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Treatment of relapsed adult T-cell leukemia/lymphoma after allogeneic hematopoietic stem cell transplantation: the Nagasaki Transplant Group experience.

Authors :
Itonaga H
Tsushima H
Taguchi J
Fukushima T
Taniguchi H
Sato S
Ando K
Sawayama Y
Matsuo E
Yamasaki R
Onimaru Y
Imanishi D
Imaizumi Y
Yoshida S
Hata T
Moriuchi Y
Uike N
Miyazaki Y
Source :
Blood [Blood] 2013 Jan 03; Vol. 121 (1), pp. 219-25. Date of Electronic Publication: 2012 Oct 24.
Publication Year :
2013

Abstract

Adult T-cell leukemia/lymphoma (ATL) relapse is a serious therapeutic challenge after allogeneic hematopoietic stem cell transplantation (allo-SCT). In the present study, we retrospectively analyzed 35 patients who experienced progression of or relapsed persistent ATL after a first allo-SCT at 3 institutions in Nagasaki prefecture (Japan) between 1997 and 2010. Twenty-nine patients were treated by the withdrawal of immune suppressants as the initial intervention, which resulted in complete remission (CR) in 2 patients. As the second intervention, 9 patients went on to receive a combination of donor lymphocyte infusion and cytoreductive therapy and CR was achieved in 4 patients. Of 6 patients who had already had their immune suppressants discontinued before the relapse, 3 patients with local recurrence received local cytoreductive therapy as the initial treatment, which resulted in CR for more than 19 months. Donor lymphocyte infusion-induced remissions of ATL were durable, with 3 cases of long-term remission of more than 3 years and, interestingly, the emergence or progression of chronic GVHD was observed in all of these cases. For all 35 patients, overall survival after relapse was 19.3% at 3 years. The results of the present study suggest that induction of a graft-versus-ATL effect may be crucial to obtaining durable remission for ATL patients with relapse or progression after allo-SCT.

Details

Language :
English
ISSN :
1528-0020
Volume :
121
Issue :
1
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
23100309
Full Text :
https://doi.org/10.1182/blood-2012-07-444372