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Efficacy of Tucidinostat Pre-emptive Therapy for Peripheral T-cell Lymphoma after Allogeneic Stem Cell Transplantation.

1/5 보강
Internal medicine (Tokyo, Japan) 📖 저널 OA 63.8% 2024: 6/6 OA 2025: 37/56 OA 2026: 50/84 OA 2024~2026 2026 Vol.65(2) p. 318-321
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
환자: refractory PTCL who underwent allo-SCT followed by preemptive therapy with tucidinostat
I · Intervention 중재 / 시술
allo-SCT followed by preemptive therapy with tucidinostat
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
The patient has maintained complete remission for 2-years. Thus, given its mechanism, tucidinostat may be a viable option for post-transplant therapy.

Takada K, Tachi N, Shonai T, Kawasaki K, Sone T, Ogata H, Kato S, Kobayashi S, Kimura F

📝 환자 설명용 한 줄

Recently, various molecular targeted therapies have been developed for peripheral T-cell lymphoma (PTCL).

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↓ .bib ↓ .ris
APA Takada K, Tachi N, et al. (2026). Efficacy of Tucidinostat Pre-emptive Therapy for Peripheral T-cell Lymphoma after Allogeneic Stem Cell Transplantation.. Internal medicine (Tokyo, Japan), 65(2), 318-321. https://doi.org/10.2169/internalmedicine.5535-25
MLA Takada K, et al.. "Efficacy of Tucidinostat Pre-emptive Therapy for Peripheral T-cell Lymphoma after Allogeneic Stem Cell Transplantation.." Internal medicine (Tokyo, Japan), vol. 65, no. 2, 2026, pp. 318-321.
PMID 40571612 ↗

Abstract

Recently, various molecular targeted therapies have been developed for peripheral T-cell lymphoma (PTCL). However, relapsed/refractory (r/r) PTCL is associated with poor outcomes. Allogeneic stem cell transplantation (allo-SCT) can be effective against r/r PTCL owing to its graft-versus-lymphoma effect. Nevertheless, a posttransplant relapse is common. Although post-transplant preemptive therapy has shown favorable outcomes in leukemia, reports on its use for PTCL are extremely limited. We herein present the case of a patient with refractory PTCL who underwent allo-SCT followed by preemptive therapy with tucidinostat. The patient has maintained complete remission for 2-years. Thus, given its mechanism, tucidinostat may be a viable option for post-transplant therapy.

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