Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Blood. 2013 Mar 7;121(10):1819-23. doi: 10.1182/blood-2012-08-451690. Epub 2013 Jan 10.
Prognostic implications of 3 imaging tools, metastatic bone survey, magnetic resonance imaging, and positron emission tomography (PET), were evaluated in 2 consecutive Total Therapy 3 trials for newly diagnosed myeloma. Data including PET at baseline and on day 7 of induction as well as standard prognostic factors were available in 302 patients of whom 277 also had gene expression profiling (GEP)-derived risk information. According to multivariate analysis, more than 3 focal lesions on day 7 imparted inferior overall survival and progression-free survival, overall and in the subset with GEP-risk data. GEP high-risk designation retained independent significance for all 3 end points examined. Thus, the presence of > 3 focal lesions on day 7 PET follow-up may be exploited toward early therapy change, especially for the 15% of patients with GEP-defined high-risk disease with a median overall survival expectation of 2 years. This trial was registered at www.clinicaltrials.gov as #NCT00081939 and # NCT00572169.
在两项连续的多发性骨髓瘤 Total Therapy 3 试验中,评估了 3 种影像学工具(转移骨扫描、磁共振成像和正电子发射断层扫描[PET])的预后意义。302 例患者中有基线和诱导第 7 天的 PET 数据以及标准预后因素,其中 277 例患者还有基因表达谱(GEP)风险信息。多变量分析显示,第 7 天有超过 3 个局灶性病变预示总体生存率和无进展生存率降低,无论是否有 GEP 风险数据。GEP 高危诊断对所有 3 个终点均具有独立意义。因此,在早期治疗改变时,特别是对于 GEP 定义的高危疾病患者,他们的中位总生存预期为 2 年,可利用第 7 天 PET 随访中出现>3 个局灶性病变的情况。该试验在 www.clinicaltrials.gov 上注册,编号分别为#NCT00081939 和#NCT00572169。