HonCode

Go Back   HER2 Support Group Forums > her2group
Register Gallery FAQ Members List Calendar Today's Posts

Reply
 
Thread Tools Display Modes
Old 04-05-2007, 05:21 PM   #1
cafe1084
Senior Member
 
Join Date: Nov 2006
Location: West Virginia
Posts: 105
Tamoxifen: Yes or No?

I have 3 weeks before I finish taxol and see the doc again. Still trying to decide about taking tamoxifen. Researching and reading Becky's posts regarding it, I m leaning toward NO, but would like to know from those of you taking it, how you are doing with it and from those of you not taking it, did you decide not to and why? I truly respect the knowledge and opinions of the women here and just need information. I have to make a decision and it has to be one I can comfortably live with- the doc has presented no further options to me and I want to know my options and I want to present an educated argument in case he doesn't want to listen.

Thanks in advance!
Steph C
cafe1084 is offline   Reply With Quote
Old 04-05-2007, 06:11 PM   #2
Andi
Senior Member
 
Join Date: Mar 2006
Location: IOWA
Posts: 243
I would recommend you follow Becky's advice and try to go the AI route if possible. I had just stopped my periods about a month before my diagnosis, so figured I would be menopausal before too long and would make the switch. I took tamoxifen for 1 year and finally tested so that I could change to Femara, but then had my recurrence. I will never know whether or not it would have made a difference for me if I would have gone the other route with things. I normally like to go the direction that if something happens, I won't have to second guess my decisions, kind of the "rather be safe than sorry" approach. As far as how I tolerated the tamoxifen, I really didn't have any problems with it while I was taking it. Best of luck to you in making your decision.
__________________
Andi
-- ------------------------
Stage IIIC, 17 of 20 Nodes +, E+, Her2+++
Diagnosed 6/30/05
Lumpectomy 7/13/05
Dose Dense A/C x 4
Weekly Taxol + Herceptin x 12
Remainder of year Herceptin Every 3 weeks (completes 9/13/06)
Radiation completed 2/28/06
Currently on Tamoxifen
Dec 06 - Pleural effusion treated with pleurodesis
Now er/pr-, her2++
1/07 started weekly Navelbine plus Herceptin
Discontinued Tamoxifen
4/27/07 CTshowed progression
5/01/07 Began Tykerb/Xeloda + Zometa
5/22/07 Stopped treatment due to great progression
Andi is offline   Reply With Quote
Old 04-06-2007, 08:59 AM   #3
Stephanie B.
Senior Member
 
Stephanie B.'s Avatar
 
Join Date: Nov 2006
Location: Bakersfield, CA
Posts: 66
The only problem I had while on Tamoxifen was weight gain and occasional hot flashes but after being on for 7 months my doctor took me off because I had a recurrance so it obviously wasn't working for me.

Stephanie
Stephanie B. is offline   Reply With Quote
Old 04-06-2007, 09:26 AM   #4
Becky
Senior Member
 
Becky's Avatar
 
Join Date: Sep 2005
Location: Stockton, NJ
Posts: 4,179
Dear Steph C

I looked at your profile so I could give additional advice but it does not list how ER or PR positive you are (for example, I am 50%ER but PR neg). Are you strongly ER+ and PR+ (I am considered moderately ER+). Anyway, it makes a difference (somewhat). Also, how long will you be on Herceptin therapy (when does it end for you). This way, I can tell you about some studies etc that can help you with questions for your oncologist.

Have a great day
__________________
Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
Becky is offline   Reply With Quote
Old 04-08-2007, 09:36 AM   #5
cafe1084
Senior Member
 
Join Date: Nov 2006
Location: West Virginia
Posts: 105
Becky,

I am ER<10% and PR-. This is why I am having such a difficult time deciding my course of action. If I were mod to high er/pr+, it may make it easier for me to decide....who knows?! Ill be on herceptin til next April.
cafe1084 is offline   Reply With Quote
Old 04-08-2007, 02:17 PM   #6
panicked911
Senior Member
 
Join Date: Oct 2005
Posts: 115
Hi:
My oncologist at a major Ny medical cancer center said no way to tamoxifen during the first 5 years or new studies are doen that revela something radically different. i am highly er nd pr positive as well as her2 positive. At age 43 - I was close enough to menapaus to be thrusted into it with lupron so i could take the AI's.
All three oncs I saw said the same thing - cuting edge reaesrch shows AI's more effective for triple positives than tamoxifen alone. The only factor that would alter this way of thiking is age. If you are in your mid 30's or younger - the docs are extremely reluctant to put you into menapaus because of unrelated issues. For her2 cancers the greatest chnace of a relapse is within the first two years, followed by 5 years. It can come back at any time but these two bench marks seem to be the biggies -

hope this helps

Susanne
panicked911 is offline   Reply With Quote
Old 04-08-2007, 08:09 PM   #7
Bev
Senior Member
 
Join Date: Dec 2005
Location: Alexandria, VA
Posts: 1,055
Steph C. I'm not the greatest scientific source. As a triple positive, I feel that tamox can work for a year or two while you wait and see if you're post menopausal. I've looked at studies and I just don't see a big difference for triple positive in the first couple of years for AI v Tamox.

