Have you had a recurrence after Herceptin or are you still NED?
Comments
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Hi Sassa,
Seems you and I have similar situations, my DX was 1.6cm and HER2+++ though. I was wondering about the CT/PET, I finished my Herceptin almost a year ago, but my Onc has not ordered me to do a CT/PET, is this standard. So far, I have only been asked to do markers and Mammi and Ultrasound.
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I know HER2 has a lot of bad press and can be a pretty scary diagnosis. However, I know a lot of women on the boards with survival beyond five years. As an encouragement, I've been NED for about 7 years. Had CMF and late Herceptin for only 9 weeks for very early stage her2+ bc, which is not the standard best treatment that others have gotten.
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Shelloz,
I believe that the use of CT/PET scan is up to the individual oncologists. Some oncologists don't believe they serve any purpose as statistics supposedly show that outcome is the same when recurrence is diagnosed when the patient presents with symptoms as opposed to picking up a problem via CT/PET scan before any symptoms occur.
I have had bilateral mastectomies so I do not do mammograms any more. Three months after I finished my herceptin, my onc sent me in for a chest x-ray, did the standard blood work (including markers) and sent me in for a baseline CT/PET scan.
Unfortunately, the CT/PET scan found a hypermetabolic mass in my spleen which was eventually diagnosed to be a probable rare congenital splenic cyst. I was sent in for a CT/Pet scan three months later to make sure there was no change in the splenic lesion. (there wasn't). I now go every 4 months for the scan. I don't know if my frequency is entirely due to the BC, I know my onc is keeping an eye on my spleen as the only way we would ever have a definitive diagnosis on the lesion is if I had my spleen removed or at autopsy. I am not volunteering for either procedure
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I finished Herceptin Aug 2008. Every time I meet with onc I ask about PET/CT scan for follow-up and he says no. Only does the tumor markers, which he himself tells me are unreliable anyway. Doesn't talk to me about when I'm at highest risk for recurrence. Naysays any interest I have in HER2+ vaccine trials. I'm going for a 2nd opinion re: my follow-up care on the 28th.
I've been very happy with all my tx at the cancer center where I was first diagnosed until it comes to follow-up. I would like for my doctor to be a little more vigilant.
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Carolina, we are at our highest risk for recurrence the first two years after finishing chemo (not the herceptin, the stuff before the herceptin). Risks drop slightly the third year, by year five we are down to about zero percent risk.
I asked my onc if the year of herceptin affects when the first two years start (stretches the highest risk into the third year). She said no, even with herceptin, it is still the first two years after finishing chemo (in my case AC).
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Sassa,
I'm soooo glad you posted that. I was very confused as when the highest recurrence is AFTER chemo or AFTER Herceptin. I did AC as well. this is what your onc confirmed?
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Thanks, Sassa, esp. for the info that it is after chemo not after herceptin. I finished chemo in Nov. 2007, so I'm going into my second year. It's so scary. Why can't we have Herceptin booster infusions once a year or once every 6 months? My concern is the LENGTH of the residual benefit of Herceptin after it is stopped. Are there any studies on that? And I mean biological studies--looking at the cells to see if the receptors are still being blocked 6 mos, 12 mos, 18 mos down the road.I have about 3 weeks left in the eligibility window for the AE37 HER2+ vaccine trial. I'm not sure I can get all the paperwork together in time or figure out the travel logistics to go to the facility every month. I wish I had found out about it earlier, but one has to enter the trial within 6 months of finishing Herceptin, and that is Feb. 15 for me. Aye yi yi.
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I did a year of herceptin and finished in April 2006. I was diagnosed Oct of 2004 and am still fine as far as I know!
Heidi
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While our highest risk is the two years after chemo, my onc started the CT/PET scans after I finished the herceptin. She is making sure that if the herceptin was holding anything in check, that we find out asap during this second year.
Carolina, pharmacokinetic studies of herceptin found that herceptin has a long half life (a mean of 11 - 23 days) so it is possible to take around three months after the last dose for the circulating levels of herceptin to clear the body. However, while there may still be circulating level for those three months, the level is of decreasing effectiveness at blocking receptors.
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Sassa, again thank you for that information. It's not very encouraging in terms of protection after the end of Herceptin tx.Do you know where I might be able to read the studies? I have a 2nd opinion appt. with a new oncologist on 1/28 and would like to be well-informed about this issue. I'll also try to google it and see what I come up with.Thanks.
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Carolina,
When I read the studies, I was a reviewer at the Center for Drugs at FDA and the information was included in the investigational drug application (not available to the public).
The following links will give you information on the drug:
The package insert has clinical pharmacology in Section 12
http://www.gene.com/gene/products/information/pdf/herceptin-prescribing.pdf
The National Cancer Institute has a information page on trastuzumab (Herceptin). There are also links to the various studies done on the drug.
http://www.cancer.gov/cancertopics/druginfo/trastuzumab
The drug company also has a website for herceptin. If you go to the section for health professionals, you will find more technical information. The section also has a nice chart that shows how the risk of recurrence levels off after three years.
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Finished one year of Herceptin 05/08 and dx'd with brain mets 4 months later. Guess it didn't work for me
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I was dx'd a year ago (had my first mammo on my remaining breast and it was clear! Yay!) I'm on Herceptin until next April and so far so good.To any of my sisters who have had a recurrence - you are in my prayers always!
