Zacharia T Thomas, Saini Sanjay, Halpern Elkan F, Sumner James E
Department of Radiology, Massachusetts General Hospital, Boston, MA 02114, USA.
AJR Am J Roentgenol. 2006 Apr;186(4):1067-70. doi: 10.2214/AJR.05.0038.
We sought to define the ideal number of target lesions to be measured to assess disease response in patients undergoing chemotherapy for colon cancer metastases to the liver.
Thirty consecutive patients were recruited for this study. Patients were part of a multisite, randomized, double-arm, phase 3 clinical trial involving chemotherapy with an investigational drug for metastatic colon cancer. Patients were recruited from U.S. and international sites. Institutional review board approval was obtained, and informed consent was obtained from all patients. Our study included CT measurements of hepatic metastases. All patients (n = 30) had a minimum of five target lesions in the liver. Target-lesion size was defined by Response Evaluation Criteria in Solid Tumors (RECIST) criteria. We calculated the patient response at 2 months and at 6 months (complete response, partial response, stable disease, and progressive disease) using RECIST. Patient response was calculated based on the percentage increase or decrease at 2 and 6 months in the greatest diameter of the single largest lesion, two large lesions, three large lesions, four lesions, and five lesions, respectively. The concordance between five-target-lesion measurement and lesser numbers of lesions was analyzed using kappa statistics (StatView, 5.0).
In 93.33% of patients (n = 28/30), there was agreement on patient response irrespective of the number of measurements made on CT. Of these 30 patients, 47% had a partial response (n = 14/30), 43% had stable disease (n = 13/30), and 10% had progressive disease at 2 months (n = 3/30). At 6 months, 43% had a partial response (n = 13/30), 47% had stable disease (n = 14/30), and 10% had progressive disease (n = 3/30). Agreement in response evaluation between lesion groups for multiple measurements was high, with values of 1.0 for multiple-lesion measurements and 0.88 for single-lesion measurements at 2 months. The concordance values were the same at 6 months.
In the majority of patients with hepatic metastases of colorectal cancer, measuring the maximal diameter of the single largest lesion yielded the same treatment-response classification as measuring up to five target lesions. This result suggests that it may be possible to reduce the number of lesions measured in clinical trials.
我们试图确定在接受化疗治疗肝转移结肠癌患者中评估疾病反应时要测量的理想靶病灶数量。
连续招募30例患者参与本研究。患者是一项多中心、随机、双臂、3期临床试验的一部分,该试验涉及使用一种研究性药物治疗转移性结肠癌。患者从美国和国际站点招募。获得了机构审查委员会的批准,并获得了所有患者的知情同意。我们的研究包括对肝转移灶的CT测量。所有患者(n = 30)肝脏中至少有5个靶病灶。靶病灶大小根据实体瘤疗效评价标准(RECIST)标准定义。我们使用RECIST计算了患者在2个月和6个月时的反应(完全缓解、部分缓解、疾病稳定和疾病进展)。患者反应是根据2个月和6个月时单个最大病灶、两个大病灶、三个大病灶、四个病灶和五个病灶最大直径的增加或减少百分比来计算的。使用kappa统计分析(StatView,5.0)分析五个靶病灶测量与较少病灶数量之间的一致性。
在93.33%的患者(n = 28/30)中,无论CT测量的病灶数量如何,患者反应的判断一致。在这30例患者中,47%有部分缓解(n = 14/30),43%疾病稳定(n = 13/30),10%在2个月时有疾病进展(n = 3/30)。在6个月时,43%有部分缓解(n = 13/30),47%疾病稳定(n = 14/30),10%有疾病进展(n = 3/30)。多次测量时不同病灶组之间反应评估的一致性很高,2个月时多个病灶测量的值为1.0,单个病灶测量的值为0.88。6个月时的一致性值相同。
在大多数结直肠癌肝转移患者中,测量单个最大病灶的最大直径与测量多达五个靶病灶产生的治疗反应分类相同。这一结果表明在临床试验中可能减少测量的病灶数量。