Skip to content
Forum IndexForum: LCIS (Lobular Carcinoma In Situ) → Topic: Just diagnosed with LCIS
« Forum: LCIS (Lobular Carcinoma In Situ): Just diagnosed, in treatment, or finished treatment for LCIS.

Topic: Just diagnosed with LCIS

Log in to post a reply
  • Posted on: Nov 1, 2009 01:52 pm
Joined: Nov 2006
Posts: 47
kristie78 wrote:

Okay, just given the dx of LCIS, waiting for a visit with an oncologist but what should I expect? I'm slightly confused as the surgical oncologist said "depending on your doctor's school of thought, this is either Stage 0 bc or just an indication of a higher risk of developing BC'

What are the treatments if any at all?

Thanks!

Kristie

Posts 1 - 8 (8 total)
Krisc
NC
Joined: Mar 2009
Posts: 21
Nov 1, 2009 03:30 pm Krisc wrote:

Hi Kristie,

I was diagnosed with LCIS this April '09.  My oncologist, breast surgeon and gyn do not consider it stage 0, but a "marker' for an increased risk of developing invasive breast cancer.  My oncologist and breast surgeon tell me that I have about a 30% chance over my lifetime of developing BC.  I am 54, and they are assuming I live to be 84:). But who knows?  After you do some research, talk with others, you will find LCIS is a very uncommon condition and there are lots of unknowns.  After my stereotactic biopsy when the LCIS was discovered, I had an MRI, then a few weeks later an excisional biopsy.  Followed by a digital mammogram 6 weeks later.  Then off to the oncologist and he prescribed Evista for me.  He decided on Evista over Tamoxifin since I am post menopause.  My treatment so far will be digital mammos and MRI every 6 months.  Breast exams every 6 months, by oncologist and breast surgeon.  So every 3 months I am having something done.  Since I am relatively new to this, not so sure how this "watch and see" course will be.  I know I do worry about invasive BC.  Many decide on bilateral mastecomies, and that is an option.  Most doctors think that is drastic unless you have other things going on along with LCIS. (Easy for them to say, right?) Good luck to you and keep us informed!

Kris


Diagnosis: LCIS, Stage 0
awb
Joined: Aug 2005
Posts: 2,764
Nov 1, 2009 04:24 pm awb wrote:

Kristie-----no wonder you're confused---there is ongoing controversy in the medical community regarding LCIS--what it should be called, what it truly is, how it should be managed, etc.... (many view it as just a marker for high risk of invasive bc in the future, while others view it as bc as it is technically a  stage 0, non-invasive in-situ bc.) The 3 standard options usually given are : 1) close monitoring 2) close monitoring with tamoxifen (or evista depending on menopausal status) 3) BPMs I was diagnosed with LCIS 6 years ago and went with option #2---I finished my 5 years of tamoxifen last year and now take Evista (since I'm postmenopausal now) for further preventative measures, and I continue with high risk surveillance of alternating MRIs with mammos every 6 months and breast exams on the opposite 6 months.  The oncologist will go over all your risk factors and try to figure out your estimated 5 year and lifetime risks--(I say try, because with LCIS they are really not exactly sure); they can also discuss all  the risks and benefits of taking tamox  or evista with you, and set up a plan for monitoring, if that is the route you choose to go. My oncologist does a breast exam every time, takes blood for tumor markers, goes over any SEs that I might be having (fortunately I tolerated tamox well and am doing well on evista), and orders any tests that are needed. Feel free to PM me if you'd like to chat.

anne

"I don't know what the future holds, but I know who holds the future"
Diagnosis: 9/5/2003, LCIS, Stage 0, 0/0 nodes
kristie78
Joined: Nov 2006
Posts: 47
Nov 1, 2009 04:30 pm kristie78 wrote:

Okay, being that I am only 31 taking these drugs will they hurt my chances of having children?

leaf
Joined: Dec 2005
Posts: 5,944
Nov 1, 2009 06:03 pm, edited Nov 1, 2009 06:07 PM by leaf leaf wrote:

Be careful  with terminology as you wander in this subject: a few places/people consider hormonal therapy 'chemotherapy'.   Most do not.  But it can get confusing.

