Department of Radiology, Dana-Farber Cancer Institute, 44 Binney St., Boston, MA 02116, USA.
AJR Am J Roentgenol. 2010 Sep;195(3):W221-8. doi: 10.2214/AJR.09.3928.
The purpose of this article is to compare the recently published revised Response Evaluation Criteria in Solid Tumors (RECIST) guidelines (version 1.1) to the original guidelines (RECIST 1.0) for advanced non-small cell lung cancer (NSCLC) after erlotinib therapy and to evaluate the impact of the new CT tumor measurement guideline on response assessment.
Forty-three chemotherapy-naive patients with advanced NSCLC treated with erlotinib in a single-arm phase 2 multicenter open-label clinical trial were retrospectively studied. CT tumor measurement records using RECIST 1.0 that were generated as part of the prospective clinical trial were reviewed. A second set of CT tumor measurements was generated from the records to meet RECIST 1.1 guidelines. The number of target lesions, best response, and time to progression were compared between RECIST 1.1 and RECIST 1.0.
The number of target lesions according to RECIST 1.1 decreased in 22 patients (51%) and did not change in 21 patients (49%) compared with the number according to RECIST 1.0 (p < 0.0001, paired Student's t test). Almost perfect agreement was observed between best responses using RECIST 1.1 and RECIST 1.0 (weighted kappa = 0.905). Two patients with stable disease according to RECIST 1.0 had progressive disease according to RECIST 1.1 criteria because of new lesions found on PET/CT. There was no significant difference in time to progression between RECIST 1.1 and RECIST 1.0 (p = 1.000, sign test).
RECIST 1.1 provided almost perfect agreement in response assessment after erlotinib therapy compared with RECIST 1.0. Assessment with PET/CT was a major factor that influenced the difference in best response assessment between RECIST 1.1 and RECIST 1.0.
本文旨在比较最近发布的修订版实体瘤反应评价标准(RECIST)指南(版本 1.1)与厄洛替尼治疗晚期非小细胞肺癌(NSCLC)的原始指南(RECIST 1.0),并评估新的 CT 肿瘤测量指南对疗效评估的影响。
回顾性研究了 43 例接受厄洛替尼单臂 2 期多中心开放性临床试验治疗的化疗初治晚期 NSCLC 患者。评估了作为前瞻性临床试验的一部分生成的 RECIST 1.0 的 CT 肿瘤测量记录。从记录中生成了第二组 CT 肿瘤测量值,以符合 RECIST 1.1 指南。比较了 RECIST 1.1 和 RECIST 1.0 之间的靶病变数、最佳疗效和疾病进展时间。
与 RECIST 1.0 相比,根据 RECIST 1.1,靶病变数减少的患者有 22 例(51%),不变的患者有 21 例(49%)(p<0.0001,配对学生 t 检验)。根据 RECIST 1.1 和 RECIST 1.0 的最佳疗效评估结果几乎完全一致(加权 Kappa=0.905)。根据 RECIST 1.0 为稳定疾病的 2 例患者,根据 RECIST 1.1 标准为疾病进展,因为 PET/CT 发现了新病变。RECIST 1.1 和 RECIST 1.0 之间的疾病进展时间无显著差异(p=1.000,符号检验)。
与 RECIST 1.0 相比,厄洛替尼治疗后,RECIST 1.1 在疗效评估中具有近乎完美的一致性。评估与 PET/CT 的结合是影响 RECIST 1.1 和 RECIST 1.0 最佳疗效评估差异的主要因素。