked” your childs cord blood? If so why and how did you go about the process of doing so?
b) Would you consider it in the future.
Any aspect of your cord cell story will be of great interest so feel free to tell us below.
The Epstein–Barr virus is mostly known as the cause of glandular fever.
But in recent years it is also has been shown to be related to a number of types of lymphoma.
Increasingly it is believed the Epstein–Barr viral infection can mean a higher risk of certain autoimmune and other diseases. In particular Parkinson’s disease, Lupus (https://patienttalk.org/?tag=lupus) , rheumatoid arthritis (https://patienttalk.org/?tag=rheumatoid-arthritis), and multiple sclerosis (https://patienttalk.org/?tag=multiple-sclerosis).
While many people (maybe 90% of the population) have been infected with the virus very few of us show any symptoms.
The purpose of this blog post is to find out to what extent our readers with autoimmune and similar conditions have had the Epstein–Barr virus . Please take the poll to give us an indication.
It would be great if you would use the comments box below to say which condition you have.
Thanks in advance
Lindsay4 | Strep several times in college (2001-2005); severe endometriosis (stage 4) at 28 that required surgery in 2009; have had 2 more surgeries since for endometriosis (stage 2 and 3 respectively); a very severe case of mono in 2010; in 2014, had my 3rd surgery for endo, and one month later I was diagnosed with LUPUS. I was only ever tested for Epstein-Barr when I got dangerously sick in 2015, and it came up positive that I’d had it. They said I didn’t have to do anything about it(???). They could never figure out what was wrong with me at that time though. Fatigue is insane. I take adderall just to be able to work, and I can STILL sleep all day on it. Don’t know what to do anymore. |
Mamad03 | I have MS, UCTD and Sjogren’s |
GironLara | HELLO, Good-day To You All Dear Viewers Brothers and Sisters ,Friends ,I want to shear a testimony on how Dr Lugard help me cured a virus called herpes simplex virus, I am so very happy today because I am free from the disease/virus of Herpes, My name is GIRON LARA from USA , I have been having Herpes since the past two years now, and I have pass through many different processes in getting cured from the diseases virus of HSV2 but nothing was working out, a friend of mine on Facebook called Harry Lura introduce me to DR LUGARD,and also give me hes email address ( or ) http://drlugardspellhome.webs.com/ that he is the only one who can helped me get cured from my Herpes and any other diseases i may have , so I contacted him and have faith on him, All thanks to the gods of DR LUGARD , after sending me the herbal medicines which he has prepared for me, my life get transformed and everything was fine and Okay with me, till now I have been going to check up and its now going to tow-months now I am still negative. All thanks Goes to DR LUGARD and My Friend called Harry Lura for what she has done for me and my family… if you are also passing true problems, pains or any type of sickness or diseases i will advice you to contact DR LUGARD now by emailing him now at:( or ) You can also call him on these Mobile number okay . TRULY DR LUGARD YOU ARE THE BEST MAY GOD-ALMIGHTY REWARD YOU FOR YOUR GOOD WORK OKAY, I WILL CONTINUOUS TO TESTIFY OF YOUR GOODNESS UNTIL MY LAST BREATH IN THESE EARTH MY BEST REGARDS SIR. whats-app also now or on his web sit http://dr-lugardspellhome.webs.com/ |
IE | I have MS Primary Progressive, had mono as a teen and spinal tap revealed EBV antibodies. |
lemonfoundation | aredmosquito MS is Lyme disease cover-up. http://www.cfsstraighttalk.blogspot.com |
aredmosquito | I have MS, have never had mono, and was tested for antibodies to EBV which came up negative. |
DebbyReaana | Relapsing Remitting Multiple Sclerosis. |
RachelSouth | Fibro with other undefined and diagnosed with asthma last year, which is still not controlled. |
andersoncarol1212 | My name is Carol Anderson, I am here to give my testimony about a doctor who helped me in my life. I was infected with HERPES SIMPLEX VIRUS in 2010, i went to many hospitals for cure but there was no solution, so I was thinking how can I get a solution out so that my body can be okay. One day I was in the river side thinking where I can go to get solution. so a lady walked to me telling me why am I so sad and i open up all to her telling her my problem, she told me that she can help me out, she introduce me to a doctor who uses herbal medication to cure HERPES SIMPLEX VIRUS and gave me his email, so i mail him. He told me all the things I need to do and also give me instructions to take, which I followed properly. Before I knew what is happening after two weeks the HERPES SIMPLEX VIRUS that was in my body got cured . so if you are also heart broken and also need a help, y |
JosephDieva | I was dx with : Mono and Infectious Heppatitius in 1982 , dx with Eppstein – Barr virus in 1986 , dx with “Leaky Gut” in 1999 , dx with Hypo thyroidism in 2010 and dx with M.S. In 2013 ( my feet started to go numb in 2008 , a sign of M.S. to come ) !!!!!! |
JackieBax | Fibromyalgia, Hypothyroidism |
TinaMulhall tinamulhall@yahoo.ie 78.17.60.113 |
Ulcerative colitis. I had EBV and chickenpox as a child. |
loulou02 lyndav1@live.com.au 49.181.78.27 |
I have fibromyalgia. Yes I have had EBV Ross River Virus and Barmah Forest Virus. |
RandiLynnHart gimmedanger87@gmail.com 66.87.78.222 |
