DCIS - cancer or Pre-cancer?
Comments
-
Hi janniexy, I don't mean to correct you. I was just a little surprised in reading your post. Pure DCIS is NOT life threatening and ALWAYS non-invasive. It biologically does NOT know how to metasticize. Pre-cancer/cancer may be just semantics between docs- whatever, but there is not a doctor on earth that should be confused about the DX. The only way a DCIS cell becomes invasive is for the cell to undergo a change in the structure. It not like the DCIS cells fill up a duct and eventually explode. That's why some DCIS cells undergo a change and become invasive, and others never change. Calling it a pre-cancer is not just one isolated opinion. About half disagree on the semantics of it. It does not really matter. I think we can call it what we want. Either definition can work. But, they ALL agree that DCIS without a micro-invasion is not life threatening and ALWAYS non-invasive.
-
louishenry, you wrote the answer that I was going to write. Regardless of whether they call DCIS cancer or pre-cancer, what all doctors agree on is that pure DCIS (i.e. without a microinvasion and without a recurrence) is always non-invasive and has a 100% survival rate.
DCIS cells are cancer cells that are contained within the milk ducts of the breast. So long as these cancer cells are in the ducts, they do not have the ability to metastasize (travel to and take hold in other parts of the body). However, when DCIS is analysed under the microscope, in anywhere from 10% - 30% of cases, a microinvasion of invasive cancer will be found. What this means is that a few of those cancer cells have broken through the milk duct and moved into the open breast tissue. Now the cancer does have the ability to metastasize. However, at this point, the diagnosis is no longer DCIS - the presence of any amount of invasive cancer, even a microinvasion, changes the staging from Stage 0 to Stage 1. Similarly, after a preliminary diagnosis of DCIS, if there is a recurrence, in 50% of cases the recurrence will be in the form of invasive cancer. Like all invasive cancer, this is potentially life threatening. But here again, with the invasive recurrence, the diagnosis will be changed and is no longer Stage 0.
Of course, just because DCIS is always non-invasive and non-life threatening does not mean that DCIS isn't serious and does not need to be removed and treated. DCIS is breast cancer caught at the earliest stage. Because it has the potential to become invasive cancer, it needs to be treated before it can become life threatening.
After reading all the articles and opinions on this, I think the clearest and least confusing definition for DCIS is non-invasive cancer. This both highlights the seriousness of the condition (it's cancer) but also communicates that it's not life threatening (non-invasive).
-
That's what my Doc said......You have Cancer.....the good kind. Pre-invasive, they know it leads to invasive, just not exactly which ones will.........yet.
-
Bumped for Gerberer.
-
This whole thing about DCIS not being cancer is bull. Sorry but it ticks me off. Yes, it is cancer, just not invasive yet. The next time a Dr tells one of us it is not cancer, I would suggest to them to have some of our 'non-cancer cells' injected into his/her breast tissue to see what happens. I'm sure they wouldn't be willing to try that experiment. Hmmmm, I wonder????
-
Just wanted to paraphrase something from a sister survivor's book: If you think DCIS is a gift, you're NOT invited to my birthday party.
Kathi
-
Wow, I am really confused about DCIS. I received a phone call from my oncologist who had my patholgy slides re-read. I already knew from the original path report that I was diagnosed with ADH. The new report came back saying ADH and also Borderline DCIS, low grade. I was told my treatment would stay the same, they are treated the same, tamoxifen for the next 5 years, and switching between mammograms and MRI's every 6 months. I had said DCIS was breast cancer from reading about it and he said no, it is the pre-curser to breast cancer. Now I realize that I am only borderline, but this is so confusing!
-
That really was close to my dx. I had some ADH and about 2mm of DCIS. It was low grade. Some docs call dcis breast cancer and some don't. Mine also said it was a pre-curser. I did not have rads recommended as the biopsy removed it all and lumpectomy was clean. I get digital mammos every year and an mri every year as well. They rotate with each other. I did not have borderline DCIS, mine was legit, but it was so tiny. I am on tamox. It has been fine.
