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异基因移植在多发性骨髓瘤中的应用——它仍有立足之地吗?

Allogeneic Transplantation in Multiple Myeloma-Does It Still Have a Place?

作者信息

Gahrton Gösta, Iacobelli Simona, Garderet Laurent, Yakoub-Agha Ibrahim, Schönland Stefan

机构信息

Department of Medicine, Karolinska Institutet, Huddinge, SE 14186 Stockholm, Sweden.

Department of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.

出版信息

J Clin Med. 2020 Jul 10;9(7):2180. doi: 10.3390/jcm9072180.

Abstract

Novel drugs have improved survival for patients with multiple myeloma in recent years. However, the disease is still fatal. Allogeneic stem cell transplantation (Allo) has proven to cure some patients with the disease, but its role is controversial due to relatively high transplant-related toxicity and mortality (nonrelapse mortality, NRM). Using nonmyeloablative reduced-intensity conditioning (RIC), both toxicity and NRM can be reduced, and RICAllo is, therefore, an option for subgroups of patients. Upfront tandem autologous/RICAllo (Auto/RICAllo) was shown to be superior to single Auto or tandem Auto/Auto in both progression-free (PFS) and overall survival (OS) in two prospective studies with long-term follow-up, while three similarly designed studies did not detect a difference. A recent update of pooled patient data from four of these studies showed significantly superior PFS and OS with Auto/RICAllo. Importantly, none of these studies showed inferior results with Auto/RICAllo in patients less than 70 years of age. Auto/RICAllo appears to overcome some poor risk cytogenetic markers. Encouraging results have also been seen in treatment of relapsed patients. Combining Allo with new proteasome inhibitors and immunomodulatory drugs may further improve results. Other encouraging new cell therapies such as with CAR T-cells, NK- and CAR NK-cells may well have a place in combination with RICAllo. Such studies are warranted.

摘要

近年来,新型药物提高了多发性骨髓瘤患者的生存率。然而,该疾病仍然是致命的。异基因干细胞移植(Allo)已被证明可以治愈一些该疾病患者,但由于相对较高的移植相关毒性和死亡率(非复发死亡率,NRM),其作用存在争议。使用非清髓性减低强度预处理(RIC),毒性和NRM均可降低,因此RICAllo是部分患者亚组的一种选择。在两项长期随访的前瞻性研究中,前期串联自体/RICAllo(Auto/RICAllo)在无进展生存期(PFS)和总生存期(OS)方面均优于单次自体移植或串联自体/自体移植,而三项设计类似的研究未发现差异。最近对其中四项研究的汇总患者数据进行的更新显示,Auto/RICAllo的PFS和OS显著更优。重要的是,这些研究均未显示Auto/RICAllo在70岁以下患者中结果较差。Auto/RICAllo似乎克服了一些不良风险细胞遗传学标志物。在复发患者的治疗中也取得了令人鼓舞的结果。将Allo与新的蛋白酶体抑制剂和免疫调节药物联合使用可能会进一步改善结果。其他令人鼓舞的新细胞疗法,如CAR T细胞、NK细胞和CAR NK细胞疗法,很可能与RICAllo联合使用。此类研究很有必要。

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