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Current Treatment Patterns and the Role of Upfront Autologous Stem Cell Transplantation in Patients with Peripheral T-Cell Lymphoma: A Korean Nationwide, Multicenter Prospective Registry Study (CISL 1404)open access

Authors
Cho, HyungwooYoon, Dok HyunShin, Dong-YeopKoh, YoungilYoon, Sung-SooKim, Seok JinDo, Young RokLee, Gyeong-WonKwak, Jae-YongPark, YongKim, Min KyoungKang, Hye JinYi, Jun HoYoo, Kwai HanLee, Won SikPark, Byeong BaeJo, Jae CheolEom, Hyeon-SeokKim, Hyo JungJeong, Seong HyunWon, Young-WoongSohn, Byeong SeokKwon, Ji-HyunSuh, CheolwonKim, Won Seog
Issue Date
Apr-2023
Publisher
KOREAN CANCER ASSOCIATION
Keywords
Peripheral T-cell lymphoma; Treatment pattern; Autologous stem cell transplantation
Citation
CANCER RESEARCH AND TREATMENT, v.55, no.2, pp.684 - 692
Indexed
SCIE
SCOPUS
KCI
Journal Title
CANCER RESEARCH AND TREATMENT
Volume
55
Number
2
Start Page
684
End Page
692
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/189358
DOI
10.4143/crt.2022.1434
ISSN
1598-2998
Abstract
PURPOSE: We conducted a nationwide, multicenter, prospective registry study for newly diagnosed patients with peripheral T-cell lymphoma (PTCL) to better define the clinical characteristics, treatment patterns, survival outcomes, and the role of upfront autologous stem cell transplantation (ASCT) in these patients. Materials and Methods: Patients with PTCL receiving chemotherapy with curative intent were registered and prospectively monitored. All patients were pathologically diagnosed with PTCL. RESULTS: A total of 191 patients with PTCL were enrolled in this prospective registry study. PTCL, not otherwise specified (PTCL-NOS) was the most common pathologic subtype (n=80, 41.9%), followed by angioimmunoblastic T-cell lymphoma (AITL) (n=60, 31.4%). With a median follow-up duration of 3.9 years, the 3-year progression-free survival (PFS) and overall survival (OS) rates were 39.5% and 60.4%, respectively. The role of upfront ASCT was evaluated in patients who were considered transplant-eligible (n=59). ASCT was performed as an upfront consolidative treatment in 32 (54.2%) of these patients. There were no significant differences in PFS and OS between the ASCT and non-ASCT groups for all patients (n=59) and for patients with PTCL-NOS (n=26). However, in patients with AITL, the ASCT group was associated with significantly better PFS than the non-ASCT group, although there was no significant difference in OS. CONCLUSION: The current study demonstrated that the survival outcomes with the current treatment options remain poor for patients with PTCL-NOS. Upfront ASCT may provide a survival benefit for patients with AITL, but not PTCL-NOS.
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