From the *Department of Nuclear Medicine and Molecular Imaging Center, †Division of Colon and Rectal Surgery, Department of Surgery, and ‡Division of Hematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Clin Nucl Med. 2015 Mar;40(3):200-5. doi: 10.1097/RLU.0000000000000693.
In metastatic colorectal cancer (mCRC) with wild-type K-ras, cetuximab-based regimen is an option for third-line therapy. The objective of this study was to assess if early response evaluation by 18F-FDG PET/CT can predict progression-free survival (PFS) and overall survival (OS) in these patients.
Patients with mCRC going to receive third-line cetuximab-based therapy were enrolled. 18F-FDG PET/CT studies were arranged at baseline and at the ends of the first and fourth weeks of therapy. Treatment response was evaluated with 2 methods: method 1 based on PET response criteria in solid tumors 1.0 and method 2 based on the assumption that an increase in peak tumor metabolism implies nonresponse. Progression-free survival was counted to tumor progression based on the Response Evaluation Criteria in Solid Tumors 1.1 or death. The predictive powers for PFS and OS were analyzed using the Kaplan-Meier method and the log-rank test.
Twenty-seven patients were eligible with a median PFS of 5.8 months and a median OS of 9.1 months. Method 2 predicts PFS (P = 0.001) and OS (P < 0.001) at the end of the first week, whereas method 1 does not. Both methods predict PFS and OS at the end of the fourth week.
Early response evaluation by 18F-FDG PET/CT predicts PFS and OS in patients with mCRC receiving third-line cetuximab-based therapy. Early therapeutic change may be possible for nonresponsive patients after 1 week of treatment.
在野生型 K-ras 的转移性结直肠癌(mCRC)中,西妥昔单抗为基础的方案是三线治疗的选择。本研究的目的是评估 18F-FDG PET/CT 早期疗效评估是否能预测这些患者的无进展生存期(PFS)和总生存期(OS)。
招募 mCRC 患者,他们将接受三线西妥昔单抗为基础的治疗。在基线、治疗第一和第四周末安排 18F-FDG PET/CT 研究。采用 2 种方法评估治疗反应:方法 1 基于实体瘤 1.0 标准,方法 2 基于假设肿瘤代谢峰增加意味着无反应。根据实体瘤疗效评价标准 1.1,将 PFS 定义为肿瘤进展或死亡。采用 Kaplan-Meier 法和对数秩检验分析 PFS 和 OS 的预测能力。
27 例患者符合条件,中位 PFS 为 5.8 个月,中位 OS 为 9.1 个月。方法 2 在第一周末预测 PFS(P = 0.001)和 OS(P < 0.001),而方法 1 则不能。两种方法均在第四周末预测 PFS 和 OS。
18F-FDG PET/CT 早期疗效评估可预测接受三线西妥昔单抗为基础治疗的 mCRC 患者的 PFS 和 OS。治疗后 1 周内,对于无反应的患者可能可以进行早期治疗改变。