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Old 04-27-2007, 10:33 AM   #1
AlaskaAngel
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Question Speculation about chemo-induced anemia (and possibly leukopenia as well)

I know some prefer to see "just the facts" but I think some speculations are worth sharing. This post is, however, pure speculation on my part.

I have been thinking about Andrea Budin's post about her chemo-induced anemia:

http://www.her2support.org/vbulletin...ad.php?t=27872

In considering Andrea Budin's circumstances (chemo-induced anemia), and reflecting only upon my own experience, I came to speculate that perhaps destruction of cancer cells by chemotherapy might not be solely (or even primarily) what produces sustained remission. I wonder whether there is any evidence of a higher rate of long remissions among those who have even mildly lower blood counts that are sustained.... My theory being, that there would then be perhaps less blood supply to support stray cancer cells in establishing the network for their further development.

If there is truth to that, maybe it would be especially helpful to not use as much of the drugs like Procrit.

Most of us do have chemo-related fatigue, some of which is related to blood counts. But perhaps some of the fatigue is not entirely a bad thing to have....

Any comments are welcome.

AlaskaAngel
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Old 04-27-2007, 11:29 AM   #2
Becky
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There is probably a difference when looking at it via low red counts versus low white counts (and what is low in those white counts – ie: neutrophils, lymphocytes etc).


My thoughts on red counts fall into 2 schools. One is the fact that the makers of Procrit (in the product literature they had in 2004 which is when I had chemo) stated that in their own studies – they found a reduced survival statistic in cancer patients who used their product versus blood transfusion. Therefore, when all the data and posts here started talking about it, it was out there already – and by the manufacturer themselves in their own product insert. Because of reading that insert (that was laying around the cancer center), I always wanted to avoid having to use that product and worried about it because my natural red blood cell count (RBC) is low to begin with and continues to be. That, plus chemo plus my last menstrual cycle (where I bled like a pig for one month – I went out with a bang) scared me that I would need some RBC assistance. I ended up not to.

<O

But before I ended up not needing anything, I did a lot of research in case I did. I did find articles contrary to Procrit’s own literature. This data says that greatly upping RBC any way you can (and they touted Procrit) would enhance cancer survival because more red cells means more oxygenation of body tissues. Cancer survives best in a nonoxygen environment so – oxygen weakens cancer. Oxygenation weaking cancer is a probable fact (and probably also one of the many reasons why exercise reduces the recurrence rate of bc). That is all I want or can say about the red cell count aspect at this moment. I am sure some of you will comment and I can then think on this more. However, the horse is out of the barn in saying that red cell boosters are not necessarily good. But, I think if you really need them, you really need them. They just should not be used willy-nilly.

<O

White blood cell (WBC) boosters are a different story. Although preliminary data says that they too are not good (to include G-CSF (Neulasta and Neupogen) and GM-CSF (Leukine)), the benefit of dense dose chemo for bc (every 2 weeks for AC followed by taxol) versus the regular dosing (every three weeks) is great (especially for Her2+ and triple negative women). There is a 38% survival benefit for dense dose overall (including all pathologies of which most are plain old ER+/PR+ cancers). So, it makes good sense for the more concerning pathologies to use dense dose chemotherapy utilizing a WBC booster. The main point is what booster to use – Neulasta or Leukine. Many of you know that I refused Neulasta and used Leukine instead. My rationale is that Neulasta (or Neupogen which is the same drug by a different company) only boosts the neutrophils (that fight short term infection) while Leukine boosts all components of the white blood cell system including monocytes and especially dendrites (the scouts that find cancer and induce the body to manufacture killer Tcells against that). Since both products could have potential negative effects, at least utilize dense dose chemo with Leukine (where one might have the potential to self vaccinate). All the Her2 vaccine trials use Leukine in conjunction with the active to further promote vaccination due to the dendritic effect.

<O

So, hopefully some of you will respond and we can have a healthy discussion on this. Hope you are doing well Angel. I am and will email you sometime this weekend.
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Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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Old 04-27-2007, 12:28 PM   #3
AlaskaAngel
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Thanks Becky. Do you know how far out the numbers for improved survival with blood boosting apply to? I'm tempted to do a poll of all of us old-timers here just to see if the blood boosting oxygenation is a short-term effect that maybe works best concurrently with chemo, or if it is a long-term one.