If you don't want to do either AI or Tamox, well I hope you tested under 5% positive. If not you have to do one or the other. Try the search tool in the purple bar above to learn more about previous AI/Tamox discussions.

Actually doing Tamox for over a year, resulted in only hot flashes.

I will be switching to an AI shortly. I am worried about the bone loss though. Have seen what it can do once you get older.

Keep on researching your options. Good Luck. BB
Bev is offline   Reply With Quote
Old 04-09-2007, 07:03 AM   #8
dlaxague
Senior Member
 
Join Date: May 2006
Posts: 221
pathology consult

Hi Steph,

I don't know where you have your treatment, but have you thought about sending your slides and blocks for a second opinion pathology on the ERPR? I sent mine to Baylor, and wished I'd done it sooner. The first report was ER 5% and PR 0%, so I allowed my onc to browbeat me into taking Arimidex for two years. Then that onc left and the new one said no Arimidex. I was in a quandary and that's when I decided to re-do the pathology. When I did the second opinion at Baylor, it came back completely negative for both. Allred at Baylor has some studies to show that it's usually the other way around - when done at an expert lab, there's more positivity, not less. But regardless, this is an important decision and you want to base it on accurate information.

Another piece of information to add to the mix is that it appears that Elizabeth Edwards' primary cancer had a very low level of ER positivity and she did not do hormonal therapy. Many oncs recommend hormonal therapy for anything more than 1% positive, and you have to wonder if it would have made a difference for Elizabeth Edwards, now having a more ER+ recurrence.

It's easy to send your slides, whether you do it yourself or have the local pathology dept. do it for you. I sent my own - let me know if you need details.

Debbie Laxague
dlaxague is offline   Reply With Quote
Old 04-09-2007, 11:37 AM   #9
Rupali
Senior Member
 
Join Date: Dec 2005
Posts: 148
Hi all,
I have been also really confused about ths topic. I was 10% ER+ and 10% PR+. I am finishing 2 years of Tamoxifen and almost a year of Zoladex. I have been always debating that when I am just 10% ER and PR positive then do I need these extra drugs and is shutting down the ovaries the best thing to do as I think it is no letting the body come back to its natural self.
My doctor is a leader in hormonal treatments and is leading lot of researchs at harvard. He said the best combination in my case would be to stay on Tamoxifen for 2 years and then move to AI for at least 3 more years together with zoladex.
I am 31 years old and dont know if my age has anything to do with this protocol.
Please comment.
Regards,
Rupali
Rupali is offline   Reply With Quote
Old 04-09-2007, 05:14 PM   #10
Becky
Senior Member
 
Becky's Avatar
 
Join Date: Sep 2005
Location: Stockton, NJ
Posts: 4,179
Dear Steph


It is such a hard call as less than 10% (in many references) is called negative. Perhaps you should have your slides read elsewhere. For example, less than 10% could be the lowest reading on that criteria at the lab it was done.

For example, 9 is less than 10 and 1 or 0 is also less than 10 but if less than 10 - is it 0 in your case?

In almost ALL cases less than 5% is negative (which is the reading for my PR and my onc considers this negative because it is the lowest reading at the pathology lab where my slides were first sent to). I sent them to Sloane Kettering for a re-read and got PR negative status of less than 1% (since I suppose that is their lowest reading)

Tamoxifen tends to not work well if you are Her2+ in general and works even less so if you are not highly ER and PR positive.
__________________
Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
Becky is offline   Reply With Quote
Old 04-09-2007, 06:13 PM   #11
Rupali
Senior Member
 
Join Date: Dec 2005
Posts: 148
One thing which was very funny in my case was that when they did needle biopsy and came back with path report then they said I was 80% ER+ and PR + and this was done at a local hospital.

But the result of matectomy path report said 10% ER+ PR+ and strobgly Her2+++. So I guess just to play a safe game they put me on Tamoxifen and zoladex for 2 years and then to move onto AI and zoladex.

