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Old 03-12-2015, 08:47 AM   #18
Mtngrl
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Join Date: May 2011
Location: Denver, CO
Posts: 1,427
Re: early Christmas present--10 yr overall & bc specific survival results just publis

This is an interesting and informative discussion. Thanks to all.

I'd like to point out that early detection of breast cancer does not actually improve overall survival. I know that goes against common sense, but it's a fact. The small drop in death rates from breast cancer in recent years is from better treatments, not from "catching it early." In less-developed countries, breast cancer is a leading cause of death. I suspect that the disparity is not so much due to the lack of mammograms as to the weakness in the health care systems in general (not to mention misogyny/undervaluing girls and women.)

Alaska Angel rightly questions the reflexive, blanket use of a drug that is never effective for some patients (for example, our beloved, dear departed Mandamoo) and becomes ineffective for many others. She says the money spent on that one-size-fits-all approach might be better spent otherwise. That goes double (at least!) for routine mammography. Billions are spent on it, yet there is no demonstrable benefit. There is also no evidence that routine breast self exams save lives.

Mammography, ultrasound, and MRI are necessary and essential for diagnosis of symptoms that might indicate that a person has breast cancer. That is a very different proposition from "let's screen everyone whether they're symptomatic or not." The main outcome of early detection is the opportunity to boast of five-year survival rates that look pretty great. Yet overall survival hasn't budged much. If you find it early you just have more years of knowing you have cancer, and being a cancer patient (and, hopefully, getting to NED and staying there.)

We are, indeed, lucky to have Herceptin and other targeted treatments for HER-2+ breast cancer. But don't fall too far down the "early detection" hole. After all, finding it "early" still means you have cancer. Chrissy was first diagnosed and treated at Stage 0. Yet her cancer metastasized, and she died. It happens.

Alaska Angel makes a great point about Herceptin that can be applied to all current cancer treatment protocols. There is no way to know if a particular person was "saved" by her specific cancer treatment. If she's alive, it's not unreasonable to assume the slash/burn/poison worked. But some cancers are slow-growing and indolent, and never become deadly. A good example is prostate cancer. Virtually all men who live into their 90s have prostate cancer, yet most of them die "with" it and not "of" it. That's true of some breast cancers. (Not HER-2+, but some other types.) Some are deadly no matter what, some are curable, and some never become deadly. We don't have a great way to tell which is which.

Substantially more research and attention should be going into preventing or curing metastatic cancer. That's what kills, and there's no known cure. All our expensive new treatments do appear to prolong survival for some people, but there's still no cure and, as the recent results published for Kadcyla, some brutally expensive new drugs are really no better than the old ones.

With cancer, an ounce of prevention is worth about a ton of cure. Lung cancer is virtually incurable. But lung cancer rates dropped substantially as smoking rates declined. Stomach cancer used to be widespread. With the advent of refrigeration and food preservatives, it's now very rare in developed countries. I'm very happy about the HPV vaccine, and hope it becomes ubiquitous.

Breast cancer doesn't seem to be caused by a specific virus. My money is on environmental pollutants and endocrine disruptors. The "vaccines" that are being studied train the body's immune system to go after the cancer cells in some way.

If we're going to spend billions of dollars on breast cancer, cleaning up toxic waste, developing clean energy, and finding safe alternatives to pesticides, herbicides, plastics, and other industrial chemicals (and ways to neutralize the ones we have dumped into the environment) appear to be better uses of the money. Increasing the budget of the NCI would be a fabulous place to start.
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Amy
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4/19/11 Diagnosed invasive ductal carcinoma in left breast; 2.3 cm tumor, 1 axillary lymph node, weakly ER+, HER2+++
4/29/11 CT scan shows suspicious lesions on liver and lungs
5/17/11 liver biopsy
5/24/11 liver met confirmed--Stage IV at diagnosis
5/27/11 Begin weekly Taxol & Herceptin for 3 months (standard of care at the time of my DX)
7/18/11 Switch to weekly Abraxane & Herceptin due to Taxol allergy
8/29/11 CT scan shows no new lesions & old lesions shrinking
9/27/11 Finish Abraxane. Start Herceptin every 3 weeks. Begin taking Arimidex
10/17/11--Brain MRI--No Brain mets
12/5/11 PET scan--Almost NED
5/15/12 PET scan shows progression-breast/chest/spine (one vertebra)
5/22/12 Stop taking Arimidex; stay on Herceptin
6/11/12 Started Tykerb and Herceptin on clinical trial (w/no chemo)
9/24/12 CT scan--No new mets. Everything stable.
3/11/13 CT Scan--two small new possible mets and odd looking area in left lung getting larger.
4/2/13--Biopsy of suspicious area in lower left lung. Mets to lung confirmed.
4/30/13 Begin Kadcyla/TDM-1
8/16/13 PET scan "mixed," with some areas of increased uptake, but also some definite improvement, so I'll stay on TDM-1/Kadcyla.
11/11/13 Finally get hormone receptor results from lung biopsy of 4/2/13. My cancer is no longer ER positive.
11/13/13 PET scan mixed results again. We're calling it "stable." Problems breathing on exertion.
2/18/14 PET scan shows a new lesion and newly active lymph node in chest, other progression. Bye bye TDM-1.
2/28/14 Begin Herceptin/Perjeta every 3 weeks.
6/8/14 PET "mixed," with no new lesions, and everything but lower lungs improving. My breathing is better.
8/18/14 PET "mixed" again. Upper lungs & one spine met stable, lower lungs less FDG avid, original tumor more avid, one lymph node in mediastinum more avid.
9/1/14 Begin taking Xeloda one week on, one week off. Will also stay on Herceptin and Perjeta every three weeks.
12/11/14 PET Scan--no new lesions, and everything looks better than it did.
3/20/15 PET Scan--no new lesions, but lower lung lesions larger and a bit more avid.
4/13/15 Increasing Xeloda dose to 10 days on, one week off.
7/1/15 Scan "mixed" again, but suggests continuing progression. Stop Xeloda. Substitute Abraxane every 3 weeks starting 7/13.
10/28/15 PET scan shows dramatic improvement everywhere. All lesions except lower lungs have resolved; lower lungs noticeably improved.
12/18/15 Last Abraxane. Continue on Herceptin and Perjeta alone beginning 1/8/16.
1/27/16 PET scan shows cancer is stable.
5/11/16 PET scan shows uptake in some areas that were resolved on the last two scans.
6/3/16 Begin Kadcyla and Tykerb combination
6/5 - 6/23 Horrible diarrhea from K&T together. Got pneumonia.
7/15/16 Begin Kadcyla only every 3 weeks.
9/6/16 Begin radiation therapy on right lung lesion that caused the pneumonia.
10/3/16 Last of 12 radiation treatments to right lung.
11/4/16 Huffing and puffing, low O2, high heart rate, on tiniest bit of exertion. Diagnosed as radiation pneumonitis. Treated with Prednisone.
11/11/16 PET scan shows significant improvement to radiated part of right lung BUT a bunch of new lung lesions, and the bone met is getting worse.
11/22/16 Begin Eribulin and Herceptin. H every 3 weeks. E two weeks on, one week off.
3/6/17 Scan shows progression in lungs. Bone met a little better.
3/23/17 Lung biopsy. Tumor sampled is ER-, PR+ (5%), HER2+++. Getting Herceptin and Perjeta as a maintenance treatment.
5/31/17 Port placement
6/1/17 Start Navelbine & Tykerb
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