3-Deoxy-3'-18F-Fluorothymidine and 18F-Fluorodeoxyglucose positron emission tomography for the early prediction of response to Regorafenib in patients with metastatic colorectal cancer refractory to all standard therapies

被引:9
作者
Kim, Jeong Eun [1 ]
Chae, Sun Young [2 ]
Kim, Jwa Hoon [1 ]
Kim, Hwa Jung [3 ]
Kim, Tae Won [1 ]
Kim, Kyu-pyo [1 ]
Kim, Sun Young [1 ]
Lee, Jae-Lyun [1 ]
Oh, Seung Jun [2 ]
Kim, Jae Seung [2 ]
Ryu, Jin-Sook [2 ]
Moon, Dae Hyuk [2 ]
Hong, Yong Sang [1 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Prevent Med, Seoul, South Korea
关键词
F-18-fluorothymidine; F-18-fluorodeoxyglucose; Positron emission tomography; Regorafenib; Metastatic colorectal cancer; IMAGING PROLIFERATION; TARGETED-THERAPY; PHASE-III; IN-VIVO; CHEMOTHERAPY; BEVACIZUMAB; LEUCOVORIN; PET; 3'-DEOXY-3'-F-18-FLUOROTHYMIDINE; FLUOROURACIL;
D O I
10.1007/s00259-019-04330-7
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
PurposeThe purpose of this study was to evaluate the value of 3-deoxy-3-F-18-fluorothymidine (F-18-FLT) and F-18-fluorodeoxyglucose (F-18-FDG) positron emission tomography/computed tomography (PET/CT) for early prediction of standard anatomic response and survival outcomes in patients with metastatic colorectal cancer (mCRC) receiving Regorafenib.MethodsSixty-eight patients with mCRC refractory to standard cytotoxic chemotherapy were enrolled and received Regorafenib (160mg/day on days 1-21, following a 7-day break). Standard anatomical response was evaluated every 8weeks. Both scans were performed before and on day 21 of Regorafenib.ResultsOf the 61 patients included in per-protocol analysis, complete response was not observed, but partial response was observed in 8.2% (n=5), stable disease in 67.2% (n=41), and progressive disease in 24.6% (n=15). The objective response rate was 8.2% and disease control rate 75.4%. Five responders (8.2%) and 13 non-responders (21.3%) met the CT and F-18-FLT PET/CT criteria (maximum standardized uptake value decrease 10.6% for responders). Forty-three (70.5%) exhibited discordant responses on CT and F-18-FLT PET/CT (McNemar test, P<0.001). At a median follow-up of 8.9months, median progression-free survival (PFS) and median overall survival (OS) were 3.6months (95% confidence interval [CI], 3.34-3.80months) and 8.5months (95% CI, 6.95-10.10months), respectively. Comparison of PFS and OS according to F-18-FLT PET/CT response revealed slightly longer PFS (P=0.015) in responders, but the correlation with OS was not significant. The PET Response Criteria in Solid Tumours (PERCIST) of F-18-FDG PET/CT revealed differences in PFS and OS between partial metabolic response (PMR) and non-PMR (P=0.048 and P=0.014, respectively), and between progressive metabolic disease (PMD) and non-PMD (P=0.189 and P=0.007, respectively).ConclusionsSurvival outcome was significantly associated with PERCIST using F-18-FDG PET/CT but the change of F-18-FLT uptake was only slightly associated with PFS. F-18-FDG PET/CT can be used as imaging biomarker to predict clinical outcomes early in patients with mCRC receiving Regorafenib.
引用
收藏
页码:1713 / 1722
页数:10
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