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Venetoclax
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Obinutumab plus venetoclax in cll
My father got diagnosed cll october 2009,was on wait and watch till mid 2014,then given R-bendamustine and was on remission till october 2016,then started ibrutinib in 2016 and stopped ibrutinib in mid 2018,in 2020 end due to fast multiplication of tlc and enlarged spleen and lymphnodes our doc suggested
My father got diagnosed cll october 2009,was on wait and watch till mid 2014,then given R-bendamustine and was on remission till october 2016,then started ibrutinib in 2016 and stopped ibrutinib in mid 2018,in 2020 end due to fast multiplication of tlc and enlarged spleen and lymphnodes our doc suggested
Rameshchag
in
CLL Support
3 years ago
Going off venetoclax
My oncologist said I could potentially go off
venetoclax
and if (or when) I have a recurrence I could go back on it. The research is sketchy because of the newness of the drug. Any thoughts?
My oncologist said I could potentially go off
venetoclax
and if (or when) I have a recurrence I could go back on it. The research is sketchy because of the newness of the drug. Any thoughts?
Lulu8581
in
CLL Support
3 years ago
Venetoclax
When add
venetoclax
to Ibrutinib in Cll Treatment
When add
venetoclax
to Ibrutinib in Cll Treatment
Chinhdo
in
CLL Support
3 years ago
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Obinutuzumab and venetoclax in relapsed cll,
My father got diagnosed cll october 2009,was on wait and watch till mid 2014,then given R-bendamustine and was on remission till october 2016,then started ibrutinib in 2016 and stopped ibrutinib in mid 2018,in 2020 end due to fast multiplication of tlc and enlarged spleen and lymphnodes our doc suggested
My father got diagnosed cll october 2009,was on wait and watch till mid 2014,then given R-bendamustine and was on remission till october 2016,then started ibrutinib in 2016 and stopped ibrutinib in mid 2018,in 2020 end due to fast multiplication of tlc and enlarged spleen and lymphnodes our doc suggested
Rameshchag
in
CLL America Support
3 years ago
Living with CLL
So I was fine until November 2019 when I started on
Venetoclax
, I have been taking 400mg everyday, my CLL under cntrol and I not having side effects. I’m lucky that I was diagnosed early and the CLL hadn’t gone into my lymph nodes.
So I was fine until November 2019 when I started on
Venetoclax
, I have been taking 400mg everyday, my CLL under cntrol and I not having side effects. I’m lucky that I was diagnosed early and the CLL hadn’t gone into my lymph nodes.
2gizzy
in
CLL Support
3 years ago
Covid Antibody Test
Best regards Reinhard from Austria Dx Jan. 2000,Tx
Venetoclax
Obinutuzumab Jun 2015 - Sep 2018 (CR, mrd- in blood and bone marrow)
Best regards Reinhard from Austria Dx Jan. 2000,Tx
Venetoclax
Obinutuzumab Jun 2015 - Sep 2018 (CR, mrd- in blood and bone marrow)
Reinhard
in
CLL Support
3 years ago
Proctitis and Venetoclax
Am wondering if anyone else has experienced this while taking
Venetoclax
or Ibrutinib?
Am wondering if anyone else has experienced this while taking
Venetoclax
or Ibrutinib?
Lady_Lymington
in
CLL Support
3 years ago
Muscle cramps as a side effect of Venetoclax
I am taking
venetoclax
at present and am suffering with muscle cramps, particularly in my back. Does anyone else have this problem? My consultant refuses to acknowledge that this is as a result of the medication but my GP has found it to be the case.
I am taking
venetoclax
at present and am suffering with muscle cramps, particularly in my back. Does anyone else have this problem? My consultant refuses to acknowledge that this is as a result of the medication but my GP has found it to be the case.
Suzy11
in
Leukaemia Support
3 years ago
Doctor wants to start Venetoclax today but recent blood work shows evidence of AIHA but Doctor still says start Ven
shouldn't AIHA be treated first? hemoglobin dropping weekly down from 14.7 2 months ago now 10.7 Haptoglobin less than 31 LDH almost 700 Doctor says still start Venclexta tomorrow but why not hold off until AIHA is controlled with steroids or Rituxan? I think the Rituxan will put him in control of
shouldn't AIHA be treated first? hemoglobin dropping weekly down from 14.7 2 months ago now 10.7 Haptoglobin less than 31 LDH almost 700 Doctor says still start Venclexta tomorrow but why not hold off until AIHA is controlled with steroids or Rituxan? I think the Rituxan will put him in control of
Palmetto
in
CLL Support
3 years ago
Ibrutinib combinations in CLL therapy: scientific rationale and clinical results
Among these strategies, ibrutinib with targeted agent
venetoclax
results in high complete response rates and, importantly, high rates of undetectable minimal residual disease.
Among these strategies, ibrutinib with targeted agent
venetoclax
results in high complete response rates and, importantly, high rates of undetectable minimal residual disease.
Jm954
Administrator
in
CLL Support
3 years ago
Aggressive CLL - Richter's Transformation
The first-line treatment was obinutuzumab/
venetoclax
but after a year on this treatment, his disease has turned to a Richter's Transformation (large cell lymphoma).