I wondered also whether maybe one reason the younger women tend to have more aggressive cancer might be because their bones are better at producing blood cells whereas the older women's systems probably produce fewer blood cells.

I enjoy sharing thoughts, and marvel that you keep the busy schedule that you do, Becky!

A.A.
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Old 04-27-2007, 07:20 PM   #4
Becky
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There were no numbers. The article was written by a guy who was touting supplements etc. The link was sent to me by my husband's cousin who is a nuceutical salesman (and the article sounded very charlitan to me) but the premise of boosting the red count to increase physiological oxygenation sounded reasonable. However, Procrit's own label states otherwise and they make the drug. The article/link was sent to me over 2 years ago but I am trying to look for it.
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Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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Old 04-27-2007, 08:40 PM   #5
Bev
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AA and Becky, I have been anemic most of my adult life. I did take iron supplements in the past 10 years as directed. Sometimes I worry that Iron could have fed things. Maybe anemic is normal. Maybe it's disastrous to feed iron to ER+. Maybe offering Procrit to cancer patients is wrong too. We just have to take our best guess. I turned down nuelasta after my first try at it. It made my counts skyrocket, but they also came back when I didn't do it either.

I just don't know. BB
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Old 04-28-2007, 04:35 AM   #6
Mary Jo
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Hello,

I never became anemic during chemo, so never needed Procrit. Not sure if that's good or bad. Thinks it's good.

Mary Jo
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Dx. 6/24/05 age 45 Right Breast IDC
ER/PR. Neg., - Her2+++
RB Mast. - 7/28/05 - 4 cm. tumor
Margins clear - 1 microscopic cell 1 sent. node
No Vasucular Invasion
4 DD A/C - 4 DD Taxol & Herceptin
1 full year of Herceptin received every 3 weeks
28 rads
prophylactic Mast. 3/2/06

17 Years NED

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Old 06-14-2007, 07:21 AM   #7
dlaxague
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Confused

I don't know why it happens but again, I wrote a long reply and when I hit submit, I was re-directed to sign in before posting (but I had already signed in), and the post disappeared. Sigh. Usually I give up at that point but this topic is really intriguing so I'll try again.

I am confused by the discussions. My understanding is that there is fairly good evidence that something about ESA's decreases survival in at least some cancer patients. The reason for that could be related to the increase in Hg, to the possible growth-stimulating effect if there are epoetin receptors on the cancer cells, or to something not-yet-understood.

The best evidence for the above seems to come from studies that took the observation that cancer cells that were operating in a hypoxic manner were resistant to chemo and rads, and they looked at the possibility that increasing Hg. might counteract that resistance. But weren't those cancer cells choosing hypoxia? Weren't they choosing not to use the already-available oxygen? Then why would increasing Hg (which is not necessarily the same as increasing oxygen) change the way they functioned? The reason that they thought that might make a difference is my first area of confusion.

Then there's my anemia/hypoxia confusion. Anemia is not the same thing as hypoxia. Anemia is less-than-normal numbers of red blood cells. Hypoxia is decreased oxygen levels in tissue. Red blood cells carry oxygen to the tissues, so sometimes these two things correlate, sometimes not. I do not think that people who are mildly anemic (Hg 10 to 12) have decreased oxygen delivery to their tissues - the body adapts pretty well, especially when the changes are gradual. Otoh, the people who DO have significantly decreased levels of oxygen in blood and tissue are those with chronic lung disease, and they typically do not raise their Hg much, to try to compensate (hmm - 'wonder why not?). Nor, to my knowledge, do they have a difference in their incidence of cancer.

So if the link in decreased survival were r/t purely to Hg levels, surely by now this would have been noticed, r/t Hg levels or to oxygenation, independent of ESA administration.

It seems possible that ESA's, while stimulating red cell production, might also stimulate angiogenesis. That could be one factor in this phenomenon.

And then there's the altitude discussion. There is less oxygen in the air at higher altitude and so over time (not days - I think it's more like months), people living at altitude produce a few more red blood cells, to compensate. This compensation, however, means that they that have exactly the same oxygen levels in their blood and available to their tissues - so why would that make a difference to cancer? Someone posted that it's well know that there's less cancer at altitude. I didn't know that. Can you post references, please?

