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Experiences with Palladia/Cytoxan
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1
31 October 2011 - 2:19 am
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Hello again,

It's been a few months since I posted on the site.  However, we got news on Friday that Capone's osteosarcoma cancer has spread to his lungs.  We knew this was going to happen, but sadly it happened much sooner than we had expected.  He is just about 4 months post amputation. He had 4 rounds of Carboplatin, which ended about 1 month ago. 

 

Our oncologist suggested this treatment to possibly slow down the growth of speed of the lung mets.  Palladia 1 day and then Cytoxan nand Rimadyl the next.  He had his first dose of Palladia on Sunday.  He does seem a bit lethargic and might be a bit sore. I know that leg lameness can be a side effect of this drug.  However, I'm not sure if it could be because the air is crisp and the fact he was not given any Rimadyl yesterday.  I just gave him some Rimadyl with his morning breakfast.  I'll see how he is later.   We're still waiting for the Cytoxan to arrive at our pharmacy.  Apparently, this will happen sometime this afternoon. 

 

We know that he only has a short time left with us and want him to be happy and comfortable.  Our oncologist was saying about 3 months without any other treatments.   I just don't want to continue the use of a drug that is going to make him feel horrible. I'm just wondering how many people have had experience with this drug/drug combination. 

 

Waiting for Capone to wake up from his nap to see if he is really limping around before I call the oncologist to discuss.  Figured I would post here in the meantime and see what everyone here has to say about it.

 

Thank you,

Tiffany and Capone.

Orange County, CA
Member Since:
28 November 2008
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2
31 October 2011 - 10:49 am
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Hi Tiffany.  I don't have any experience with Palladia, as it was not available when Max was on metronomics .  I'm sure others who are currently using it will post.  We did use Cytoxan while on metronomics , and I can tell you Max did not have any bad side effects from it.  However, we used it directly after his chemo (6 rounds of carbo) ended, and the cancer had not yet spread.  Once mets were discovered in his lungs, we discontinued metronomics .  I have heard great things about Palladia, so I hope it works well for you and Capone.  Please give your boy a good ear rub from me when he's feeling a bit better, and please keep us updated on his progress.

San Diego, CA
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29 October 2010
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3
31 October 2011 - 12:48 pm
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Hi Tiffany and Capone, you'll see in my sig that we did Palladia and cytoxan, but then had to drop the palladia due to GI issues. Abby now takes the cytoxan every day. I can't really say whether the Palladia helped her - it may have slowed down the progression of her mets, but it certainly didn't stop them. But even if it was slowing them down, we had to give it up because she was having diarrhea too often, which was also affecting her energy level (which was still pretty crazy high, but not as crazy high as it is w/out being on the palladia). She's had no ill effects from the cytoxan. Right now we are doing cytoxan and artemisinin . I don't really know what effect this combo is having on the mets, because we haven't done an xray since July. (Although he lungs still sound clear as a bell.) We are still considering whether or not to do one... Probably will decide this week or next. If we do one and the cytoxan/arte is slowing the mets down, then we'll just stick with that. If we do an xray though and it shows bad news, we might drop all that and try masitinib - which is basically the French version of Palladia. (Our onc. said he's seen some dogs do well on palladia, but not masitinib, or vice versa, so just because she did badly on the palladia doesn't mean she'll be sick on the masit.) Anyway, I mention that because masitinib is something else you could consider if you do find that Capone doesn't do well on the pallladia.

 

Also, "luckypup" just posted this blog update yesterday - they had AMAZING results with palladia:

http://luckypup.....ainly-ups/

I don't think they visit the site very often, but maybe you could PM them if you have questions.

Also, feel free to PM me if you want to know more about what we are doing w/ Abby.

All the best to Capone!
Jackie, Abby's mom

Abby: Aug 1, 2009 – Jan 10, 2012. Our beautiful rescue pup lived LARGE with osteosarcoma for 15 months – half her way-too-short life. I think our "halflistic" approach (mixing traditional meds + supplements) helped her thrive. (PM me for details. I'm happy to help.) She had lung mets for over a year. They took her from us in the end, but they cannot take her spirit! She will live forever in our hearts. She loved the beach and giving kisses and going to In-N-Out for a Flying Dutchman. Tripawds blog, and a more detailed blog here. Please also check out my novel, What the Dog Ate. Now also in paperback! Purchase it at Amazon via Tripawds and help support Tripawds!

Chicago, IL
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5 March 2011
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4
31 October 2011 - 7:28 pm
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Tiffany, I'm so sorry for the diagnosis - what a punch in the stomach.  Our onc recommended that protocol for Tate's metronomics for his histiocytic sarcoma.  We opted just for Cytoxan + Rimadyl because I'd heard about Palladia side effects with many dogs, plus it was really expensive.  Now I'm rethinking it based on Lucky's blog post but that doesn't solve the $$$ thing.

Tate hasn't really had any side effects with C+R.  Even when we started we decided if he did have side effects, we'd just quit and let him be a dog til his time came.  I'm with you 100% on the happy and comfortable part.

Keep us posted, okay?  Is Capone still limping? 

