Children's Oncology Group, University of Florida, Gainesville, Florida, USA.
Pediatr Blood Cancer. 2011 Jul 1;56(7):1041-5. doi: 10.1002/pbc.22991. Epub 2011 Feb 15.
¹²³I-metaiodobenzylguanidine (MIBG) scans are preferable to ¹³¹I-MIBG for neuroblastoma imaging as they deliver less patient radiation yet have greater sensitivity in disease detection. Both ¹²³I-MIBG and ¹³¹I-MIBG scans were used for disease assessments of neuroblastoma patients enrolled on Children's Oncology Group (COG) high-risk study A3973. The hypothesis was that ¹²³I-MIBG and ¹³¹I-MIBG scans were sufficiently similar for clinical purposes in terms of ability to predict survival.
Patients enrolled on COG A3973 with stage 4 disease who completed ¹²³I-MIBG or ¹³¹I-MIBG scans at diagnosis, post-induction, post-transplant, or post-biotherapy were analyzed. The performance of the Curie score for each MIBG scan type in predicting survival was evaluated. At each time point, survival curves for ¹²³I-MIBG versus ¹³¹I-MIBG were compared using the log-rank test.
Of the 413 patients on A3973 with at least one MIBG scan, 350 were stage 4. The 5-year event-free survival (EFS) and overall survival (OS) rates were 33.4 ± 3.6% and 45.6 ± 4.0% (N = 350). At post-induction, EFS (P = 0.3501) and OS (P = 0.5337) for ¹²³I-MIBG versus ¹³¹I-MIBG were not significantly different. Similarly, comparisons at the three other time points were non-significant.
We found no evidence of a statistically significant difference in outcome by type of scan. For future survival analyses of MIBG Curie scores, ¹²³I-MIBG and ¹³¹I-MIBG results may be combined and analyzed overall, without adjustment for scan type.
¹²³I-间碘苄胍(MIBG)扫描在神经母细胞瘤成像方面优于¹³¹I-MIBG,因为前者为患者提供的辐射较少,且在疾病检测方面具有更高的敏感性。¹²³I-MIBG 和 ¹³¹I-MIBG 扫描均用于入组儿童肿瘤学组(COG)高危研究 A3973 的神经母细胞瘤患者的疾病评估。假设¹²³I-MIBG 和 ¹³¹I-MIBG 扫描在预测生存方面对于临床目的来说足够相似。
入组 COG A3973 且具有 4 期疾病的患者,在诊断时、诱导后、移植后或生物治疗后完成¹²³I-MIBG 或 ¹³¹I-MIBG 扫描,对其进行分析。评估每种 MIBG 扫描类型的 Curie 评分在预测生存方面的表现。在每个时间点,使用对数秩检验比较 ¹²³I-MIBG 与 ¹³¹I-MIBG 之间的生存曲线。
在 A3973 中,有 413 名患者至少进行了一次 MIBG 扫描,其中 350 名患者为 4 期。5 年无事件生存率(EFS)和总生存率(OS)分别为 33.4 ± 3.6%和 45.6 ± 4.0%(N = 350)。在诱导后,¹²³I-MIBG 与 ¹³¹I-MIBG 之间的 EFS(P = 0.3501)和 OS(P = 0.5337)没有显著差异。同样,其他三个时间点的比较也没有显著差异。
我们没有发现扫描类型对结果有统计学意义上的显著差异。对于未来 MIBG Curie 评分的生存分析,¹²³I-MIBG 和 ¹³¹I-MIBG 结果可以合并分析,无需调整扫描类型。