Song Moo-Kon, Chung Joo-Seop, Lee Je-Jung, Lee Jae-Hoon, Song Ik-Chan, Lee Sang-Min, Shin Dong-Yeop, Lee Gyeong-Won, Lee In-Sook
Department of Hematology-Oncology, Pusan National University Hospital Medical Research Institute, Busan, Korea.
Acta Haematol. 2015;134(1):7-16. doi: 10.1159/000370235. Epub 2015 Mar 28.
The International Staging System (ISS) does not take into consideration the clinical role of imaging modalities in multiple myeloma (MM), even though these are important. Some studies have indicated a lack of impact of ISS in MM patients who receive novel agents. Therefore, accessible novel risk stratification might be needed in elderly MM patients receiving conventional therapy or novel agents. We analyzed 198 newly diagnosed and symptomatic MM patients who were not eligible for transplantation. The initial treatment regimen was therapy with melphalan-prednisone (MP, n = 44), thalidomide-cyclophosphamide-dexamethasone (n = 89) or bortezomib-MP (VMP, n = 65). The magnetic resonance imaging (MRI) pattern was normal in 34 patients, focal in 30 and diffuse/variegated in 134. High-risk cytogenetic abnormalities were not associated with the diffuse/variegated MRI pattern (p = 0.182). ISS stage III [progression-free survival (PFS) p = 0.005; overall survival (OS) p = 0.027], high-risk cytogenetic abnormalities (PFS p = 0.001; OS p < 0.001) and diffuse/variegated MRI pattern (PFS p < 0.001; OS p < 0.001) were independently associated with poorer PFS and OS. Patients were further stratified according to the 3 prognostic factors. The PFS and OS of the 3 groups differed significantly. The addition of the diffuse/variegated MRI pattern may improve the prognostic potential of the current staging system which includes ISS and cytogenetic abnormalities.
国际分期系统(ISS)未考虑到影像学检查在多发性骨髓瘤(MM)中的临床作用,尽管其很重要。一些研究表明,ISS对接受新型药物治疗的MM患者没有影响。因此,对于接受传统治疗或新型药物治疗的老年MM患者,可能需要一种易于获得的新型风险分层方法。我们分析了198例新诊断且有症状但不适合移植的MM患者。初始治疗方案为美法仑-泼尼松治疗(MP,n = 44)、沙利度胺-环磷酰胺-地塞米松治疗(n = 89)或硼替佐米-美法仑治疗(VMP,n = 65)。34例患者的磁共振成像(MRI)表现正常,30例为局灶性表现,134例为弥漫/多样表现。高危细胞遗传学异常与弥漫/多样MRI表现无关(p = 0.182)。ISS III期[无进展生存期(PFS)p = 0.005;总生存期(OS)p = 0.027]、高危细胞遗传学异常(PFS p = 0.001;OS p < 0.001)和弥漫/多样MRI表现(PFS p < 0.001;OS p < 0.001)均与较差的PFS和OS独立相关。根据这3个预后因素对患者进行进一步分层。3组的PFS和OS有显著差异。增加弥漫/多样MRI表现可能会提高当前包括ISS和细胞遗传学异常的分期系统的预后评估能力。