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Old 01-20-2012, 11:44 AM   #1
AlaskaAngel
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Question Explanations welcome

Can someone explain what the rationale is that is being used to hold up progress?

TEN years ago when I was diagnosed, it was possible to do comparison studies in other countries that showed the effectiveness of such treatment as ovarian ablation plus "X" drug, versus standard chemotherapy for early stage bc:


http://jncimonographs.oxfordjournals...001/30/67.full

and


http://jncimonographs.oxfordjournals...expansion.html

How long will it take for us to get a comparison of either ovarian ablation and trastuzumab alone (or possibly trastuzumab plus lapatinib) for premenopausal early stage bc patients, versus standard chemotherapy, in this country?

-AlaskaAngel
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Dx 2002 age 51
bc for granny, aunt, cousin, sister, mother.
ER+/PR+/HER2+++, grade 3
IDC 1.9 cm, some DCIS, Stage 1, Grade 3
Lumpectomy, CAFx6 (no blood boosters), IMRT rads, 1 3/4 yr tamoxifen
Rads necrosis
BRCA 1 & 2 negative
Trials: Early detection OVCA; 2004 low-dose testosterone for bc survivors
Diet: Primarily vegetarian organic; metformin (no diabetes), vitamin D3
Exercise: 7 days a week, 1 hr/day
No trastuzumab, no taxane, no AI
NED
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Old 01-20-2012, 02:26 PM   #2
Lani
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Re: Explanations welcome

That is because EVERYONE got chemo if their tumor was invasive in the US for years and years (still today!) as it was the standard of care and trials could only ADD treatments onto the standard of care or the doctors could be sued for denying patients "their best hope"
Europeans tried to determine with yearly St. Gallen qualification modifications which ER+ tumors benefited from chemo and ADDED chemo onto the basic standard of care and were unencumbered by malpractice suit considerations.

Endocrine therapy is also cheaper than chemo in general and European countries' national health services had trouble paying for chemos like taxanes and platinum agents.

It was difficult to get US oncologists to look seriously into the possibility that the ONLY benefit premenopausal ER+ patients might be getting from the chemo was the early menopause they were put into ( a result which could be arrived at much more simply)

THere are different cultural attitudes towards oophorectomy, GNRH injections as well as different women's willingness to suffer with symptoms of lack of estrogens...many things come into play.

And this does not even entertain entering into the realm of paranoia about manipulation by/influece of " big pharma"
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Old 01-22-2012, 01:32 PM   #3
tricia keegan
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Re: Explanations welcome

Lani,

Just to clarify, up to '05 when I was dx chemo was always given if a tumour was over 1cm or had nodes positive or was her2+, usually the gold standard of that time a/c followed by Taxol/herceptin same as the U.S!

Most Onc's in Ireland would never suggest an ooph but when I suggested it myself my onc agreed it was a good idea
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Tricia
Dx July '05 IDC 1.9cm Triple positive 3/9 nodes positive
A/C X 4 ..Taxol/Herceptin x 12 wks then herceptin 1 yr
Rads x 36 ..oophorectomy August '06
Currently taking Arimidex..
June 2011 osteopenia/ zometa x1 yearly- stopped Zometa 2015 as Dexa show normal bone density.
Stopped Arimidex July 2014- Restarted Arimidex 2015 for a further two years on the advice of my Onc.
2014 Normal Dexa scan
2018 Mammo all clear, still NED!
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Old 01-22-2012, 01:42 PM   #4
Adriana Mangus
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Re: Explanations welcome

Hi Angel,

What's a pink ribbon diet?

Love,

Adriana
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1994 - rt brst, .lump, underarm node dissection,chemo+rad 1.2 cms, Grade 3.
28 nodes neg
Er,Pr, Positive HER2 status unknown
2003- Recur to rt lung.July 16 ( B-Day!)
Her2+++ Er,Pr, Negative
2003 - Aug04--Navelbine + Herceptin
2004- 2007--
NED - Herceptin, only
2007 Feb-April Xeloda added to hereceptin
2007-May Back on Navelbine+Herceptin
2008-Feb-Mar 15 Ses Rad to Rt. Lung
2008- Oc 17 Add Tykerb to Herceptin
2009- June-- Discont Tykerb
2009 July 7--Current Taxol + Herceptin
2009 Dec--Discontinued treatment due to progression. Looking into cyberknife.
2010-Aug Accepted to TDM1, no SE, except liver count went up.
2010-2011 September got kicked out of the trial, due to a small spot found on lung.
2011- 2012 September thru early 2013 on Herceptin
2013- March Bone density shows small spot on 5th rib.
2013 - April 4th appt with onc. will post after discussing course of treatment.
2013-March-April Cyber knife to brain and radiation to rib. Chest --base line before chemo-CT-Scan stable for lung issue. CA2729 Normal.
2013 April Herceptin- TDMI
2013 Sept Herceptin + Perjeta . CA2729 within normal range. Brain and Pet scans October 31st. will post results.
2013 October Brain MRI- mixed response. Will see Onc/rad on Halloween.
2013 October/November Brain-MRI nothing new. Repeat MRI next year in May.

2013 December Continue Herceptin and Perjeta. Stable at the moment.
2014 February Brain MRI -clear!
2014 January Added Taxotere to Perjeta+Herceptin.
2014 March Stopped chemo-chest ct-scan next.

2014- March Scans shows tumor's larger, CA2729 higher. Discontinue Herceptin.
2014 April Perjeta+ Halaven
2014 April CA2729 went down 60 points after one cycle. Cough does not want to go away.
2014 June Continue on Perjeta + Halaven-- no more cough. Stable
2014 June Back on Herceptin + abraxane
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Old 01-22-2012, 11:23 PM   #5
Rich66
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Re: Explanations welcome

Not sure it matters which country a given study is done in so long as it is largely viewed to be valid and in a similar population. As long as the treatments are available/covered here at Dr. discretion.
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