Dont know if this was the best approach or not. I now feel that it might be a good idea to send my slides to SLoan and get a 2nd opinion. What do u think.
Rupali is offline   Reply With Quote
Old 04-09-2007, 07:59 PM   #12
Becky
Senior Member
 
Becky's Avatar
 
Join Date: Sep 2005
Location: Stockton, NJ
Posts: 4,179
My first pathology was done at a community hospital so I didn't feel comfortable without a big cancer center's assessment since they do tens of thousands of these every year. In many cases, (like grade of cancer), the tests are subjective and done by a human being's opinion. Therefore, you want someone who's seen thousands of slides because then that person's opinion is not subjective anymore but becomes more objective. My cancer was downgraded to Grade 2 (and reconfirmed by Johns Hopkins) and I feel very comfortable with this versus the community hospital.


If yours was done at a big cancer center, you should feel comfortable BUT - you did get 2 very conflicting reports. Which one is right? What if you couldn't tolerate antihormonals? With the 10% ER and PR - it wouldn't be so dangerous to not take something but at 80% - you better try to tolerate any and all side effects (I think you get what I mean). So - maybe a tie breaking opinion is what you need.

I hope this helps.
__________________
Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
Becky is offline   Reply With Quote
Old 04-10-2007, 12:42 AM   #13
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
A little off subject, but maybe still relevant, but has anyone else heard the theory or read research that suggests that having been on Herceptin might make Her2 patients more treatable with Tamoxifen later on?
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 04-12-2007, 08:54 AM   #14
saleboat
Senior Member
 
saleboat's Avatar
 
Join Date: Sep 2005
Location: NYC
Posts: 250
I went to three Oncs regarding the anti-hormonal decision. I am not menopausal and all three Oncs recommended Tamox. I think my age was a big factor in the decision-- absent the decision to do an ooph, I don't think the shots would be a sure thing to make me menopausal.

Given that I was strongly both ER+ and PR+ the decision to do Tamox was an easier one-- the AIs are only slightly better than Tamox in this situation, and the risks of an early menopause are not ones that I want to take-- bone issues, heart issues, etc.

Jen
__________________
dx 4/05 @ 34 y.o.
Stage IIIC, ER+ (90%)/PR+ (95%)/HER2+ (IHC 3+)
lumpectomy-- 2.5 cm 15+/37 nodes
(IVF in between surgery and chemo)
tx dd A/C, followed by dd Taxol & Herceptin
30 rads (or was it 35?)
Finished Herceptin on 7/24/06
Tamox
livingcured.blogspot.com

"Keep your face to the sunshine and you cannot see the shadow." -- Helen Keller
saleboat is offline   Reply With Quote
Old 04-12-2007, 06:33 PM   #15
Debra
Senior Member
 
Join Date: Dec 2006
Posts: 136
I am 41-diagnosed at 40. Was 19% ER+ and 20% PR+. I had a total hysterectomy in December and I am still on tamoxifin. I too am confused if I should be. Both my oncologists recommend to stay on tamoxifin for a total of one year for sure if not two, then switch to an AI. I feel like I should switch having had the hyst. but am quite confused as well.

I am also concerned about bone loss etc. Tamoxifin actually helps your bones whereas AI's decrease bone density from what I am told. I do believe age plays a big factor. I don't have any estrogen anymore anyways so I am already taking that risk so I think I should be on an AI. I would guess tamoxifin is what your docs are leaning towards due to your age. The difficult part is all the studies don't take everything into consideration that we do!
__________________
Debra

Diag. 11/05 at age 40 triple positive
3.8 cm tumor and 9 mm tumor
Stage IIb/SN positive(no other nodes)Grade 3
Bilat. mastect. 12/05 (Rt.prophylactic) followed with AC/taxol/Herceptin/tamoxifen then switched to arimidex after hysterectomy in 12/06. August 07 switched to Aromasin due to severe jt. pain from Arimidex. Nov. 2011 No more meds and NED!
Debra is offline   Reply With Quote
Old 04-12-2007, 06:53 PM   #16
Jackie
Senior Member
 
Jackie's Avatar
 
Join Date: Mar 2006
Location: (Hill Country) Texas
Posts: 72
Cool

I am 48 and on Tamoxifen. I was pre-menopause before chemo. I feel like I and post menopause now. Haven't had hormone tests to confirm, but no periods for 21 months. I asked my onc about switching to AI and he said he wanted me to stay on Tamoxifen for 2 years then switch to AI. I'm sure bone loss is a concern since I am osteopenia in my hips already (was a year ago after completing chemo) and AIs don't protect that like Tamoxifen.
__________________
Jackie
Stage II, Grade 2, DX 4-05
EP +, HER2 +++,
1 node+, 1.6cm
46 yrs. old at time of dx.
Completed Chemo 11-05
Completed 1 yr. Herceptin 8-06
Jackie is offline   Reply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


All times are GMT -7. The time now is 03:47 PM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2024, vBulletin Solutions, Inc.
Copyright HER2 Support Group 2007 - 2021
free webpage hit counter