Disappointing Appointment
I noticed on his blood work that the calcium level is slightly elevated. This has me wondering if there is bone involvement. He has no symptoms of it. No one has brought it up, but it concerns me.
All in all, it was very disappointing. I always go into these appointments prepared for the worse. Steve is a very positive thinker. Always thinks everything will just work out. He is very disappointed. Expected to hear lots of shrinkage, let's operate.
Thanks for "listening".
Chelsea
Comments
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Wow these boards are weird
Wow these boards are weird today! I keep trying to post and get knocked off.
I'm sorry to hear about the appt.
Just keep listening to that cure word and let the doctors do their thing. I know how stressed and anxious you are feeling, but lets keep hoping for the best. Do some googling and ask about the liver biopsy - I think I remember reading that many recommend against them...
DAMN! I could have gotten Steve a mouse for free - one of five, he could have taken his pick! I bet their mouse will cost top dollar.
Hugs Chels!
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The Air Just Went Out of the Room....
Hi Chels:)
I'm disappointed right along with you. Steve has taken a harsh beating and I was optimistic as well that some kind of surgical intervention would be done.
This is hard news.....I went from High to Low in a complete free-fall with your update. Just saddens me to see people I care about getting hurt so badly when they are trying so hard. Makes my stomach tie up in knots.
That's a tough combo of chemo alright...I know that TaraHK did this one I believe and experienced some positive response, but I don't want to speak for her.
Your guy is hard as nails and I so much hope that this new plan will yield the expected results this time:) You both deserve some good news!
For what it's worth, give Steve my best....we're in your corner and wish we could do more.
It's just so upsetting to watch all of us having to suffer so much.
I'm just about to finish up this post and was higher than a kite.....then I read the reality of what's happening to my friends and want to just hit the Delete key on what I wrote. It just seems so not important anymore...
Glad to be here 'listening' with you...
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On HoldSundanceh said:The Air Just Went Out of the Room....
Hi Chels:)
I'm disappointed right along with you. Steve has taken a harsh beating and I was optimistic as well that some kind of surgical intervention would be done.
This is hard news.....I went from High to Low in a complete free-fall with your update. Just saddens me to see people I care about getting hurt so badly when they are trying so hard. Makes my stomach tie up in knots.
That's a tough combo of chemo alright...I know that TaraHK did this one I believe and experienced some positive response, but I don't want to speak for her.
Your guy is hard as nails and I so much hope that this new plan will yield the expected results this time:) You both deserve some good news!
For what it's worth, give Steve my best....we're in your corner and wish we could do more.
It's just so upsetting to watch all of us having to suffer so much.
I'm just about to finish up this post and was higher than a kite.....then I read the reality of what's happening to my friends and want to just hit the Delete key on what I wrote. It just seems so not important anymore...
Glad to be here 'listening' with you...
Chelsea,
So sorry for this latest news. Let's just believe that the liver surgery is "on hold" and as soon as these pesky lung mets are under control, the surgery will be "on" again. The dang road just seems to be filled with so many boulders.
Wishing you both the strength to keep climbing over the boulders and onto a clear highway of success.
Luv,
Wolfen
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Very interested in this
Very interested in this information about KRAS not necessarily being the same on the matastases as it is on the primary tumor as I have never heard that before. I will ask my oncologist about this when I see her on June 20th. In fact, I think I will e-mail her NP right now and ask about this. Was this the same with BRAF, or did he just never get BRAF testing done on the primary? Very interested to hear more...
Tedd
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When Steve was diagnosed twotachilders said:Very interested in this
Very interested in this information about KRAS not necessarily being the same on the matastases as it is on the primary tumor as I have never heard that before. I will ask my oncologist about this when I see her on June 20th. In fact, I think I will e-mail her NP right now and ask about this. Was this the same with BRAF, or did he just never get BRAF testing done on the primary? Very interested to hear more...
Tedd
When Steve was diagnosed two years ago they tested for KRAS but not BRAF. If he tests positive for BRAF the anti egfr drugs may be effective, after all. They are now testing a piece of the metastasized tumor (liver) for both mutations. But even if they had already tested the primary for BRAF, they would still retest the met as it could be a completely different genetic makeup. Interting, isn't it? I knew about the first part but this was the first I had heard of there being any benefit to testing metastasis.
