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噻替派、白消安、环磷酰胺:中枢神经系统淋巴瘤自体造血干细胞移植前有效但有毒的预处理方案。

Thiotepa, Busulfan, Cyclophosphamide: Effective but Toxic Conditioning Regimen Prior to Autologous Hematopoietic Stem Cell Transplantation in Central Nervous System Lymphoma.

机构信息

Hématologie Clinique et Thérapie Cellulaire, Centre Hospitalier Universitaire Amiens-Picardie, 80000 Amiens, France.

Hématologie Clinique, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.

出版信息

Med Sci (Basel). 2023 Jan 29;11(1):14. doi: 10.3390/medsci11010014.

DOI:10.3390/medsci11010014
PMID:36810481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9944873/
Abstract

In primary central nervous system lymphoma, two-year progression-free survival rates of up to 63 percent have been reported for first-line autologous stem cell transplantation after conditioning with the thiotepa busulfan cyclophosphamide regimen. However, 11 percent of the patients died due to toxicity. Besides conventional survival, progression-free survival and treatment related mortality analyses, a competing-risk analysis was applied to our cohort of twenty-four consecutive patients with primary or secondary central nervous system lymphoma who underwent autologous stem cell transplantation after thiotepa busulfan cyclophosphamide conditioning. The two-year overall survival and progression-free survival rates were 78 percent and 65 percent, respectively. The treatment-related mortality rate was 21 percent. The competing risks analysis demonstrate that age 60 or over and the infusion of less than 4.6 × 106/kg CD34+ stem cells were significant adverse prognostic factors for overall survival. Autologous stem cell transplantation with thiotepa busulfan cyclophosphamide conditioning was associated with sustained remission and survival. Nevertheless, the intensive thiotepa busulfan cyclophosphamide conditioning regimen was highly toxic, especially in older patients. Thus, our results suggest that future studies should aim at identifying the subgroup of patients who will really benefit of the procedure and/or to reduce the toxicity of future conditioning regimen.

摘要

在原发性中枢神经系统淋巴瘤中,采用噻替哌、白消安和环磷酰胺方案预处理后进行一线自体干细胞移植,两年无进展生存率高达 63%。然而,有 11%的患者因毒性而死亡。除了常规生存、无进展生存和治疗相关死亡率分析外,我们对 24 例原发性或继发性中枢神经系统淋巴瘤患者进行了竞争风险分析,这些患者在接受噻替哌、白消安和环磷酰胺预处理后接受了自体干细胞移植。两年总生存率和无进展生存率分别为 78%和 65%。治疗相关死亡率为 21%。竞争风险分析表明,年龄 60 岁或以上和输注的 CD34+干细胞少于 4.6×106/kg 是总生存的显著不良预后因素。用噻替哌、白消安和环磷酰胺预处理的自体干细胞移植与持续缓解和生存相关。然而,密集的噻替哌、白消安和环磷酰胺预处理方案毒性很高,尤其是对老年患者。因此,我们的结果表明,未来的研究应旨在确定真正受益于该手术的患者亚组,和/或降低未来预处理方案的毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/1142b285babb/medsci-11-00014-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/c5faa711aba2/medsci-11-00014-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/63c6b208281b/medsci-11-00014-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/1142b285babb/medsci-11-00014-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/c5faa711aba2/medsci-11-00014-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/63c6b208281b/medsci-11-00014-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848d/9944873/1142b285babb/medsci-11-00014-g003.jpg

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