Matic, Zometa for your mom?

Gitane
Gitane Member Posts: 1,885

Hi Matic,

You mentioned that you were waiting for the St. Gallen's meeting in March to make the decision about Zometa for your mom.  What did you find out?

Hope you are checking in with us from time to time.  We'd love to hear from you.  

Comments

  • matic22
    matic22 Member Posts: 132
    edited May 2009

    Hi dear Gitane!

    It is strange but I have decided to check these sites today and I see your headline, so I am very happy to see you are doing fine.Well as far as Zometa is concerned i asked one oncologist about Mum, and she said if mum has osteopenia (which she has!) , she would give her Zometa 2 a year.So, I have not decided yet if that would be good , because in some ways I would not mess up her body with more and more drugs, because she is all right.She is on Aromasin and doing fine, and I believe we are going to continue with it for more than 2 years, maybe later on switch to Femara, but for now this is a drug of choice.

    I will think about that and I will tell you my decision.

    How are you all ladies doing?

    I have been working a lot with women with breast cancer and am enjoying it.

    Kind regards from Slovenia!:)))It is quite hot here...

  • Gitane
    Gitane Member Posts: 1,885
    edited May 2009

    Matic,  Thank you for posting. I understand that you might hesitate to add a medication when your mother is stable and healthy. We, of course, appreciate it very much when you come here to share your experience and knowledge with us.  Best of luck to you and good health to your mother.   G.

  • nash
    nash Member Posts: 2,600
    edited May 2009

    Yes, thanks for posting, Matic. Glad your mom is doing well.

    Wanted to add that my new onc (I switched followup care in January of this year) started me on Zometa, which I'll get every six months for 3 years (assuming the insurance will pay for it). The insurance picked up the first infusion, and I'm waiting to hear on approval for the infusion I'm supposed to have in June. I don't have osteopenia, so my onc is using it off-label for me.

  • hlya
    hlya Member Posts: 484
    edited May 2009

    I heard Zometa was for bone mets patients and now the early stage patients can only get it twice a year.  But the drug company is applying for approval to get this under doctor's prescribed drugs.

    Nash, are you on tamoxifen now?  Is it working well on you?  Did you get ovaries removed or not? 

  • nosurrender
    nosurrender Member Posts: 2,019
    edited May 2009

    Me too!

    I am on Femara and twice yearly Zometa....

    I feel good having the extra protection!

    Hello to all my fellow IL pals and our dear Matic!

  • nash
    nash Member Posts: 2,600
    edited May 2009

    Lucky, I am on Tamoxifen. I started it 14 months ago. I'm taking a little break from it right now b/c of the side effects--I've read it's OK to go off of it for a few weeks. Still have my ovaries and plan to hang on to them for awhile.

    Don't know if the Tamoxifen is working or not, and I have been reading article lately about how some ILC seems to be Tamoxifen resistant due to the number of estrogen gamma receptors ILC tends to have. IDC has more alpha receptors, which is what Tamoxifen targets. But then I wonder if my pleomorphic ILC, which is supposed to act more like a high grade IDC, falls into the category of having more gamma receptors or not.

    I'm glad to hear that the drug company is applying to get approval for Zometa for early stagers--that's where I am with it right now, and it will be interesting to see if my insurance covers my second dose. My onc said they usually cover the first one b/c they think the patient is metastatic, but when they figure out it's being given every six months, then they tend to balk on covering it since it's off-label in that setting.

  • hlya
    hlya Member Posts: 484
    edited June 2009

    Nash!

    I heard chemo doesn't work for ILC, now Tamoxifen doesn't work for ILC either, then what works for us???



    nosurrender:

    What's the difference between Femara and Zometa? Is Femara for postmeno women or premeno?

  • LizM
    LizM Member Posts: 963
    edited June 2009

    I am thinking about asking my oncologist about Zometa at my six month follow-up this month.  I have been on Arimidex/Femara for almost 3 years.  My bone density scan two years ago showed osteopenia and I have been on Fosomax.  Wating for my test results to discuss with Oncologist.  If no improvement, I am going to ask for Zometa. 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2009

    This is an interesting article about the negative issues pertaining to Tamoxifen:

    http://www.all-natural.com/tamox.html 

    I have an appt in August with a Dr who specializes in natural alternative hormonal meds. I3C and DIM are two that I will be considering in place of Tamoxifen.

    matic - Hi!

  • nash
    nash Member Posts: 2,600
    edited June 2009

    LuckyA, there are several women on the boards who had neoadjuvant chemo work very well on their ILC, so we've got evidence here in our little group that chemo can work. And I wouldn't say that Tamoxifen doesn't work for ILC--it's just that I read several research papers that questioned its efficacy due to the gamma receptor issue. But who knows what other issues comes into play.

    I think it comes down to the fact that there is no drug that works for all women (either ILC or IDC) all the time, and that's the problem with treating cancer in general.

  • nash
    nash Member Posts: 2,600
    edited June 2009

    Laura, keep us posted on what the naturopath has to say--I'd be interested.

  • hlya
    hlya Member Posts: 484
    edited June 2009

    Hi, Nash or any other ladies,



    Could anybody explain what gamma receptor mean? I read a post before but didn't get it...and can't find that post anymore. Or a link would help. thanks.

  • nash
    nash Member Posts: 2,600
    edited June 2009

    Lucky, here's a link to info on Tamoxifen/ILC/gamma receptors that is from this site:

    http://www.breastcancer.org/treatment/hormonal/new_research/20081030b.jsp

  • lemont
    lemont Member Posts: 31
    edited June 2009

    I'm an early-stager who gets Zometa twice a year. I'm treated at an NCCN institution so they are usually cutting-edge. I've heard from two sources that at some point Zometa will become standard care for most bc patients. The reason is that recent studies have shown it reduces recurrence rates. They don't know why. It was not intended for that purpose. It's in the same "family" of drugs as Boniva, to help prevent and restore bone loss.

    Reclast and Zometa are exactly the same drug. They call it Reclast when it's given to non-bc patients for osteopenia or osteoporosis. They call it Zometa when it's given to bc patients. It has been used for bone metastasis for quite some time, but then it's given more often.

    Hope this helps,

    Cinda 

  • mreilley99
    mreilley99 Member Posts: 149
    edited June 2009

    hi matic, and everyone! i fortunately did need tochecktheboardsbut since my bone scan last weeki amonce againliving on here! uptake was found on my right rib (orginal cancer side of breast)  and uptake in my skull along uppercheek bone and towrds right ear. i am gettinga cat and mri this week. my symptoms are a focal pain between my r temple and r ear. bout the size of a quater.itisvery specificpain,pressure, little bitof numbness,no vision changes just a feeling of pressure if i try to lay onmyright side, pain is worse at night.no vomiting or nasea , just pain which can ast times be severve and others a dull throb. ihave eliminated theusual- sinus infection,isssues fromTMJ and normalheadaches.i have been having this pain since january. any others with single mets to skull, rib fracture ?? thanks for allyourhelp.

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