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PCNA gene attack -- for solid tumors
City of Hope’s groundbreaking translational research history includes developing the technology underlying synthetic human insulin and monoclonal antibodies, which are integral to widely used, lifesaving cancer drugs, such as trastuzumab, rituximab and
cetuximab
.
City of Hope’s groundbreaking translational research history includes developing the technology underlying synthetic human insulin and monoclonal antibodies, which are integral to widely used, lifesaving cancer drugs, such as trastuzumab, rituximab and
cetuximab
.
Derf4223
in
Advanced Prostate Cancer
11 months ago
Rituximab Update
Had first Rituximab infusion yesterday and all good. Blood pressure high on arrival but came down OK. No allergic reactions. This morning I have woken to greatly reduced swelling, no aches, pains or sore joints . Completely on a high. Hope it lasts. Next infusion 8th July. Problem now is getting
Had first Rituximab infusion yesterday and all good. Blood pressure high on arrival but came down OK. No allergic reactions. This morning I have woken to greatly reduced swelling, no aches, pains or sore joints . Completely on a high. Hope it lasts. Next infusion 8th July. Problem now is getting
SALI
in
NRAS
11 days ago
Disease Progression on Pirtobrutinib
After my last two CT scans (3 months apart) the oncologist told me the lymph nodes have grown and the dark monster is back. I was confused because my blood work was well within normal range. Been taking LOXO 305 for 18 months with virtually no side effects so I am unhappy with this news. My oncologist
After my last two CT scans (3 months apart) the oncologist told me the lymph nodes have grown and the dark monster is back. I was confused because my blood work was well within normal range. Been taking LOXO 305 for 18 months with virtually no side effects so I am unhappy with this news. My oncologist
steve_canada
in
CLL Support
11 days ago
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Seven-year-old girl with autoimmune encephalitis help
Hi, I'm Fernanda, mother of a girl with autoimmune encephalitis. We live in Italy. Is there anyone here who has recovered from this disease? I am really scared. It all started in April. In May, everything seemed fine, but now in June she has relapsed. She has started Rituximab and needs to have 4 infusions
Hi, I'm Fernanda, mother of a girl with autoimmune encephalitis. We live in Italy. Is there anyone here who has recovered from this disease? I am really scared. It all started in April. In May, everything seemed fine, but now in June she has relapsed. She has started Rituximab and needs to have 4 infusions
FernandaDuval12
in
Encephalitis International
13 days ago
Rituximab Infusions
My Rheumatologist advised to stop the adalimumab injections because of my hair loss and has recommended a six monthly Rituximab infusion. Has anyone experienced this treatment - for better, or, worse?
My Rheumatologist advised to stop the adalimumab injections because of my hair loss and has recommended a six monthly Rituximab infusion. Has anyone experienced this treatment - for better, or, worse?
Nannalyn
in
NRAS
13 days ago
Eye troubles
Hi my lupus community I need your thoughts on my dilemma. I have had a lupus diagnosis for 20 years now and have been on lots of different meds over the years and have had to stop they for different reasons. The most significant being Hydroxicloriquine and chloroquine which have caused retinopathy.
Hi my lupus community I need your thoughts on my dilemma. I have had a lupus diagnosis for 20 years now and have been on lots of different meds over the years and have had to stop they for different reasons. The most significant being Hydroxicloriquine and chloroquine which have caused retinopathy.
littlemissp
in
LUPUS UK
15 days ago
Month 21 of 24 Rituximab and Venetoclax
I'm doing well with this treatment CLL wise with all bloods within normal range. Antibody levels are however below being of much use.Past 10 weeks I've had chronic diarrhoea with stool tests coming up negative. Blood tests all negative including C diff. I've been advised to stop Venetoclax for 2 weeks
I'm doing well with this treatment CLL wise with all bloods within normal range. Antibody levels are however below being of much use.Past 10 weeks I've had chronic diarrhoea with stool tests coming up negative. Blood tests all negative including C diff. I've been advised to stop Venetoclax for 2 weeks
Fastbike14
in
CLL Support
20 days ago
has anyone experienced neuropathy as a result of rituximab
Has anyone experienced neuropathy as a result of rituximab for non hodgkins lymphoma
Has anyone experienced neuropathy as a result of rituximab for non hodgkins lymphoma
PossumPracticalCat
in
Non Hodgkin's Lymphoma Friends
24 days ago
infusion
Hi, I am currently on 40mg of Adalimumab every 2 weeks but it is not working, the hospital have decided that an infusion of Rituximab is the next step, has anybody else had this treatment and did it work?
Hi, I am currently on 40mg of Adalimumab every 2 weeks but it is not working, the hospital have decided that an infusion of Rituximab is the next step, has anybody else had this treatment and did it work?
LTC1607
in
NRAS
24 days ago
Leukemia-associated macrophages, their role in the CLL Tumor Micro-environment and how they affect progression and therapy response
Understanding how the CLL Tumor Micro-environment (TME) functions is crucial to improving CLL therapy. CLL cells are not as robust as healthy B cells and they rely on their created TME in the nodes and bone marrow for their survival. That's why it's so easy to kill CLL cells with in vitro testing - checking
Understanding how the CLL Tumor Micro-environment (TME) functions is crucial to improving CLL therapy. CLL cells are not as robust as healthy B cells and they rely on their created TME in the nodes and bone marrow for their survival. That's why it's so easy to kill CLL cells with in vitro testing - checking
AussieNeil
Partner
in
CLL Support
27 days ago
rituximab
any of you has personal or otherwise experiences with rituximab use in combination with prednison. Like many of us, I keep on “ flaring” when I diminish my dose of prednison. There might be better out ome with a combination. But not widespread a aila le, and expensive. Thanks.
any of you has personal or otherwise experiences with rituximab use in combination with prednison. Like many of us, I keep on “ flaring” when I diminish my dose of prednison. There might be better out ome with a combination. But not widespread a aila le, and expensive. Thanks.
