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A tunnelling ulcer in Sweet's syndrome after chemotherapy
He had received immune-chemotherapy with a BV-CHP regimen, including brentuximab vedotin (BV, 1.8 mg/kg on day 1),
cyclophosphamide
(750 mg/m2 on day 1), doxorubicin (50 mg/m2 on day 1), and prednisone (100 mg on days 1–5) (4) for four cycles and achieved complete remission (CR) during the second cycle
He had received immune-chemotherapy with a BV-CHP regimen, including brentuximab vedotin (BV, 1.8 mg/kg on day 1),
cyclophosphamide
(750 mg/m2 on day 1), doxorubicin (50 mg/m2 on day 1), and prednisone (100 mg on days 1–5) (4) for four cycles and achieved complete remission (CR) during the second cycle
Shell567
Sweet's Syndrome UK
in
Sweet's Syndrome UK
11 months ago
POST 3 - CAR-T cell therapy
Lymphodepletion {chemotherapy} will also commence:
Cyclophosphamide
{D-6} also Fludarabine for four days {D-6 to D-3} followed by two days rest and then Day 0 {14th June} will be the exciting day that I receive the first small dose of the modified T-cells.
Lymphodepletion {chemotherapy} will also commence:
Cyclophosphamide
{D-6} also Fludarabine for four days {D-6 to D-3} followed by two days rest and then Day 0 {14th June} will be the exciting day that I receive the first small dose of the modified T-cells.
casanova
in
CLL Support
1 year ago
Unrelenting pain post chemo dose
Commenced on 3 weekly epirubicin and
cyclophosphamide
. I'm on my 2nd cycle but during the 2 cycles I have the most horrendous, unrelenting pain in my upper back area which is also very tender. I have 15mg slow release morphine and more for breakthrough but despite this the pain continues.
Commenced on 3 weekly epirubicin and
cyclophosphamide
. I'm on my 2nd cycle but during the 2 cycles I have the most horrendous, unrelenting pain in my upper back area which is also very tender. I have 15mg slow release morphine and more for breakthrough but despite this the pain continues.
Cazdf
in
SHARE Metastatic Breast Cancer
1 year ago
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UK NICE Approves Ibrutinib +Venetoclax for First Line treatment for ALL Patients from today
[/i] [i]
A: During scoping consultation, a consultee highlighted an urgent need for access to novel treatments for younger, fitter patients with chronic lymphocytic leukaemia as currently only fludarabine,
and rituximab (FCR) or venetoclax plus obinutuzumab via the Cancer Drugs
[/i] [i]
A: During scoping consultation, a consultee highlighted an urgent need for access to novel treatments for younger, fitter patients with chronic lymphocytic leukaemia as currently only fludarabine,
and rituximab (FCR) or venetoclax plus obinutuzumab via the Cancer Drugs
Jm954
Administrator
in
CLL Support
1 year ago
tapering off azathioprine
Initially had
cyclophosphamide
infusions and have been maintained on azathioprine since, Last rituximab was 2 yrs ago, been in remission for 2 yrs now.
Initially had
cyclophosphamide
infusions and have been maintained on azathioprine since, Last rituximab was 2 yrs ago, been in remission for 2 yrs now.
stuc
in
Vasculitis UK
1 year ago
Relative risk for secondary bone marrow cancer within 5 years after initial CLL chemoimmunotherapy treatment (typically BR or FCR)
In countries where targeted therapies ('brutinibs, venetoclax, obinutuzumab/rituximab) are now available, the remaining reason that FCR (Fludarabine+
Cyclophosphamide
+Rituximab) is still sometimes recommended for the treatment of CLL is that it can be curative* about 55% of the time - but [u]
only[
In countries where targeted therapies ('brutinibs, venetoclax, obinutuzumab/rituximab) are now available, the remaining reason that FCR (Fludarabine+
Cyclophosphamide
+Rituximab) is still sometimes recommended for the treatment of CLL is that it can be curative* about 55% of the time - but [u]
only[
AussieNeil
Partner
in
CLL Support
11 months ago
Cyclophosphamide & Niraparib
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Hidden
in
OvaCare
2 years ago
Cyclophosphamide & Niraparib
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Hidden
in
My Ovacome
2 years ago
cyclophosphamide
She is trying me on
Cyclophosphamide
, please let me know of any successes with this drug. Thank you. Xxx
She is trying me on
Cyclophosphamide
, please let me know of any successes with this drug. Thank you. Xxx
Clipper15
in
My Ovacome
2 years ago
Asymptomatic Trandmission
Does anyone have any data or medical journal articles, addressing the contagious for either Pre symptomatic infections or individuals that have asymptomatic viral infections.. Also, in my home state of Utah in the USA, I have not been able to find any published data on the current incident or presence
Does anyone have any data or medical journal articles, addressing the contagious for either Pre symptomatic infections or individuals that have asymptomatic viral infections.. Also, in my home state of Utah in the USA, I have not been able to find any published data on the current incident or presence
skipro
in
CLL Support
6 days ago
V + O for R/R CLL post FCR
I sent this to skyshark based on some info he posted but I was[u] hoping for the whole group to chime in.[/u] I had 3 rounds of FCR in 2018 stopped because of profound neutropenia. I relapsed exactly 2 years later and though I did not start Tx until the 5 year point in 2023, would have gladly started
I sent this to skyshark based on some info he posted but I was[u] hoping for the whole group to chime in.[/u] I had 3 rounds of FCR in 2018 stopped because of profound neutropenia. I relapsed exactly 2 years later and though I did not start Tx until the 5 year point in 2023, would have gladly started
skipro
in
CLL Support
17 days ago
Burning tongue and metallic taste .
