Waag, 77, is on the immunotherapy Keytruda, a new type of drug that
enlists the body's defenses in the fight. The first new
immunotherapy drug for cancer was introduced in 2011, so long term
efficacy is unknown. But the approach is showing promise. Before
these drugs, the prognosis for most patients with advanced melanoma
was a year at best. In one study of Keytruda, 40 percent of such
patients survived at least three years, and 10 percent showed no
evidence of cancer. "The prospect that more and more patients will
be cured is becoming a reality," said Waag's oncologist Dr Lynn
Schuchter, chief of hematology oncology at Philadelphia's Penn
Medicine who has no current financial ties to drug companies.
After decades in which progress meant eking out weeks or months at
the end of life, such treatments are changing the dialogue around
cancer. Leading cancer experts are beginning to talk about the
possibility some patients will beat diagnoses once considered death
sentences. The White House calls it an "inflection point" with
cancer science apparently poised for big gains. In his state of the
union address in January, President Barack Obama announced a federal
initiative to "cure cancer once and for all," including up to $1
billion to boost the best ideas in prevention, early detection and
treatment. Silicon Valley innovators are joining the effort too.
Napster founder Sean Parker has endowed a foundation aimed at
accelerating the development of promising treatments. For the most
difficult cancers, the day that the word "cure" can be used with
confidence remains a long way off, top oncologists and drug company
executives said in interviews with Reuters. But as they gather
Friday at the annual meeting of American Society of Clinical
Oncology in Chicago, a new optimism is expected to permeate many
conversations. Talking about recent progress against melanoma, the
first cancer to be targeted by immunotherapy, Dr Daniel Hayes,
incoming ASCO president, summed up the cautious shift: "It makes us
wonder if we can use the word "cure.'"
'RAISING THE BAR FOR SURVIVAL'
Doctors at the ASCO meeting will hear about efforts to attack the
toughest cancers with immunotherapy, including another potential
game-changer that tweaks a patient's own cells to become more
effective cancer-killers, as well as other drugs and combinations.
Merck & Co's Keytruda and Opdivo, a rival drug made by Bristol Myers
Squibb, work by blocking a protein tumors use to evade detection by
the immune system. Roche Holding AG recently received U.S.
regulatory approval for a similar drug, Tecentriq, for treating
bladder cancer. One study of Opdivo in patients with a type of
advanced lung cancer found that 23 percent were alive two years
after starting the drug, compared to 8 percent of those given
standard chemotherapy. "We are raising the bar for overall
survival," said Fouad Namouni, head of medical research at Bristol
Myers. "How can we do more? We are looking at combining
immunotherapy agents." Researchers are also trying to determine
which patients will respond best to immunotherapy and how long they
need to continue treatment. In the recent Keytruda study, the
melanoma in two patients got worse after their treatment was
stopped. Waag, a retired professor of engineering at New York's
University of Rochester, is wary of stopping treatment. First
diagnosed in 1998, Waag's skin lesions were surgically removed, and
he was apparently disease-free for 13 years. "Then it came back -
and with a vengeance," he said. Some patients, including Waag,
experience no apparent side effects. But immunotherapy drugs can
cause liver inflammation and other problems linked to revving up the
body's immune system, requiring patients to stop treatment. A
substantial portion of patients do not respond to the drugs at all.
Immunotherapy is "the first broad spectrum anti-cancer agent" since
radiation, said Roger Perlmutter, head of research at Keytruda maker
Merck. "We are just scratching the surface," he said. "When we are
able to treat patients with earlier-stage disease we would expect an
even better response and longer durability." Still, Perlmutter said
he was reluctant to use the word "cure" because people who have had
cancer are at higher risk of recurrence than people who have not. "I
prefer to say we can treat this malignancy - remove any symptoms so
daily living is as normal as possible," he said.
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BIG AMBITIONS, BIG PRICE
For many oncologists, a real cure will be realized only after
decades of follow-up study show significant numbers of patients
survive with no signs of cancer. The current benchmark for patients
to be considered cancer free is five years. That is a low bar, said
Michael Postow, an oncologist at New York's Memorial Sloan Kettering
Cancer Center whose research is supported by Bristol Myers and other
companies. "If the patient is 38, for example, we need even more
than five years," Postow said. "We have high hopes that the survival
benefits from these drugs will extend well beyond five years." At
around $150,000 a year, Keytruda and Opdivo are expensive. Another,
still experimental, immunotherapy approach that is generating
excitement could cost much more.
Chimeric antigen receptor T-cell, or CAR-T, therapies are made by
extracting a patient's immune system T cells, altering their DNA to
sharpen their ability to spot and kill cancer cells, and infusing
them back into the same patient.
Early studies have shown them apparently eliminating blood cancers,
such as leukemia and lymphoma, in 40 to 90 percent of patients. But,
in some cases, there were potentially life-threatening side effects.
At the ASCO meeting, Kite Pharma Inc, Juno Therapeutics Inc will
present more results from trials using CAR-T cell drugs to treat
patients with advanced lymphoma. "All the preliminary clinical data
that have been generated, both by us and by our competitors indicate
that the treatment benefit will be transformative," said David
Chang, Kite's chief medical officer. If a single CAR-T treatment
safely wipes out a patient's lymphoma - something not yet proven -
Wall Street analysts have estimated Kite could charge up to
$450,000.
(Reporting By Deena Beasley; Editing by Michele Gershberg and Lisa
Girion)
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