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Acalabrutinib + Ruxolitinib interactions
Hello I have CLL (taking Acalabrutinib ) I also have Myelofibrosis and my Dr might put me on Ruxolitinib..... I am Looking for interactions between both drugs. I have checked drugs.com and Epocrates Looking for someone with more info or someone taking this combination Thank you
Hello I have CLL (taking Acalabrutinib ) I also have Myelofibrosis and my Dr might put me on Ruxolitinib..... I am Looking for interactions between both drugs. I have checked drugs.com and Epocrates Looking for someone with more info or someone taking this combination Thank you
antonb
in
CLL Support
2 years ago
Ruxolitinib and NSAIDs
Would anyone care to comment on the Jakafi label warnings against using NSAIDs? There is reportedly an increased risk of bleeding. If this is really the case, I guess I'm limited to acetaminophen for pain management.
Would anyone care to comment on the Jakafi label warnings against using NSAIDs? There is reportedly an increased risk of bleeding. If this is really the case, I guess I'm limited to acetaminophen for pain management.
sbs_patient
in
MPN Voice
2 years ago
COVID update: Who remains at higher risk? by LLS.org
People with the following types of blood cancer are less likely to develop protective antibodies and they are less able to fight off an infection because the cancer affects immune B-cells: • Chronic
lymphocytic
leukemia
• Diffuse large B-cell lymphomas • Follicular lymphoma • Marginal zone lymphoma
People with the following types of blood cancer are less likely to develop protective antibodies and they are less able to fight off an infection because the cancer affects immune B-cells: • Chronic
lymphocytic
leukemia
• Diffuse large B-cell lymphomas • Follicular lymphoma • Marginal zone lymphoma
lankisterguy
Volunteer
in
CLL Support
2 years ago
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Managing the cardiovascular risk of Bruton's Tyrosine Kinase Inhibitors in chronic lymphocytic leukemia
The American Society of Hematology journal [i]Blood Advances[/i] published an important "[i]International Consensus Statement on the Management of Cardiovascular Risk of Bruton's Tyrosine Kinase Inhibitors in CLL[/i]" on 5 July 2022. It provides "[i]a management guideline for CV[/i] [i]toxicities of
The American Society of Hematology journal [i]Blood Advances[/i] published an important "[i]International Consensus Statement on the Management of Cardiovascular Risk of Bruton's Tyrosine Kinase Inhibitors in CLL[/i]" on 5 July 2022. It provides "[i]a management guideline for CV[/i] [i]toxicities of
CLLerinOz
Administrator
in
CLL Support
2 years ago
Dietary factors and risk of chronic lymphocytic leukemia and small lymphocytic lymphoma
I'm posting this in a separate thread for more people to see. The publication is freely accessible and covers a large array of people. I will not participate in a discussion (I do not have the strength). This is for information only and because I have quoted it several times and I promised to share
I'm posting this in a separate thread for more people to see. The publication is freely accessible and covers a large array of people. I will not participate in a discussion (I do not have the strength). This is for information only and because I have quoted it several times and I promised to share
Yalokin
in
CLL Support
2 years ago
Further evidence that even moderate exercise is good for your long term health - particularly when you have CLL!
, chronic
lymphocytic
(CLL), according to new research from the University of Surrey.
, chronic
lymphocytic
(CLL), according to new research from the University of Surrey.
AussieNeil
Partner
in
CLL Support
1 year ago
Atypical CF -diagnosed in UK? Results back
After the better part of a year, I finally received my results for CF and PCD testing. The initial brush biopsy for PCD indicated no mucociliary clearance amongst other things. However, they regrew the cilia and decided this was caused by mucus trapping the cilia. I was told they had to retest the
After the better part of a year, I finally received my results for CF and PCD testing. The initial brush biopsy for PCD indicated no mucociliary clearance amongst other things. However, they regrew the cilia and decided this was caused by mucus trapping the cilia. I was told they had to retest the
Person99
in
Lung Conditions Community Forum
2 years ago
Save the date! Our first conference for over two years! We're very pleased to invite you to our conference in Glasgow later this month.
