Bone Pain fr Herceptin
 

Hello. Just found this site. So glad I did.

I am experiencing some pretty bad bone pain. Started Herceptin in June. Had already completed chemo in Feb.

Doc says it's probably from Arimidex...not Herceptin but I was on Arimidex for 3 months and had no bone pain until I started Herceptin.

Any and all comments and replies appreciated.

UPDATE: Forgive me I'm just learning how to use these message boards (used to chat rooms) and not sure how to answer what.

I thank you all for your input. Although I wouldn't wish this on anyone, it is somewhat comforting to know others are experiencing same effects. Appreciate the input from everyone.

I also would like to see if any have had this problem as well.

I am having some bone pain as well, my Onc did say it could be the Herceptin, I have been taking Herceptin weekly since the end of August.


Vicki

I started herceptin in June '05. I've been having increased joint pain, hands , feet, knees sometimes elbows and hips. I was blaming it on Taxol or post chemo arthritis if there is such a thing. My onc. has offered no opinion as to etiology other than to order an EMG for possible neuropathy which was negative.
It's a big question still ...
Carol

Ditto...
 

though mine isn't really pain, but aches along my lower back. They didn't start until I started doing some new stomach exercises.

Hi Vicki
 

Thanks for your reply. Are you taking Arimidex or any other hormone therapy as well as the Herceptin or Herceptin only?

Gina

Gina
 

<<<<

Thanks for your reply. Are you taking Arimidex or any other hormone therapy as well as the Herceptin or Herceptin only?

Gina>>>>


Gina, No I am not taking any Arimidex or any hormone theraphy as I am ER/PR Negative.

I am taking just the Herceptin only. I had dose dense 4AC, followed by dose dense 4 Abraxane, started Herceptin the next week after Chemo was finished.

Bone Pain fr Herceptin
 

I have been on weekly Herceptin since August 2004 w/o associated bone pain. Only bone pain I've experienced during all of my treatments (4 rounds AC, 6 mos of wkly [3 wks on/1 wk off] Navelbine, 63 treatments of Herceptin, 1 dose Zometa, 2 doses Aridia) occurred after taking the Zometa that had many horrible side effects including widespread bone pain, continuous fever, etc. I have also had localized bone pain on my sternum due to tumors on it. Hope this is helpful.

I have just started on herceptin-every 3 weeks-and arimidex. Within about 5 days of the first arimidex I started to experience pain in my hip. I already have osteoporosis so am aware of the bone thinning side effects of arimidex...my onc and I are at opposite ends of the spectrum on this. I cannot get in to see a bone specialist until mid-Jan. Don't know if the side effects of arimidex are going to be worth it. Wishing for the crystal ball...!!!

I started Arimidex in April 03. Have had on and off aches in the back since then. The "aches" sometimes feel more like a pain. It is most noticable in the ribs. Sometimes it is felt in the front ribs, and sometimes back.

I started Herceptin in May 05. The aches/pain are still in the rib area, but seem more pronounced since starting the Herceptin. For a while, it seemed the 5th day brought a more achy feeling (I take weekly Herceptin). But I had a treatment yesterday, and the aches have been quite noticeable today.

If it's bad enough, I take a Tylenol, and try not to worry. The Tylenol seems to help some.

About a year after starting the Arimidex, my onc and I were discussing bone aches and he commented that he thought the aches would go away after my body got used to the Arimidex, but that hasn't happened. Maybe he was just making an assumptin.

Blessings, Barbara

Hi All,

I check this site a few times a week and was relieved to read today that other women out there have bone pain on Herceptin. I am on weekly herceptin, and 3 out of 4 carboplatin and abraxane. Just got my 5th treatment in a 24 week regimen Tuesday and was so upset by back pain last night in bed that I hardly slept at all. Of course, every bit of pain equates to a met in my mind but the pain moves around sort of across the back of my rib cage. Had scans (PET, Bone and CAT) just 6 weeks ago showing two liver mets but no bone mets and my rational mind tells me it's not a progression but I feel ruled by my irrational emotions lately. Anyway, I will go take two tylenol and try to GET A GRIP.
This site is a constant source of comfort to me. Thank you all for your honesty and support.
Donna

I had the same thing, and the doctors told me no it was NOT the herceptin. But my study nurse told me that another lady who was on the study was recieving Herceptin and she stopped taking it, because she was convinced it was the Herceptin that was causing it. Her pain did stop after taking it. I however just took pain pills and when they stopped giving me those, I just indured it. There was no way I wasn't getting the only thing I had in my arsenal that I could take for HER2. That was just her, I don't know if it was or not. I was also on Carboplatin and Taxotere. I did the neuropathy studies and thank goodness, I had none. I am 2 years NED and with no pain now. It did take a while for it to stop. But if it was the Herceptin and I don't know that it was, I am NED because of it, I would do it all over again.

