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    <title>Reflections from ASH 2011</title>
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    <id>tag:myeloma.org,2011-12-12:/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011//26</id>
    <updated>2011-12-13T16:04:21Z</updated>
    <subtitle>Pat Killingsworth is attending the 53rd American Society of Hematology Annual Meeting in San Diego, California with a group of other patients and caregivers.</subtitle>
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<entry>
    <title>I am finding some salvage therapy options here at ASH...</title>
    <link rel="alternate" type="text/html" href="http://myeloma.org/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011/2011/12/i-am-finding-some-salvage-therapy-options-here-at-ash.html" />
    <id>tag:myeloma.org,2011:/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011//26.659863</id>

    <published>2011-12-13T02:12:37Z</published>
    <updated>2011-12-13T16:04:21Z</updated>

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    <author>
        <name>Pat Killingsworth</name>
        
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In my last blog I attempted to describe what it's like to cover an important
conference like ASH as a patient.<br />
<br />
I used my experience at Saturday's poster session to set the stage for some
important news from the San Diego Convention Center.<br />
<br />
So let's get back to my research poster experience that I started to share with
you yesterday.<br /><br /></span><img alt="posters1.jpg" src="http://myeloma.org/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011/posters1.jpg" class="mt-image-center" style="text-align: center; display: block; margin: 0 auto 20px;" height="375" width="500" /><span style="font-size:12.0pt;
font-family:&quot;Times New Roman&quot;,&quot;serif&quot;;mso-fareast-font-family:Calibri;
mso-fareast-theme-font:minor-latin;mso-ansi-language:EN-US;mso-fareast-language:
EN-US;mso-bidi-language:AR-SA">As I walked up and down the rows--flanked by posters of different colors and
sizes on both sides--I found my mind wondering back to my recent "close call"
following my stem cell transplant this summer.<br />
<br />
Even though it looks like my RVD (Revlimid/Velcade/dex) therapy is working
post-transplant, I can't shake that "close call" experience of realizing I
might be running out of treatment options.<br />
<br />
What was I looking for?&nbsp; New therapy ideas for patients (like me!) who are
facing difficult salvage therapy decisions in the near future.<br />
<br />
Mmm.&nbsp; Here's a poster with Phase 2 study results which combines a
traditional leukemia and lymphoma drug, bendamustine, with Velcade.&nbsp; I
wonder if bendamustine, might be the answer?<br />
&nbsp; <br />
I have a friend who has run out of therapy options.&nbsp; As a last ditch
effort, his Mayo Clinic oncologist started him on bendamustine--and it seems to
be working so far.<br />
<br />
Here's another poster with research data about Cytoxan, another alkaloid class
"blast from the past."&nbsp; I think Cytoxan has been around longer than
bendamustine.<br />
<br />
I have another myeloma patient friend who is doing wonderfully on nothing but
Cytoxan and prednisone.&nbsp; It has worked for him for over a year.<br />
<br />
Of course, there are some new novel therapy agent options represented on
posters here as well, like carfilzomib, pomalidomide and elotuzumab.<br />
<br />
Now if these hard working researchers and clinicians can get the FDA to approve
some of this stuff, a lot of my fellow patients will benefit.<br />
<br />
As a post script, I would like to note one advantage of studying older,
established drugs like Cytoxan and bendamustine:&nbsp; They can be prescribed "off label" for use almost immediately outside a clinical trial setting.<br />
<br />
Time to have fun, kick-back and read some of these study results...&nbsp; <br />
<br />
Until next time, feel good and keep smiling!&nbsp; <br /><br />Pat<br style="mso-special-character:
line-break" />
<br style="mso-special-character:line-break" />
</span> ]]>
        
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</entry>

<entry>
    <title>Reflections from an emotional Saturday at ASH.</title>
    <link rel="alternate" type="text/html" href="http://myeloma.org/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011/2011/12/reflections-from-an-emotional-saturday-at-ash.html" />
    <id>tag:myeloma.org,2011:/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011//26.659858</id>

    <published>2011-12-11T19:41:14Z</published>
    <updated>2011-12-13T16:09:00Z</updated>

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    <author>
        <name>Pat Killingsworth</name>
        
