Clinical features and treatment outcomes of peripheral T-cell lymphoma in children. A current data report from Polish Pediatric Leukemia/Lymphoma Study Group (PPLLSG)

被引:13
|
作者
Maciejka-Kemblowska, Lucyna [1 ]
Chaber, Radoslaw [2 ]
Wrobel, Grazyna [2 ]
Maldyk, Jadwiga [3 ]
Kozlowska, Marta [1 ]
Kulej, Dominika [2 ]
Kazanowska, Bernarda [2 ]
Bubala, Halina [4 ]
Dembowska-Baginska, Bozena [5 ]
Karolczyk, Grazyna [6 ]
Koltan, Andrzej [7 ]
Wyrobek, Elzbieta [8 ]
机构
[1] Med Univ Gdansk, Dept Pediat Hematol & Oncol, Ul Debinki 7, PL-80952 Gdansk, Poland
[2] Wroclaw Med Univ, Dept & Clin Pediat Oncol Hematol & Bone Marrow Tr, Wroclaw, Poland
[3] Med Univ Warsaw, Dept Dev Pathol, Warsaw, Poland
[4] Med Univ Silesia, Dept Pediat Hematol & Oncol Zabrze, Katowice, Poland
[5] Childrens Mem Hlth Inst, Dept Pediat Oncol, Warsaw, Poland
[6] Wladyslaw Buszkowski Childrens Hosp Kielce, Dept Pediat Hematol & Oncol, Kielce, Poland
[7] Nicolaus Copernicus Univ, Coll Med Bydgoszcz, Dept Pediat Hematol & Oncol, Bydgoszcz, Poland
[8] Jagiellonian Univ, Coll Med, Inst Pediat, Dept Pediat Oncol Hematol, Krakow, Poland
来源
ADVANCES IN MEDICAL SCIENCES | 2016年 / 61卷 / 02期
关键词
Non-Hodgkin lymphoma; Children; Treatment; Peripheral T-cell lymphoma; RETROSPECTIVE ANALYSIS; CHILDHOOD; CLASSIFICATION; TRANSPLANTATION; EXPERIENCE; CHEMOTHERAPY; ADOLESCENCE; TRIALS;
D O I
10.1016/j.advms.2016.03.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: Peripheral T-cell lymphomas (PTCL) are lymphoproliferative disorders derived from post-thymic cells, that occur extremely rarely in children. The optimal treatment of pediatric PTCL remains still unclear. Patients and methods: Ten children with PTCL from 3 up to 18 years of age registered by the Polish Pediatric Leukemia/Lymphoma Study Group (PPLLSG) were retrospectively analyzed. All patients were treated with different regimens including protocols: for lymphoblastic lymphoma in 7 cases, for anaplastic large cell lymphoma in 1, CHOP in 1. Five of the 10 patients with PTCL were classified as stage II; 4 as stage III and 1 as stage IV due to extralymphatic organs (bone marrow) involvement. Four histological subtypes of PTCL were recognized: extranodal NK/T-cell lymphoma, nasal type (ENTNT), peripheral T-cell lymphoma not otherwise specified (PTCL-NOS), subcutaneous panniculitis-like T-cell lymphoma (SPL), Sezary syndrome (SS). After first-line therapy 9 patients initially achieved complete remission, 4 relapsed, 5 died. One patient achieved remission spontaneously. Three children (1 with stage IV and 2 in relapse) underwent high-dose chemotherapy with allogeneic bone marrow stem cell transplantation and all of them are alive and in CR. Results: The cumulative probability of 5-year overall survival (OS) for our whole group was 63.9% (95% CI: 35.2-88.2%) with a median follow-up time of 48.4 months (range 24-90+ months). The 5-year event free survival (EFS) was 81%. PTCLs are a heterogeneous and rare group of childhood NHLs. Conclusions: According to our experience the standard chemotherapy for precursor lymphomas seems to be a beneficial treatment option for children with PTCL. Allogeneic stem cell transplantation may improve the outcome in selected patients. (C) 2016 Medical University of Bialystok. Published by Elsevier Sp. z o.o. All rights reserved.
引用
收藏
页码:311 / 316
页数:6
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