-
Need to chime in here. The ACS says that DCIS is non-invasive cancer, pre-cancer.
Here is the link - look for breast cancer general terms and then for carcinoma in situ
http://www.cancer.org/docroot/CRI/content/CRI_2_4_1X_What_is_breast_cancer_5.asp?sitearea=
Gentle Hugs,
Trish
-
msdede...I have the exact dx as you..I had the biopsy saying ADH so then I had a lumpectomy on a palpable lesion (that was there for 6 yrs but biopsied and found to be benign so they left it and I noticed it changed) so ...the pathologist couldnt agree with half stating DCIS and the other half saying borderline ...so it was sent to Yale for a 2nd opinion and good thing ...it came back that the margins werent clean so I had to have a re-excision (2 wks ago) and now they are saying clean margins and I dont need radiation....I have to have an MRI in Dec and then screenings every 6 months...what is your treatment? Hope all goes well...Beth ..
-
Beth1128....I did not need radiation, probably because it was borderline DCIS and such a small amount. I have started Tamoxifen, a week ago , for the next five years. My first MRI is scheduled for Feb. and then I will be alternating every 6 months with mammograms. When I first met with the Dr., she was going by my first path report and spent the time giving me information all about how I am at High Risk because of my age, have ADH, dense breasts, that I should go on Tamoxifen and so on. I left understanding what was wrong with me and knowing what I needed to do. I received a call a week ago with results to the path report being re-read and how it is still ADH, but, Borderline DCIS. Because it was a phone call I was not prepared to ask questions, all I know is that the treatment plan is the same as discussed for the ADH and follow up in Dec. I do have to call back, I forgot to ask for a copy of my new report. Hope all goes well with you too!
-
AMEN sister!
If you look up the definition for dcis you can clearly see that carcinoma is cancer. It is just contained and hasn't spread.
-
I'd really like to know why I have no breasts if I didn't have cancer!
-
Yes..after talking to all my doctors this week I have confirmed that DCIS is cancer. It is contained and non-invasive and therefore again yes, we are the lucky ones. I don't think there was any such thing as 'pre-cancer'.....some people call it that as a 'comfort term' because it has not spread, but it is cancer. Makes me mad to see that some of you had issues with your insurance! That is unbelievable 8( I'm so sorry that you've had to deal with that. Hugs to you and love this website, so far it has been my best support 8)
-
i to had DCIS and my doctor described it as breast cancer but with no lymph nodes removed and now i question that as they have found a lymph node on my ct scan that is suspicious. Hang in there and know you are loved. Sending you a hug.
Keta
-
Donna....I like that...pre-invasive cancer...It does say it all, doesn't it? Now I know how to describe DCIS to people who ask about it......Thanks.
Sandy
-
I have the same question ... I just started looking up what my path report means and found cancer sites saying DCIS is "pre cancer" ??? so what the??? i just had mastectomy... for pre cancer or cancer...they told me it was cancer...i am so confused by some of this and very annoyed at this point...why do some cancer sites say it is not cancer but could be....I have read your responses but when u research the cancer sites it says "pre cancer" .
-
I was told that I have cancer. It is pre invasive cancer because it has not moved from it's original site....the ducts. I had grade 3 with lots of comedo necrosis. I was told by my docs that this type of DCIS is probably very close to becoming invasive.
I'm confused by your dx signature. It says that you had IDC not DCIS?
-
My goodness this is an old thread! 2008!
