HonCode

Go Back   HER2 Support Group Forums > her2group
Register Gallery FAQ Members List Calendar Today's Posts

Reply
 
Thread Tools Display Modes
Old 06-26-2007, 12:14 PM   #1
Lani
Senior Member
 
Join Date: Mar 2006
Posts: 4,783
Exclamation FDA asked to reconsider aspartame due to link to breast ca and lymphoma

FDA Should Reconsider Aspartame Cancer Risk, Say Experts: New Rat Study Links Artificial Sweetener with Lymphomas, Breast Cancer [Center for Science in the Public Interest]
WASHINGTON—A new long-term animal test from an Italian cancer institute raises serious safety questions about the artificial sweetener aspartame, which is marketed generically as well as under the NutraSweet and Equal brand names. A dozen toxicology and epidemiology experts and the nonprofit Center for Science in the Public Interest are calling on the Food and Drug Administration (FDA) to immediately review the study, which found increases in lymphomas, leukemias, and breast cancers in rats. If FDA concludes that aspartame does cause cancer in animals, the agency is required by law to revoke its approval for the controversial sweetener, which is used in Diet Pepsi, Diet Coke, tabletop packets, and countless other foods.
The new study, conducted by the respected Ramazzini Foundation and published in the journal Environmental Health Perspectives, found statistically significant increases in lymphomas and leukemias in rats that were fed as little as 20 milligrams of the sweetener per kilogram of body weight—an amount that's in the ballpark of what some people consume. The new study is superior to a similar one released in 2005 in that it began exposing the rats to aspartame before their birth.
"Because aspartame is so widely consumed, it is urgent that the FDA evaluate whether aspartame still poses a 'reasonable certainty of no harm,' the standard used for gauging the safety of food additives," said CSPI executive director Michael F. Jacobson. "But consumers, particularly parents, shouldn't wait for the FDA to act. People shouldn't panic, but they should stop buying beverages and foods containing aspartame."
The Acceptable Daily Intake of aspartame in the United States is 50 mg per kg of body weight. The new study looked at doses less than that (20 mg per kg) and greater (100 mg per kg). Though few people would consume aspartame at the higher dose, the lower does is equivalent to a 50-pound child drinking 2½ cans of diet soda per day, or a 150-pound adult drinking about 7½ cans of diet soda per day. But aspartame also enters the diet through sugar-free or reduced-sugar gums, candies, yogurts, and hundreds of other products. Many aspartame-containing products are likely to be consumed by kids, including sugar-free Kool-Aid, Jell-O gelatin dessert and pudding mixes, and some Popsicles.
A 2006 National Cancer Institute study seemed to ease cancer fears related to aspartame, but that study had major limitations, including its reliance on imprecise food-frequency questionnaires, and it included only subjects between the ages of 50 and 69 who first consumed aspartame as adults. The effects of consuming aspartame from infancy or childhood might be very different, says CSPI, as suggested by the new animal study.
Among those who today called on FDA Commissioner Andrew von Eschenbach to review the new aspartame study are former Occupational Safety and Health Administration officials John Froines (now at UCLA) and Peter F. Infante (now at George Washington University); James Huff, current Associate Director for Chemical Carcinogenesis at the National Institute of Environmental Health Sciences (NIEHS); and Kamal M. Abdo, a toxicologist formerly at the National Toxicology Program of the NIEHS.
As a result of the new study, for the first time CSPI downgraded aspartame on its online Chemical Cuisine directory from a "use caution" rating to "everyone should avoid." CSPI also urges everyone to avoid the artificial sweeteners acesulfame potassium and saccharin. It rates sucralose, also known by the brand name Splenda, as safe.
CSPI also called on the food industry to voluntarily switch to other sugar substitutes.
"Switching to safer ingredients now could be a wise precautionary action," Jacobson wrote to Cal Dooley, president of the Food Products Association/Grocery Manufactures Association.
According to a 1996 report in the Minneapolis Star Tribune, the FDA rejected repeated proposals by NIEHS to test aspartame using more modern methods than were originally used. David Rall, the former director of NIEHS and its National Toxicology Program, said, "any compound that is that widely used needs to be retested with modern methods every once in a while." The State of California, too, has urged new testing of aspartame. The FDA also rejected NIEHS's proposal to test acesulfame potassium, which CSPI says was "abysmally tested" by its manufacturer and showed signs of causing cancer in animals.

The abstract:

