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Posts tagged as “sickle cell disease”

Chicago Woman Iesha Thomas Becomes 1st Adult Cured of Sickle Cell Disease With Chemo-Free Technique

Ieshea Thomas, a Chicago woman, is the first adult to be cured of sickle cell disease with the chemotherapy-free procedure at UI Hospital. Photo: UI News Release
Ieshea Thomas, a Chicago woman, is the first adult to be cured of sickle cell disease with the chemotherapy-free procedure at UI Hospital. (Photo: UI News Release)

Iesha Thomas has been in and out of hospitals battling sickle cell disease since she was only 8 months old. This summer, 33-year-old Thomas became the first adult to be cured of sickle cell disease with a chemotherapy-free procedure at University of Illinois Hospital & Health Sciences System (UI Health), the University reported. Thomas is one of 12 adult patients cured of sickle cell disease as part of a clinical trial at UI Health that used a unique procedure for stem cell transplantation from healthy tissue matched from a sibling donor.

Findings from phase I/II of the clinical trial are published online in the journal Biology of Blood & Marrow Transplantation.
Stem cell transplants have been used for years as a means of possibly curing sickle cell disease. However, before the stem cell transplant could be completed patients would have to endure a taxing course of drugs to kill the cancer cells, otherwise known as chemotherapy.
The more traditional form of stem cell transplant uses chemotherapy to destroy the patient’s own bone marrow, which shuts down their immune system and makes them vulnerable to infections.
The new technique – first developed and performed at the National Institutes of Health campus in Maryland – eliminates the need for chemotherapy to prepare the patient to receive the transplanted cells and offers the prospect of cure for tens of thousands of adults suffering from sickle cell disease – many of them Black Americans.
According to the National Heart, Lung & Blood Institute (NIH), about 1 in 13 African American babies is born with sickle cell trait. About 1 in every 365 black children is born with sickle cell disease.
About 90 percent of the approximately 450 patients who have received stem cell transplants for sickle cell disease have been children. Chemotherapy has been considered too risky for adult patients, who are often more weakened than children by the disease.
“Adults with sickle cell disease are now living on average until about age 50 with blood transfusions and drugs to help with pain crises, but their quality of life can be very low,” says Dr. Damiano Rondelli, chief of hematology/oncology and director of the blood and marrow transplant program at UI Health, and corresponding author on the paper.
“Now, with this chemotherapy-free transplant, we are curing adults with sickle cell disease, and we see that their quality of life improves vastly within just one month of the transplant,” said Rondelli, who is also the Michael Reese Professor of Hematology in the UIC College of Medicine.

Julius and Desmond Means were cured of sickle cell disease at UI Health through a chemotherapy-free stem cell transplant in 2013. Their older brother, Clifford (center), was the donor. Photo: UIC News Release
Julius and Desmond Means were cured of sickle cell disease at UI Health through a chemotherapy-free stem cell transplant in 2013. Their older brother, Clifford (center), was the donor. Photo: UIC News Release

The chemo-free transplant performed by UI is described in a news release:

In the reported trial, the researchers transplanted 13 patients, 17 to 40 years of age, with a stem cell preparation from the blood of a tissue-matched sibling. Healthy sibling donor-candidates and patients were tested for human leukocyte antigen, a set of markers found on cells in the body. Ten of these HLA markers must match between the donor and the recipient for the transplant to have the best chance of evading rejection.
In a further advance of the NIH procedure, physicians at UI Health successfully transplanted two patients with cells from siblings who matched for HLA but had a different blood type.
In all 13 patients, the transplanted cells successfully took up residence in the marrow and produced healthy red blood cells. One patient who failed to follow the post-transplant therapy regimen reverted to the original sickle cell condition.

In Thomas’ case, her sister was a match and following the transplantation she no longer required blood transfusions.
Further research on this type of stem cell transplant is needed, but doctors are hopeful for what early trials show for adults.
“Adults with sickle cell disease can be cured without chemotherapy – the main barrier that has stood in the way for them for so long,” Rondelli said. “Our data provide more support that this therapy is safe and effective and prevents patients from living shortened lives, condemned to pain and progressive complications.”
To learn more about ongoing sickle cell transplant trials at NIH (a participant in a trial will not be charged for a procedure) call 1-800-411-1222 or visit the NIH clinical trials registry at www.clinicaltrials.gov and search under ‘sickle cell disease.”
article by Gwendolyn Harris via blackdoctor.org

Through the Pain, 25 Year-Old Eric Williams and Others Speak Out During National Sickle Cell Awareness Month

Sickle Cell Disease sufferers from around Southern California banded together Wednesday to bring awareness for September’s National Sickle Cell Awareness Month, like Eric Williams, a 25-year-old who suffers from the genetic disease. (photo via nbclosangeles.com)

“You get slow throbs and it builds and then feels like someone is punching you, then stabbing you, then a building is coming down on you,” said Eric Williams, a 25-year-old living with the genetic disease.

As a child, Williams said he had more access to pediatricians who specialized in the disease.  As an adult, it’s considerably harder for him to find specialists in Los Angeles County, where he lives, that treat adults.

Dr. Susan Claster is one hematologist in Orange County who does treat adults, but has trouble handling a huge flux of patients by herself.  “I can’t see everybody, and we need to find others who are interested in seeing these patients,” Claster said. “That really frustrates me.”

California and eight other states recently received grant funding to expand treatment for sickle cell patients.

Williams, set to attend nursing school, said he won’t let the disease slow him down, and hopes to inspire others.  “I would like to inspire them by having them see you can go to college and get a job and be part of mainstream society – you just have to figure out your way to do it,” Williams said.

To learn more about Sickle Cell Disease, go to: http://sicklecelldisease.org/index.cfm?page=news&id=94

original article by Angie Crouch and Heather Navarro via nbclosangeles.com; additions by Lori Lakin Hutcherson

NFL’s McCourty Twins Raise Awareness and Funds via "Tackle Sickle Cell" Campaign (VIDEO)