Aphinity Trial Pertuzumab

Options
2456

Comments

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited September 2012

    Felt really good today - went to lunch with a friend, had a massage and felt pretty normal - yea!!! What sucks is knowing that next week at this time I won't :(

    I wish we all knew if we were getting Perjeta or not - it's just plain scary having cancer and then getting the bonus round with the Her2 thing - and not really understanding how the treatment we're getting being in the study will impact us long term.

    Who wanted to be in this club anyway?????? 

  • damiana9
    damiana9 Member Posts: 389
    edited September 2012

    I started my first treatment on Sept 5.  So far it seems to be going well.  While getting my infusion I felt sort of pissed because I didn't have any side effects during my Pertuzemab portion...Then I realized I didn't have any side effects during the Herceptin either, so who knows.  I really don't feel as bad as I thought I would, yet on saturday I felt like a zombie and I sure didn't want to think of feeling that bad for the next 5 months...At least we have good days too, right?

  • damiana9
    damiana9 Member Posts: 389
    edited September 2012

    Just had #2 yesterday. Feel pretty blah today. I had 1 day of big D last cycle, constipated the rest of the time, so who knows. My research nurse said she hasn't had anyone on the study with any noteable side effects. Guess we just cross our fingers!

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited September 2012
    Hi - I'm having #5 Tuesday - had another MUGA yesterday and felt whiny Yell and angry - I am tired of getting poked!!!!!!!!!!!!!!! Anyway - I wouldn't say I have diahrea but I'm not constipated either.  So who knows... I'm just really tired a lot more than before.  Sol can you believe you only have 2 to go? ll of a sudden it seems like things are going fast.  I cannot wait to get done with the chemo and onto radiation - oh boy! Are you all doing that too?
  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited September 2012

    Hi - I don't know about the Tamox - I'm thinking maybe July when we're all done with the Herceptin/P regimen. I am so tired lately - I'm wondering if it's all those lovely chemicals finally doing their thing on me. Have you thought about what happens next? What I mean is for months the treatment has been the primary focus and then once the chemos done there's the rad, but it seems like it'll be less of a big deal on our poor systems - it's all sureal - still. But emotionally I think I am doing better. I don't cry as much - just once in a while - anyway...I am so glad that you are doing OK. I think about you. Are you still working? That's amazing - I don't think I could.

    Take care-

    Marilyn 

  • damiana9
    damiana9 Member Posts: 389
    edited September 2012

    I wonder about how it will go when it's over also.  How closely we are watched and such.  That is one of the good things about being in a drug trial is that we WILL be watched more closely and by more people than the people not doing the trials- so hopefully it will be enough tests that we feel safe, yet not so many we are constantly overwhelmed by these demanding cancer doctors :(

    Finished #2 wednesday.  I feel pretty crappy now.  I have the racing heart thing too....

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited September 2012

    Interesting - I too have had the racing heart thing. I really notice it when I have a lot of salty stuff - the first time was when my friend was visiting and we ate out more than I normally do. I wish I knew if I was gettign Perjeta and I know you all do too. Is your hair gone? Mine went and now is coming back - the whites are the longest and I even had to shave my legs yesterday. I went to the acupuncturist and I think it really helped last time. Today I had a lot of energy - not so much yesterday - do you think it was the Muga? I will get the results probably Monday when I see The Oncologist. WHen I've tried to get him to tell me the likelihood of recurrence he never has said just basically that we're going after it like it was a big deal and it's not - easy for him to say.  I am going to this group and there's a young woman (34 I think) who has stage 4 and she has 3 kids - so scary. It is sooo good to have you to "talk" to.

    Write soon I hope....

    <3

    Marilyn

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    My chemo was cancelled yesterday because my white blood count was low - UGH! Then last night I fell over my dog. Dog is black. Room was dark. Hardwood floor. Double UGH!  I cried - not because I was hurt so much as it was EVERYTHING. I just want to get this over with. Question - how do basketball players fall on hardwood floors and just get up?

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    Actually dog (Oso) was VERY scared of me afterwards. I had to coax him over with treats - but now he is back to normal.

    I just reread my pathology report - and fund mixed (good/bad) info on line about prognosis. UGH. Iknow I shouldn't do this but the dr won't tell me ANYTHING. Oh BTW he will be gone for the next month+ so I am seeing other doctors. WOndering if I should just switch as I've only seen him about 2 times out of 5.  This will be chemo #5 on Tuesday - so I'm only one ahead of you. The may decrease the dosage which makes me nervous too. I want the WHOLE thing.  What do you think about changing doctors?