IV chemotherapy (i.e. antimetabolite/anti-Herceptin therapy) is NOT considered appropriate for LCIS and nothing worse. Normally radiation is not done, but we have 1 sister here who got radiation for LCIS and nothing worse.

The National Cancer Institute considers the term 'LCIS' as misleading.  That's because LCIS was identified BEFORE they knew the natural history (i.e. how many LCIS women got bc.)  Risk estimates for LCIS are complex, because before the 1990s, it was fairly routine to treat LCIS with bilateral mastectomies.http://www.cancer.gov/cancertopics/pdq/treatment/breast/HealthProfessional/page6

Different docs have different feelings about LCIS. On my first visit to my breast surgeon, before she even asked about my family history, she said, "If you are interested in PBMs, I will fall over in my chair."  I had an excision, but she refuses to consider PBMs on me.

I am probably among the least monitored among the LCIS women I've seen in this forum.  I get clinical exams twice a year, and annual mammograms.  I'm on tamoxifen.  I just want you to be prepared, because different doctors apparently have very different ideas about LCIS.  There is little in LCIS that is NOT controversial.

RE: fertility: Tamoxifen is contraindicated during pregnancy.  

Recently developed ovarian stimulation protocols with aromatase inhibitor letrozole and tamoxifen appear to provide a safe stimulation with endogenous estrogen levels comparable with those achieved in the natural cycle.http://www.ncbi.nlm.nih.gov/pubmed/19806518

Many of these patients will use adjuvant endocrine therapy. This treatment has no direct impact on their fertility, but postpones a possible pregnancy, since pregnancy is contra-indicated during Tamoxifen treatment.http://www.ncbi.nlm.nih.gov/pubmed/18411579

I am not an expert on this;  I don't know how representative these papers are. You really need to talk to your doc, and probably go to a high risk clinic, probably at a large institution. Research yourself, and come to an informed decision.   You may also want to ask on the Young Women with bc forum.

 Many papers estimate the incidence of breast cancer in (LCIS and nothing worse) patients is about 0.5-1% per year, so most women have some time to decide.

If you're going through hell, keep going-Winston Churchill
chris38
Joined: Jan 2009
Posts: 13
Nov 3, 2009 06:04 pm chris38 wrote:

Hi Kristie,

My name is Christine... I am 39 and was diagnosed almost a year ago with LCIS...  Take your time to decide whats best for you...  My BS and onologist consider LCIS to be a marker for getting cancer in the future.. They dont consider it cancer... Call me i would love to chat with u further.  Its hard to make a decision its still taking me awhile...  914-391-6764

chris38

penguin1
Joined: Feb 2009
Posts: 44
Nov 4, 2009 10:12 pm penguin1 wrote:

Hi Leaf!

I read so many of your posts as they are so interesting and near to my heart.  I think we are taking the same path with LCIS- I kind of felt that my breast surgeon was under-monitoring me, but it seems your's said the same.  I had the excisional for DCIS and now LCIS remains- went on Tamoxifin about 4 months ago and will have my next mammo in September- no sooner unless needed.  My doctor doesn't feel MRIs are necessary unless something new arises.  I really felt I should be monitored more closely, but I truly love my surgeon and will go with what she feels is right... which seems to be what your doctor said as well- that makes me feel better.  Do you happen to be from the NY area?  That would be strange if it was the same doctor!

Take care, Leaf.


Diagnosis: 3/11/2009, DCIS, <1cm, Stage 0, Grade 2, 0/0 nodes
leaf
Joined: Dec 2005
Posts: 5,944
Nov 5, 2009 01:12 pm leaf wrote:

 Hi, penguin! No, I'm not from the NY area.  I can't stand my bs - I go to my onc for my breast exams.  

If you're going through hell, keep going-Winston Churchill
chris38
Joined: Jan 2009
Posts: 13
Nov 14, 2009 10:57 pm chris38 wrote:

Hi Kristie,

Please give me a call would love to talk to you. 914-391-6764

christine

© 2009 Breastcancer.org. All rights reserved.