No EBV related anything for me. |
Roxannestanbridge Roxanne_caldwell@hotmail.co.uk 46.254.249.208 |
Glandular fever at 18, MS diagnosed at 30 although had a few relapses from 18 yo |
GinnyIckle pickledginger@gmail.com 208.103.65.134 |
Hx of Ebv, cmv, chicken pox, shingles x2, Lyme disease. Have celiac, multinodular thyroid, cf, fm, Sjogrens, t2diabetes, Dysautonomia. |
Pam Crittenden plwc@comcast.net 98.209.15.5 |
Severe case of mono at 17 (1978) diagnosed with MS at 32 (1993). |
GillianCunninghamWright gilldusty2@btinternet.com 86.146.4.251 |
I had EBV, chicken pox, scarlet fever, mumps, tonsillitis. Diagnosed with glandular fever in 2006, never recovered, now have M.E. Fibro and Type 2 Diabetes. |
thequeenkat | I Contracted Mononucleosis When I Was 15, Which I Am Certain Was Followed By Me Developing Narcolepsy. I Also Have PCOS, Hyposmia, Auditory Processing Disorder And Now Am being Evaluated For Multiple Sclerosis. Narcolepsy And All Other Conditions Were Diagnosed In My Early Twenties, Although I Know I Had Them Most Of My Life. The MS Is A Recent Development. Sorry If My Post Is Typed Oddly, I Am Having Problems With This Android Phone. |
KathyHastings | I was infected with EBV along with many other viruses in my body; prior to also dx with Celiac Disease. |
JosephDieva | Yes , I was diagnosed with Eppstein – Barr Virus in 1986 ! |
CheyMcKenzie | Gladular Fever aged 13, diagnosed MS aged 41 but believed to have had it a few years by then. |
JosephDieva | Was diagnosed with Mono and Hepatitis in April of 1982 , diagnosed with Eppstein – Barr virus in April of 1986 , developed first sign of M.S. IN SUMMER OF 2008 and finally diagnosed with M.S. in March if 2013 ! |
touzell | Had glandular fever 30 years ago.. 2.5 years ago diagnosed with psorathic arthritis and this year ensinophilic esophagus. Interested to further studies relating it all. |
lemonfoundation | HIV-Negative AIDS: Is it CFS, GWS, or AIDS? Allied NATO Government is hiding millions of infectious NON HIV AIDS cases (like mine) under the “Chronic Fatigue Syndrome (CFS)” ICD-code. – Dr. Lorraine Day on Joyce Riley’s military show THE POWER HOUR (09/12): “…HIV-Negative AIDS cases falsely reported and treated as CFS cases may be one of the biggest cover-ups we have seen.” – In 1992 “…Newsweek made an even more shocking announcement: …CFS patients who had the same immune system deficiencies as the NON-HIV AIDS cases…”– Dr. Judy Mikovits stated on In Short Order (11/12) about CFS & Myalgic Encephalopathy (ME): “…consider this as NON HIV AIDS.” – Neenyah Ostrom’s book “America’s Biggest Cover-up: 50 |
NancyD64 | Diagnosed with EBV at 16 after a year of being sick, missed a semester of high school. Diagnosed with RRMS just shy of 36 y.o. living, with it 14 yrs.
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shurl Stirling | my son was diagnosed with neuro sarcoid, if was treated with steroids.if was diagnosed with other conditions because the neuro s mimics other conditions.checkout Joe Stirling on Google. He’s a rare case (less than 2 people suffer the neuro sarcoid in 100,000 ) nobody, not even professors know what causes it. ???? i can’t believe that. |
virgo54 | Had a very severe case of Glandular Fever over 30 years ago, was hospitalised for a week. 10 years ago developed Primary Progressive Multiple Sclerosis (PPMS) |
CameoCamylMassey | Diagnosed with EBV in 1987. Had it for many years but none of the doctors knew to look for it. They just gave me antibiotics and amphetamines to keep me going, until my immune system collapsed. Wound up bedridden for 3 years, unable to use arms or legs, unable to chew food, no short or long term memory, lymph nodes swelled like ping pong balls and turned purple/blue, and would sleep 72 hours and still be exhausted. I finally overcame that and rehabilitated myself, but was then told I had Fibromyalgia and a compromised immune system. Since then I have had shingles that turned into MRSA, and a systemic infection that has led to 8 major surgeries to remove major parts of my body. Was just told by a Rheumatologist, that my Fibro is back in full flare. |
graceg | In reply to MelissaKisnerSouthard.MelissaKisnerSouthard Hi my name is grace,what is Auto Immune Hepatitis,or can u tell me where to find the information on it. Thank you I have sle,ra,fibro, diabetes,etc. I have just found out over the phone about me having hep c. I just don’t get it?? Thanks for your posts. 🙂 |
Roxannestanbridge | I had glandular fever in 2000 and been treated for Labrynthitus x3 times since – until I got my MS diagnosis in 2011 |
Taneesa | I’ve had mono, phenomena several times and fevers out of the blue for no apparent reason since i was a child |
KathyHastings | Yes on EBV, also Chicken Pox Virus, Herpes Virus; many were running rampant in my body, because my body was so busy trying to attack the gluten….all these virus attacked my CNS. Result Celiac Disease….anti-viral med….3yrs later….levels are down, but still considered high. So, I also have dx of CFS.
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katieg | glandular fever at 18, hypothyroidism for 20 years, psoraitic arthritis over 10 years, MS diagnosed 2011 but optic neuritis in mid 1990’s |
SallyNickle | I had Mono when I was 17. |
MelissaKisnerSouthard | Yes! I had EBV when I was 18. never sick a day before that. Now I have Hypothyroidism, fibromyalgia, Lupus and Auto Immune Hepatitis. I have always thought it was connected to the EBV!!! |