Home         Forums  

Go Back   Marrowforums > Treatments > Drugs and Drug Treatments
Register FAQ Search Today's Posts Mark Forums Read

Drugs and Drug Treatments ATG, Cyclosporine, Revlimid, Vidaza, Dacogen, ...

Reply
 
Thread Tools Search this Thread
  #1  
Old Fri Sep 26, 2014, 01:01 AM
Faye R Faye R is offline
Member
 
Join Date: Feb 2013
Location: New Zealand
Posts: 60
Vidaza

Please tell me how many have gone into remission after taking Vidaza who are RCMD Advanced Thanks
Reply With Quote
  #2  
Old Fri Sep 26, 2014, 06:56 AM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Vidaza

Hi Faye!
You know in Europe Vidaza isn’t approved for low risk MDS. I have seen results between 67% response to 38% response for low risk patients.

Here is one study: http://www.ncbi.nlm.nih.gov/pubmed/23596104

High risk patients have better results often a little more than 50%.

Combinations of Vidaza with other drugs show much better results for example Vidaza + Pracinostat 89% response: https://ash.confex.com/ash/2012/webp...aper50414.html . Only 9 patients had participated in this study when this report was written.

Vidaza + Revlimid has showed 72% response rate: http://www.ncbi.nlm.nih.gov/pubmed/22915641
Kind regards
Birgitta-A
Reply With Quote
  #3  
Old Sun Sep 28, 2014, 01:14 AM
Faye R Faye R is offline
Member
 
Join Date: Feb 2013
Location: New Zealand
Posts: 60
Smile vidaza

Many thanks tomorrow I go and have 2 units of blood and meet up with the Australian people who are going to go through the procedures with our nurses and myself. Looking more positive about my future now.
Reply With Quote
  #4  
Old Sun Sep 28, 2014, 12:06 PM
MarianneS MarianneS is offline
Member
 
Join Date: Sep 2013
Location: nassau county, new york
Posts: 12
vidaza

hubby MDS high risk so far in remission 13 cycles too old for sct dr. stretching out now between cycles.....good luck.
Reply With Quote
  #5  
Old Fri Oct 3, 2014, 01:40 PM
mitch mitch is offline
Member
 
Join Date: Mar 2014
Location: St John, Indiana, USA
Posts: 10
I am not in the high risk group, but I am RCMD Intermediate-1 and have been on Vidaza for nine months/cycles. I am on the 5 day IV treatment plan, with three weeks off between treatments. I had a BMB after the sixth cycle and the doc said I am currently in remission. So they are keeping me on it for the foreseeable future. Hopefully it continues to work. Good luck to you....

Mitch
Reply With Quote
  #6  
Old Wed Oct 8, 2014, 08:11 PM
Faye R Faye R is offline
Member
 
Join Date: Feb 2013
Location: New Zealand
Posts: 60
vidaza

Many thanks every one vidaza is very new here in N.Z. in fact I am the first to have it here and count myself lucky (question) I get 2 files injected into 2 different sites the nurses here want to inject both files into the same site how many of you have this done, I was with the Vidaza rep when she was telling the doctors and nurses on how to administer the drug 2 files injected subcutaneously 2cm apart. This is what has been done so far what would happen if they did it their way.
Reply With Quote
  #7  
Old Wed Oct 8, 2014, 09:03 PM
bailie bailie is offline
Member
 
Join Date: Dec 2013
Location: McMinnville,OR
Posts: 825
I had eight cycles of Vidaza. There were strict instructions to keep the injections at least one inch apart. It is important to plan the injection sites for each day ahead of time. I would run out of room by the seventh injection. I would alternate from side to side each day.
__________________
age 70, dx RAEB-2 on 11-26-2013 w/11% blasts. 8 cycles Vidaza 3w/Revlimid. SCT 8/15/2014, relapsed@Day+210 (AML). Now(SCT-Day+1005). Prepping w/ 10 days Dacogen for DLI on 6/9/2017.
Reply With Quote
  #8  
Old Wed Oct 8, 2014, 09:04 PM
Helen L Helen L is offline
Member
 
Join Date: Oct 2014
Location: Melbourne
Posts: 2
My husband was on Vidaza for 2 years. He found that if the injection sites were too close together he would get a large inflamed area and took 2 weeks to heal. I do not think 2 vials at once is a good idea. He used a map similar to what is used for Betaferon. Space the 2 injection sites as far apart as possible each day. He used his stomach and top of thighs and it worked well.
Reply With Quote
  #9  
Old Thu Oct 9, 2014, 06:23 AM
Cheryl C Cheryl C is offline
Member
 
Join Date: Dec 2011
Location: Lake Macquarie, Australia
Posts: 843
All the best with the Vidaza, Faye. I have avoided doing any chemo so far - don't think it would be very good for me since I'm quite sensitive to even mild drugs.