    </author>
    
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<![endif]--><br /><span style="font-size: 12pt; font-family: &quot;Calibri&quot;,&quot;serif&quot;;">I was excited to
learn that the IMF had selected me to represent them as a patient blogger at
this year's American Society of Hematology (ASH) annual meeting in San Diego.<br />
<br />
I have covered a number of ASH and ASCO (American Society of Clinical Oncology)
meetings in the past.&nbsp; By far the least glamorous, yet very important
component of the five day event are the poster sessions.<br /><br /></span><img alt="posters2.jpg" src="http://myeloma.org/MtEntryPage.action?source=/imf_blogs/reflections_from_ash_2011/posters2.jpg" class="mt-image-center" style="text-align: center; display: block; margin: 0 auto 20px;" height="375" width="500" /><br /><span style="font-size:12.0pt;font-family:&quot;Calibri&quot;,&quot;serif&quot;;
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Poster sessions are open daily for peer and media review.&nbsp; Each day, as
many as 1000 large posters are mounted on flat bulletin board style backdrops
in a large hall which looks a lot like an airplane hanger.<br />
<br />
The posters are grouped by category.&nbsp; For example, Saturday there was a
row filled with nothing but stem cell transplant related research results the
length of a football field.<br />
<br />
Think that's a lot?&nbsp; There were three rows of multiple myeloma related
posters.&nbsp; That's almost 100 research study posters!&nbsp; <br />
<br />
Years of hard work, all summarized on a 3 ft X 5 ft poster. They may not
represent the most dramatic advances in hematological research--those are saved
for oral presentations in the afternoon and evening sessions.<br />
<br />
But the research displayed in the poster exhibit hall are the heart and soul of
ASH.&nbsp; There are lots of diamonds in the rough here.&nbsp; You just have to
know where to look and what to look for.<br />
<br />
That was my job Saturday; to carefully work my way through the rows of posters,
looking for study results which might impact my fellow patients.<br />
<br />
Keeping this in mind, I usually look for data on new and promising emerging
myeloma therapies.&nbsp; These can be hard to find, since the majority of
posters aren't about clinical trials.&nbsp; Instead, they reflect very
specific, genetic related studies with tiles like "Gene mutations detected by
whole-exome sequencing," or "Prognostic significance of focal lesions in whole
body MRIs."<br />
<br />
But every fifth or sixth poster usually reflects therapy results, and Saturday
was no exception.<br />
<br />
At first I was a bit disappointed.&nbsp; Nothing was jumping out at me--just a
bunch of highly technical study results which didn't seem like they would be
relevant to patients.<br />
<br />
But soon I noticed several posters that I considered significant.&nbsp; Then I
found another and another...<br />
<br />
There were indeed some significant therapy-related study results here.&nbsp;
But I found myself losing focus.&nbsp; <br />
<br />
You see, after over four years on Revlimid, this summer I underwent an
autologous stem cell transplant.<br />
<br />
The results of my transplant were disappointing.&nbsp; Not only hadn't it
slowed my multiple myeloma down, but it had made things worse!&nbsp; My doctors
were concerned--and so was I.<br />
<br />
What if Revlimid and/or Velcade had stopped working for me as well?&nbsp; What
would I do then?<br />
<br />
Long suffering multiple myeloma patients face this reality every day.&nbsp;
Once standard anti-myeloma therapies stop working, the next step is what
oncologists called salvage therapy.<br />
<br />
Salvage therapy is a catch-all term used to describe the mad scramble as your
myeloma docs try and come-up with a drug or drug combination that can keep a
strengthening, angry myeloma at bay.<br />
<br />
Fortunately, it looks like a combination of Revlimid, Velcade and dexamethasone
(RVD) is going to work for me a while longer.<br />
<br />
But this experience profoundly changed how I view the world of multiple myeloma
therapy.&nbsp; We need new drugs which enhance the way Revlimid and/or Velcade
works--or can stand alone when they are no longer effective--and we need them
NOW!<br />
<br />
As I strolled up and down the rows of posters Saturday,&nbsp; I found myself
drawn to posters about new therapies for relapsed myeloma patients like me.<br />
<br />
<b>I was therapy shopping!</b><br />
<br />
I was walking up and down the rows, looking for therapy options like I was
shopping at Target or Kohls.<br />
<br />
What a strange, surreal experience!&nbsp; <br />
<br />
OK.&nbsp; That's the poignant, emotional side of Saturday's assignment.&nbsp;
Hopefully I have set the stage for you so you can understand my frame of
reference here at ASH.<br />
<br />
But what did I find?&nbsp; Did I locate any diamonds in the rough which might
give relapsed multiple myeloma patients hope?<br />
<br />
YES!&nbsp; Yes I did.<br />
<br />
I will share my impressions and some specifics I found in my next blog
post.&nbsp; Until then, let me say I was very encouraged by what I saw
Saturday.<br />
<br />
Until next time, Feel good and keep smiling!&nbsp; Pat<br style="mso-special-character:
line-break" />
<br style="mso-special-character:line-break" />
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