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成人晚期 T 淋巴细胞白血病/淋巴瘤或伯基特淋巴瘤患者的早期自体和/或同种异体干细胞移植。一项回顾性单中心分析。

Early autologous and/or allogeneic stem cell transplantation for adult patients with advanced stage T- lymphoblastic leukemia/lymphoma or Burkitt lymphoma. A retrospective single-centre analysis.

机构信息

University Hospital of Internal Medicine V Hematology and Oncology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

出版信息

Ann Hematol. 2024 Nov;103(11):4701-4705. doi: 10.1007/s00277-024-05979-3. Epub 2024 Sep 3.

Abstract

T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) and Burkitt lymphoma (BL) are uncommon, highly aggressive diseases originating either from immature precursor T cells or from mature B cells in BL. We retrospectively analyzed the outcome of an early autologous and/or allogeneic stem cell transplantation (SCT) concept in 28 patients with advanced stage T-ALL/LBL and BL after three to four remission induction/consolidation chemotherapy cycles. Considering only patients in first complete remission (CR), the 5-year overall survival (OS) and event-free survival (EFS) was 91% in patients with BL and 73% in patients with T-ALL/LBL with a 5-year relapse incidence (RI) of 9% in patients with BL and 27% in patients with T-ALL/LBL. All relapsing patients finally succumbed to the disease (n = 10) or complications/toxicity after having received a salvage allogeneic transplant (n = 5). Despite the low patient number our retrospective single-centre analysis by incorporating an early intensive high-dose chemo-/radiotherapy strategy with either autologous or allogeneic stem cell transplantation, although preliminary, show promising long-term outcome. Further studies are highly warranted to better define those patients who might benefit most from such a treatment approach.

摘要

T 细胞急性淋巴细胞白血病/淋巴瘤(T-ALL/LBL)和伯基特淋巴瘤(BL)是罕见的高度侵袭性疾病,起源于不成熟的前体 T 细胞或 BL 中的成熟 B 细胞。我们回顾性分析了 28 例经过三到四个缓解诱导/巩固化疗周期后处于晚期的 T-ALL/LBL 和 BL 患者早期自体和/或同种异体干细胞移植(SCT)方案的结果。仅考虑处于首次完全缓解(CR)的患者,BL 患者的 5 年总生存率(OS)和无事件生存率(EFS)为 91%,T-ALL/LBL 患者为 73%,BL 患者的 5 年复发率(RI)为 9%,T-ALL/LBL 患者为 27%。所有复发的患者最终死于疾病(n=10)或接受挽救性同种异体移植后发生并发症/毒性(n=5)。尽管患者数量较少,但我们的回顾性单中心分析表明,通过早期强化高剂量化疗/放疗联合自体或同种异体干细胞移植,尽管初步结果显示出有希望的长期疗效。需要进一步的研究来更好地确定那些最有可能从这种治疗方法中获益的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11534969/e6104ddce8a0/277_2024_5979_Fig1_HTML.jpg

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