Outcomes of adult patients with early T-cell precursor (ETP) acute lymphoblastic leukemia/lymphoma (ALL) and non-ETP T-ALL

Early T-cell precursor (ETP) acute lymphoblastic leukemia/lymphoma (ALL) is generally considered to be a high-risk subtype. We retrospectively analyzed the clinical outcomes of adult patients diagnosed with ETP-ALL or other T-cell ALL (non-ETP T-ALL). The subjects were 82 patients (ETP-ALL: n  = 18,...

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Published inInternational journal of hematology Vol. 117; no. 5; pp. 738 - 747
Main Authors Onishi, Yasushi, Furukawa, Eijiro, Kamata, Mayumi, Fukatsu, Masahiko, Kameoka, Yoshihiro, Hatta, Shunsuke, Hamada, Hiroyuki, Oyake, Tatsuo, Kai, Tatsuyuki, Sukegawa, Masumi, Nakajima, Shinji, Yanagiya, Ryo, Yamaguchi, Kohei, Takahashi, Taro, Harazaki, Yoriko, Izumi, Toru, Murai, Kazunori, Ito, Shigeki, Ikezoe, Takayuki, Ishizawa, Kenichi, Takahashi, Naoto, Harigae, Hideo
Format Journal Article
LanguageEnglish
Published Singapore Springer Nature Singapore 01.05.2023
Springer Nature B.V
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Summary:Early T-cell precursor (ETP) acute lymphoblastic leukemia/lymphoma (ALL) is generally considered to be a high-risk subtype. We retrospectively analyzed the clinical outcomes of adult patients diagnosed with ETP-ALL or other T-cell ALL (non-ETP T-ALL). The subjects were 82 patients (ETP-ALL: n  = 18, non-ETP T-ALL: n  = 64) for whom relevant immunophenotype data needed for classification were available. ETP-ALL patients were older (median age, 50.5 vs. 33.5 years, P  = 0.042) and had less mediastinal involvement (27.8 vs. 73.4%, P  < 0.001). The rate of complete remission (CR) with the first induction therapy was significantly lower in the ETP group (33.3 vs. 64.0%, P  = 0.03), but the CR rate within 2 cycles of chemotherapy did not differ significantly (61.1 vs. 76.6%, P  = 0.232). The 3-year overall survival (OS) rate was also similar in both groups (43.2 vs. 45.8%, P  = 0.992). The ETP phenotype had no impact on survival in the transplant group or the non-transplant group. A multivariate analysis identified the male sex as a poor prognostic factor (HR: 4.43, P  < 0.01), but not the immunophenotype of ETP. The prognosis for adult patients with ETP-ALL was comparable to that of non-ETP T-ALL patients. However, further studies aimed at improving the remission rate for ETP-ALL are needed.
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ISSN:0925-5710
1865-3774
DOI:10.1007/s12185-023-03546-6