Szendrei Tamás, Plander Márk, Szabó Zsuzsanna, Kereskai László, Kajtár Béla, Papp Gergely, Iványi János László
Hematológia Osztály, Markusovszky Egyetemi Oktatókórház Szombathely, Markusovszky Lajos u. 5., 9700.
Pathologiai Intézet, Pécsi Tudományegyetem, Általános Orvostudományi Kar Pécs.
Orv Hetil. 2019 Mar;160(13):502-508. doi: 10.1556/650.2019.31353.
Prognostic impact of the detection of minimal residual disease (MRD) in multiple myeloma (MM) has been confirmed in numerous studies.
Retrospective examination of our patient database (107 newly diagnosed multiple myelomas between 2007 and 2017). Flow cytometry (FCM) was performed as MRD assessment.
MRD assessment was performed in 56 patients (median age: 68 years), after induction treatment of multiple myeloma. The treatment contained bortezomib in 91%, autologous haematopoetic stem cell transplantation (ASCT) was perfomed in 50%. MRD detection was performed on bone marrow samples, predominantly in our hospital (BD FACScan, 3 colour, panel: CD38, CD138, CD19, CD45, CD56, CD28, CD117, cyKappa, cyLambda, 100 000 events).
SPSS 13.0.
The progression-free survival (PFS) and the overall survival (OS) were significantly longer in MRD negative (n = 22) patients (PFS: 54 months, OS: 79% after 5 years) than MRD positive patients (n = 34, PFS: 22 months, OS 21% after 5 years, p = 0.001). Patients achieving complete response (CR) (n = 29) have different PFS (MRD negative CR: 60 months, MRD positive CR: 21 months, p<0.001). Patents achiving MRD negative very good partial response (n = 5) have similar PFS (54 months) as patients with MRD negative CR. The longest PFS (68 months) was observed in MRD negative patients, after ASCT (n = 11), while the PFS was significantly (p<0.001) shorter in patients who were MRD positive after ASCT (n = 18, PFS: 25 months), similarly in MRD positive patients without ASCT (n = 15, PFS 21 months). Cox regression analysis (stage, cytogenetic risk, ASCT) confirmed that MRD is an independent prognostic factor of PFS and OS. We did not find significant relationship between MRD and stage, cytogenetic risk, number of treatment cycles, ASCT.
The depth of response after induction treatment of MM is an independent predictor of survival. MRD assessment with FCM is recommended to define response. Consideration of maintenance treatment in MRD positive patients and eradication of MRD are also recommended. Orv Hetil. 2019; 160(13): 502-508.
多项研究已证实检测多发性骨髓瘤(MM)微小残留病(MRD)对预后的影响。
回顾性分析我们的患者数据库(2007年至2017年间107例新诊断的多发性骨髓瘤患者)。采用流式细胞术(FCM)进行MRD评估。
对56例患者(中位年龄:68岁)进行多发性骨髓瘤诱导治疗后的MRD评估。91%的治疗方案包含硼替佐米,50%的患者接受了自体造血干细胞移植(ASCT)。MRD检测在骨髓样本上进行,主要在我院(BD FACScan,三色,检测组合:CD38、CD138、CD19、CD45、CD56、CD28、CD117、胞质κ轻链、胞质λ轻链,100000个事件)。
使用SPSS 13.0。
MRD阴性患者(n = 22)的无进展生存期(PFS)和总生存期(OS)显著长于MRD阳性患者(n = 34,PFS:54个月,5年后OS:79%)(PFS:22个月,5年后OS:21%,p = 0.001)。达到完全缓解(CR)的患者(n = 29)有不同的PFS(MRD阴性CR:60个月,MRD阳性CR:21个月,p<0.001)。达到MRD阴性非常好的部分缓解的患者(n = 5)的PFS(54个月)与MRD阴性CR患者相似。在接受ASCT后的MRD阴性患者中观察到最长的PFS(68个月)(n = 11),而在ASCT后MRD阳性的患者中PFS显著缩短(p<0.001)(n = 18,PFS:25个月),在未接受ASCT的MRD阳性患者中情况类似(n = 15,PFS 21个月)。Cox回归分析(分期、细胞遗传学风险、ASCT)证实MRD是PFS和OS的独立预后因素。我们未发现MRD与分期、细胞遗传学风险、治疗周期数、ASCT之间存在显著关系。
MM诱导治疗后的缓解深度是生存的独立预测因素。建议采用FCM进行MRD评估以定义缓解情况。还建议考虑对MRD阳性患者进行维持治疗并清除MRD。《匈牙利医学周报》。2019年;160(13):502 - 508。