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RE: Re: BMT- Coralee

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Coralee:

and I have been thinking about your family, if I remember right, Cam is

doing a BMT very soon--correct?

We keep your family in our thoughts and prayers....

Please keep us posted on his success!

Regards

@...: coralee.williams@...: Wed, 20 Feb

2008 21:07:59 -0700Subject: Re: [ ] Re: BMT- Donna

Donna,Please consider getting regular BMB's. My husband had mutations and weird

things going on his marrow. He went from an ok response to blast crisis in two

weeks. Very important to stay on top of things and prepared. We were so thankful

he had already lined up his siblings for HLA matching and had a donor just in

case. Unfortunately his " just in case " came very abruptly when he went into

blast crisis. He is now on the eve of his transplant. Somewhere we never thought

we would be.On Wed, 20 Feb 2008 16:50:23 -0500, Dorothy Emery

<doemery@...> wrote:> Hi Donna,>> It sounds like the kind of mutations

you are talking about is not a> mutation of the Gleevec binding site (ie T315I)

but mutations of the> chromosomes other than the Philadelphia chromosome (ie you

might have> 3 chromosome 8's instead of 2). Often patients get those 2 types of>

mutations confused with each other but they do have different meanings> for

treatment. The type you have might mean possible clonal evolution> and is often

associated with the advanced phases of cml. Drug> treatments don't always work

as well in advanced phases. You were> wise to see a specialist like Dr. Cortes

(he is a top cml doctor) and> it sounds like he is on top of things by

recommending you get your> siblings tested so you will be ready if you need to

get a transplant.> If you are responding well to Gleevec and continue responding

well you> will probably never need that transplant, but it will be good to know>

whether or not you have a sibling matched donor because the extra> mutations

might make your disease a higher risk than a more plain> vanilla type with just

the Ph+ chromosome. If I were you I would> continue being seen & tested at MDACC

as they have a very sensitive> PCR test and Dr. Cortes will know what you should

do. You should> probably get a BMB more often than a more typical case as that

is the> only way they can see if these extra mutations are disappearing or not>

with Gleevec treatment (the pcr won't show that). That extra testing> won't be

necessary forever but you are still less than a year from> diagnosis and this is

a critical time for them to see how you are> going to respond. And please

remember that there are patients who> have had transplants who are doing very

well--it shouldn't be done> without good reason but there is still a place for

this treatment.> I'm glad to hear you seem to be responding well to Gleevec (but

it's> not clear from your post what your current remission state is). Best>

wishes to you.>> Dorothy> dx 5/2000>> On Feb 20, 2008, at 2:41 PM, donnaberry99

wrote:>>> -Dear All>> The posts on BMT have been a wealth of info as always. I

too was>> recommended that this may be a route I would have to take by >>

Cortes (MD )and to get my Brothers HLA in place. This info>> is all now

at MD and waiting to be matched up. I wandered>> if he suggested this

to me as I have 7 other mutations beside PH ones>> hence cloning evolution.

Please let me know what you all think. I>> have already decided myself that I

will just keep taking the>> wonderful Gleevec (have already reached PCR..dx May

07) until it is>> no longer working, then try another medication and only as a

last>> resort a BMT (I am 48).>> BTW Dr. Cortes also wanted me to get BMB every

3 mos, which I have>> opted not to do and intend to get one on my DX anniversary

instead.>> Thanks always for your wealth of information.>> Regards Donna x>>>

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Hey Donna:

My prayers are with you and your husband. I had cml and did a MUD transplant

on 2/16/07. The road of recovery is full of ups and downs. I had to learn a

whole lot of patience with the process. The good news, I have not show any

signs of CML for 10 months and the cells are 100% in. I am still on full

immunosupressants and dealing now with cGVHD issues. I am trying to recover my

life completely but that goal make be too much for me to make happen, I take

life one day at a time. Let us know how it goes, I hope he is a great survivor.

Therese

Cervera <weez_555@...> wrote:

Coralee:

and I have been thinking about your family, if I remember right, Cam is

doing a BMT very soon--correct?

We keep your family in our thoughts and prayers....

Please keep us posted on his success!

Regards

@...: coralee.williams@...: Wed, 20 Feb

2008 21:07:59 -0700Subject: Re: [ ] Re: BMT- Donna

Donna,Please consider getting regular BMB's. My husband had mutations and weird

things going on his marrow. He went from an ok response to blast crisis in two

weeks. Very important to stay on top of things and prepared. We were so thankful

he had already lined up his siblings for HLA matching and had a donor just in

case. Unfortunately his " just in case " came very abruptly when he went into

blast crisis. He is now on the eve of his transplant. Somewhere we never thought

we would be.On Wed, 20 Feb 2008 16:50:23 -0500, Dorothy Emery

<doemery@...> wrote:> Hi Donna,>> It sounds like the kind of mutations

you are talking about is not a> mutation of the Gleevec binding site (ie T315I)

but mutations of the> chromosomes other than the Philadelphia chromosome (ie you

might have> 3 chromosome 8's instead of 2). Often patients get those 2 types of>

mutations confused with each other but they do have different meanings> for

treatment. The type you have might mean possible

clonal evolution> and is often associated with the advanced phases of cml.

Drug> treatments don't always work as well in advanced phases. You were> wise to

see a specialist like Dr. Cortes (he is a top cml doctor) and> it sounds like he

is on top of things by recommending you get your> siblings tested so you will be

ready if you need to get a transplant.> If you are responding well to Gleevec

and continue responding well you> will probably never need that transplant, but

it will be good to know> whether or not you have a sibling matched donor because

the extra> mutations might make your disease a higher risk than a more plain>

vanilla type with just the Ph+ chromosome. If I were you I would> continue being

seen & tested at MDACC as they have a very sensitive> PCR test and Dr. Cortes

will know what you should do. You should> probably get a BMB more often than a

more typical case as that is the> only way they can see if these extra mutations

are disappearing or not> with

Gleevec treatment (the pcr won't show that). That extra testing> won't be

necessary forever but you are still less than a year from> diagnosis and this is

a critical time for them to see how you are> going to respond. And please

remember that there are patients who> have had transplants who are doing very

well--it shouldn't be done> without good reason but there is still a place for

this treatment.> I'm glad to hear you seem to be responding well to Gleevec (but

it's> not clear from your post what your current remission state is). Best>

wishes to you.>> Dorothy> dx 5/2000>> On Feb 20, 2008, at 2:41 PM, donnaberry99

wrote:>>> -Dear All>> The posts on BMT have been a wealth of info as always. I

too was>> recommended that this may be a route I would have to take by >>

Cortes (MD )and to get my Brothers HLA in place. This info>> is all now

at MD and waiting to be matched up. I wandered>> if he suggested this

to me as I have 7 other mutations beside PH

ones>> hence cloning evolution. Please let me know what you all think. I>> have

already decided myself that I will just keep taking the>> wonderful Gleevec

(have already reached PCR..dx May 07) until it is>> no longer working, then try

another medication and only as a last>> resort a BMT (I am 48).>> BTW Dr. Cortes

also wanted me to get BMB every 3 mos, which I have>> opted not to do and intend

to get one on my DX anniversary instead.>> Thanks always for your wealth of

information.>> Regards Donna x>>> [Non-text portions of this message have been

removed]>>>

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