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Letters to the Editor

Indian Pediatrics 2006; 43:922

First-Cousin BMT in Thalassemia with Thymogam Conditioning


Allogeneic bone marrow transplantation (BMT) is the only curative therapy for thalassemia major. The cure rates in class 1 thalassemia are 90-95% and about 70-80% in class 3 thalassemiac children(1). However, only 25-30% of these children have a HLA identical sibling available as a donor for possible BMT(2). In such a situation the parents and first cousins are an option as a donor, when a history of consanguineous marriages is a custom in certain families. We had one such situation where a sibling donor was not available, but a first cousin of the patient was HLA identical, and was hence used as the donor.

The conditioning regimen used for bone marrow transplant in thalassemia involves the usage of ATGAM (Equine antithymocyte globulin). This drug is used as an immuno-suppressive agent to suppress the T-lymphocytes. Thymogam is anti-thymocyte globulin harvested from horses immunized with T- lymphocytes and is manufactured in India. Thymogam costs half the price of ATGAM and has been used in the treatment of aplastic anemia in India(3) and also in allogeneic peripheral blood stem cell transplant(4). However it has not been used as conditioning agent in BMT. We recently used thymogam (30 mg/kg/d from day 4 to day 2) for conditioning regimen in BMT for thalassemia with an intention of reducing costs. The effort was successful and we recommend this conditioning as one option in patients with thalassemia major.

Sharat Damodar,
Emami National Institute for
Bone Marrow Transplantation,
Narayana Hrudayalaya,
Anekal Taluk,
Bangalore 560099, Karnataka, India.
E-mail: [email protected]

References

1. Lucarelli G, Andreani M, Angelucci E. The cure of thalassemia by bone marrow transplantation. Blood Rev 2002; 16: 81-85.

2. Richard K Burt,H. Joachim Deeg, Scott Thomas, George W. Santos. Bone marrow transplanatation (Vademecum). 1996); 133-135. Landes Biosciences. USA.

3. Choudhry DR, Kumar R, Mishra P, Mahapathra M, Chatterjee T, Saxena R, et al. Response to antithymocyte globulin therapy in severe aplastic anemia: A single center study from India. Turk J Haematol (supplement) 2005; 22: Abstract.

4. Kumar R, Prem S, Mahapatra M, Seth T, Chowdhary DR, Mishra P, et al. Fludarabine, Cyclophosphamide and horse antithymocyte globulin conditioning regimen for allogeneic peripheral blood stem cell transplanatation performaed in non-HEPA filter rooms for multiply transfused patients with severe aplastic anemia. Bone Marrow Transplant. 2006 Mar 6; [Epub ahead of print].

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