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单倍体相合异基因细胞移植治疗复发/难治性多发性骨髓瘤

英文原题:Haploidentical Allogeneic Cell Transplantation in Relapsed/Refractory Multiple Myeloma.

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Haploidentical Allogeneic Cell Transplantation in Relapsed/Refractory Multiple Myeloma.

PubMed 2026/02/04(内容时间) Cancer Manag Res Q3 · IF 2.6(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

在这一小型、经选择的队列中,采用个体化预处理和清髓方案的半相合异基因 HCT 与经过大量既往治疗的 r/r MM 患者的疾病控制相关。

研究思路结论见上方概要

尽管多发性骨髓瘤(MM)的新兴疗法改善了治疗选择,但复发/难治性(r/r)MM的长期疾病控制仍是一个挑战。虽然NK 细胞同种异体反应性在单倍体相合异基因造血细胞移植(HCT)中以移植后环磷酰胺(PTCy)作为移植物抗宿主病(GvHD)预防的效果被认为是几种血液肿瘤的标准治疗选择,但其在MM中的应用存在争议。在这项回顾性分析中,我们评估了一小队列连续接受单倍体相合异基因HCT联合PTCy的MM患者。

中位随访68个月(范围2-109个月),7例连续r/r MM患者接受了单倍体相合HCT。所有患者均经过大量预处理,接受过蛋白酶体抑制剂、抗CD38抗体、免疫调节药物以及至少一次自体HCT。3例患者接受了基于化疗的减低强度预处理方案联合放射免疫治疗。所有患者的GvHD预防均包括PTCy联合他克莫司和霉酚酸酯。

所有患者均显示稳定植入并达到完全供者嵌合。单倍体相合HCT使所有患者获得初始缓解,其中4例在HCT后首次疾病评估时达到完全缓解(CR),3例达到非常好的部分缓解(VGPR)。所有存活超过+100天的个体均出现疾病复发或进展。在6例存活患者中,中位复发时间为26.5个月(范围,5-81个月)。末次随访时,5例存活患者中有4例维持CR,1例维持非常好的部分缓解,均在接受后续个体化治疗后。2例患者观察到III-IV级急性GvHD,4例发生轻至中度慢性GvHD,末次随访时无GvHD相关死亡。

展开英文摘要原文

Although emerging therapies for multiple myeloma (MM) have improved treatment options, long-term disease control in relapsed/refractory (r/r) MM remains a challenge. While the effect of natural killer cell alloreactivity in haploidentical allogeneic hematopoietic cell transplantation (HCT) with post-transplantation cyclophosphamide (PTCy) as graft-versus-host disease (GvHD) prophylaxis is considered a standard treatment option for several hematologic neoplasms, its use in MM is controversial. In this retrospective analysis, we evaluated a small cohort of consecutive patients with MM who underwent haploidentical allogeneic HCT with PTCy.

With a median follow-up of 68 months (range, 2-109 months), seven consecutive patients with r/r MM underwent haploidentical HCT. All were heavily pre-treated, having received proteasome inhibitors, anti-CD38 antibody, immunomodulatory drugs, and at least one autologous HCT. Three patients received a chemotherapy-based reduced-intensity conditioning regimen combined with radioimmunotherapy. GvHD prophylaxis in all patients consisted of PTCy in combination with tacrolimus and mycophenolate mofetil.

All patients showed stable engraftment with complete donor chimerism. Haploidentical HCT resulted in initial response in all patients, with four patients achieving a complete remission (CR) and three a very good remission (VGPR) at first disease assessment post- HCT. All individuals surviving beyond day +100 experienced disease relapse or progression. Among the six surviving patients median time to relapse was 26.5 months (range, 5-81 months). At last follow-up, four of five surviving patients maintained a CR, while one patient remained in a very good partial remission, all following subsequent individualized therapies. Acute GvHD grades III-IV were observed in two patients, while four developed mild-to-moderate chronic GvHD, with no GvHD-related deaths at the last follow-up.

In this small, selected cohort, haploidentical allogeneic HCT with individualized pre-treatment and conditioning regimens was associated with disease control in heavily pretreated patients with r/r MM.

论文信息

作者
Frimmel J、Morgner A、Brogsitter C、Trautmann-Grill K、Kunadt D、Teipel R、Röllig C、Hänel M
第一作者单位
Division of Stem Cell Transplantation and Cellular Immunotherapies, Department of Internal Medicine II, University Hospital Schleswig Holstein, University Kiel, Kiel, Germany.Germany
通讯作者单位
Department of Internal Medicine I, University Hospital Dresden, University Dresden, Dresden, Germany.Germany
期刊
Cancer management and research2026
原文标识
PubMed 41883989 · DOI 10.2147/CMAR.S564588