Medical Imaging Center, The First Affiliated Hospital of Jinan University, 613 Huangpu Street, Guangzhou, 510630, China.
Department of Radiology, Affiliated Hospital of Xiangnan University (Clinical College), 25 Renmin West Road, Chenzhou, 423000, China.
Abdom Radiol (NY). 2021 Mar;46(3):894-908. doi: 10.1007/s00261-020-02770-6. Epub 2020 Sep 25.
To evaluate and compare the diagnostic performance of percentage changes in apparent diffusion coefficient (∆ADC%) and slow diffusion coefficient (∆D%) for assessing pathological complete response (pCR) to neoadjuvant therapy in patients with locally advanced rectal cancer (LARC).
A systematic search in PubMed, EMBASE, the Web of Science, and the Cochrane Library was performed to retrieve related original studies. For each parameter (∆ADC% and ∆D%), we pooled the sensitivity, specificity and calculated the area under summary receiver operating characteristic curve (AUROC) values. Meta-regression and subgroup analyses were performed to explore heterogeneity among the studies on ∆ADC%.
15 original studies (804 patients with 805 lesions, 15 studies on ∆ADC%, 4 of the studies both on ∆ADC% and ∆D%) were included. pCR was observed in 213 lesions (26.46%). For the assessment of pCR, the pooled sensitivity, specificity and AUROC of ∆ADC% were 0.83 (95% confidence intervals [CI] 0.76, 0.89), 0.74 (95% CI 0.66, 0.81), 0.87 (95% CI 0.83, 0.89), and ∆D% were 0.70 (95% CI 0.52, 0.84), 0.81 (95% CI 0.65, 0.90), 0.81 (95% CI 0.77, 0.84), respectively. In the four studies on the both metrics, ∆ADC% yielded an equivalent diagnostic performance (AUROC 0.80 [95% CI 0.76, 0.83]) to ∆D%, but lower than in the studies (n = 11) only on ∆ADC% (AUROC 0.88 [95% CI 0.85, 0.91]). Meta-regression and subgroup analyses showed no significant factors affecting heterogeneity.
Our meta-analysis confirms that ∆ADC% could reliably evaluate pCR in patients with LARC after neoadjuvant therapy. ∆D% may not be superior to ∆ADC%, which deserves further investigation.
评估并比较表观扩散系数(∆ADC%)和慢扩散系数(∆D%)的变化百分比在评估局部晚期直肠癌(LARC)患者新辅助治疗后病理完全缓解(pCR)方面的诊断性能。
在 PubMed、EMBASE、Web of Science 和 Cochrane 图书馆中进行系统检索,以获取相关的原始研究。对于每个参数(∆ADC%和∆D%),我们汇总了敏感性、特异性,并计算了汇总受试者工作特征曲线下面积(AUROC)值。进行了荟萃回归和亚组分析,以探索∆ADC%研究之间的异质性。
共纳入 15 项原始研究(804 例患者,805 处病灶,15 项关于∆ADC%的研究,4 项研究同时关于∆ADC%和∆D%)。213 处病灶观察到 pCR(26.46%)。对于 pCR 的评估,∆ADC%的汇总敏感性、特异性和 AUROC 为 0.83(95%置信区间[CI] 0.76,0.89)、0.74(95% CI 0.66,0.81)、0.87(95% CI 0.83,0.89),而∆D%则为 0.70(95% CI 0.52,0.84)、0.81(95% CI 0.65,0.90)、0.81(95% CI 0.77,0.84)。在 4 项同时涉及这两个指标的研究中,∆ADC%的诊断性能与∆D%相当(AUROC 0.80 [95% CI 0.76,0.83]),但低于仅涉及∆ADC%的研究(n=11)(AUROC 0.88 [95% CI 0.85,0.91])。荟萃回归和亚组分析表明,没有显著因素影响异质性。
我们的荟萃分析证实,∆ADC%可可靠地评估新辅助治疗后 LARC 患者的 pCR。∆D%可能并不优于∆ADC%,值得进一步研究。