We are excited to announce that our first conference for over two years will be held in Glasgow.
Topic: 'Managing CLL in 2022- Treatment guidelines explained'
When:
Tuesday 18 October
Where:
Voco Grand Central, 99 Gordon Street, Glasgow, G1 3SF. The centre is within the
We are excited to announce that our first conference for over two years will be held in Glasgow.
Topic: 'Managing CLL in 2022- Treatment guidelines explained'
When:
Tuesday 18 October
Where:
Voco Grand Central, 99 Gordon Street, Glasgow, G1 3SF. The centre is within the
pkguk2
CLL Support Association
in
CLL Support
2 years ago
COVID: Staying Safe As The Virus Evolves - LLS Podcast / CLL Society’s COVID-19 Update December 5th, 2022 / Dec 15 2022 end Antibody Study
People with the following types of blood cancer are less likely to develop protective antibodies and they are less able to fight off an infection because the cancer affects immune B-cells: • Chronic
lymphocytic
leukemia
• Diffuse large B-cell lymphomas • Follicular lymphoma • Marginal zone lymphoma
People with the following types of blood cancer are less likely to develop protective antibodies and they are less able to fight off an infection because the cancer affects immune B-cells: • Chronic
lymphocytic
leukemia
• Diffuse large B-cell lymphomas • Follicular lymphoma • Marginal zone lymphoma
lankisterguy
Volunteer
in
CLL Support
2 years ago
pre fibrotic myelofibrosis
Hi all hope your well. Could anyone help me I had a BMB nad results say I have Pre Fibrotic myelofibrosis changes not sure what this means I have ET My Haemotoligist has suggested changing to Pegylated Interferon Has anyone had same diagnosis Is anyone on htis medication to and can tell
Hi all hope your well. Could anyone help me I had a BMB nad results say I have Pre Fibrotic myelofibrosis changes not sure what this means I have ET My Haemotoligist has suggested changing to Pegylated Interferon Has anyone had same diagnosis Is anyone on htis medication to and can tell
JeniMac
in
MPN Voice
2 years ago
PV and CML?
hi just diagnosed with PV JAK2+ve. I also have 1 type of my white cells slightly high. Could I have CML at the same time as PV. My hospital notes had CML?
hi just diagnosed with PV JAK2+ve. I also have 1 type of my white cells slightly high. Could I have CML at the same time as PV. My hospital notes had CML?
DougyW
in
MPN Voice
2 years ago
1st day on Ruxolitinib
The doctor took me off both Hydroxy and Anagrelide to start on new medication Ruxolitinib 20mg x2 daily. im a bit nervous about it, as I gained a lot of weight with the other medication and shielding, I don’t want to gain more. I know I have to lose some weight (I’ve done it before and I’ll do it again
The doctor took me off both Hydroxy and Anagrelide to start on new medication Ruxolitinib 20mg x2 daily. im a bit nervous about it, as I gained a lot of weight with the other medication and shielding, I don’t want to gain more. I know I have to lose some weight (I’ve done it before and I’ll do it again
wendycu
in
MPN Voice
2 years ago
Meet Henry
Spot Leukaemia News!!! Us and Leukaemia UK are excited to launch our new Spot Leukaemia video which aims to make the signs and symptoms the most memorable yet! Introducing Henry! He’s here to make the signs and symptoms of leukaemia memorable. In the video, you will see Henry the Macaw parrot as
Spot Leukaemia News!!! Us and Leukaemia UK are excited to launch our new Spot Leukaemia video which aims to make the signs and symptoms the most memorable yet! Introducing Henry! He’s here to make the signs and symptoms of leukaemia memorable. In the video, you will see Henry the Macaw parrot as
NicoleLeukaemiaCare
in
Leukaemia Support
2 years ago
EVOLVE trial for high risk chronic lymphocytic leukemia - CLL patients will test an early treatment intervention Vs watch and wait
'[i]The goal of the S1925 [EVOLVE] trial is to find out if early treatment can help people with chronic
lymphocytic
leukemia
(CLL) or small
lymphocytic
lymphoma (SLL) live longer and have a better quality of life.
