Thanks Peg, my problem was that the onc I had at the time,  decided to put 
me back on Gleevec and Gleevec has quit working for me  before.  Here I was 
taking all these meds and my platelets and WBC were  still too high.  The 
doctor was giving me prilosec twice a day due to my  complaining about the 
pain in my side.  I never had heartburn.  If I  had, I could have understood 
why they were giving it to me.
Hang in there with Tasi; it could be the one for  you.
Jeanie<3
 
 
 
In a message dated 12/2/2013 11:07:12 A.M. Eastern Standard Time,  
[email protected] writes:

Hi Jeanie,

You are right about the proton pump  inhibitors...they are designed to work 
over a 24 hour period, meaning that  there is no good time to take them 
around TKI's.  All the TKI's carry a  warning about this, because if the 
stomach acid is reduced too much the TKI  will never reach full absorbtion.  
However, having said this, on Sprycel,  I did have to take prilosec for the 
first 
week or so until I adjusted to  taking Sprycel.  The heartburn would have 
killed me.  However, it  was only for about a week or so.  I have also had to 
do the same thing  for a few days with Tasigna.  It is a trade off, as the 
TKI may be  impaired by it.  However, I did find that once I adjusted to 
taking the  TKI I no longer required prilosec except on the rare occasion.  
Good for  you for standing your ground.  Most docs never check the interaction  
checker far enough to see that things like proton pump inhibitors can 
affect  absorption or other drugs that are liver enzyme inducers can affect 
metabolism  of the TKI's.  It pays for us to be patient active!

Fight  on,

Peg 

On Tuesday, November 26, 2013 1:58:38 PM UTC-8, Jeanie  wrote:  
 
Hi all and just wanted to say a few words about  Prilosec.  The Sprycel 
leaflet does say specifically do not take proton  pump inhibitors.  I had to 
fight with my doctors while in the hospital  as they were giving me this twice 
a day and the meds I was on for CML were  not working.  I finally told the 
nurse when she brought them in that I  would not be taking them anymore and 
showed her the leaflet.
And I had no indigestion or anything just the pain in my  right side that I 
always had.
We are all different so maybe some people can take them  without any side 
effects.
Happy Thanksgiving Everyone,
Jeanie<3
 
 
In a message dated 11/25/2013 3:58:03 P.M. Eastern Standard Time, 
[email protected]_ (javascript:)  writes:

 
Hi Peg and thank you.  As for the Prilosec, all of my doctors  and I have 
discussed it and feel that the benefits of me continuing to  take it outweigh 
the risk.  I don't take the prilosec with the TKIs,  there's at least a 
couple of hours in between.  Given my health  history, it's an unfortunate 
necessity.  
 
I agree with you and have been battling my doctors since March  regarding 
the whole "minimal effective dosing" issue.  I see no need  to take the 
maximum dose if the minimum is doing what it needs to be  doing.  At this point 
of my life, it's quality over quantity and if I  can't actually live and 
enjoy my life, I really don't see much  point.  Being sick and living in the 
shadows isn't really my  way.  
 
Suzanne
 

On Monday, November 25, 2013 2:31:42 PM UTC-5, peg wrote:

Hi Suzanne,

Like you I have been on Gleevec (8 mos),  Sprycel (3 yrs) and have just 
recently switched to a low dose Tasigna  (200mg once daily).  When on Sprycel I 
 had esophageal spasms,  where what I swallowed would not go down.  This 
may be similar to  what you are experiencing.  I do use liquid Donnatal for 
this and  other stomach problems, but I use it sparingly as it can inhibit the 
 metabolism of Tasigna!  There is not much point in taking a TKI,  and 
suffering the side effects, if you take another drug for the side  effects that 
renders the TKI useless!  Which brings up a  concern...your Prilosec.  While 
I will use that only very  occasionally, acid inhibitors like prilosec are 
contraindicated with TKI  drugs as they impair the absorbtion.  There is 
mounting evidence  that too little stomach acid will result in too little 
absorbtion of the  TKI's.  

As far as your oncologist wanting to increase your  dose to the standard 
recommended dose, there is also growing evidence  that dosage can be tailored 
to the actual need for each patient, but  because CML is absolutely fatal 
without treatment and too low a dose can  sometime lead to resistance, many 
oncologists are afraid to reduce the  dose below the standard in the absence 
of absolute medical  necessity.  However, were medical necessity has 
prevailed many  patients are being maintained fine on lower than standard 
dosing, 
myself  included.  

Since you are already on a low dose, you might  want to ask your oncologist 
to wait through at least 2 or 3 PCR's to see  what your numbers are doing.  
They recommend at least 2 PCR's  before making any changes as PCR's can 
fluctuate, so you would not ever  want to make a change based on any one, but 
rather a trend of two or  three, and they must be from the same lab!!! You 
cannot compare a PCR  from one lab to that of another.  It is like apples and  
oranges.  However, if your numbers are good, there may be no need  to put 
you on a higher dose.  Just one school of thought...you may  find others who 
disagree.  I have just had such extreme side  effects on TKI's that I have 
to hope and pray that low dosing will  work.  I PCR every month to monitor 
this.  

Like you I  also have a complicated diagnosis, and balancing drugs and side 
effects  is at the least challenging and sometimes depressing.  I have had  
Multiple Sclerosis for 25 years, was diagnosed with CML and Melanoma at  
almost exactly the same time, almost four years ago, and this year have  been 
diagnosed with an unrelated abdominal tumor and possible lung  tumors.  
Through all the years of my MS I barely took any  medication, but now pop 
handfuls of pills several times a day...very  disheartening.  I encourage you 
to 
find the lowest dose of  everything that works for you and try to find a way 
to make it all work  for your life. Some times for me this has taken a bit 
of life  modification.  I know first hand how tired and worn out you are...I  
get there too.  Try to take one day at a time...and when that  doesn't 
work, one hour at a time.  Know that you are not in this  alone.  

Fight  on,
Peg







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