  • damiana9
    damiana9 Member Posts: 389
    edited October 2012

    everything on my pathology report was POOR prognosis.  ugh!  We have a better chance though because we are in this trial and we are watched very closely.  I do not see my onc every time either but the people I do see on those off days are on top of everything and still make me feel informed and taken care of.  I have no idea how difficult it would be to change doctors mid treatment.

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    Wow - I am having a BLUE day - I hate these - I know I am supposed to grab life by its' tail and live every moment - instead I feel like crawling up in a ball and crying - Just did a little of that and decided to see what was going on here. Doesn't it just suck? I think I will go and either paint or sew. I feel like I do need to make every moment count and then I get so tired... I think I either want someone to say yes this will get me or I am home free until a ripe old age where I'll pass in my sleep. I know this is impossible - but I want to have a direction. Maybe I need to make my own??? How do you handle your BLUE moments?

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    Sol- I have Kaiser too, and the study nurse made me appts with 2 different women drs - so I am taking that as she is steering me towards someone else.  When I asked her about it she said that she thought I had said I didn't like him. I told her that that wasn't it - exactly... I think he's nice - but I feel that he tries to be funny and light, and geez I have Flipin' cancer... hello???? And, yes, maybe it's not metastized Stage 20 (yes, I know there's no such thing) but to me it is VERY scary and I need attention. My son has Cererbral Palsy so I have been dealing with Kaiser docs on that for 20 years and so this ain't my first rodeo with doctors. I guess I need to put my money where my mouth is -so to speak.

  • Nurse76
    Nurse76 Member Posts: 15
    edited October 2012

    I just saw an oncologist today in Chicago who offered me the chance to participate in the Aphinity trial. They are obtaining my tissue samples to send to Italy to see if I am a good candidate. If I am, I will need to start treatment by November 9.

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    Yea! Nurse - then you can join our group too!

  • MaryClairewalsh
    MaryClairewalsh Member Posts: 3
    edited October 2012

    Hi i living in Ireland and saw your posts. Currently i seem to have most of the side effects just after one treatment.

    Nose bleeds

    Diarrhea

    metal taste in my mouth

    Heart palpitations

    hair loss- getting it shaved this saturday

    No nausea or problems with fatigue. Still working every day, second treatment tomorrow.

    Fingers crossed it will go better than first one as my heart hit over 220 and they had to stop treatment for 24hours.... long day that was.

  • damiana9
    damiana9 Member Posts: 389
    edited October 2012

    MaryClair- that's terrible!  Of all the things in life to have to make more long and drawn out- chemo is not one anyone would choose :( ick!  I hope your next treatment goes smoothly. 

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    Hi Mary Claire~ I am so sorry to hear about your problems with your first chemo :( not a great way to start.... but I will send you good thoughts that the next one will go better and that this was your body saying what the heck are you doing to me?

    My hair went pretty much after the 2nd chemo and is now sprouting! Its encouraging to see - like blossoms after the winter.

    I hope you will write us - we are a good group and I have found the compansionship incredibly helpful.

    Take care,

    Marilyn 

  • MaryClairewalsh
    MaryClairewalsh Member Posts: 3
    edited October 2012

    Hi Everyone, well thankfully 2nd round chemo went without a hitch, no heart problems this time... shaved my head on saturday its easier than scooping up piles of hair after me!! At work today, taste buds in tact which is great as its really hard to eat when everything was tasting like carboard!!

    I am in the lovely west of Ireland, very good medical center here so i am lucky. I hope everyone is doing well and i will keep in touch..

    Byee

    Mary Claire

  • damiana9
    damiana9 Member Posts: 389
    edited October 2012

    Getting ready for #3 tomorrow.  Then I will be half done!  Yipee!

  • damiana9
    damiana9 Member Posts: 389
    edited October 2012

    Soltantio- wooohoooo! 1 more for you!

    trying to make it through today- then I will be on the upswing again. 

  • damiana9
    damiana9 Member Posts: 389
    edited October 2012

    #3 has been much easier on me than 1 &2.  Right now I am dealing with mild acheyness and cardboard tongue. 