I know it stinks to be hurting and I have no answers for you, but I did see a great massage therapist who could get it to stop hurting for a while. Hang in there, maybe we will find out more on side effects on this next meeting that is coming up?

Thanks Kristen. Appreciate the information.

I am not considering stopping the herceptin. Like you I'm going for the gold and the herceptin is the only thing available to battle the her2. But my oncologist thinks it's strictly the Arimidex that's causing the pain and is talking about switching me to another drug. So I'm trying to find out if other women are experiencing bone pain with the herceptin too. Doesn't seem like the medical community is willing to concede that it may be the herceptin yet.

God Bless you in your battle!

Gina

Gina

I have been on Herceptin for 2 years, and I think the pain I have is from arthritis....I had it before the Herceptin. I do know that when they switched my Mom from Tamoxifen to Arimidex, she experienced awful joint pain...after 2 months they had to take her off it....she was miserable....
Side effects can be different on each of us...just wanted to let you know of her experience with the Arimidex....maybe if you switched to Tamoxifen with the Herceptin, the pain would go away, and you would know whether it was the Arimidex or the Herceptin.....Just a thought....Some people say Tamoxifen & Herceptin are not a good combo, but I have several friends who did great on the combo.

bone pain from Herceptin
 

I started getting some bone pain after my 2nd dose of Herceptin (1 dose every three weeks). I had completed dose dense ac and T at the end of June and started, Herceptin the beginning of July. My back pain started in August and now elbow pain in October. I have had a bone scan, to rule out any pathology and only just now, started Arimidex. So I cannot blame it on the AI. My doctor said it could be post taxol pain which is very common and can last up to, two years after treatment.

Karen

I have bone pain in my hips. I am only taking Herceptin and I have no history of arthritis . I thought it was from the taxol that I finished in Aug.
Laurie

I think the bone pain could be from the Arimidex. I was on Arimidex on and off for 18 months. I say 'off', as I had so much bone pain that it became intolerable so I had to have breaks from it. It seemed to accumulate in my system. Yet, I know others who are on Arimidex and have little trouble with it. I have also been on Herceptin for 2 years now and have no problems with it, other than extreme tiredness half way through my day.

Hi all~
Just wanted to share my experience w/Herceptin & that awful whole-body-arthritis! I just had my 2nd dose of q3week Herceptin last week.I've been feeling so creaky & achy for the past 6 weeks-bones feel like they're just grinding on each other from the base of my neck to my sacrum, across my pelvis, even my feet-when stand up to walk after sitting for any length of time, it takes me a couple of steps before I'm up-right & my feet & ankles snap,crackle & pop!
It just occured to me today the reason...that triple dose of Herceptin! I experienced this same thing 2 yrs ago-after 49 weeks of weekly Herceptin+chemo, I was NED! I was so excited that I would be on Herceptin q3weeks & not every single week. After my first triple dose, I experienced flu-like symps for ~24 hrs & then the achy,creaky, arthritic feeling settled in.Tylenol didn't really help, hot baths, massage, stretching, nothing! After feeling this way for ~2 1/2 weeks, the achiness subsided...just in time for my next triple dose!
I teach Pilates full time & feeling the way I was feeling made it virtually impossible for me to teach. I remember lying on the floor, prone, setting up an exercise & I could barely lift my head my neck & shoulders hurt so badly!Additionally, I got these little bumps all over my torso. Ultimately, I had to go back to the weekly dosing b/c I was miserable. I decided I'd rather go in for treatment once a week & feel good, than have the "freedom" of the q3week regimen & feel crappy for 2 1/2 weeks!
After my recurrence last September ('04), my Herceptin+chemo treatments were again weekly. Since NED again (YEAH!) 8 weeks ago, we dropped the chemo & switched to the q3week Herceptin. Since I've been on q3week Herceptin, I've got those little bumps again AND awful achiness. I feel like some one stuck me in a little box & shipped me across the ocean!
I'm going to call my doc on Monday to talk about changing my dosing schedule. I really do like the freedom of the q3week dosing, but I can't handle the physical discomfort! Maybe I'll see if things are better on the q2week dosing...I'll keep you posted!

Dear Jessica and others,

Do you think that if the infusion time was lengthened the side effects would be less? When I was treated at Cancer Treatment Centers of America they used what is called "fractunated dose chemotherepy" where they divided a powerful dose of drugs into smaller doses over several days. This approach supposedly exposes the cancer cells for a longer period of time to maximize their efficacy, while reducing unpleasant side effects experienced with larger doses. While I did not have chemo there, I knew many who had with positive results. I know most hospitals probably won't infuse patients over several days, but they can increase the drip time and make some difference.

I too have been having bone pain that I was blaming entirely on the compression fracture in my back. I'm kind of thinking that it might be the herceptin and the combination of other drugs I'm on.

Blessings, Lu Ann.

No Evidence of Disease
 

I wondered myself when I first came on board.

Blessings, Lu Ann.

Thanks
 

And please do keep us posted.

Take care.

Gina