'[i]The goal of the S1925 [EVOLVE] trial is to find out if early treatment can help people with chronic
lymphocytic
leukemia
(CLL) or small
lymphocytic
lymphoma (SLL) live longer and have a better quality of life.
CLLerinOz
Administrator
in
CLL Support
2 years ago
essential thrombocytosis
I was diagnosed with et almost 4 years ago,had all the tests investigations etc,my platelets are now almost normal but apparently my hb is slightly low.i am very worried in case I have myelofibrosis which apparently is quite serious, can anyone help . Thanks.
I was diagnosed with et almost 4 years ago,had all the tests investigations etc,my platelets are now almost normal but apparently my hb is slightly low.i am very worried in case I have myelofibrosis which apparently is quite serious, can anyone help . Thanks.
glyndale
in
MPN Voice
2 years ago
Fibrosis, Grade 0 does not mean None
In another thread we've been discussing cellularity and fibrosis. I've found an unexpected (to me) result in my study. None is not an answer, we all need some fibers of fibrosis to support the marrow. The MPN condition starts when "some" becomes "more". "Structural fibrils constitute a physiological
In another thread we've been discussing cellularity and fibrosis. I've found an unexpected (to me) result in my study. None is not an answer, we all need some fibers of fibrosis to support the marrow. The MPN condition starts when "some" becomes "more". "Structural fibrils constitute a physiological
EPguy
in
MPN Voice
2 years ago
Optimizing Treatment of Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
This is a short paper setting out the non trial option for patients needing treatment after a targeted therapy https://jnccn.org/view/journals/jnccn/20/5.5/article-p581.xml Jackie
This is a short paper setting out the non trial option for patients needing treatment after a targeted therapy https://jnccn.org/view/journals/jnccn/20/5.5/article-p581.xml Jackie
Jm954
Administrator
in
CLL Support
2 years ago
Does Covid boost ALS?
I'm W&W for 2 years. Abs lymphs (ALS) were 82K in July. Got 1st Evusheld 8/23. Got Covid 8/31 and started Paxlovid same day. 5 days later, 9/5, felt great then went on a vigorous 31 miles bike ride (probably too soon for such exercise). Then rebound on 9/12 with positive home test. Never got fever but
I'm W&W for 2 years. Abs lymphs (ALS) were 82K in July. Got 1st Evusheld 8/23. Got Covid 8/31 and started Paxlovid same day. 5 days later, 9/5, felt great then went on a vigorous 31 miles bike ride (probably too soon for such exercise). Then rebound on 9/12 with positive home test. Never got fever but
JDG45
in
CLL Support
2 years ago
ET progression to MF - anxiety issues
My ET is now progressing to Post ET Myelofibrisis. My hemo has recommended I start on Ruxolitinib & also to be considered for a stem cell transplant. I know some of you have been in the same situation. Am I correct in thinking MF is life limiting? Also how have any of you coped on Rux? I feel very
My ET is now progressing to Post ET Myelofibrisis. My hemo has recommended I start on Ruxolitinib & also to be considered for a stem cell transplant. I know some of you have been in the same situation. Am I correct in thinking MF is life limiting? Also how have any of you coped on Rux? I feel very
SRH55
in
MPN Voice
2 years ago
Rapamycin
I have friends using low doses of this drug and I have an appointment with a doctor that prescribes it. When I asked my Hematologist at Mayo about it they said this drug may be get approved sooner than later for MPN’s. Has anyone researched this or used it. It is a drug used for organ transplants but
I have friends using low doses of this drug and I have an appointment with a doctor that prescribes it. When I asked my Hematologist at Mayo about it they said this drug may be get approved sooner than later for MPN’s. Has anyone researched this or used it. It is a drug used for organ transplants but
MDI55
in
MPN Voice
2 years ago
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