Newer Treatments Are Transforming the Lives of Thalassemia Patients Worldwide,

Newer Treatments Are Transforming the Lives of Thalassemia Patients Worldwide, Says Cleveland Clinic Children’s Expert Ahead of International Thalassemia Day on May 8

Bone marrow transplants, a new medication and gene therapy are collectively helping to eliminate or reduce the need for patients to undergo time-consuming and potentially risky blood transfusions

5 May, 2022, CLEVELAND: Alternative approaches to bone marrow transplants, new medications and successful gene therapy trials are all promising to transform the lives of thalassemia patients by helping to stop or significantly reduce their reliance blood transfusions, says an expert from a leading global health system, Cleveland Clinic, ahead of International Thalassemia Day on May 8.

Thalassemia is the most common inherited single-gene disorder in the world and occurs most frequently in people from the Middle East, Mediterranean countries, North Africa, India, Central Asia, and Southeast Asia. There are two types, alpha and beta, depending on the genetic defects that can occur in the protein chains that make up hemoglobin. Patients with alpha thalassemia tend to be silent carriers without symptoms, while patients with beta thalassemia major will have major symptoms early after birth and traditionally require frequent blood transfusions, which can lead to iron overload with the potential to damage the liver, heart, and endocrine system.

“There have been great advancements in treatments and research in recent years,” says Dr. Rabi Hanna, a pediatric hematologist-oncologist at Cleveland Clinic Children’s. “Thalassemia is now viewed as a disease that can be cured, with gene therapy as a novel step that uses the patients’ own hematopoietic stem cells to produce healthier red blood cells and cure their blood disorder.”

Dr. Hanna points adds that from a global perspective, gene therapy is more commonly found in research settings than in clinical practice, but that the clinical trials show very promising results. “Thalassemia patients who have received gene therapy have either eliminated or significantly reduced the amount of blood transfusions needed to manage their condition. With gene therapy, we can remove the challenges that thalassemia patients face and give them the courage to pursue their goals and dreams,” he says.

While gene therapy is seen as a viable, one-off treatment for thalassemia, Dr. Hanna points out that it is a complicated process, which includes chemotherapy to get rid of the old bone marrow and create space for new, modified stem cells. He says this could require admission to hospital for four to six weeks until new the stem cells are working and able to produce white blood cells, platelets and healthier red blood cells.

Dr. Hanna adds, however, “We are hopeful that in the future we can target the bone marrow more selectively using reduced-intensity chemotherapy or other medication to avoid the acute and long-term toxicity associated with high doses of chemotherapy.”

Other recent developments that have transformed the treatment options available to patients include a medication with the generic name luspatercept-aamt, given in the form of an injection every three weeks. In the US, this was approved by the FDA in 2019 and works by enhancing erythroid (red blood cell) maturation and reducing the need for blood transfusions by up to 50% in some patients.

While luspatercept-aamt is not in itself a cure, Dr. Hanna points out that it can also be used to enhance outcomes in curative bone marrow transplantations, which have also become more widely accessible in recent years thanks to a new transplant approach. Dr. Hanna was among the pioneers of the haplo-identical bone marrow transplant that allows for non-identical-HLA (human leukocyte antigen) donors. He explains that the reduction in blood transfusions means the patient has better health prior to the procedure, and also has fewer antibodies that could potentially attack transplanted bone marrow. 

“With the wider adoption of gene therapy on the horizon and the use of luspatercept-aamt to improve bone-marrow transplant outcomes, almost any patient can be cured,” Dr. Hanna says.

Worldwide, there are 270 million carriers with abnormal hemoglobin and thalassemia, with 300,000-400,000 babies born with serious hemoglobin disorders annually, according to the US National Institute of Health. The International Thalassemia Federation has declared this year’s awareness theme as “Be Aware. Share. Care: Working with the global community as one to improve thalassemia knowledge.”


About Cleveland Clinic Children’s

Cleveland Clinic Children’s is a part of the Cleveland Clinic health system and offers full medical, surgical and rehabilitative care for infants, children and adolescents. Cleveland Clinic Children’s supports 389 beds in four acute care hospitals and one post-acute specialty hospital. In addition, pediatric services are available at more than 50 outpatient clinic locations across Northeast Ohio. A staff of more than 300 full-time pediatricians and sub-specialists see 750,000 pediatric visits each year and provide hospital care for 13,000 children per year. Cleveland Clinic Children’s is a non-profit, multi-specialty academic medical center integrating clinical care, research, and education. Cleveland Clinic Children’s consistently ranks among the “Best Children’s Hospitals” by U.S. News & World Report. Visit us online at and on Facebook at

About Cleveland Clinic

Cleveland Clinic is a nonprofit multispecialty academic medical center that integrates clinical and hospital care with research and education. Located in Cleveland, Ohio, it was founded in 1921 by four renowned physicians with a vision of providing outstanding patient care based upon the principles of cooperation, compassion and innovation. Cleveland Clinic has pioneered many medical breakthroughs, including coronary artery bypass surgery and the first face transplant in the United States. U.S. News & World Report consistently names Cleveland Clinic as one of the nation’s best hospitals in its annual “America’s Best Hospitals” survey. Among Cleveland Clinic’s 72,500 employees worldwide are more than 5,050 salaried physicians and researchers, and 17,800 registered nurses and advanced practice providers, representing 140 medical specialties and subspecialties. Cleveland Clinic is a 6,500-bed health system that includes a 173-acre main campus near downtown Cleveland, 22 hospitals, more than 220 outpatient facilities, including locations in northeast Ohio; southeast Florida; Las Vegas, Nevada; Toronto, Canada; Abu Dhabi, UAE; and London, England. In 2021, there were 10.2 million total outpatient visits, 304,000 hospital admissions and observations, and 259,000 surgical cases throughout Cleveland Clinic’s health system. Patients came for treatment from every state and 185 countries. Visit us at Follow us at News and resources available at

Editor’s Note: Cleveland Clinic News Service is available to provide broadcast-quality interviews and B-roll upon request.


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