Jan & Tate

http://tate.tripawds.com/
August 16, 2006 to November 28, 2011
TATE ~ Forever in our hearts.

Member Since:
15 March 2011
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5
31 October 2011 - 8:10 pm
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Hi Tiffany - I'm so sorry about Capone's mets - I know how it feels to have it take the wind out of your sails. Sam had a similar timing of his mets....he did 6 rounds of carboplatin and immediately following, developed mets. We considered Palladia, but he had so many mets (more than a dozen) and didn't tolerate carbo real well, so we didn't want to risk side effects. We put him on metronomics (including Cytoxin) and just hoped to slow the mets and keep him comfortable - our oncologist's estimate was 8 weeks. And that was 13 weeks ago. We pulled him off all meds 5 weeks ago because the mets continued to multiply - he has well over 25 at this point. He's on artemisinin , k9 immunity and fish oil....and he's doing well. The estimates our doctor's give are just that, estimates, so try not to dwell on it. We never know how much time we have left. Also, anything you put Capone on, you can always stop if it does't agree with him. Sam swam for a 1/2 hour just last week...pretty great for a dog with so many mets and 5 weeks past his "estimate"! Hang in! Xo sue and Sammy

6
1 November 2011 - 12:23 pm
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Should have given Capone his 2nd dose of Palladia today.  However, he was coughing a lot yesterday.  More than he ever has without the drug.  Anyways, around 12:30 am while snuggling on the couch he hacked up a bile-like glob with bright red blood included.  Not the way you want to end your day.  I told my husband that I was going to sleep downstairs on the couch to keep an eye on Capone.  He coughed a few more times until about 5am but no more blood.  Whew.  Capone slept great after that.... me not so much!  I did find his snoring and his stinky toots somewhat comforting. : )

 

I called the oncologist first thing this AM. She agreed that we should stop the Palladia until Thursday to see if the coughing up blood stops.  So far today he has only coughed 2 times for a very short period of time.  No other signs of blood.  We're still waiting for the Cytoxan to be delivered to our pharmacy.  We too will hold off on starting this drug until after Thursday.  My oncologist thinks that if we don't have any other problems we should give Capone a lower dose of Palladia to see if that ceases the side effects.   She still says that the Palladia could not be the cause of the coughing/blood but I'm optimistic as to the onset after giving the drug.   

 

While out on a walk last night, my husband asked me if I could have a superpower what would it be... My reply was to take pain away from anyone and everything.  Mainly speaking of my Capone. No one should have to suffer.  I want nothing more than to have my sweet Capone just pass peacefully in his sleep.  Man, cancer sucks!!

 

Hoping that we have a much more peaceful day/night. 

-Tiffany and Capone.

San Diego, CA
Member Since:
29 October 2010
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7
1 November 2011 - 1:57 pm
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Sorry to hear about the coughing/blood. That must have been terribly scary. I hate cancer too! This whole thing sucks and you just want to scream sometimes because it is so unfair.

Hope a lower dose helps and that he is not coughing anymore!

Hang in there,

Jackie, Abby's mom

Abby: Aug 1, 2009 – Jan 10, 2012. Our beautiful rescue pup lived LARGE with osteosarcoma for 15 months – half her way-too-short life. I think our "halflistic" approach (mixing traditional meds + supplements) helped her thrive. (PM me for details. I'm happy to help.) She had lung mets for over a year. They took her from us in the end, but they cannot take her spirit! She will live forever in our hearts. She loved the beach and giving kisses and going to In-N-Out for a Flying Dutchman. Tripawds blog, and a more detailed blog here. Please also check out my novel, What the Dog Ate. Now also in paperback! Purchase it at Amazon via Tripawds and help support Tripawds!

8
3 November 2011 - 1:11 pm
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We are scheduled to start Palladia again tomorrow at a lower dose of 100 mg instead of 115 mg. We shall see how it goes. If we have other negative siide effects we will have determined that Palladia is not going to work.  It would be awesome if the Palladia can be continued and slowed down the progression of the lung mets or better yet made them smaller.   We will just have to see how things go with the dosage.

We're also going to hold off on starting the Cytoxan until he goes into the oncologist for a repeat CBC.  We want to just be sure than any side effects he is having is most certainly from the Palladia.  I totally agree with our oncologist.  Better ease into things. 

 

Keep sending good vibes to Capone.  He can definitely use them 🙂

Happy Thursday-- Have a great day!

-Tiffany and Capone.

San Diego, CA
Member Since:
29 October 2010
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9
3 November 2011 - 1:22 pm
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Sounds like you are taking a good approach. Sometimes it is tempting to try to throw everything at the cancer, but you have to go slow and add things in one at a time so that you can figure out what work's with your pup's system and what doesn't. It took me FOREVER to get Abby on to her current list of 'goodies' because she can sometimes have a sensitive system so I had take a lot of time when adding in each new thing. THen we'd have a little set-back (not necessarily from the drug/supplement) and have to ease off and start again.

