CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Pseudo-autologous Stem Cell Transplant for the Treatment of Secondary Central Nervous System Lymphoma.
Pseudo-autologous Stem Cell Transplant for the Treatment of Secondary Central Nervous System Lymphoma.
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既往接受异基因干细胞移植的患者,若之后采集干细胞用于自体移植,所采集细胞有时称为“假自体”细胞,以表明其来源于供者。假自体干细胞移植(pASCT)鲜有报道。本文描述一例 pASCT:一名 66 岁男性弥漫性大 B 细胞淋巴瘤(DLBCL)患者,既往接受CAR-T 细胞治疗及随后无关供者相合移植,但仍多次复发。异基因移植后的最近一次复发仅累及中枢神经系统(CNS),表现为多发脑神经麻痹。虽然既往已采集自体干细胞,且有供者来源的异基因干细胞可用,研究团队仍在患者接受改良挽救化疗(甲氨蝶呤、阿糖胞苷、噻替哌和利妥昔单抗,MATRix)后恢复期间采集假自体干细胞。随后患者接受白消安和噻替哌大剂量治疗,并进行 pASCT。尽管移植物抗宿主病(GVHD)预防仅持续较短时间(<1 个月),患者未发生 GVHD,且移植后 23 个月仍无病生存期。作者讨论了在已有冻存自体和异基因干细胞可用时,仍选择 pASCT 的依据。
In patients who have previously undergone allogeneic stem cell transplantation and later have stem cells collected for an autologous transplant, the collected cells are sometimes referred to as "pseudo-autologous" to indicate that they are donor-derived. The use of pseudo-autologous stem cell transplantation (pASCT) has rarely been reported.
We describe a case of pASCT in a 66-year-old man with multiple relapses of diffuse large B-cell lymphoma (DLBCL) despite prior chimeric antigen receptor T-cell (CAR T) therapy and a subsequent matched unrelated donor transplant. His most recent relapse after allogeneic transplantation was limited to the central nervous system (CNS) and presented with multiple cranial nerve palsies.
Although previously collected autologous stem cells and donor-derived allogeneic stem cells were available, pseudo-autologous stem cells were collected during recovery from a modified salvage chemotherapy regimen (methotrexate (MTX), cytarabine, thiotepa, and rituximab (MATRix)). He subsequently received high-dose therapy with busulfan and thiotepa followed by pASCT. Despite receiving only brief (<1 month) graft-versus-host disease (GVHD) prophylaxis, he did not develop GVHD and remains disease-free 23 months after transplant.
We discuss the rationale for selecting pASCT despite the availability of stored autologous and allogeneic stem cells.
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