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Drug slows Alzheimer's but can it make a real difference?

An experimental Alzheimer鈥檚 drug modestly slowed the brain disease鈥檚 inevitable worsening 鈥 but the anxiously awaited new data leaves unclear how much difference that might make in people鈥檚 lives. Japanese drugmaker Eisai and its U.S.
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FILE - This Oct. 7, 2003 file photo shows a closeup of a human brain affected by Alzheimer's disease, on display at the Museum of Neuroanatomy at the University at Buffalo in Buffalo, N.Y. An experimental Alzheimer鈥檚 drug modestly slowed the brain disease鈥檚 inevitable worsening, researchers reported Tuesday, Nov. 29, 2022 - and the next question is how much difference that might make in people鈥檚 lives. Japanese drugmaker Eisai and its U.S. partner Biogen had announced earlier this fall that the drug lecanemab appeared to work, a badly needed bright spot after repeated disappointments in the quest for better Alzheimer鈥檚 treatments. (AP Photo/David Duprey)

An experimental Alzheimer鈥檚 drug modestly slowed the brain disease鈥檚 inevitable worsening 鈥 but the anxiously awaited new data leaves unclear how much difference that might make in people鈥檚 lives.

Japanese drugmaker Eisai and its U.S. partner Biogen had announced that the drug lecanemab appeared to work, a badly needed bright spot after repeated disappointments in the quest for better treatments of the incurable disease.

Late Tuesday, the companies provided full results of the study of nearly 1,800 people in early stages of the mind-robbing disease. The data was presented at an Alzheimer鈥檚 meeting in San Francisco and published in The New England Journal of Medicine.

Lecanemab delayed patients鈥 worsening by about five months over the course of the 18-month study, Eisai鈥檚 Dr. Michael Irizarry told The Associated Press. Also, lecanemab recipients were 31% less likely to advance to the next stage of the disease during the study.

鈥淭hat translates to more time in earlier stages鈥 when people function better, Irizarry said.

Every two weeks, study participants received intravenous lecanemab or a dummy infusion. Researchers tracked them using an 18-point scale that measures cognitive and functional ability.

The study's key finding: Those given lecanemab declined more slowly, a difference of not quite half a point on that scale over the 18 months, concluded the research team led by Dr. Christopher van Dyck at Yale University.

Doctors are divided over how much difference that may make for patients and families -- especially as the drug carries some worrying potential safety risks including brain swelling.

鈥淚t is unlikely that the small difference reported in this trial will be noticeable by individual patients,鈥 said Dr. Madhav Thambisetty of the National Institute on Aging, who noted he wasn鈥檛 speaking for the government agency.

He said many researchers believe a meaningful improvement would require at least a difference of a full point on that 18-point scale.

But Dr. Ron Petersen, an Alzheimer鈥檚 expert at the Mayo Clinic, said the drug鈥檚 effect was 鈥渁 modest one but I think it鈥檚 clinically meaningful鈥 -- because even a few months鈥 delay in progression could give someone a little more time when they鈥檙e functioning independently.

The trial is important because it shows a drug that attacks a sticky protein called amyloid -- behind Alzheimer鈥檚 -- can delay disease progression, said Maria Carrillo, chief science officer for the Alzheimer鈥檚 Association.

鈥淲e all understand that this is not a cure and we鈥檙e all trying to really grasp what it means to slow Alzheimer鈥檚, because this is a first,鈥 Carrillo said.

But any delay in cognitive decline early on could be meaningful for 鈥渉ow much time we have with our loved ones in a stage of disease where we can still enjoy family and outings, vacations, bucket lists,鈥 she said.

Amyloid-targeting drugs can cause side effects that include swelling and bleeding in the brain, and lecanemab did as well. One type of this swelling was seen in about 13% of recipients. Eisai said most were mild or asymptomatic.

Also, two deaths have been publicly reported among lecanemab users who also were taking blood-thinning medications for other health problems. Eisai said Tuesday the deaths can鈥檛 be attributed to the Alzheimer鈥檚 drug.

But Mayo鈥檚 Petersen said if lecanemab is approved for use in the U.S., he鈥檇 avoid prescribing it to people on blood thinners at least initially.

And Thambisetty said the death reports raise concern about how the drug may be tolerated outside of research studies 鈥渨here patients are likely to be sicker and have multiple other medical conditions.鈥

The Food and Drug Administration is considering approving lecanemab under its fast-track program, with a decision expected in early January. If approved, it would be the second anti-amyloid drug on the market.

Nearly all treatments available for the 6 million Americans with Alzheimer鈥檚 鈥 and millions more worldwide with the most common form of dementia 鈥 only temporarily ease symptoms. Scientists don鈥檛 yet know exactly how Alzheimer鈥檚 forms but one theory is that gunky amyloid buildup plays a key role, although drug after drug that targets it has failed.

In a contentious move last year, the FDA , Biogen鈥檚 Aduhelm, despite lack of evidence of better patient outcomes. Insurers and many doctors have -- another reason experts have anxiously awaited word of how well the newer lecanemab may work.

If the FDA approves lecanemab, patients and their families will need a voice in deciding whether it鈥檚 worth the hassle of IV infusions and the risk of side effects for the chance of at least some delay in progression, Petersen said.

鈥淚 don鈥檛 think we鈥檙e going to stop the disease in its tracks鈥 with just amyloid-targeting drugs, he added, saying it will take a combination of medications that target additional Alzheimer鈥檚 culprits.

Researchers are preparing to test lecanemab with other experimental drugs, and how it works in high-risk people before they show the first signs of memory problems.

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The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute鈥檚 Department of Science Education. The AP is solely responsible for all content.

Lauran Neergaard, The Associated Press