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I had read that primary CRC and subsequenttachilders said:Very interested in this
Very interested in this information about KRAS not necessarily being the same on the matastases as it is on the primary tumor as I have never heard that before. I will ask my oncologist about this when I see her on June 20th. In fact, I think I will e-mail her NP right now and ask about this. Was this the same with BRAF, or did he just never get BRAF testing done on the primary? Very interested to hear more...
Tedd
liver mets are genetically different,which would imply mets elsewhere would differ too. PIK3CA should also be tested for. Further, tho i may be wrong here, i recall reading that if KRAS mutant,you won'tbe BRAF mutant and vice versa...
http://clincancerres.aacrjournals.org/content/early/2012/01/17/1078-0432.CCR-11-1965.abstract
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Thanks Steve.coloCan said:I had read that primary CRC and subsequent
liver mets are genetically different,which would imply mets elsewhere would differ too. PIK3CA should also be tested for. Further, tho i may be wrong here, i recall reading that if KRAS mutant,you won'tbe BRAF mutant and vice versa...
http://clincancerres.aacrjournals.org/content/early/2012/01/17/1078-0432.CCR-11-1965.abstract
Thanks Steve.
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I wish the results had been better, Chels-
I've had a couple of these "worse than expected" scans, and it sucks. I guess the one thing I would say is that it sounds like you have a great team who are not giving up on Steve, and in my experience with doctors the "c" word doesn't get thrown around lightly. If they think there is still hope for a cure for Steve, I would try to put trust in that for now, as best you can. It's not easy, I know. Sending strength your way~AA
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My primary tumor was KRASChelsea71 said:When Steve was diagnosed two
When Steve was diagnosed two years ago they tested for KRAS but not BRAF. If he tests positive for BRAF the anti egfr drugs may be effective, after all. They are now testing a piece of the metastasized tumor (liver) for both mutations. But even if they had already tested the primary for BRAF, they would still retest the met as it could be a completely different genetic makeup. Interting, isn't it? I knew about the first part but this was the first I had heard of there being any benefit to testing metastasis.
My primary tumor was KRAS mutant, BRAF wild-type, according to the info I have. They biopsied some peritoneal mets, but all I know about them is that they were confirmed to be adenocarcinoma and thus were mets from the colon tumor and not a different type of cancer. I will have to ask my oncologist about all of this in more detail, as it could be very important with regard to treatment options. Thank you so much for this information. It could literally be a life-saver, or at least a life-extender....
Tedd
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Sorry
Sorry you didn't get better news. I'm hoping that his new treatment works better for him and his next scan shows a big improvement.
Kim
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chances of both kras and brafcoloCan said:I had read that primary CRC and subsequent
liver mets are genetically different,which would imply mets elsewhere would differ too. PIK3CA should also be tested for. Further, tho i may be wrong here, i recall reading that if KRAS mutant,you won'tbe BRAF mutant and vice versa...
http://clincancerres.aacrjournals.org/content/early/2012/01/17/1078-0432.CCR-11-1965.abstract
chances of both kras and braf mutations being present are statustically low, but they are not mutually exclusive. I had this argument with one of my oncs and eventually dug up the data and I got my braf test,despite being a kras mutant.
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sorry
ah so so sorry about those results Chelsea.....indeed i know you must have hoping for so much more. I do agree with the thinking that the cure word is still wonderful .....glad it is still floating around the room. Sorry too that you now have this added to Montreal ....what a blessing to have fresh opportunities though.....
sending love to you both, mags
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I found a 2011 paper where
I found a 2011 paper where they looked at 305 cases from patients that they had been able to biopsy bot the primary colon tumor site and the liver, and the results are below:
197/305 were KRAS wild type at both sites
108/305 had a KRAS mutation at one or both sites
5 had KRAS mutant at primary and KRAS wild type in liver
1 had KRAS wild type at primary and KRAS mutant in liver
5 had a different KRAS mutation between primary and liver site
In summary, there is only about a 3.6% chance of having a different KRAS at the primary site and the liver (they didn't look at lung or peritoneum). Wish the chances were better....
