Multi focal disease
I had five individual tumors ranging from .25mm-1.1cm. Does anyone have any information on how the size is staged? Is it a cumulative number achieved by adding all the foci together, or is it the size of the largest foci? My surgeon says the largest foci, my onc say add them up. I've tried to research this without much definitive success.
Many thanks,
mooboojack
Comments
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There is not a definate answer. It was discussed at the San Antonio Breast Cancer Symposium in December but I don't know that they came up with a definative answer. I, too, had mutifocal (1 and 1..6 cm). In my case it didnt matter since I had positive nodes but in my head I always consider it as 2.6 cms of bc.
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I had 3 tumors, 2 cm 1cm and .50cm I was staged according to the largest tumor. Because the tumors were in separate quadrants of the breast, a lumpectomy was not an option. Had bmx Oct 9th, chemo, but did not need radiation.
Hugs, Karen
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They stage and treat according the one largest and the most aggressive tumour. Although as Karen stated, IF they are in different quadrants, then a mast is preferrable to a lumpectomy. Good Luck with your test!
What is your next step of treatment? Have you had surgery yet?
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I also had 3 lesions, then a tiny (1mm) 4th one was found @ path. From what I'd read on-line, I was afraid they would total them for a combined size, and one onc I spoke to even threw in what they took during my initial biopsy when we were discussing this. But my BS (@UCLA) said no, they just go by the largest one, and having 2 or 3 additional smaller ones did not change that.
On the other hand, I've heard some docs use the term "tumor load" when disussing multicentric or multifocal disease, so I think the total load or scope of the disease can somewhat impact their thinking on chemo regimens and rads. Deanna
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Thanks for your responses. I had a unilateral mastectomy,6 rounds of TCH, and am now getting Herceptin every 3 weeks until April. I am on Femara for 5 years.
There was no lymph infiltration.
The tumors were all in the same quadrant. Do any of you know how common multi focal disease is?
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KinAZ,
Why did you opt for a bmx?
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I had two tumors....8 cm and .5 cm. For purposes of this board, I added the sizes together. It was called multi focal and the surgeon and oncologist staged them by the size of the largest tumor. I ended up with a lumpectomy. The first surgeon was adament that it had to be a mastectomy but the 3 others I saw said it was a good case for a lumpectomy. Whatever you do, get a second (or even third) opinion. And then don't look back and second guess yourself. Your decision is the right decision.
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mooboojack
I felt the bmx was best for me....for the affected side, my tumors were just too far apart and not much breast would be left after trying to get clean margins... as for the unaffected side, that was just my preference. I did not want any chance of going through this again. I still miss my breasts, but hope to have recon by the end of the year.
I dont know how common multi focal bc is.
Karen
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I was multifocal and multicentric. tumor 2.2cm but also 4 DCIS in other quadrents.
Being small breasted to start with I went for a mast but all quadrents were afected anyway.
Reading on the net I have read that it is very rare.
Aly
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I had 1 tumor 2.2cm and 4 DCIS in all quadrents. I went for a mast.
I read on the net Multifocal and Multicentric bc is very rare!
Aly
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Don't know how common or uncommon it is, but I had 2 areas of IDC along with 8 mm of DCIS. My take on the doctor's opinion was that it was more cause for concern.
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Hi there,,
I had 2 tiny "buggers"... 4mm and 1mm idc and dcis in the area....i had a lumpectomy and radiation.......
I also read, different from Emily, that in can be quite common.
My "buggers" were referred to a 4mm focus and a 1mm satellite ....apparently that meant that the satellite was a part of the other tumour....
i dunno ?
hugs ...kosh
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My understanding is that multi focal just means suspicious but not necessarily malignant. At least that is what my mri report said. My bc was staged in respect to my main tumor and nodes. I bet if you look at the stats, the chemo tx is the same. It is really more protocol, than I would like. All in all... you just have to listen to the doctors..... do your own research and trust your "inner self" to make the decision you are comfortable with.
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