HEMATOPOIETIC STEM CELL TRANSPLANT IN AGGRESSIVE T AND NK/T CELL LYMPHOMA - ROLE OF UPFRONT AUTOLOGOUS TRANSPLANT IN NODAL PERIPHERAL T-CELL LYMPHOMA.

Lawrence Cheng Kiat Ng, Christopher Shwei Wen Tham, Francesca Wei Inng Lim, Yunxin Chen, Shin Yeu Ong, Chandramouli Nagarajan, Jing Jing Lee, Yeow Tee Goh, Yeh Ching Linn, Yuh Shan Lee, Colin Diong Phipps, Jeffrey Kim Siang Quek, Than Hein, Jordan Chung Cheng Hwang, Nicholas Grigoropoulos, William Ying Khee Hwang, Aloysius Yew Leng Ho
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引用次数: 1

Abstract

Aggressive T and NK/T-cell lymphoma are known to have a high risk of relapse and poor long-term prognosis. Hematopoietic stem cell transplantation has been performed as part of consolidation or salvage treatment. We retrospectively studied the outcomes of autologous (A) and allogeneic (allo) hematopoietic stem cell transplantation (SCT) in aggressive T and NK/T-cell lymphoma at our center between 2010 to 2020. Patients with nodal peripheral T-cell lymphoma (PTCL) that were younger than 65 years old who did not receive upfront autologous SCT (ASCT) at first complete remission were selected from our registry data for further comparison. Thirty-six patients underwent ASCT, and 16 patients underwent alloSCT. In the ASCT cohort, 18 patients with nodal PTCL who underwent upfront ASCT at first complete remission (upfront ASCT) were compared with 15 patients with nodal PTCL who were in first complete remission after single-line induction but did not receive ASCT. The two-year progression-free survival (PFS) and overall survival (OS) rates for the ASCT cohort were 58% and 73%, respectively. The two-year PFS and OS for the alloSCT cohort were 47% (P=0.35, P=0.02, respectively). Twenty-four patients who received SCT at first remission (21 ASCT and three alloSCT) had a two-year PFS and OS of 75% and 89%, respectively. In comparison, 28 patients who received SCT at relapse/refractory (15 ASCT and 13 alloSCT) had a two-year PFS and OS of 40% and 50%, respectively (P=0.047, P=0.024, respectively). Patients in complete remission prior to transplantation (n=42) had a two-year PFS and OS of 59% and 73%, respectively. In contrast, patients in partial remission prior to transplantation (n=10) had a two-year PFS and OS of 40% and 48%, respectively (p>0.05). Non-relapse mortality occurred in 6% and 43% of ASCT and AlloSCT, respectively. Multivariate analysis revealed that EBV-positivity at diagnosis indicated poorer PFS. EBV-positivity at diagnosis and more than two prior lines of treatment at transplant were associated with poorer OS. For nodal PTCL, the two-year PFS and OS were 79% and 100% for the upfront ASCT cohort and 78% and 92% for the non-upfront ASCT cohort, respectively (p>0.05). Hematopoietic SCT is a feasible treatment option for aggressive T and NK/T-cell lymphoma. Patients who underwent SCT at first remission had better survival rates than those who underwent SCT at relapse/refractory. Nevertheless, due to the limited sample size of the current study, the role of upfront ASCT in patients with nodal PTCL who achieved first complete remission remains unclear.

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造血干细胞移植在侵袭性t和nk / t细胞淋巴瘤中的作用——前期自体移植在淋巴结周围t细胞淋巴瘤中的作用
侵袭性T和NK/T细胞淋巴瘤复发风险高,长期预后差。造血干细胞移植已被作为巩固或挽救治疗的一部分。我们回顾性研究了2010年至2020年在我们中心进行的自体(A)和同种异体(allo)造血干细胞移植(SCT)治疗侵袭性T和NK/T细胞淋巴瘤的结果。年龄小于65岁且首次完全缓解时未接受前期自体SCT (ASCT)的结性周围t细胞淋巴瘤(PTCL)患者从我们的注册数据中选择进行进一步比较。36例患者行ASCT, 16例患者行同种异体细胞移植。在ASCT队列中,18例淋巴结性PTCL患者在首次完全缓解(ASCT)时接受了前期ASCT,与15例单线诱导后首次完全缓解但未接受ASCT的淋巴结性PTCL患者进行了比较。ASCT队列的两年无进展生存率(PFS)和总生存率(OS)分别为58%和73%。同种异体移植队列的两年PFS和OS分别为47% (P=0.35, P=0.02)。24例首次缓解时接受SCT的患者(21例ASCT和3例同种异体SCT)的两年PFS和OS分别为75%和89%。相比之下,28例复发/难治性患者(15例ASCT和13例同种异体SCT)接受SCT的两年PFS和OS分别为40%和50% (P=0.047, P=0.024)。移植前完全缓解的患者(n=42)的两年PFS和OS分别为59%和73%。相比之下,移植前部分缓解的患者(n=10)的两年PFS和OS分别为40%和48% (p>0.05)。ASCT和AlloSCT的非复发死亡率分别为6%和43%。多因素分析显示,诊断时ebv阳性表明PFS较差。诊断时ebv阳性和移植时超过两条既往治疗线与较差的OS相关。对于淋巴结型PTCL,前期ASCT队列的2年PFS和OS分别为79%和100%,非前期ASCT队列的2年PFS和OS分别为78%和92% (p>0.05)。造血SCT是侵袭性T和NK/T细胞淋巴瘤的可行治疗选择。首次缓解期接受SCT的患者比复发/难治期接受SCT的患者生存率更高。然而,由于目前研究的样本量有限,前期ASCT在淋巴结性PTCL患者首次完全缓解中的作用尚不清楚。
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