Kushner Brian H, Kramer Kim, Modak Shakeel, Cheung Nai-Kong V
Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, 1275 York Ave, New York, NY 10065, USA.
J Clin Oncol. 2009 Mar 1;27(7):1041-6. doi: 10.1200/JCO.2008.17.6107. Epub 2009 Jan 26.
Relapse-free survival (RFS) is a powerful measure of treatment efficacy. We describe the sensitivity of standard surveillance studies for detecting relapse of neuroblastoma (NB).
The patients were in complete/very good partial remission of high-risk NB; routine monitoring revealed asymptomatic and, therefore, unsuspected relapses in 113 patients, whereas 41 patients had symptoms prompting urgent evaluations. Assessments every 2 to 4 months included computed tomography, iodine-131-metaiodobenzylguanidine (131)I-MIBG; through November 1999) or iodine-123-metaiodobenzylguanidine ((123)I-MIBG) scan, urine catecholamines, and bone marrow (BM) histology. Bone scan was routine through 2002.
(123)I-MIBG scan was the most reliable study for revealing unsuspected relapse; it had an 82% detection rate, which was superior to the rates with (131)I-MIBG scan (64%; P = .1), bone scan (36%; P < .001), and BM histology (34%; P < .001). Among asymptomatic patients, (123)I-MIBG scan was the sole positive study indicating relapse in 25 (27%) of 91 patients compared with one (4.5%) of 22 patients for (131)I-MIBG scan (P = .04) and 0% to 6% of patients for each of the other studies (P < .001). Patients whose monitoring included (123)I-MIBG scan were significantly less likely than patients monitored by (131)I-MIBG scan to have an extensive osteomedullary relapse and had a significantly longer survival from relapse (P < .001) and from diagnosis (P = .002). They also had significantly longer survival than patients with symptomatic relapses (P = .002).
(123)I-MIBG scan is essential for valid estimation of the duration of RFS of patients with high-risk NB. Without monitoring that includes (123)I-MIBG scan, caution should be used when comparing RFS between institutions and protocols.
无复发生存期(RFS)是衡量治疗效果的一项重要指标。我们描述了标准监测研究在检测神经母细胞瘤(NB)复发方面的敏感性。
患者为高危NB完全缓解/非常好的部分缓解状态;常规监测发现113例患者有无症状且因此未被怀疑的复发,而41例患者有症状促使进行紧急评估。每2至4个月的评估包括计算机断层扫描、碘-131-间碘苄胍(¹³¹I-MIBG;至1999年11月)或碘-123-间碘苄胍(¹²³I-MIBG)扫描、尿儿茶酚胺以及骨髓(BM)组织学检查。2002年之前骨扫描为常规检查。
¹²³I-MIBG扫描是发现未被怀疑复发最可靠的检查;其检出率为82%,优于¹³¹I-MIBG扫描(64%;P = 0.1)、骨扫描(36%;P < 0.001)和BM组织学检查(34%;P < 0.001)。在无症状患者中,¹²³I-MIBG扫描是91例患者中25例(27%)显示复发的唯一阳性检查,相比之下,¹³¹I-MIBG扫描在22例患者中有1例(4.5%)(P = 0.04),其他检查在患者中的比例为0%至6%(P < 0.001)。监测包括¹²³I-MIBG扫描的患者发生广泛骨髓复发的可能性明显低于接受¹³¹I-MIBG扫描监测的患者,且复发后的生存期(P < 0.001)和诊断后的生存期(P = 0.002)明显更长。他们的生存期也明显长于有症状复发的患者(P = 0.002)。
¹²³I-MIBG扫描对于准确评估高危NB患者的RFS持续时间至关重要。如果没有包括¹²³I-MIBG扫描的监测,在比较不同机构和方案的RFS时应谨慎。