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We give you many useful information about health

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We give you many useful information about health

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Tampilkan postingan dengan label Major. Tampilkan semua postingan
Tampilkan postingan dengan label Major. Tampilkan semua postingan

Sabtu, 24 September 2011

Bayer drug a "major new player" in prostate cancer

AppId is over the quota
AppId is over the quota
By Kate Kelland

STOCKHOLM | Fri Sep 23, 2011 6:12pm EDT

STOCKHOLM (Reuters) - An experimental drug from Germany's Bayer and Norwegian biotech Algeta that prolongs the lives of patients with advanced prostate cancer is a major step forward in treatment of the disease, cancer experts said on Saturday.

A late stage trial of Alpharadin, a new type of drug that delivers minute, highly-charged doses of radiation to secondary tumors in the bone, was halted early after researchers saw patients on the new treatment living almost three months longer on average than those on standard treatment plus placebo.

"It would have been unethical not to offer the active treatment to those taking placebo," Chris Parker, who led the trial at Britain's Royal Marsden Hospital, told delegates at the European Multidisciplinary Cancer Congress (EMCC) in Stockholm.

Alpharadin is based on the active ingredient radium 223 and is designed to treat patients with advanced disease whose cancer has spread to their bones.

Parker said he expected the drug to become a new standard treatment for these patients. Both Jean Charles Soria, a co-chair of the EMCC congress, and Michael Baumann, president of the European Cancer Organization, said Alpharadin was "a major new player" and likely to be "practice changing."

Kemal Malik, Bayer's head of global development, has described the success of Alpharadin -- which first showed promise in headline data released in June -- as a "transforming moment" for the company.

Sales of Alpharadin are expected to reach $662 million by 2015, according to consensus forecasts from Thomson Reuters Pharma. The drug's performance is also particularly important for Algeta, whose fortunes are tied closely its success.

Parker said the two firms now intend to use the data to submit the drug for regulatory approval.

TARGETED

Alpharadin is from a class of drugs called alpha-pharmaceuticals which work by sending tiny, charged, targeted doses of damaging radiation to a secondary tumour -- known as a metastasis -- in the bone.

Because it is so targeted, side effects are minimal in comparison with more conventional treatments, a factor that is likely to boost its popularity with patients and doctors.

"Compared to chemotherapy, which affects all the tissues of the body, radium-223 is highly targeted to the bone metastases, and it has a completely different safety profile," Parker explained. In the trial, he said, the drug was "extremely well tolerated."

Radium is similar to calcium in that it sticks to bone, particularly to where new bone is being formed, so it is a highly effective way of delivering radiation to a target.

"It takes only a single alpha particle to kill a cell," Parker said. "And collateral damage is minimised because the particles have such a tiny range -- a few millionths of a meter -- so we can be sure that the damage is being done where it should be, to the metastasis."

Parker's team studied the drug in patients with prostate cancer because it has a high tendency to spread to the bones. Around 90 percent of all men with prostate cancer will develop bone metastases in the advanced stages of the disease.

Prostate cancer is also the second most common cancer in men after lung cancer, killing an estimated 255,000 men each year.

Complete data from the trial showed that the median overall survival period for patients on the new drug was 14 months compared with 11.2 months for the placebo. The hazard ratio was 0.695, meaning that patients taking Alpharadin had a 30 percent lower rate of death compared to patients taking placebo.

(Reporting by Kate Kelland)



View the original article here



Peliculas Online

Senin, 12 September 2011

HEALTH MANAGEMENT. Major brain stent study: Experts say procedures effectively for some patients

An article in the New England Journal of medicine, says report on national institutes of health research on brain of stents, that aggressive treatment without Stenting better for high-risk patients.
But experts at the Cedars-Sinai Medical Center, who believe in the study, that this is suitable for some patients. You express concern that those who could benefit from minimally invasive placement of a mesh tube or stent blocked brain arteries open from this report can be discouraged. They say this study is a helpful start, and concerns about multiple study but not likely to understand the last word when Stenting may be appropriate, restrictions and exclusions.
"Get far greater than those generally patients in the study of received aggressive management of risk factors." Only with these heroic measures benefit the type of average patients, as have the study, ", says Patrick D. LYD, MD, Chairman of the Department of Neurology and Carmen and Louis Warsaw Chair of Neurology at Cedars-Sinai, expert on medical intervention and management of the stroke."
Michael j. Alexander, MD, Professor and clinical Chief of the Department of neurosurgery, and Director of Neurovascular Cedars-Sinai Center comments: "for certain patients - in particular for the drugs are not effective - most experts believe Stenting is a viable option." "We have many patients had had dramatic, immediate improvement in neurological function after intracranial stenting."
LYD and Alexander, the Cedars-Sinai led part of the clinical trial of 50-Center, expressed concern about this study including: sicker patients - such as those with multiple blockages of arteries or long blocks - were excluded; Some patients are probably benefit stenting. Most patients in the study had blockages in smaller arteries, which are more difficult to treat with stenting. "It is common in clinical trials of interventionellen or surgical procedures for patients of treatment to a higher rate of event" "have in the first 30 days." Long-term results provide more valid information. "Angioplasty and stenting has become commonplace in the treatment of blocked heart arteries, but Stenting in the brain is more difficult, because cerebral arteries are more sensitive than that of the heart," said Alexander, Member of the first NIH Steering Committee for this study. Evaluated the wingspan stent - the study - designed to more flexible too fragile cerebral arteries will start.
"This is the first study, which closely analyzed patient outcomes with intracranial Stenting longer-term." First trials with coronary (heart) Artery Stenting and Carotid Artery Stenting also were not very successful. However, as we could, to determine which patients are the best candidates for these treatments, and the technology has improved, they become very successful. I think the same is true of the intracranial Artery Stenting it, "Alexander said.
Alexander has more than 500 intracranial Stenting procedures and was involved in early testing of the device in the study, intrakranialer angioplasty and stenting system used gateway span. He is a consultant and device Proctor for Stryker Neurovascular, manufacturer of the gateway balloon and wingspan stent. He has no other financial interest in the company.
The device is approved by the food and drug administration.
The New England Journal of Medicine article is on the Stenting vs. aggressive medical management for recurrent stroke study, prevent in intracranial stenosis (SAMMPRIS) funded by the National Institute of neurological disorders and stroke, part of NIH.