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

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 ins...

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Published inBlood Vol. 121; no. 1; pp. 219 - 225
Main Authors Itonaga, Hidehiro, Tsushima, Hideki, Taguchi, Jun, Fukushima, Takuya, Taniguchi, Hiroaki, Sato, Shinya, Ando, Koji, Sawayama, Yasushi, Matsuo, Emi, Yamasaki, Reishi, Onimaru, Yasuyuki, Imanishi, Daisuke, Imaizumi, Yoshitaka, Yoshida, Shinichiro, Hata, Tomoko, Moriuchi, Yukiyoshi, Uike, Naokuni, Miyazaki, Yasushi
Format Journal Article
LanguageEnglish
Published Washington, DC Elsevier Inc 03.01.2013
Americain Society of Hematology
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Summary: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. •ATL patients who relapsed after allogeneic HSCT have a very high mortality rate and present a serious therapeutic challenge.•No large study exists that assesses the role of salvage therapies for relapsed ATL after HSCT; this is the first report summarizing the outcome.
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ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2012-07-444372