    Soltantio- do you actually HAVE hair to wash???   I have had lightheadedness when I have been too active- like yesterday after grocery shopping, I had my mom drive us home because I didn't feel like I could drive.  I have also had ear ringing...  as for the bathroom- you may have just gotten out of bed too quickly- that has happened to me often, without chemo- but the chemo probably just made it worse.

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited October 2012

    Hi ~ Sol, so sorry to hear about the dizziness and ear ringing - must have been scary :(

    Glad to hear that today is better.

    Damiana~ I'm a little ahead of Sol - my 6th chemo is scheduled for next week - and hopefully it'll happen. My 5th one ws delayed because my white blood cells hadn't recovered. So what Sol wrote about protein and excercise is important. I feel like I can eat anything and haven't gained weight. Also what's weird for me is that no matter what I eat I poo. Sorry if that's TMI but I find it interesting. I sure hope that's a sign I'm getting Perjeta. I hope we all are so that none of us have to deal with this again and can just go onto happily ever after.

    Take care everyone~

    M

  • Nurse76
    Nurse76 Member Posts: 15
    edited November 2012

    I finally found out that I was approved for the Aphinity Trial and started treatment two days ago. So far only side effects are rash on face and neck and headache. My chemo nurse feels that the symptoms could be related to the Decadron. Only other symptoms are mild abdominal cramps and fatigue. One chemo treatment down, 5 to go.... Waiting for the loss of hair bothers me more than anything else right now - kind of sounds vain, but it bothers me more than the surgery and reconstruction!

  • Nurse76
    Nurse76 Member Posts: 15
    edited November 2012

    Well the mild symptoms disappeared over the weekend - felt like I was hit by a truck! Mostly flu- like symptoms, no appetite, could't get warm, abdominal cramps, headache and body aches (could be from Neulasta). Yuck...

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited November 2012

    Hi - it sounds like the Neulasta to me too. Can you do Neupogen instead? It's 5 shots instead of one but I think the side effects weren't nearly as bad. And the onc. told me to take Claritin so I did a half hor before the shot and there were no side effects except low back on the 5th one.

    I am done with the chemo part and will start on just the Herceptin and study drug (hopefully it's the real deal) next week. It'll be interesting to see how that goes. I miss my hair sooo much - feel pretty good otherwise - tired but that is manageable. What are you taking for the nausea?

    I went to the radiologist yesterday and go on the 28th to get set up - tatoos (oh boy) and measurements. I really liked him he gave me ots of info so I feel relieved about the side effects which sounds like there aren't a whole lot and the info I got from the internet is old. 

    Take good care-

    Marilyn

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited November 2012

    So tomorrow I do the Herceptin/P drug thing - no more Taxo...(whatever it is) or carboplatin!!! I am wondering how I'll feel? I have my hopes up that it won't be a big deal anymore.... I will keep you posted.

    Hope you are all doing OK. Would love to hear from you guys that are doing the study to compare notes.

  • damiana9
    damiana9 Member Posts: 389
    edited November 2012

    CV- Yeah!  No more chemo!!! You will have to let us know how you feel after just the herceptin/pertuzemab.

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited November 2012

    Hi - So first thing they did was take some blood to go to Milan for the study. Really??? Don't they want fresh? I'd be more than happy to go - I'm considerate like that....

    It seemed like it took forever. I got there at 9:30 and between all the stuff including wait times I got out at 1:30. Right away I noticed a weird kind of sour taste and thick feeling at the back of my tongue. I felt abit nauseous too :( By the time I got home I took a Pepcid the study nurse recommended I take it as I've had some reflux pblms and she said that I don't want to end up with esphogul ( is that how you spell that?) cancer so take it! But that didn't fix the nausea so I took an ativan when I went to bed - slept really good and now that I'm up I'm feeling much better! So hopefully that was it. Also noticved my pee smelled weird - hope that's not TMI - but i relly hate that smell. That too was not as strong this morning.

    On that note - I hope you are all doing well. What are you doing for Thanksgiving?

    Marilyn

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited November 2012

    Yep I thought so too - but it was only a short time and I have felt perfectly fine since - so who knows. I will be interested to see how your goes. I go in for my rad set up Wed.

  • cvmarilyn
    cvmarilyn Member Posts: 179
    edited November 2012

    Hadn't thought of that Soltiano - could be - I guess check with your nurse. Hope it goes well for you - please let us know.

    Hope everyoe else is doing well - it would be really great to hear how others on the study are fairing.

Categories