The first-line treatment was obinutuzumab/
venetoclax
but after a year on this treatment, his disease has turned to a Richter's Transformation (large cell lymphoma).
Phs2385
in
CLL Support
3 years ago
CLL responses to Pfizer’s Covid vaccines.
In patients treated with either Bruton tyrosine kinase inhibitors or
venetoclax
with or without anti-CD20 antibody, response rates were low (16.0% and 13.6%, respectively): https://ashpublications.org/blood/article/doi/10.1182/blood.2021011568/475742/Efficacy-of-the-BNT162b2-mRNA-COVID-19-Vaccine-in
In patients treated with either Bruton tyrosine kinase inhibitors or
venetoclax
with or without anti-CD20 antibody, response rates were low (16.0% and 13.6%, respectively): https://ashpublications.org/blood/article/doi/10.1182/blood.2021011568/475742/Efficacy-of-the-BNT162b2-mRNA-COVID-19-Vaccine-in
Twin21
in
CLL Support
3 years ago
Chronic Lymphocytic Leukemia - CLL: When Being Fully Vaccinated for Covid-19 Doesn’t Mean Fully Protected
The article continues, "In patients treated with either Bruton's tyrosine kinase inhibitors or
venetoclax
± anti-CD20 antibody, responses are relatively low." Results are expected to be similar for those with CLL regardless of the type of vaccine.
The article continues, "In patients treated with either Bruton's tyrosine kinase inhibitors or
venetoclax
± anti-CD20 antibody, responses are relatively low." Results are expected to be similar for those with CLL regardless of the type of vaccine.
KatieBlue
in
CLL Support
3 years ago
New CLL Regimen after 6 years on Imbruvica
Then I will start Veneteclax early in May, preceded by taking a pill called Allopurinol 4 days before the
Venetoclax
to protect by kidneys. All this matches all the webinars I have watched on Patient Power and LLS.org so I am praying that my body responds in the right way.
Then I will start Veneteclax early in May, preceded by taking a pill called Allopurinol 4 days before the
Venetoclax
to protect by kidneys. All this matches all the webinars I have watched on Patient Power and LLS.org so I am praying that my body responds in the right way.
Gisygirl
in
CLL Support
3 years ago
Worthwhile: an article, a presentation, and a table
The presentation talks about identifying resistance to
Venetoclax
. The table quantifies the risk of factors associated with the development of secondary cancers in CLL. https://cllsociety.org/2018/06/cll-markers-and-what-they-mean-a-patient-perspective-part-ii-notch1/ https://duckduckgo.com/?
The presentation talks about identifying resistance to
Venetoclax
. The table quantifies the risk of factors associated with the development of secondary cancers in CLL. https://cllsociety.org/2018/06/cll-markers-and-what-they-mean-a-patient-perspective-part-ii-notch1/ https://duckduckgo.com/?
Luap001
in
CLL Support
3 years ago
I've just recently worked my way up to Venetoclax 400mg. I'm curious if anyone had similar side effects:
I've just recently worked my way up to
Venetoclax
400mg. I'm curious if anyone had similar side effects: 1. When I inhale, at times I will experience a shortness of breath (of sorts) it's hard to explain.
I've just recently worked my way up to
Venetoclax
400mg. I'm curious if anyone had similar side effects: 1. When I inhale, at times I will experience a shortness of breath (of sorts) it's hard to explain.
Nook120
in
CLL Support
3 years ago
Nausea with venetoclax
Just started the
venetoclax
ramp up. I am taking the
venetoclax
at night with food but experiencing at lot of nausea with the
venetoclax
. Has anybody had this nausea and what did you do about it?
Just started the
venetoclax
ramp up. I am taking the
venetoclax
at night with food but experiencing at lot of nausea with the
venetoclax
. Has anybody had this nausea and what did you do about it?
jjaarons
in
CLL Support
3 years ago
Working while on treatment O&V
Venetoclax
and Obinutuzumab for a year has been put forward & having read about the efficacy of this combo now for the last few months, I am happy with this.
Venetoclax
and Obinutuzumab for a year has been put forward & having read about the efficacy of this combo now for the last few months, I am happy with this.
Fergusaims
in
CLL Support
3 years ago
Covid Vaccine after obinutuzumab
Hello, My dad started
Venetoclax
+ obinutuzumab treatment July of 2020. and his last obinutuzumab infusion was 1 December 2020. (so 4 months ago), he is still on venetolax until June.
Hello, My dad started
Venetoclax
+ obinutuzumab treatment July of 2020. and his last obinutuzumab infusion was 1 December 2020. (so 4 months ago), he is still on venetolax until June.
atiatamer
in
CLL Support
3 years ago
Rasburicase/Allopurinol
Hi, I am in the first week of ramp up of
Venetoclax
. I was hospitalized for 2 days for the first dose. I had Rasburicase IV, but I am not sure if I should be taking Allopurinol daily at home. I should have asked, too stressed. I am at high risk of TLS, but very little effect on large node yet.
Hi, I am in the first week of ramp up of
Venetoclax
. I was hospitalized for 2 days for the first dose. I had Rasburicase IV, but I am not sure if I should be taking Allopurinol daily at home. I should have asked, too stressed. I am at high risk of TLS, but very little effect on large node yet.
Hidden
in
CLL Support
3 years ago
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