Wolf Robert J, Foerster Robert, Bruckner Thomas, Bostel Tilman, Schlampp Ingmar, Debus Juergen, Rief Harald
Department of Radiation Oncology, University Hospital Heidelberg, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany.
Department of Medical Biometry, University Hospital Heidelberg, Im Neuenheimer Feld 305, 69120, Heidelberg, Germany.
BMC Cancer. 2016 Jul 25;16:528. doi: 10.1186/s12885-016-2571-z.
Adequate prediction of survival plays an important role in treatment decisions for patients with spinal bone metastases (SBM). Several prognostic factors are already used in daily clinical practice, but factors related to stability of SBM are still unknown. Therefore, we designed this study to identify these prognostic factors.
We retrospectively assessed 915 patients from solid tumors with commonly metastased into the bone treated at our department between January 2000 and January 2012. Lung cancer (NSCLC), breast and renal cancer listed in Table 1 are the most common solid tumors with bone metastasis in this study. Prostate carcinoma was excluded due to osteoblastic SBM with no influence for stability. We calculated overall survival (OS) and bone survival (BS; time between first diagnosis of bone metastases until death) with the Kaplan-Meier method and assessed prognostic factors for BS with the log-rank test and a Cox regression model separately for patients with stable and unstable SBM.
Median follow-up was 9.3 months. OS after 6 months, 1, 2, and 5 years was 81, 62, 42, and 25 % in patients with stable SBM and 78, 57, 38, and 22 % in patients with unstable SBM (p = 0.851). BS was 57, 38, 22, and 5 % in the group of stable SBM after 6 months, 1, 2, and 5 years. For patients with unstable SBM BS after 6 months, 1, 2, and 5 years was 59, 39, 19, and 8 % (p = 0.755). In multivariate analysis we found male gender (HR = 1.27 [95 % CI 1.01-1.60], p = 0.04), Karnofsky performance status (KPS) <80 % (HR = 1.27 [95%CI 1.04-1.55], p = 0.02) and non-small cell lung cancer (NSCLC; HR = 2.77 [95%CI 1.99-3.86], p < 0.0001) to be independent prognostic factors for shortened survival in patients with stable SBM. Independent prognostic factors for unstable SBM were age per year (HR = 1.01 [95 % CI 1.0-1.02], p = 0.025), multiple SBM (HR = 1.35 [95 % CI 1.1-1.65], p = 0.003), and NSCLC (HR = 2.0 [95 % CI 1.43-2.80], p < 0.0001). Additionally, not wearing an orthopedic corset (HR = 0.77 [95 % CI 0.62-0.96], p = 0.02) was associated with prolonged BS in patients with unstable SBM and in both groups BS was significantly longer in patients without liver metastases (stable SBM: HR = 0.72 [95 % CI 0.56-0.92], p = 0.008; unstable SBM: HR = 0.71 [95 % CI 0.54-0.92], p = 0.01).
Survival was equal for patients with stable and unstable SBM. However, prognostic factors differed in both groups and stability should therefore be considered in treatment decision-making.
准确预测生存期在脊柱骨转移(SBM)患者的治疗决策中起着重要作用。目前日常临床实践中已使用多种预后因素,但与SBM稳定性相关的因素仍不清楚。因此,我们设计了本研究以确定这些预后因素。
我们回顾性评估了2000年1月至2012年1月在我科接受治疗的915例实体瘤骨转移患者。表1中列出的肺癌(非小细胞肺癌)、乳腺癌和肾癌是本研究中最常见的骨转移实体瘤。前列腺癌因成骨性SBM对稳定性无影响而被排除。我们采用Kaplan-Meier法计算总生存期(OS)和骨生存期(BS;从首次诊断骨转移到死亡的时间),并分别用对数秩检验和Cox回归模型评估稳定和不稳定SBM患者的BS预后因素。
中位随访时间为9.3个月。稳定SBM患者6个月、1年、2年和5年的OS分别为81%、62%、42%和25%,不稳定SBM患者分别为78%、57%、38%和22%(p = 0.851)。稳定SBM组6个月、1年、2年和5年的BS分别为57%、38%、22%和5%。不稳定SBM患者6个月、1年、2年和5年的BS分别为59%、39%、19%和8%(p = 0.755)。多因素分析中,我们发现男性(HR = 1.27 [95%CI 1.01 - 1.60],p = 0.04)、卡氏评分(KPS)<80%(HR = 1.27 [95%CI 1.04 - 1.55],p = 0.02)和非小细胞肺癌(NSCLC;HR = 2.77 [95%CI 1.99 - 3.86],p < 0.0001)是稳定SBM患者生存期缩短的独立预后因素。不稳定SBM的独立预后因素为年龄每年增长(HR = 1.01 [95%CI 1.0 - 1.02],p = 0.025)、多发SBM(HR = 1.35 [95%CI 1.1 - 1.65],p = 0.003)和NSCLC(HR = 2.0 [95%CI 1.43 - 2.80],p < 0.0001)。此外,不稳定SBM患者未佩戴矫形束腰(HR = 0.77 [95%CI 0.62 - 0.96],p = 0.02)与BS延长相关,两组中无肝转移患者的BS均显著延长(稳定SBM:HR = 0.72 [95%CI 0.56 - 0.92],p = 0.008;不稳定SBM:HR = 0.71 [95%CI 0.54 - 0.92],p = 0.01)。
稳定和不稳定SBM患者的生存期相当。然而,两组的预后因素不同,因此在治疗决策中应考虑稳定性。