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

Author:

Itonaga Hidehiro12,Tsushima Hideki2,Taguchi Jun2,Fukushima Takuya3,Taniguchi Hiroaki2,Sato Shinya12,Ando Koji24,Sawayama Yasushi2,Matsuo Emi24,Yamasaki Reishi25,Onimaru Yasuyuki12,Imanishi Daisuke2,Imaizumi Yoshitaka2,Yoshida Shinichiro24,Hata Tomoko2,Moriuchi Yukiyoshi12,Uike Naokuni6,Miyazaki Yasushi2

Affiliation:

1. Department of Hematology, Sasebo City General Hospital, Sasebo, Japan;

2. Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan;

3. School of Health Sciences, University of the Ryukyus, Nishihara, Japan;

4. Department of Internal Medicine, National Hospital Organization Nagasaki Medical Center, Ohmura, Japan;

5. Department of Internal Medicine, Nagasaki Rousai Hospital, Sasebo, Japan; and

6. Department of Hematology, National Kyushu Cancer Center, Fukuoka, Japan

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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