| Literature DB >> 26361794 |
Hiroo Katsuya1, Kenji Ishitsuka1, Atae Utsunomiya2, Shuichi Hanada3, Tetsuya Eto4, Yukiyoshi Moriuchi5, Yoshio Saburi6, Masaharu Miyahara7, Eisaburo Sueoka8, Naokuni Uike9, Shinichiro Yoshida10, Kiyoshi Yamashita11, Kunihiro Tsukasaki12, Hitoshi Suzushima13, Yuju Ohno14, Hitoshi Matsuoka15, Tatsuro Jo16, Masahiro Amano17, Ryosuke Hino18, Mototsugu Shimokawa19, Kazuhiro Kawai20, Junji Suzumiya21, Kazuo Tamura1.
Abstract
Adult T-cell leukemia/lymphoma (ATL) is a malignancy of mature T lymphocytes caused by human T-lymphotropic virus type I. Intensive combination chemotherapy and allogeneic hematopoietic stem cell transplantation have been introduced since the previous Japanese nationwide survey was performed in the late 1980s. In this study, we delineated the current features and management of ATL in Japan. The clinical data were collected retrospectively from the medical records of patients diagnosed with ATL between 2000 and 2009, and a total of 1665 patients' records were submitted to the central office from 84 institutions in Japan. Seventy-one patients were excluded; 895, 355, 187, and 157 patients with acute, lymphoma, chronic, and smoldering types, respectively, remained. The median survival times were 8.3, 10.6, 31.5, and 55.0 months, and 4-year overall survival (OS) rates were 11%, 16%, 36%, and 52%, respectively, for acute, lymphoma, chronic, and smoldering types. The number of patients with allogeneic hematopoietic stem cell transplantation was 227, and their median survival time and OS at 4 years after allogeneic hematopoietic stem cell transplantation was 5.9 months and 26%, respectively. This study revealed that the prognoses of the patients with acute and lymphoma types were still unsatisfactory, despite the recent progress in treatment modalities, but an improvement of 4-year OS was observed in comparison with the previous survey. Of note, one-quarter of patients who could undergo transplantation experienced long survival. It is also noted that the prognosis of the smoldering type was worse than expected.Entities:
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Year: 2015 PMID: 26361794 DOI: 10.1182/blood-2015-03-632489
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113