Tedd
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Well, my oncologist at NW hastachilders said:I found a 2011 paper where
I found a 2011 paper where they looked at 305 cases from patients that they had been able to biopsy bot the primary colon tumor site and the liver, and the results are below:
197/305 were KRAS wild type at both sites
108/305 had a KRAS mutation at one or both sites
5 had KRAS mutant at primary and KRAS wild type in liver
1 had KRAS wild type at primary and KRAS mutant in liver
5 had a different KRAS mutation between primary and liver site
In summary, there is only about a 3.6% chance of having a different KRAS at the primary site and the liver (they didn't look at lung or peritoneum). Wish the chances were better....
Tedd
Well, my oncologist at NW has agreed that it might make sense to test my mets for KRAS and BRAF, so now I just have to hope they kept enough of the omental tumors that they did biopsy (to make sure they were colon cancer) to do the testing....
Tedd
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Current research seems to indicate that MET may have atachilders said:I found a 2011 paper where
I found a 2011 paper where they looked at 305 cases from patients that they had been able to biopsy bot the primary colon tumor site and the liver, and the results are below:
197/305 were KRAS wild type at both sites
108/305 had a KRAS mutation at one or both sites
5 had KRAS mutant at primary and KRAS wild type in liver
1 had KRAS wild type at primary and KRAS mutant in liver
5 had a different KRAS mutation between primary and liver site
In summary, there is only about a 3.6% chance of having a different KRAS at the primary site and the liver (they didn't look at lung or peritoneum). Wish the chances were better....
Tedd
greater influence on anti-EGFR treatment
www.mdanderson.org/newsroom/news-releases/2013/met-protein-levels.html
and
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Chelsea
I wish you folks got better news but it's pretty cool that they are using a mouse as a guinea pig so to speak. Being able to test treatments for effectiveness seems to me to be a positive step in the right direction... The roller coaster gets old, I understand how you folks must feel
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Sorry
Sad to hear the news, no sadder then you to be sure. Most of all thanks for sharing with us.
Sudance said it best I think. I hate to try and speak for everyone. However, for me, it is hard to accept that this could be happening. For the two of your it must be especially hard after so much hard and dedicated effort.
Hugs and hope that there is a "Cure" in the future.
Art
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Wow! I wasn't expecting so
Wow! I wasn't expecting so many responses to my post. Thank you so much for all your kind words.
The positive side of all this is that Steve will now be treated at a new hospital by a new oncologist. He will now be treated in our neighboring province where they seem to take a more aggressive approach to cancer treatment. I couldn't help but be impressed by this whole mouse idea. Hopefully it will work out. It is very important when doing the biopsy that they extract a piece of the tumor that contains active cancer cells. Anyways, I really like this hospital (McGill Health Care Centre) and I like the team of doctors.
Steve seems to be feeling better about it all. He was pretty discouraged the first couple days after learning about the progression. Talking about not renewing his magazine subscriptions etc.... It was upsetting to see him in this state of mind. He has always been so positive. I do worry about the Folfirinox. Mostly because of the Oxilaplatin. He plays the guitar and puts together model planes and has many other activities that involve fine motor
skills. These hobbies keep him sane and occupy a lot of his time. So I am
worried about how the neuropathy will affect his quality of life. We booked a trip to Vegas. We leave on Wednesday. Going all out. The helicopter ride over the Grand Canyon, Crisscross Angel, Cirque de Soleil etc... It may be a while before he feels well enough to do a trip like this. I feel that we just can't put these things off anymore.
Thanks again to everybody for the support. Don't know what I'd do without you guys.
Chelsea0 -
Hey Jen. Ha ha. Steve and Ijen2012 said:Wow these boards are weird
Wow these boards are weird today! I keep trying to post and get knocked off.
I'm sorry to hear about the appt.
Just keep listening to that cure word and let the doctors do their thing. I know how stressed and anxious you are feeling, but lets keep hoping for the best. Do some googling and ask about the liver biopsy - I think I remember reading that many recommend against them...
DAMN! I could have gotten Steve a mouse for free - one of five, he could have taken his pick! I bet their mouse will cost top dollar.
Hugs Chels!
Hey Jen. Ha ha. Steve and I have had many laughs over the mouse thing. He has named it Bravo. Sorry to hear your still wrestling with the mouse situation.
As for the liver biopsy, I did inquire about the risk of seeding. We weighed it out. They say it's less risky for him due to The HIPEC surgery that he's had. (No peritoneal membrane etc).
Thanks and good luck with those mice.0
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