I have more to ramble about but this is too long already. I'll save further comments for responses to other's thoughts on this.

Debbie Laxague
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3/01 ~ Age 49, occult primary announced by large axillary node found by my husband. Multiple CBE's, mammogram, U/S could not find anything in the breast. Axillary node biopsy - pathology said + for "mets above diaphragm, probably breast".
4/01 ~ Bilateral mastectomies (LMRM, R simple) - 1.2cm IDC was found at pathology.
5 of 11 axillary nodes positive, largest = 6cm. Stage IIIA
ERPR 5%/1% (re-done later at Baylor, both negative at zero).
HER2neu positive by IHC and FISH (8.89).
Lymphovascular invasion, grade 3, 8/9 modified SBR.
TX: Control of arm of NSABP B-31's adjuvant Herceptin trial (no Herceptin): A/C x 4 and Taxol x 4 q3weeks, then rads. Arimidex for two years, stopped after second patholgy opinion.
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Old 06-14-2007, 08:01 AM   #8
Margerie
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Debbie,

I ran across lots of anecdotal evidence in my search. Can't get access to the good articles. Talked to a couple of families in the mountain area where we bought our vacation home. Their stories were the same: member of family dx with cancer (one was a child), diagnosis grim, moved to mountains and all went into remission. I figure it could be more than the altitude: less pollution, tendency for less fast food/better diet, more opportunity for exercise, more vit D, etc.

It may be all in my head- but I definitely feel a difference in my cardio abilitites for a few days on my return from the mountains (after just a 4 day trip).

A smattering of altitude/cancer discussions: (Will look more when I get back- out the door today)

http://www.asco.org/portal/site/ASCO...stractID=30083

http://carcin.oxfordjournals.org/cgi...stract/3/5/461

http://members.westnet.com.au/pkolb/peat3.htm
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Dx 10/05 IDC, multi-focal, triple +, 5 nodes+
MRM, 4 DD A/C, 12 weekly taxol + herceptin
rads concurrent with taxol/herceptin
finished herceptin 01/08
ooph, Arimidex, bilateral DIEP reconstruction
NED
Univ. of WA, Seattle vaccine trial '07
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Old 06-14-2007, 03:25 PM   #9
TSund
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thread

This is fascinating. Has there been a simple study of whether there is less cancer at high altitudes?


Terri
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Old 06-16-2007, 07:01 AM   #10
dlaxague
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Hi Margerie and all,

Thanks for the links. This is my favorite kind of discussion where we are all thinking, thinking, and sharing ideas.

I looked around a bit with google, also. I didn't find much, and most of what I found was looking at increased cosmic or ionizing radiation at high altitude and an increase in cancer incidence. One study of mice showed an increase in cancer at altitude over time (1969). There does not seem to be much interest in this subject (judging by the lack of research). There was a lot of interest in studying airline personnel, again r/t mostly to radiation exposure at altitude but also to interrupted circadian rhythms and other lifestyle factors.

Your first two links were interesting but hardly conclusive. The last one was pretty out-there - this MD evidently has his own theories and a very pricey clinic where people learn his special technique for relieving asthma, but his theories are not supported by mainstream medicine (which is not to say he might not be onto something but if he is, he needs to show some evidence.).

So I'd say that while it is intriguing and could be true (or not), it would not be accurate at this point to say that it is "pretty well known" that there is less cancer at altitude. And I'm not sure it will ever be known, given the many confounders that would exist when comparing populations.

Debbie Laxague
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Old 06-17-2007, 06:19 PM   #11
Margerie
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Debbie-

Thanks for calling me out! Yes- I would say that it is not right for me to say "it is pretty well-known..." I was thinking about the incidence breast cancer of women living at altitude (mountains of Japan, other rural areas, indigenous populations) are low, versus the women with a very high incidence (Marin, CA) which is at or below sea level. Of course, more than just altitude playing with these numbers.

Anyway, like I said before- love to speculate.
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Are we there yet?


Dx 10/05 IDC, multi-focal, triple +, 5 nodes+
MRM, 4 DD A/C, 12 weekly taxol + herceptin
rads concurrent with taxol/herceptin
finished herceptin 01/08
ooph, Arimidex, bilateral DIEP reconstruction
NED
Univ. of WA, Seattle vaccine trial '07
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