Hematopoietic stem cell transplantation for primary cutaneous γδ T-cell lymphoma and refractory subcutaneous panniculitis-like T-cell lymphoma

被引:25
|
作者
Gibson, Juliet Fraser [1 ]
Alpdogan, Onder [2 ]
Subtil, Antonio [3 ]
Girardi, Michael [4 ]
Wilson, Lynn D. [5 ]
Roberts, Kenneth [5 ]
Foss, Francine [6 ]
机构
[1] Yale Univ, Sch Med, New Haven, CT 06511 USA
[2] Thomas Jefferson Univ, Jefferson Med Coll, Dept Med Oncol, Philadelphia, PA 19107 USA
[3] Yale Univ, Sch Med, Dept Dermatol & Pathol, New Haven, CT 06511 USA
[4] Yale Univ, Sch Med, Dept Dermatol, New Haven, CT 06511 USA
[5] Yale Univ, Sch Med, Dept Therapeut Radiol, New Haven, CT 06511 USA
[6] Yale Univ, Sch Med, Hematol & Bone Marrow Transplantat, New Haven, CT 06511 USA
关键词
gamma-delta; hematopoietic stem cell transplantation; primary cutaneous gamma delta T-cell lymphoma; subcutaneous panniculitis-like T-cell lymphoma; T-cell lymphoma; PROGNOSTIC-FACTORS;
D O I
10.1016/j.jaad.2015.01.003
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: The panniculitic T-cell lymphomas (TCLs) comprise 2 distinct entities, alpha beta subcutaneous panniculitis-like TCL (SPTCL) and the gamma delta cutaneous TCLs with pannicular involvement primary cutaneous gd (PCGD)-TCL. Although outcomes for most patients with SPTCL are favorable, those with PCGD-TCLs generally have an inferior outcome, and treatment strategies have not been well defined. Allogeneic hematopoietic stem cell transplantation (HSCT) has been shown to be a potentially curative strategy in aggressive TCLs and in refractory and advanced-stage mycosis fungoides. Objective: We sought to analyze the outcomes of HSCT for panniculitic cutaneous TCL. Results: Fourteen patients (4 SPTCL, 10 PCGD-TCL) presented with primarily pannicular T-cell infiltrates. Seven patients underwent allogeneic HSCT from matched-related donors and matched-unrelated donors of which 4 (57%) are alive (1 SPTCL, 3 PCGD-TCL) at 7.8, 6.9, 6.2, and 0.25 years. Two patients underwent autologous HSCT (1 SPTCL, 1 PCGD-TCL) and both are alive at a median follow-up of 1.91 years. Limitations: This study is limited by its retrospective nature and small sample size because of the rarity of SPTCL and PCGD-TCL. Conclusion: Aggressive therapy followed by allogeneic HSCT is a promising treatment modality for patients with PCGD-TCL.
引用
收藏
页码:1010 / +
页数:11
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