Kaaswinkel
in
PMRGCAuk
28 days ago
Contact with child vaccinated against chicken pox
Hi, Hope all are doing well. Making slow progress here, but all going in the right direction so I am told. Feel better than the beginning of the year for sure! Got next rituximab in August 🤞 I have not seen my great niece for quite some time and had hoped to visit her as she is growing fast.
Hi, Hope all are doing well. Making slow progress here, but all going in the right direction so I am told. Feel better than the beginning of the year for sure! Got next rituximab in August 🤞 I have not seen my great niece for quite some time and had hoped to visit her as she is growing fast.
lollypocket
in
Vasculitis UK
28 days ago
Long term predisolone
Hi All I’d really interested in hearing from anyone who has been told they’ll be on predisolone for good. I’ve been on it for 13 years, varying doses but never got off it. I was on mycophenloate and then rituximab but have been advised that just steroids will be my recommended medication to control
Hi All I’d really interested in hearing from anyone who has been told they’ll be on predisolone for good. I’ve been on it for 13 years, varying doses but never got off it. I was on mycophenloate and then rituximab but have been advised that just steroids will be my recommended medication to control
Galaxy2
in
Vasculitis UK
1 month ago
Will spleen shrink after Rituximab treatment?
Just wondering if spleen will shrink after having 4 Rituximab treatments? Is this usually what happens?
Just wondering if spleen will shrink after having 4 Rituximab treatments? Is this usually what happens?
Redkatt
in
CLL Support
1 month ago
flowers
Hi folks thought I would post this pic of the lupins In my garden, they have self seeded all over the path and look beautiful . An update on me, I’m due to start Rituximab soon as Methotrexate has stopped working on me and my lupus is not under control at all, I’m also on steriods at the moment. I’ve
Hi folks thought I would post this pic of the lupins In my garden, they have self seeded all over the path and look beautiful . An update on me, I’m due to start Rituximab soon as Methotrexate has stopped working on me and my lupus is not under control at all, I’m also on steriods at the moment. I’ve
svfarmer
in
LUPUS UK
1 month ago
Rituximab blood results after 3rd treatment
Just finished 4 cycles of Rituximab over 4 weeks. Blood tests were taken two days before each treatment. Lymphocytes 2.1/1.3/1.3/1.5 Platelets 139/153/135/214/216 Haemoglobin 103/101/97/104/113 Neutrophils 1.7/1.6/1.0/1.0/0.8 RBC 4.21/3.99/3.93/4.19/4.55 HCT 0.32/0.31/0.30/0.32/0.35 Hoping
Just finished 4 cycles of Rituximab over 4 weeks. Blood tests were taken two days before each treatment. Lymphocytes 2.1/1.3/1.3/1.5 Platelets 139/153/135/214/216 Haemoglobin 103/101/97/104/113 Neutrophils 1.7/1.6/1.0/1.0/0.8 RBC 4.21/3.99/3.93/4.19/4.55 HCT 0.32/0.31/0.30/0.32/0.35 Hoping
Redkatt
in
CLL Support
1 month ago
Methotrexate and Prednisolone GPA
Hi everyone. I have been on methotrexate and prednisolone for nearly three years for Vasculitis GPA along with blood thinners and statins etc, was also on Mycophenolate for first 2 years. I have been told Rituximab not suitable for me. GPA symptoms are currently under control, have not been able to get
Hi everyone. I have been on methotrexate and prednisolone for nearly three years for Vasculitis GPA along with blood thinners and statins etc, was also on Mycophenolate for first 2 years. I have been told Rituximab not suitable for me. GPA symptoms are currently under control, have not been able to get
Wyllow
in
Vasculitis UK
1 month ago
Rituximab and Denosumab
Has anyone had a Denosumab injection after having a Retuximab infusion. I have just had my second infusion and due a Denosumab injection soon. Just read that Denosumab can increase the risk of serious infection with Rituximab. Rheumatology have said that it's OK, but I don't trust them.
Has anyone had a Denosumab injection after having a Retuximab infusion. I have just had my second infusion and due a Denosumab injection soon. Just read that Denosumab can increase the risk of serious infection with Rituximab. Rheumatology have said that it's OK, but I don't trust them.
Jacko37
in
NRAS
1 month ago
Finally...🥳
Hi I hope everyone is doing well and if not hang on in there and reach out as there is misch support on here! I've had the toughest few months since last November the worse flare since being diagnosed in 2013, shadow on lung picked on a routine Chest X Ray at screening for new meds, so couldn't start
Hi I hope everyone is doing well and if not hang on in there and reach out as there is misch support on here! I've had the toughest few months since last November the worse flare since being diagnosed in 2013, shadow on lung picked on a routine Chest X Ray at screening for new meds, so couldn't start
3LittleBirds2
in
NRAS
1 month ago
Rituximab operation
OPERATION, can you have have an operation while on Rituximab?
OPERATION, can you have have an operation while on Rituximab?
65_women
in
NRAS
1 month ago
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