Validation of the iATL-PI prognostic index in therapeutic decision-making for patients with smoldering and chronic ATL: a multicenter study
Validation of the iATL-PI prognostic index in therapeutic decision-making for patients with smoldering and chronic ATL: a multicenter study
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冒烟型和慢性 ATL 患者治疗决策中 iATL-PI 预后指数的验证:一项多中心研究
DOI:
10.1007/s12185-022-03473-y
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发表时间:
2022
影响因子:
2.1
通讯作者:
Tsukasaki Kun
中科院分区:
文献类型:
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作者:
Imaizumi Yoshitaka;Iwanaga Masako;Nosaka Kisato;Ishitsuka Kenji;Ishizawa Kenichi;Ito Shigeki;Amano Masahiro;Ishida Takashi;Uike Naokuni;Utsunomiya Atae;Ohshima Koichi;Tanaka Junji;Tokura Yoshiki;Tobinai Kensei;Watanabe Toshiki;Uchimaru Kaoru;Tsukasaki Kun
Adult T cell leukemia-lymphoma (ATL) is clinically heterogeneous and is classified into four subtypes: acute, lymphoma, chronic, and smoldering. Recently, a new prognostic index based on the value of soluble interleukin-2 receptor, denoted the “iATL-PI,” has been proposed for patients with smoldering and chronic ATL. To evaluate the effectiveness of the iATL-PI, we re-analyzed our previously published data on 176 patients with smoldering or chronic ATL (76 smoldering, 100 chronic) diagnosed between 2010 and 2011, as well data from the subsequent follow-up study on prognosis between 2016 and 2017. The proportions for the low-, intermediate-, and high-risk iATL-PI groups at the time of ATL diagnosis were 44.7%, 48.7%, and 5% for smoldering ATL; 6.3%, 71.9%, and 21.9% for favorable chronic ATL; and 5.9%, 27.9%, and 66.2% for unfavorable chronic ATL, respectively. The survival of patients with smoldering or chronic ATL as a whole was significantly stratified according to the three iATL-PI groups. Most patients with unfavorable chronic ATL in the low iATL-PI risk group had indolent clinical courses. Our results showed that iATL may become a useful tool to predict the prognosis of smoldering and chronic ATL, which have diverse clinical courses.
DOI:
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发表时间:
--
期刊:
影响因子:
--
作者:
通讯作者:
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影响因子:
64.8
作者:
Kataoka, Keisuke;Shiraishi, Yuichi;Ogawa, Seishi
通讯作者:
Ogawa, Seishi
影响因子:
6.5
作者:
SHIMOYAMA, M
通讯作者:
SHIMOYAMA, M