Umbilical cord blood transplants become standard
| By Marie McCullough, The Philadelphia Inquirer | |
| McClatchy-Tribune Information Services |
That's when his parents,
Nonprofit cord-blood banking is a complicated, costly network, but it has been growing steadily, thanks to federal support, stem-cell research -- and families like the Shaffers.
Sarah and Marc discovered that in the
This month,
Three years ago,
Of the 3,200 babies delivered at
"Ethnically diverse groups are underrepresented as cord-blood donors and have a lower chance of finding a matched donor," said
"Our biggest challenge is building diversity," echoed
Mrowiec spoke at a
"Do you know why we're here?" his mother asked him.
"Because I got cells that fixed my bones," the precocious preschooler piped up.
Then, to her mild mortification, he used her smartphone to play his favorite song --
Standard of care
The stem cells in cord blood, though not as versatile as stem cells from embryos, can spawn the whole blood and immune system, including oxygen-carrying red blood cells and disease-fighting white blood cells.
More than 80 cancers and disorders, including leukemia, can be treated with a blood stem-cell transplant.
The usual source of such stem cells is bone marrow from a donor. The
Not until 1988 in
Umbilical cords have the disadvantage of yielding only a tiny amount of stem-cell-laden fluid. Mason was fortunate to be matched to three stored cord-blood units.
In fact, the vast majority of donated cords are rejected as too small, though they can still be used for research, Mrowiec said. (That barrier may be lifted soon; researchers are developing ways to multiply blood stem cells in the lab.)
But cord blood also has advantages over bone marrow. It is painless to collect, and less likely to cause complications if the tissue match is imperfect.
That's why cord-blood transplantation has gone from experimental to standard of care over the last decade. About 25,000 have been done worldwide, 10 times more than in 2003.
Only a small fraction of these transplants have been done through private, for-profit storage banks, which charge a collection fee of up to
Mason's parents and brother were not a match for him.
Paying it forward
Mason's form of malignant infantile osteopetrosis, or MIOP, is ultra-rare, afflicting an estimated 1 in 500,000 babies. It causes bones to be abnormally dense. That can interfere with bone marrow, causing recurrent infections, bleeding, anemia. The skull, meanwhile, gets too large and heavy and often presses on nerves within the head, causing vision loss, hearing loss, and facial paralysis.
Given the rarity and varied problems of MIOP, babies may be misdiagnosed until the disease has done irreparable or lethal damage.
In Mason's first five months of life, he was treated for seizures, acid reflux, a severe respiratory infection, and eye problems.
His parents rationalized that it could be worse, and that his glasses looked "cute," but they were increasingly worried. Sarah, a former oncology unit social worker, is a project manager for insurance giant UnitedHealthcare. Marc has master's degree in business administration and works for
It was Mason's abnormally large belly that prompted his pediatrician to order diagnostic tests at A.I. duPont
"First," his mother recalled, "they said it might be leukemia. Marc and I cried. The next morning, they said, 'It's not leukemia. We need to think outside the box.'
"When they told us it was MIOP, they said he would die by age 2 without treatment. But if he had a stem-cell transplant, that could kill him, too."
Indeed, destroying a baby's native blood system with high-dose chemotherapy is a risky last resort. But Mason's transplant went as smoothly as such terrifying things can go, and after 50 days in the hospital, he went home, effectively reborn.
That was also the birth of his mother's idea for promoting public cord-blood donation, and for an online support group for MIOP families worldwide.
The foundation "was born out of this absolute desperation to make sense of what Mason went though, and pay our blessings forward," Sarah said. Her reaction was not unusual. A cord-blood collection program at
Verter praised the Shaffers for educating expectant parents about an altruistic option they may not know about and facilitating that option.
"They're doing a huge public service," she said.
In the three years since their foundation was launched, it has helped collect 1,700 cord-blood units, of which 226 have been banked and three used for transplant, a "very good" record, Sarah said.
"I think cord-blood collection is going to boom and take off as the research finds more diseases that can be treated," she said. "The possibilities are endless for this tissue that is normally thrown in the trash."
INFORMATION
For an overview of cord-blood medical therapies and storage options, see parentsguidecordblood.org.
It shows how private and public cord-blood banks work and which U.S. hospitals accept donations of umbilical cords. If there is no donation site near you, you can find out how to send your baby's cord blood to a mail-in donation program.
mmccullough@
215-854-2720
@repopter
___
(c)2014 The Philadelphia Inquirer
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