| Literature DB >> 35032188 |
Akio Onishi1,2, Shigeo Fuji3, Shigehisa Kitano4, Akiko Miyagi Maeshima5, Kinuko Tajima1, Junko Yamaguchi1, Ichiro Kawashima1, Akihisa Kawajiri1, Tomonari Takemura1, Ayumu Ito1, Takashi Tanaka1, Keiji Okinaka1, Yoshihiro Inamoto1, Saiko Kurosawa1, Sung-Won Kim1, Wataru Munakata6, Dai Maruyama6, Kensei Tobinai6, Takahiro Fukuda1.
Abstract
The prognosis of patients with aggressive adult T cell leukemia-lymphoma (ATLL) is dismal even with intensive chemotherapy. Allogeneic hematopoietic stem cell transplantation (HSCT) is a promising option for patients with aggressive ATLL, but the posttransplant outcome remains unsatisfactory. Hence, to further improve clinical outcomes, novel therapeutic approaches are needed. The clinical significance of immune checkpoint protein expression has not been well-established in aggressive ATLL. This study aims to identify the association between the expression profile of immune checkpoint proteins on ATLL cells and clinical outcomes. This retrospective study cohort included 65 patients with aggressive ATLL diagnosed between 2001 and 2015 at the National Cancer Center Hospital, Tokyo, Japan. Formalin-fixed paraffin-embedded tissue was used to immunohistochemically determine the expression of immune checkpoint proteins and assess the impact of expression profile on the probability of overall survival from diagnosis or HSCT. The current analysis shows that cytotoxic T lymphocyte antigen-4 (CTLA-4), programmed death-1 (PD-1), and programmed death-ligand 1 (PD-L1) expressions were adverse prognostic factors in patients with aggressive ATLL. Experiments that assess the efficacy of immune checkpoint inhibitors are warranted to alleviate the adverse impacts associated with negative immune checkpoints.Entities:
Keywords: Adult T cell leukemia–lymphoma; Cytotoxic T lymphocyte antigen-4; Programmed death-1; Programmed death-ligand 1
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Year: 2022 PMID: 35032188 DOI: 10.1007/s00277-022-04760-8
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673