From the Departments of Radiology (Y.T., A.G., D.M.K., A.S.) and Medical Oncology (R.F., H.L., J.L.), Royal Marsden Hospital, Downs Road, Sutton, Surrey SM2 5PT, England.
Radiology. 2014 Nov;273(2):452-61. doi: 10.1148/radiol.14132702. Epub 2014 May 26.
To compare revised Choi criteria that incorporate concurrent size and attenuation changes at early follow-up imaging with Response Evaluation Criteria in Solid Tumors ( RECIST Response Evaluation Criteria in Solid Tumors ) 1.1 and original Choi criteria in stratification of clinical outcomes in patients with metastatic renal cell carcinoma ( mRCC metastatic renal cell carcinoma ) treated with sunitinib.
Institutional review board approved this retrospective study and waived informed consent. Baseline and first follow-up computed tomographic scans in 69 patients (50 men, 19 women; mean age, 60.3 years; range, 19-83 years) with mRCC metastatic renal cell carcinoma treated with sunitinib from October 1, 2008, to March 1, 2013, were evaluated for tumor response by using RECIST Response Evaluation Criteria in Solid Tumors 1.1, original Choi criteria, and revised Choi criteria. Correlations with overall survival ( OS overall survival ) and progression-free survival ( PFS progression-free survival ) were compared and stratified according to each radiologic criteria with Kaplan-Meier and multivariate Cox regression analysis.
Median follow-up time was 29.7 months (95% confidence interval [ CI confidence interval ]: 18.9, 45.9). Response according to revised Choi criteria was independently correlated with OS overall survival (hazard ratio, 0.47 [95% CI confidence interval : 0.23, 0.99]; P = .046) and PFS progression-free survival (hazard ratio, 0.53 [95% CI confidence interval : 0.29, 0.99]; P = .047). Response according to RECIST Response Evaluation Criteria in Solid Tumors was not significantly correlated with OS overall survival (hazard ratio, 0.65 [95% CI confidence interval : 0.27, 1.58]; P = .344) or PFS progression-free survival (hazard ratio, 0.89 [95% CI confidence interval : 0.42, 1.91]; P = .768). Response according to original Choi criteria was not significantly correlated with OS overall survival (hazard ratio, 0.60 [95% CI confidence interval : 0.32, 1.11]; P = .106) or PFS progression-free survival (hazard ratio, 0.59 [95% CI confidence interval : 0.34, 1.02]; P = .060). Median OS overall survival and PFS progression-free survival in responders according to revised Choi criteria was 39.4 months (95% CI confidence interval : 9.1, upper limit not estimated) and 13.7 months (95% CI confidence interval : 6.4, 24.6), respectively, compared with 12.8 months (95% CI confidence interval : 8.7, 18.0) and 5.3 months (95% CI confidence interval : 3.9, 8.4), respectively, in nonresponders.
Contemporaneous reduction in tumor size and attenuation were correlated with favorable clinical outcomes. Response according to revised Choi criteria showed better correlation with clinical outcomes compared with that according to RECIST Response Evaluation Criteria in Solid Tumors or original Choi criteria in patients with mRCC metastatic renal cell carcinoma treated with sunitinib.
比较纳入早期随访影像学中同时发生的大小和衰减变化的修订 Choi 标准与实体瘤反应评估标准 1.1(Response Evaluation Criteria in Solid Tumors,RECIST)和索坦治疗转移性肾细胞癌(metastatic renal cell carcinoma,mRCC)患者的原始 Choi 标准在临床结局分层中的作用。
本回顾性研究获得机构审查委员会批准,并豁免了知情同意。对 2008 年 10 月 1 日至 2013 年 3 月 1 日接受舒尼替尼治疗的 69 例 mRCC 患者(50 名男性,19 名女性;平均年龄 60.3 岁;范围 19-83 岁)的基线和首次随访 CT 扫描进行肿瘤反应评估,使用 RECIST 标准、原始 Choi 标准和修订 Choi 标准。通过 Kaplan-Meier 和多变量 Cox 回归分析比较与总生存期(overall survival,OS)和无进展生存期(progression-free survival,PFS)的相关性,并根据每个影像学标准进行分层。
中位随访时间为 29.7 个月(95%置信区间[CI]:18.9,45.9)。根据修订 Choi 标准的反应与 OS 独立相关(危险比,0.47[95%CI:0.23,0.99];P=0.046)和 PFS(危险比,0.53[95%CI:0.29,0.99];P=0.047)。根据 RECIST 标准的反应与 OS 无显著相关性(危险比,0.65[95%CI:0.27,1.58];P=0.344)或 PFS(危险比,0.89[95%CI:0.42,1.91];P=0.768)。根据原始 Choi 标准的反应与 OS 无显著相关性(危险比,0.60[95%CI:0.32,1.11];P=0.106)或 PFS(危险比,0.59[95%CI:0.34,1.02];P=0.060)。根据修订 Choi 标准,反应者的中位 OS 为 39.4 个月(95%CI:9.1,上限未估计),PFS 为 13.7 个月(95%CI:6.4,24.6),而非反应者的中位 OS 为 12.8 个月(95%CI:8.7,18.0),PFS 为 5.3 个月(95%CI:3.9,8.4)。
肿瘤大小和衰减的同时减少与良好的临床结局相关。与 RECIST 标准或原始 Choi 标准相比,修订 Choi 标准在接受舒尼替尼治疗的 mRCC 患者中与临床结局的相关性更好。