Percutaneous vertebroplasty/kyphoplasty contributes to the improved outcome in patients with newly diagnosed multiple myeloma: A single center cohort study

IF 3.4 2区 医学 Q2 Medicine
Fujing Zhang , Shuzhong Liu , Xi Zhou , Wei Wang , Congwei Jia , Qin Wang , Yong Liu , Junling Zhuang
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引用次数: 0

Abstract

Objective

To evaluate the efficacy and prognosis of percutaneous vertebroplasty/kyphoplasty (PVP/PKP) in patients with newly diagnosed multiple myeloma (NDMM).

Methods

Clinical data of NDMM patients who underwent PVP/PKP during front-line regimen at Peking Union Medical College Hospital from January 1, 2003, to June 30, 2023, were analyzed. Patients with comparable bone diseases not receiving orthopedic surgery were selected as controls. Visual analogue scale (VAS) score, progression-free survival (PFS), and overall survival (OS) were compared.

Results

Baseline characteristics were matched between the surgical group (n = 51 with 56 surgeries) and non-surgical group (n = 102), including demographics, tumor load, International Staging System (ISS), bone diseases, cytogenetic abnormalities, first-line treatment, and autologous stem-cell transplantation (ASCT). Bone lesions for PVP/PKP were located at thoracic vertebrae (53.6 %, 30/56) or lumbosacral vertebrae (46.4 %, 26/56). The postoperative VAS score was significantly improved (2.25 ± 0.81 vs 5.92 ± 1.05, P < 0.001). The median follow-up time was 51[38–70] months. Kaplan-Meier survival analysis suggested that both PFS (37[17–89] vs 23[12–61] months, HR 0.648, 95 %CI 0.431–0.973, P = 0.047) and OS (not reached vs 66[28-NR] months, HR 0.519, 95 %CI 0.296–0.910, P = 0.045) were significantly prolonged in the surgical group. COX multivariate analysis suggested that PVP/PKP was an independent prognostic factor for PFS (P = 0.021, HR 0.589, 95 %CI 0.376–0.922) and OS (P = 0.038, HR 0.496, 95 %CI 0.255–0.963). Subgroup analysis confirmed that patients with ISS II/III or non-ASCT achieved better PFS and OS in the surgical group (PFS: P = 0.033, P = 0.040; OS: P = 0.024, P = 0.018 respectively), while similar survival outcome was observed in patients with ISS I or ASCT between two groups.

Conclusion

For NDMM patients, not only does PVP/PKP alleviate bone pain, meanwhile, it improves the PFS and OS in advanced subpopulation or non-transplant myeloma patients, which suggests that shortening the gap from symptom onset to diagnosis by orthopedic surgery favors clinical prognosis.

经皮椎体成形术/椎体后凸成形术有助于改善新诊断多发性骨髓瘤患者的预后:单中心队列研究
目的 评价经皮椎体成形术/椎体后凸成形术(PVP/PKP)在新诊断多发性骨髓瘤(NDMM)患者中的疗效和预后。方法 分析北京协和医院自 2003 年 1 月 1 日至 2023 年 6 月 30 日在一线治疗期间接受 PVP/PKP 的 NDMM 患者的临床数据。对照组为未接受骨科手术的同类骨病患者。结果手术组(n = 51,56次手术)和非手术组(n = 102)的基线特征相匹配,包括人口统计学、肿瘤负荷、国际分期系统(ISS)、骨病、细胞遗传学异常、一线治疗和自体干细胞移植(ASCT)。PVP/PKP的骨病变位于胸椎(53.6%,30/56)或腰骶椎(46.4%,26/56)。术后 VAS 评分明显提高(2.25 ± 0.81 vs 5.92 ± 1.05,P < 0.001)。中位随访时间为 51[38-70] 个月。Kaplan-Meier 生存分析表明,手术组的 PFS(37[17-89] 个月 vs 23[12-61] 个月,HR 0.648,95 %CI 0.431-0.973,P = 0.047)和 OS(未达到 vs 66[28-NR] 个月,HR 0.519,95 %CI 0.296-0.910,P = 0.045)均显著延长。COX多变量分析表明,PVP/PKP是PFS(P = 0.021,HR 0.589,95 %CI 0.376-0.922)和OS(P = 0.038,HR 0.496,95 %CI 0.255-0.963)的独立预后因素。亚组分析证实,在手术组中,ISS II/III 或非 ASCT 患者的 PFS 和 OS 更好(PFS:P = 0.033,P = 0.040;OS:P = 0.024,P = 0.018),而在两组间,ISS I 或 ASCT 患者的生存结果相似。结论对于NDMM患者,PVP/PKP不仅能缓解骨痛,同时还能改善晚期亚群或非移植骨髓瘤患者的PFS和OS,这表明通过骨科手术缩短从症状出现到确诊的时间差有利于临床预后。
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来源期刊
CiteScore
7.20
自引率
2.90%
发文量
50
审稿时长
34 days
期刊介绍: The Journal of Bone Oncology is a peer-reviewed international journal aimed at presenting basic, translational and clinical high-quality research related to bone and cancer. As the first journal dedicated to cancer induced bone diseases, JBO welcomes original research articles, review articles, editorials and opinion pieces. Case reports will only be considered in exceptional circumstances and only when accompanied by a comprehensive review of the subject. The areas covered by the journal include: Bone metastases (pathophysiology, epidemiology, diagnostics, clinical features, prevention, treatment) Preclinical models of metastasis Bone microenvironment in cancer (stem cell, bone cell and cancer interactions) Bone targeted therapy (pharmacology, therapeutic targets, drug development, clinical trials, side-effects, outcome research, health economics) Cancer treatment induced bone loss (epidemiology, pathophysiology, prevention and management) Bone imaging (clinical and animal, skeletal interventional radiology) Bone biomarkers (clinical and translational applications) Radiotherapy and radio-isotopes Skeletal complications Bone pain (mechanisms and management) Orthopaedic cancer surgery Primary bone tumours Clinical guidelines Multidisciplinary care Keywords: bisphosphonate, bone, breast cancer, cancer, CTIBL, denosumab, metastasis, myeloma, osteoblast, osteoclast, osteooncology, osteo-oncology, prostate cancer, skeleton, tumour.
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