Hoping all goes well for Capone! Keep us posted! Abby sends kisses,
Jackie, Abby's mom

Abby: Aug 1, 2009 – Jan 10, 2012. Our beautiful rescue pup lived LARGE with osteosarcoma for 15 months – half her way-too-short life. I think our "halflistic" approach (mixing traditional meds + supplements) helped her thrive. (PM me for details. I'm happy to help.) She had lung mets for over a year. They took her from us in the end, but they cannot take her spirit! She will live forever in our hearts. She loved the beach and giving kisses and going to In-N-Out for a Flying Dutchman. Tripawds blog, and a more detailed blog here. Please also check out my novel, What the Dog Ate. Now also in paperback! Purchase it at Amazon via Tripawds and help support Tripawds!

Chicago, IL
Member Since:
5 March 2011
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10
3 November 2011 - 6:14 pm
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sending good vibes...

http://tate.tripawds.com/
August 16, 2006 to November 28, 2011
TATE ~ Forever in our hearts.

11
9 November 2011 - 3:16 pm
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Well... too many side effects with Palladia. : ( Now the question is do we try something else? I have a vet friend who recommended Kinavet.  Anyone have experience with this drug?  Some other options: if the Kinavet can't be tolerated we could try Cytoxan (which is better given when no mets are present) which unfortunately is not the case for Capone. We could try a IV dose of doxorubicin administered every 2 weeks.  Chest x-rays again in couple of weeks to see if more mets are present.   UGH. 

 

Capone is coughing more which totally breaks my heart. During the conversation with the oncologist today this was discussed. She has called in a cough medicine to our pharmacy.  I'm planning on sleeping on the couch to see how much he is coughing at night.  I guess the cough medicine is just something we can give him during the evening.  I don't remember the name currently but I think it starts with a "B" --I'll have the details once I pick up the prescription.

krun15
12
9 November 2011 - 3:36 pm
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Hi ,

I know Rio used Kinavet for internal mast cell cancer.  You could PM her mom Micki, she posts as riosmom. 

I think Rio tolerated the drug OK but it didn't help her situation.

I briefly discussed Kinavet with our oncologist, but again it was for mast cell cancer.  I have not yet tried it.

 

Karen and the pugapalooza

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15 March 2011
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13
9 November 2011 - 4:16 pm
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We've been on a very similar path with our Sam. We ultimately went with metronomics (with Cytoxan) - he had so many mets we were confronted with trying to find a balance with slowing the mets he had and using meds that were most tolerable if he only had a little time left. It unfortunately didn't slow things down so we took him off (7 weeks ago) and only have him on arteminisin, K9 immunity and fish oil. We did just also add Prednisone about 3 weeks ago. Sam also has a cough and at times he does cough blood. We decided to start the prednisone hoping if he was breathing easier then he would cough less. The cough medicine our oncologist will prescribe is a narcotic and the side effects are sleepiness. Sam still has really good energy so we want to wait to use that for when he appears in distress - for now, he's still calm and can figure out how to slow himself down when he's coughing. So sorry you're dealing with this....I know how stressful it is! Hang in there. Xoxo sue and Sammy

14
9 November 2011 - 5:10 pm
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I'm curious what exactly you mean by "metronomics " -- I feel silly for even asking.  I feel like I've become a slight expert with the terms and medications.  Capone has been good about slowing down when he does cough. At this point, he has coughed up a small amount of blood in his bile 2 times in the past two weeks. He is coughing multiple times each day and night.  So upsetting.  It sounds like we're getting the same cough medicine.  His oncologist said it would make him sleepy and should only be given at night.  I'm thinking I'll wait until the cough worsens but at least I'll have it on hand if needed.  We have Capone on fish oil 1 time each day, I end up putting it on his breakfast.  He takes Rimadyl 75 mg x2 a day. 

San Diego, CA
Member Since:
29 October 2010
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15
9 November 2011 - 5:44 pm
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Sorry to hear the palladia didn't work out for Capone.

Metronomics (sometimes you'll see people just write MP - metronomic protocol) is named for the metronome like in music - because you are dosing out a little bit of chemo every day (or every other) like a metronome. At-home chemo pills - like Palladia or Cytoxan - are "MP".

I don't have any experience w/ kinavet so can't help there.

We are having new xrays done this week. If Abby's mets have gotten worse with her current routine (mainly cytoxan & artemisinin ) then we are going to try masitinib, which is supposed to be similar to palladia - but according to our onc. he's seen dogs that didn't do well on palladia do fine on masitinib (and vice versa). So the masitinib might be another thing to consider??

Hang in there! Hope sweet Capone is still a happy boy, even while dealing with all this! Give him some extra loving from us!
Jackie, Abby's mom

Abby: Aug 1, 2009 – Jan 10, 2012. Our beautiful rescue pup lived LARGE with osteosarcoma for 15 months – half her way-too-short life. I think our "halflistic" approach (mixing traditional meds + supplements) helped her thrive. (PM me for details. I'm happy to help.) She had lung mets for over a year. They took her from us in the end, but they cannot take her spirit! She will live forever in our hearts. She loved the beach and giving kisses and going to In-N-Out for a Flying Dutchman. Tripawds blog, and a more detailed blog here. Please also check out my novel, What the Dog Ate. Now also in paperback! Purchase it at Amazon via Tripawds and help support Tripawds!

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