Barzenje Dlawer Abdulla, Kolstad Arne, Ghanima Waleed, Holte Harald
Department of Oncology, Ostfold Hospital Trust, Grålum, Norway.
Department of Oncology, Oslo University Hospital, Oslo, Norway.
Hematol Oncol. 2018 Feb;36(1):217-223. doi: 10.1002/hon.2415. Epub 2017 Apr 9.
In this single-center, population-based, and retrospective study, we analyzed the outcome of 49 patients with solitary bone plasmacytoma (SBP) and 28 patients with solitary extramedullary plasmacytoma (SEP), all treated with radiotherapy. Laminectomy was performed in 18/30 SBP patients with vertebral involvement and tumour resection in 10 SEP patients. Overall survival and cause of death for each patient were compared to 5 sex-, age-, and residency-matched individuals from the normal population. Response (complete and partial) was achieved in 94% of SBP and 96% of SEP patients. Relapse rates were higher in SBP (65%) compared to patients with SEP (18%) (P < .01). Only one in-field relapse was identified for the whole series. Ten- and 15-year overall survival, progression free survival (PFS) and multiple myeloma free survival (MMFS) for patients with SBP were 60%/41%, 25%/17%, and 33%/33%. Corresponding values for patients with SEP were 67%/54%, 57%/44%, and 91%/91%. SBP patients had significantly shorter PFS and MMFS compared to SEP patients (P < .01 for both). Only two of the SEP patients developed multiple myeloma and no patient in the whole series progressed to multiple myeloma later than 10 years after diagnosis. Unlike for SEP, the major cause of death among SBP patients was multiple myeloma (49%). Compared to matched normal population, no increased risk of death from secondary malignancies or cardiovascular disease was observed. Positive predictors in SBP patients were for overall survival age <60 years, combined laminectomy and radiotherapy and radiotherapy dose >40 gray, for PFS tumour size <6 cm and combined laminectomy and radiotherapy and for MMFS tumour size <6 cm. Radiotherapy confers excellent local control in both SEP and SBP patients; however, the challenge is to prevent development of multiple myeloma in patients with SBP.
在这项单中心、基于人群的回顾性研究中,我们分析了49例孤立性骨浆细胞瘤(SBP)患者和28例孤立性髓外浆细胞瘤(SEP)患者的治疗结果,所有患者均接受了放射治疗。18/30例椎体受累的SBP患者接受了椎板切除术,10例SEP患者接受了肿瘤切除术。将每位患者的总生存期和死亡原因与5名年龄、性别和居住地匹配的正常人群个体进行比较。94%的SBP患者和96%的SEP患者获得了缓解(完全缓解和部分缓解)。SBP患者的复发率(65%)高于SEP患者(18%)(P <.01)。整个系列中仅发现1例野内复发。SBP患者的10年和15年总生存期、无进展生存期(PFS)和无多发性骨髓瘤生存期(MMFS)分别为60%/41%、25%/17%和33%/33%。SEP患者的相应值分别为67%/54%、57%/44%和91%/91%。与SEP患者相比,SBP患者的PFS和MMFS显著缩短(两者P均<.01)。仅2例SEP患者发展为多发性骨髓瘤,整个系列中无患者在诊断后10年以上进展为多发性骨髓瘤。与SEP不同,SBP患者的主要死亡原因是多发性骨髓瘤(49%)。与匹配的正常人群相比,未观察到继发性恶性肿瘤或心血管疾病导致的死亡风险增加。SBP患者总生存期的阳性预测因素为年龄<60岁、椎板切除术联合放疗以及放疗剂量>40格雷,PFS的阳性预测因素为肿瘤大小<6 cm、椎板切除术联合放疗,MMFS的阳性预测因素为肿瘤大小<6 cm。放射治疗在SEP和SBP患者中均能实现良好的局部控制;然而,挑战在于预防SBP患者发生多发性骨髓瘤。