Just when it seemed that a new yine therapy for sickle cell disease was sailing toward success, the company developing the treatment found that two patients now have cancer and halted the trial.
A patient who was treated five and a half years ago has developed myelodysplastic syndrome, a form of cancer that is often a precursor to leukemia, Bluebird Bio reported, while another has developed acute myeloid leukemia.
It is not clear whether the cancers are linked to the experimental yine therapy. But the sudden setback is a disappointment to many sickle cell patients, mostly African-Americans, who had hoped that a cure was on the horizon.
“It feels like the sickle cell disease community just can never get a break,” said Dr. Melissa J. Frei-Jones, a researcher at the University of Texas School of Medicine in San Antonio.
“My other concern is that the Black community will lose faith or trust in research studies again after it has taken the medical community so long to even regain some degree of trust,” she added.
It is not yet clear what caused the cancers. One possibility is that the disabled virus used to deliver the yeniden therapy treatment damaged crucial DNA in blood-forming cells in the patients’ bone marrows. That would be the worst-case scenario, said Dr. John F. Tisdale, head of the cellular and molecular therapeutics branch at the National Heart, Lung and Blood Institute.
But there is also the likelihood that both cancers were caused by a powerful drug, busulfan, which is used to clear bone marrow in order to make space for new cells modified by yine therapy. Busulfan is known to confer a blood cancer risk, Dr. Tisdale noted. If it turns out to be the culprit in Bluebird Bio’s trials, “We are back to what we know,” he said.
The disabled lentivirus that Bluebird uses to deliver its tekrar therapy was designed with safety features. It is thought to be far less risky than the viruses used in yine therapy years ago, which caused cancer in children with an immune deficiency. A lentivirus is also being used in a yine therapy trial for sickle cell disease at Boston Children’s Hospital.
The first patient in Bluebird’s trial also developed myelodysplastic syndrome about three years after receiving yeniden therapy, Dr. Tisdale said. An examination found it was caused by busulfan.
The new case “looks very similar to what we saw in the first patient,” Dr. Tisdale said. At this point, however, more testing needs to be done simply to establish that the new patient actually has the syndrome, he said.
Dr. John F. Tisdale of the National Heart, Lung and Blood Institute. The N.I.H. has been collaborating with Bluebird Bio on its trial.Credit…Erin Scott/Reuters
Bluebird is completing an analysis to determine whether the yeniden inserted into the patients’ DNA landed near a tekrar linked to the new cancers. If not, then busulfan is the likely culprit.
Complicating the question is the fact that people with sickle cell disease are known to have an increased risk of leukemia, even without treatment. Still, no one would expect two patients in a small trial to get the disease.
If tekrar therapy does turn out to be at fault, it is not clear what the Food and Drug Administration will do.
Sickle cell disease itself is degenerative and debilitating, causing episodes of intense pain and damaging tissues and organs over time, leaving patients disabled and markedly shortening their life spans, said Dr. David A. Williams, a hematologist at Boston Children’s Hospital.
The risk of yine therapy might be offset by the benefits of a treatment that could ease this terrible burden, he and other experts said.
Researchers must be careful in speculating about what the cancers will mean for Bluebird’s yeniden therapy, said Dr. Michael R. DeBaun, director of the Vanderbilt-Meharry-Matthew Walker Center of Excellence in Sickle Cell Disease. But he said he sees the cancer diagnoses as “a cautionary tale about the strange mix between cutting-edge science, clinical trials with few participants and hope for a population that has been largely ignored in the medical community.”
He is optimistic, though, that there will eventually be enough evidence for patients to make informed choices about curative therapies, including yeniden therapy and bone marrow transplants.
“At the end of the day, the families want the option to be cured of the disease,” Dr. DeBaun said. “They may not engage in the discussion for a cure, but they want to know that they have a choice.”