Angi, whether DCIS is considered to be cancer or pre-cancer simply depends on how one defines cancer. The definition of cancer often includes 3 criteria (from the National Cancer Institute: What Is Cancer?):
1) Abnormality of the cells
2) Uncontrolled growth of the cells
3) Invasiveness/the ability to metastasize
DCIS cells meet the first two criteria, but not the third. This is why some doctors consider DCIS to be a pre-cancer. Often it's oncologists who take this position, and that actually makes some sense when you consider that most of their patients have invasive cancer and face the risk of metastasis and death, and their job is to work with the patient to keep that from happening. With DCIS patients, oncologists only have to be concerned about local (i.e. in the breast area) recurrences so it's not surprising that many classify DCIS as a pre-cancer.
Whether a doctor considers DCIS to be cancer or pre-cancer, the treatment recommendations are usually the same. First and foremost, it's usually recommended that the DCIS be removed, either with a lumpectomy, or if the DCIS is too widespread (as it was in my case), with a mastectomy. Surgical removal is recommended because DCIS can over time develop to become invasive cancer. So removal of DCIS while it's still DCIS is a way to avoid a diagnosis of IDC.
Angi, your signature line indicates that you had IDC, not DCIS. I realize that most women who have IDC also have some DCIS, but because IDC is the more serious condition, the diagnosis, staging and treatment plan is all based on the IDC. While there may be a debate within the medical community on what to call DCIS (pre-cancer, cancer, pre-invasive cancer....), there's no debate that IDC is cancer. When DCIS and IDC are found together, the DCIS has to be removed (and sometimes that might mean that the patient needs to have a mastectomy), but other than that, whatever is done to treat the IDC will be more than sufficient to treat the DCIS. So after the surgical removal, the presence of the DCIS can pretty much be ignored and the treatment plan can focus on the IDC.
-
This is always an interesting topic.
When I was first Dx, I was told I had DCIS. My surgeon explained it, just as Beesie does. He added that this is the type of "cancer" that is not life threatening, if it has remained in this form, and that won't be known, till the final pathology results are in. I had a mix of both intermediate, and high grade, but after my UMx it was confirmed that I had pure DCIS, no microinvasion.
When I went back to get my final pathology results, my surgeon told me that "I was effectively cured!" that my choice to remove the breast, took all the offending material. He gave me the option of Tamox, but said that he saw no pressing need for me to take it. I was very pleased with that because, my Mother had taken it for 5 years, and had lots of SE's from it.
I find the easiest way to explain to people what I have had, is to say that I had a "form of breast cancer" that was removed by a UMX. If anyone says anything about DCIS not being BC, I simply ask them if they would like to play Russian Roulette, and leave it there to see what transpires?
Not something that I would ever consider. I sacrificed a breast for this beast. I am not letting anyone make me feel uncomfortable about my DX which is really just semantics, anyway.
Don't get me wrong, I am grateful every day that I was Dx with DCIS over anything else. We all go through the exact same terror when we hear that Dx, and while we wait for test results, and surgery, and then that final path report.
For me, it was over two months of waiting. The relief, when I got the final path was the most amazing feeling I have ever had. I am one of the really,really fortunate ones. I haven't had any negative feelings, and have adjusted to being a Unibooober really well, but I am, probably older than most of you at almost 60, so I am sure that makes a difference.
I have definitely changed, from all this, but not in a bad way. The new "normal" isn't bad at all!
-
So well said, Bessie and Ariom!!!
When I share my experience, I tell people I have stage 0 breast cancer. When I'm in a situation where there is more interest, I will say it is non-invasive, the kind of breast cancer you want, if you're going to get it. If I want to get fancy, I'll throw out DCIS. I explain that it is an unknown whether it will become invasive which is why it is treated like more advanced breast cancer. I think it's important to think in terms of educating folks...
I'm with you, Axiom! I like this new-normal. This has been a growing experience. And for that reason, I am grateful! xo Lisa
-
I also have the Aflac Cancer policy and it has been fantastic. I was just diagnosed with DCIS in March 2013 and had the policy for 8 years. I had a lumpectomy and I just finished 10 treatments of radiation so I don't know much about how they do with that.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team