I was dx 10 years ago. Had FCR, Ibrutinib, and Venetoclax. I am on Venetoclax now for 18 months after 6 times of V+O. A year ago I lost my taste sense and everything tastes metallic,but the worse is a burning tongue sensation. Does it have any connetion to CLL or Venetoclax ?Gidi
I was dx 10 years ago. Had FCR, Ibrutinib, and Venetoclax. I am on Venetoclax now for 18 months after 6 times of V+O. A year ago I lost my taste sense and everything tastes metallic,but the worse is a burning tongue sensation. Does it have any connetion to CLL or Venetoclax ?Gidi
GIDI
in
CLL Support
28 days ago
IFN-1 levels before treatment may be biomarker of SLE activity: Study
Organ damage also was associated with the use of methylprednisolone pulse therapy or intravenous (into-the-vein)
cyclophosphamide
(IVCY) pulse therapy.
Organ damage also was associated with the use of methylprednisolone pulse therapy or intravenous (into-the-vein)
cyclophosphamide
(IVCY) pulse therapy.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 year ago
Is it the time for initial treatment?
As I previously stated, my wife was diagnosed with CLL in 2020. Her markers are 13q deletion, 12 trisomy, and TP53, with IGHV muted. She is still in W&W form. So far, I've learned via reading literature and numerous posts about lymphocyte doubling time, lactate dehydrogenase, and lymph nodes. Her lymphocyte
As I previously stated, my wife was diagnosed with CLL in 2020. Her markers are 13q deletion, 12 trisomy, and TP53, with IGHV muted. She is still in W&W form. So far, I've learned via reading literature and numerous posts about lymphocyte doubling time, lactate dehydrogenase, and lymph nodes. Her lymphocyte
Sagarcanada
in
CLL Support
1 month ago
Second Treatment -Feeling scared
My husband has CLL and finished FCR in April 2019. Due to low platelets, enlarged spleen and ALC doubling he needs to start his next treatment even though he feels wellV&R is the treatment starting on 15th May. I have researched extensively including within this group, and am aware of the treatment
My husband has CLL and finished FCR in April 2019. Due to low platelets, enlarged spleen and ALC doubling he needs to start his next treatment even though he feels wellV&R is the treatment starting on 15th May. I have researched extensively including within this group, and am aware of the treatment
Sanders9
in
CLL Support
1 month ago
Wendy
My husband was diagnosed in 2010 at the age of 40. 2013 he had FCR. 11 years later, he is in week 5 of venteclax, Rituximab to follow next month. Swollen lymph nodes have disappeared.
My husband was diagnosed in 2010 at the age of 40. 2013 he had FCR. 11 years later, he is in week 5 of venteclax, Rituximab to follow next month. Swollen lymph nodes have disappeared.
Fluxthecat10
in
CLL Support
1 month ago
Reply to issues with Spleen
Hi, I agree with most of these comments on here that the enlargement of your spleen is an indication perhaps that you are ready for some form of treatment, not removal. I had chemotherapy in 2020 and my spleen was massive. After a treatment cycle of FCR for 6 months and neutropenia sepsis for 10
Hi, I agree with most of these comments on here that the enlargement of your spleen is an indication perhaps that you are ready for some form of treatment, not removal. I had chemotherapy in 2020 and my spleen was massive. After a treatment cycle of FCR for 6 months and neutropenia sepsis for 10
Roseneath69
in
CLL Support
2 months ago
Recently started Acalabrutinib
Hi everyone, My father has recently started Acalabrutinib 5 days ago. He was diagnosed with CLL in 2007 and has received FCR (twice) and Benda-Ritux once. His CLL only went into partial remission on benda-ritux and has come back after one year since his last cycle of BR. I am worried regarding the
Hi everyone, My father has recently started Acalabrutinib 5 days ago. He was diagnosed with CLL in 2007 and has received FCR (twice) and Benda-Ritux once. His CLL only went into partial remission on benda-ritux and has come back after one year since his last cycle of BR. I am worried regarding the
Healthgiddy
in
CLL Support
2 months ago
uMRD 6
I have been living for the one year point on V plus O to get the clonal sequence uMRD6 bone marrow test done so I could decide if I wanted to continue with a Venetaclax. Technically, I consider myself partially treated rather than relapsed or refractory, because I only received three of the six cycles
I have been living for the one year point on V plus O to get the clonal sequence uMRD6 bone marrow test done so I could decide if I wanted to continue with a Venetaclax. Technically, I consider myself partially treated rather than relapsed or refractory, because I only received three of the six cycles
skipro
in
CLL Support
3 months ago
Wife getting MMR vaccine booster - isolate or not?
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
xpro3
in
CLL Support
3 months ago
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