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Sassa, thank you for those links. Very helpful.EGAL, I am so sorry to hear of your experience. That sucks. Breast cancer sucks. I hope you are hanging in there and getting the best tx possible. You will be in my thoughts.Best,Carolina
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Hi Carolina,
My diagnosis is very similar to yours. Did you choose to do a ooph due to BRCA tests? I haven't had surgery yet, but I have also chose bilateral mast. Any side effects from the herceptin?
Thank you so much for your advice. I am so new at this...P.
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Hi pdlc, I'm sorry you are here, but I know you'll find lots of support and info--it's very overwhelming right after diagnosis.My BRCA2 came back with a variant of uncertain signifcance. It may turn out to be insignificant, but I do have a history of bc on my paternal side. The ovarian onc strongly recommended the ooph. I was 48 at diagnosis. I have a 4 yo dd, and I wasn't planning on more children. I was already in pregnancy- /nursing- /chemo-induced menopause, so as the onc. said, "it's a no-brainer." I may have neen more reluctant if I were younger and not ready to give up the option of more children.No side effects from the Herceptin. Are you having it with chemo? Herceptin has been shown to work synergystically with chemo for a better outcome.Good luck and keep us posted. You'll get through this. If you haven't already, read the thread entitled "Thumbs up from doctor" in this forum. It will help you feel better.Best, Carolina
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hi egal, sorry the herceptin failed you. What treatments did you initially receive? and have you tried tykerb? wishing well. Tina
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Hi all,
I was dx'ed 3/11/04 and was in the trial when the news broke about the good results. FInished Herceptin in November of 2005 following chemo and rads. NED and I are still tight.
Hugs, Janie
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Tina,
I initially had mastectomy on right breast with expander, 4 AC's, 4 Taxotere, 6 weeks rads, one year Herceptin and profilactic mastectomy with expander on left breast. Had saline impants on each and cancer side is SO uncomfortable. No one knows why! Last Herceptin was May of 2008 and on Sept. 30th, 2008 I was dx'd with brain mets. Had GAMMA Knife radiation October 6th and had an MRI on Dec. 6th. The large tumor (4 cm) has shrunk by nearly 1/2. Now have rib tenderness and pain in lower abdomen. Had rib x-ray, no cracks or breakage. I had scans in November 2008 of bones, abdomen, and lungs...they were clear. So onc doesn't think the rib and abdomen is cancer. I see him next week and we'll decide what to do next. IT does SUCK!!!
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egal, your right-it definatly does suck. It sounds that you are doing well. what's next for you? Will you go back on herceptin? I heard tykerb was able to cross the blood brain barrier, unlike herceptin. Is that an option for you? Love your kitty picture. Tina
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bump back up - Who has had a recurrence since completing a year of herceptin?
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Hi
Dx Jan 1999, so in 10th year. Stage IIIa, one year of Herceptin. NED.
Keep the faith.
-Gabrielle
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Gabrielle
How did you get Herceptin in 1999, or did you have it years after diagnoses? I am so happy for your 10 year NED what a true celebration?
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Sassa, I was told differently. I was told by the John's Hopkins Breast Center's "ask an expert" nurse that answers the website questions (Lillie Shockney) that the 2 years starts after active treatment and she said Herceptin is considered active treatment.
edit- I found the post and am reposting it here-
Dear Lillie, I just read in another post about starting the ''2 year time out countdown'' after the completion of herceptin. Can you give a little more detail why? I also was StageIII, and received chemo, rads, and 1 year herceptin, and have been counting my ''time out'' from my surgery. I will be 2 years out from surgery this Dec, but am only 6 months out from completing Herceptin. Thanks Lillie.
A:
Herceptin is still considered active treatment and for women with locally advanced disease, stage 3, it is usually recommended to start the counting after active treatment (excluding hormonal therapy) has been completed. LS
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What about the whole 9 weeks of Herceptin to be just as good as 52? * Still waiting for those results* but just an example
I respect Lilly and her expertise..BUT I don't know why a woman with locally advanced cancer time out from recurrence would be different than a woman with earlier breast cancer. If 2 woman have the same size tumor, grade 3 cancer, same chemo and are Her2 + BC..... but 1 woman has 4 lymph nodes involved the other had 2 lymph nodes....why are they any different?
I dunno.....it just seems "quaky" to me...
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I dunno either, lexislove. Lol
What does make sense to me is that while you are getting Herceptin, any bc cells are being held at bay (starved of their enzyme). By the end, you hope it knocked all the stray cells. I know I felt a "ohh, I'm not being protected anymore" after finishing Herceptin, but maybe it's state of mind. Now I'm just kind of confused.
Oh, I wasn't early stage but I am ned.
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Brenda,
That is the difference between you and I. I am Stage 1, so I was told by my onc here in Florida and the onc that gave me herceptin in Maryland when I visited my daughter (he is also affiliated with Hopkins), that for me, my two years started at the end of my AC chemo (no radiation), not at the end of my herceptin.
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Makes sense to me.
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Hi Her2+ Sisters: I finish Herceptin next Thursday. After that, my onc will schedule a PET/CT. It's his standard operating procedure with Her2+.
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