A case series of adult T-cell leukemia-lymphoma, associated with human T-cell leukemia virus type-1, at a single center in a non-viral-endemic metropolitan area

Autor: Kunihiro Tsukasaki, Mika Kohri, Yu Akuzawa, Nobutaka Kawai, Naoki Takahashi, Norio Asou, Daisuke Okamura, Tomoya Maeda, Akira Matsuda, Tsuyoshi Saeki, Maho Ishikawa
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
non-viral-endemic metropolitan area
Male
medicine.medical_specialty
Referral
medicine.medical_treatment
Hematopoietic stem cell transplantation
Single Center
Adult T-cell leukemia/lymphoma
Disease-Free Survival
human T-cell leukemia virus type I (HTLV-1)
03 medical and health sciences
0302 clinical medicine
Adult T-cell leukemia-lymphoma (ATL)
immune system diseases
Internal medicine
hemic and lymphatic diseases
Antineoplastic Combined Chemotherapy Protocols
medicine
metropolitan region
Humans
Leukemia-Lymphoma
Adult T-Cell

Aged
Aged
80 and over

Human T-lymphotropic virus 1
Performance status
business.industry
Hematopoietic Stem Cell Transplantation
Combination chemotherapy
General Medicine
Middle Aged
medicine.disease
Allografts
Lymphoma
Survival Rate
Leukemia
030104 developmental biology
030220 oncology & carcinogenesis
Original Article
Female
business
Zdroj: Journal of Clinical and Experimental Hematopathology : JCEH
ISSN: 1880-9952
1346-4280
Popis: We examined 13 patients with adult T-cell leukemia-lymphoma (ATL) diagnosed between 2007 and 2018 at a single center in a metropolitan area non-endemic for human T-cell leukemia virus type I (HTLV-1). The median age of the patients (eight male, five female) was 65 years (range, 48-83). The time from onset of symptoms to referral to our center was relatively short (median, 2 months; range, 1-9 months). Upon referral, all patients were suspected to have lymphoma, five were examined for soluble IL-2 receptor and two were examined for anti-HTLV-1 antibody. In ten of the 13 (77%), the patient themselves or their relatives were born in Kyushu. The birth places of the remaining three patients were unknown. Three patients (23%) had family histories of lymphoma. They all exhibited aggressive ATL (five acute, eight lymphoma type); however, the disease status was generally stable, with relatively stable performance status and low scores for prognostic indices. After combination chemotherapy, eight (62%) achieved remission. However, long-term remission was achieved in only one patient with localized lymphoma-type ATL and one young patient after allogeneic hematopoietic stem cell transplantation. In conclusion, at a center in a metropolitan and HTLV-1 non-endemic area in Japan, patients with ATL were relatively young and mainly presented with aggressive subtypes. At initial referral to our center, all 13 patients were suspected of having lymphoma but only two of having ATL. For centers in similar areas of Japan, prompt diagnosis and appropriate treatment of ATL patients will become increasingly necessary following the recent migration of HTLV-1 carriers to non-endemic areas.
Databáze: OpenAIRE