Can someone kindly define the three levels of RCMD for me please. I didn't realise that there are different levels within that category. Thank you.
__________________
Dx MDS RAEB 10% blasts + hypogammaglobulinemia, Sep 2011. Jan 2012 BMB - blasts down to 2% w/out treatment so BMT cancelled. Re-diagnosis RCMD. Watch and wait from Feb 2012. IVIg 5-weekly. New diagnosis Oct 2019 AML 23% blasts in marrow, 10% blasts in peripheral blood.
Reply With Quote
  #10  
Old Sat Oct 11, 2014, 09:42 PM
Faye R Faye R is offline
Member
 
Join Date: Feb 2013
Location: New Zealand
Posts: 60
Cool vidaza

A great many thanks to all who have replied the first 3 days went well bruising and inflammation around the injection sites however 4th day I was not well hospitalized for 2 nights (BMU) all is well again I have found out you have to watch constipation kiwi crush etc for me from now on.
Reply With Quote
  #11  
Old Sat Oct 11, 2014, 11:25 PM
Leigh Ann B Leigh Ann B is offline
Member
 
Join Date: Oct 2014
Location: AUSTIN
Posts: 3
Vidaza

Quote:
Originally Posted by bailie View Post
I had eight cycles of Vidaza. There were strict instructions to keep the injections at least one inch apart. It is important to plan the injection sites for each day ahead of time. I would run out of room by the seventh injection. I would alternate from side to side each day.
How much discomfort was there with vidaza. Mom has stomach problems and so has avoided all chemo. she is 77 and is starting to have infections and severe weakness, platelets 2000, hemo 7.9, transfusing 2-3 weeks.
Reply With Quote
  #12  
Old Sat Oct 11, 2014, 11:39 PM
DanL DanL is offline
Member
 
Join Date: Dec 2010
Location: Denver, CO
Posts: 590
@Cheryl,

Last I checked, RCMD is a classification under the WHO or WPSS classifications system. It is difficult to keep them all straight because doctors will use them interchangeably depending on what they are trying to tell you, but there are three other systems, two of which utilize a staging type of classification - the IPSS and the IPSS-R. The last system in use is the old French, American, British or FAB.

There is a pretty good resource right here on the forums, although it is missing the IPSS-R, which is a revised version of the IPSS and includes more prognostic data.

http://www.marrowforums.org/mds.html

Here is something on the IPSS-R

http://www.mdsbeacon.com/news/2012/0...ystem-decoded/

RCMD can be associated with a lower risk, intermediate risk, or high risk assessment, depending on blast percentage, chromosomal abnormalities, and severity of cytopenias associated with the dysplasia.

I started out as RCUD - only platelets affected, and moved to RCMD, which was accompanied by being considered low risk on the IPSS-R, but later moved to Intermediate-2 as the disease progressed prior to transplant, still being RCMD.

Hope that helps.
__________________
MDS RCMD w/grade 2-3 fibrosis. Allo-MUD Feb 26, 2014. Relapsed August 2014. Free and clear of MDS since November 2014 after treatment with Vidaza and Rituxan. Experiencing autoimmune attack on CNS thought to be GVHD, some gut, skin and ocular cGVHD. Neuropathy over 80% of body.
Reply With Quote
  #13  
Old Mon Oct 13, 2014, 06:10 AM
Cheryl C Cheryl C is offline
Member
 
Join Date: Dec 2011
Location: Lake Macquarie, Australia
Posts: 843
Thanks DanL. I appreciate the time you took to provide this info. According to the IPSS-R score calculator I am Low risk at present (providing my blast count hasn't risen in the last 9 months) so that's a big improvement on 3 years ago! Not sure whether my associated hypogammaglobulinemia would affect this risk level. To me the hypo is almost a blessing because it means I have an infusion of IgG every 4 weeks. Since my white cells (neuts and lymphs) are my biggest issue I believe that these infusions are compensating for my low immune system to a significant degree. See http://primaryimmune.org/treatment-i...bulin-therapy/ if you are interested.

I do hope that the Vidaza is providing you with relief from the GVHD and that your counts are improving now.
__________________
Dx MDS RAEB 10% blasts + hypogammaglobulinemia, Sep 2011. Jan 2012 BMB - blasts down to 2% w/out treatment so BMT cancelled. Re-diagnosis RCMD. Watch and wait from Feb 2012. IVIg 5-weekly. New diagnosis Oct 2019 AML 23% blasts in marrow, 10% blasts in peripheral blood.

Last edited by Cheryl C : Mon Oct 13, 2014 at 07:34 AM.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
Greg H - Vidaza as a Bridge to Transplant Greg H Transplants 54 Sun May 7, 2017 10:42 PM
What to do When the Vidaza Stops Working? mitch Drugs and Drug Treatments 4 Wed Mar 9, 2016 03:48 PM
Terrible Blood Counts after Vidaza joesmith MDS 11 Tue Aug 12, 2014 04:34 PM
When to stop Vidaza? Paolo D. Drugs and Drug Treatments 5 Sun Jun 26, 2011 03:15 AM
Vidaza Vs. Transplant Vera W MDS 18 Fri Apr 3, 2009 10:54 PM


All times are GMT -4. The time now is 02:57 AM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org