Robert Waag is alive and apparently cancer free more than two years after advanced melanoma reached his lungs, hips and other parts of his body – a feat only recently considered unthinkable for such patients.
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.
"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.
"The prospect that more and more patients will be cured is becoming a reality."
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.
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.
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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.'"
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.
"How can we do more? We are looking at combining immunotherapy agents."
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.
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.
"We have high hopes that the survival benefits from these drugs will extend well beyond five years."
"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."
But there is a cost. 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.