Lifespan Exposure to Low Doses of Aspartame Beginning During Prenatal Life Increases Cancer Effects in Rats [Environmental Health Perspectives]
Background: In a previous study conducted at the Cesare Maltoni Cancer Research Center of the European Ramazzini Foundation (CMCRC/ERF), we demonstrated for the first time that aspartame (APM), administered with feed at various doses to 8 week-old Sprague Dawley rats for the lifespan, is a multipotent carcinogenic agent.
Objective: The aim of this second study is to better quantify the carcinogenic risk of APM, beginning treatment during fetal life.
Methods: The study was conducted on groups of 70-95 male and female Sprague Dawley rats, administered APM with feed at concentrations of 2000, 400, or 0 ppm from the 12th day of fetal life until natural death.
Results: The results of the study show: a) a significant dose-related increase of malignant tumor-bearing animals in males (p<0.01), in particular in the group treated at 2000 ppm (p<0.01); b) a significant increase of the incidence in lymphomas/leukemias in males treated at 2000 ppm (p<0.05) and a significant dose-related increase of the incidence of lymphomas/leukemias in females (p<0.01), in particular in the group treated at 2000 ppm (p<0.01); c) a significant dose-related increase of the incidence of mammary cancer in females (p<0.05), in particular in the group treated at 2000 ppm (p<0.05).
Conclusions: The results of this carcinogenicity bioassay not only confirm, but also reinforce the first experimental demonstration of APM's multipotential carcinogenicity at a dose level close to the acceptable daily intake (ADI) for humans. Furthermore, the study demonstrates that when lifespan exposure to APM begins during fetal life, its carcinogenic effects are increased.
Lani is offline   Reply With Quote
Old 06-26-2007, 12:48 PM   #2
KellyA
Senior Member
 
KellyA's Avatar
 
Join Date: Sep 2006
Location: Savannah, Georgia
Posts: 301
VERY SCAREY I had been a heavy long term user of diet products, beginning around the age of fifteen (dx'd at 37). I really was like a smoker as far as diet cokes go- I always had a "big gulp" of diet coke in my hand and drank several a day in addition to consuming other sugar free items. I have stopped this for the most part since diagnosis, but now don't even want to use Splenda, even though its supposed to be safe. I have been shocked at the number of very young women I know that have been diagnosed with breast cancer and generallly would say that diet items are used by many young women and have really only been around for the last 25 years or so. The rates of bc certainly have skyrocketed since then. Definitely something to take note of.

Kelly
__________________
dx'd 05/06, 37 years old
er/pr-, Her2+, grade 3
double mastectomy, immediate reconstruction- implants
Stage 2b, 2 tumors- 2.2 cm and 0.6 cm, 3/5 + nodes
all scans clear
genetic testing- negative
06/06 began dd A/C x 4, 12 weekly Taxols w/ Herceptin
30 rads
Herceptin weekly x 1 year
Herceptin completed 08/07
Port removed 12/26/07 MERRY CHRISTMAS!!!!!!
05/17/08 Two year anniversary NED

"We gain strength, courage, and confidence by each experience in which we really stop to look fear in the face... you must do the thing that you think you cannot do."

-Eleanor Roosevelt

KellyA is offline   Reply With Quote
Old 06-26-2007, 03:36 PM   #3
CLTann
Senior Member
 
Join Date: Oct 2005
Posts: 476
My hunch is that FDA will not act on this. The agency is noted for its link with big businesses. For an alarming case like this, they probably would just ignore the subject and hope no one will notice its ineptness.
__________________
Ann

Stage 1 dx Sept 05
ER/PR positive HER2 +++ Grade 3
Invasive carcinoma 1 cm, no node involvement
Mastec Sept 05
Annual scans all negative, Oct 06
Postmenopause. Arimidex only since Sept 06, bone or muscle ache after 3 month
Off Arimidex, change to Femara 1/12-07, ache stopped
Sept 07 all tests negative, pass 2 year mark
Feb 08 continue doing well.
Sep 09 four year NED still on Femara.
CLTann is offline   Reply With Quote
Old 06-26-2007, 03:59 PM   #4
RhondaH
Senior Member
 
RhondaH's Avatar
 
Join Date: Sep 2005
Location: Grand Rapids, MI
Posts: 1,516
Smile One more example of...

"progress" setting us back. I would prefer to have a little "real" sugar than something that could possible kill me. Artificial this, that and the other...this is why I cook from scratch Take care and God bless.

Rhonda
__________________
Rhonda

Dx 2/1/05, Stage 1, 0 nodes, Grade 3, ER/PR-, HER2+ (3.16 Fish)
2/7/05, Partial Mastectomy
5/18/05 Finished 6 rounds of dose dense TEC (Taxotere, Epirubicin and Cytoxan)
8/1/05 Finished 33 rads
8/18/05 Started Herceptin, every 3 weeks for a year (last one 8/10/06)

2/1/13...8 year Cancerversary and I am "perfect" (at least where cancer is concerned;)


" And in the end, it's not the years in your life that count. It's the life in your years."- Abraham Lincoln
RhondaH is offline   Reply With Quote
Old 06-26-2007, 08:04 PM   #5
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
I seem to remember that aspartame has been implicated in recent years as a potential cause of brain cancers... and the FDA has fought to deny that possibility and has swept it under every rug they can find.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 06-26-2007, 11:15 PM   #6
Barbara H.
Senior Member
 
Join Date: Sep 2005
Location: Newton, MA
Posts: 951
My father in-law (now deceased) was a biochemist, and always warned me against using artificial sweetners. My children went to one of the best pediatricians in Boston, and he also felt very, very strongly about not using them. I know we have to limit sugar, but I would not eat that artificial stuff. Interestingly, when I had my CAT scan two weeks ago, I had to drink the mixture in a sugar free drink. I complained and was told that it was easier to have a drink that diabetics could also drink.
Best regards,
Barbara H.
Barbara H. is offline   Reply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


All times are GMT -7. The time now is 09:05 AM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2026, vBulletin Solutions, Inc.
Copyright HER2 Support Group 2007 - 2021
free webpage hit counter