Yesterday I spent a little while looking at the peculiarities and similarities of CLL and SLL and found a great article by the late Professor Hamblin, further reviewed by CLL Topics in patient friendly language SLL Versus CLL: How Different Are They?. updates.clltopics.org/1993-...
I am on a quest to find current reviewed patient friendly writing about SLL, has anyone got any favorites that may help others?,
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The MOST IMPORTANT difference between CLL and SLL is that as Terry Hamblin pointed out, SLL may be CURED if caught early enough when it is confined to a few nodes that can be dealt with by targeted radiation treatment. (I'm ignoring the much higher risk possible cure for CLL of a Stem Cell Transplant.) Unfortunately, as is pointed out in the references below, SLL is generally diagnosed at a much later stage than CLL, as the growing nodes aren't usually obvious until SLL has become more systemic. It seems that the possibility of a cure for SLL is also not well known by oncologists and probably even haematologists, which is a good reason to try and a specialist that specialises in SLL/CLL if that is at all possible.
Dr Sharman provides a good but brief patient friendly overview of SLL in his article
The SLL section includes a link to his CLL topics.
Some far more detailed, though not as patient friendly references were included in Al Janski's recent CLL posting regarding Ibrutinib lymphocytosis: SLL vs. CLL to the Yahoo CLLResearch Health Group:
In 15 years I haven't met a single SLL patient that was diagnosed early enough to be treated.
Hypothetically it may be possible to irradicate it, but how often does this actually happen, if ever.
Clearly, people need to be proactive and seek medical attention for tiny lumps... however they go to their GPs and he hands then antibiotics...for some unknown infection.
And I've still got my lump mid thigh that my GP dismissed years before my SLL diagnosis as something of no consequence and my haematologist subsequently said was a swollen lymph node. It hasn't changed much in size, but I will always be wondering 'what if'...
The Australian Leukaemia Foundation reckons GPs here see on average 6 - 7 CLL patients in their entire practice history, so you just have to hope that you get the right timing or a less dismissive GP.
Thanks for doing this work and providing these links Neil,
Thanks Chris it must be rare. ( :
The latest British Committee for Standards in Haematology, Guidelines on the diagnosis, investigation and management of chronic lymphocytic onlinelibrary.wiley.com/doi...
They also confirm “The rare patient in whom SLL is diagnosed following biopsy of an enlarged lymph node in the absence of detectable disease at any other site, may be offered local radiotherapy with curative intent."
It was a shame you could not attend the conference at Liverpool, Dr Pettit was most helpful in explainng things in a way that we could easily understand and answered questions in an open manner.it was also good to meet people face to face and compare notes and experiences with them, I strongly recomend you try and make the next one.I hope to see you there.
Thanks for your feedback from the day, I was disappointed I was unable to make Liverpool and very pleased that you found the day helpful. Meeting other patients in real time and learning from each other and expert speakers does make a difference. (it has for me), I hope we get to meet too at the next..
You may be interested to know, It was the UK's CLL research community's gathering today at the UK CLL Forum's Annual Scientific Day, where Professor Pettitt was awarded The Annual Catovsky Prize by the Forum in recognition of the outstanding contribution that he has made with his recent Clinical Research studies treating 17p deleted CLL..
My SLL was casually revealed after more than 2 years of 'CLL diagnosis'....the Doctors here acted as if the two usually 'go together' that usually when you find one you find the other....I was being 'treated' for C-Diff (a miserable 8 months) when they decided I had the C-diff because of the CLL-SLL....with a compromised immune system, it's hard to fight just about anything in the region...
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