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핵의학
- 2017년 06월호
[Eur J Nucl Med Mol Imaging.] Total lesion glycolysis (TLG) as an imaging biomarker in TMPstatic colorectal cancer patients treated with regorafenib.서울의대 / 임유주, 방지인, 한세원*, 팽진철*
- 출처
- Eur J Nucl Med Mol Imaging.
- 등재일
- 2017 May
- 저널이슈번호
- 44(5):757-764. doi: 10.1007/s00259-016-3577-0. Epub 2016 Nov 25.
- 내용
Abstract
PURPOSE:
This study was performed to evaluate whether fluorine-18 fluorodeoxyglucose positron-emission tomography/computed tomography (FDG PET/CT) could predict treatment outcome of regorafenib in metastatic colorectal cancer (mCRC).
METHODS:
Previously treated refractory mCRC patients were enrolled into a prospective biomarker study of regorafenib. For this sub-study, the results of FDG PET/CT scans at baseline and after two cycles of treatment were analyzed. Various metabolic parameters obtained from PET images were analyzed in relation to treatment outcome.
RESULTS:
A total of 40 patients were evaluable for PET image analysis. Among various PET parameters, total lesion glycolysis (TLG) measured in the same target lesions for RECIST 1.1 analysis were the most significant in predicting prognosis, with the lowest p-value observed in TLG calculated using the margin threshold of 40 % (TLG40 %). Further analysis using TLG40 % showed significantly longer overall survival (OS) in patients with lower baseline TLG40 % (<151.8) (p = 0.003, median 14.2 vs. 9.1 months in <151.8 and ≥151.8, respectively). Patients showing higher decrease in TLG40 % after treatment showed significantly longer progression-free survival (PFS) (p = 0.001, median 8.0 vs. 2.4 months in %ΔTLG40 % < -9.6 % and ≥ -9.6 %, respectively) and OS (p = 0.002, median 16.4 vs. 9.1 months in %ΔTLG40 % < -9.6 % and ≥ -9.6 %, respectively). The same cutoff could discriminate patients with longer survival among the patients who were under the stable disease category according to RECIST 1.1 (median PFS 8.4 vs. 6.8 months, p = 0.020; median OS 18.3 vs. 11.5 months, p = 0.049).
CONCLUSION:
Measurement of TLG can predict treatment outcome of regorafenib in mCRC.
Author information
Lim Y1, Bang JI2, Han SW3,4, Paeng JC5, Lee KH1, Kim JH6, Kang GH7, Jeong SY8, Park KJ8, Kim TY1,9,10.
1 Department of Internal Medicine, Seoul National University Hospital, 101 Daehang-ro, Jongno-gu, Seoul, 03080, South Korea.
2 Department of Nuclear Medicine, Seoul National University Hospital, 101 Daehang-ro, Jongno-gu, Seoul, 03080, South Korea.
3 Department of Internal Medicine, Seoul National University Hospital, 101 Daehang-ro, Jongno-gu, Seoul, 03080, South Korea. saewon1@snu.ac.kr.
4 Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea. saewon1@snu.ac.kr.
5 Department of Nuclear Medicine, Seoul National University Hospital, 101 Daehang-ro, Jongno-gu, Seoul, 03080, South Korea. paengjc@snu.ac.kr.
6 Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam-si, Geyonggi-do, South Korea.
7 Department of Pathology, Seoul National University Hospital, Seoul, South Korea.
8 Department of Surgery, Seoul National University Hospital, Seoul, South Korea.
9 Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
10 Department of Molecular Medicine & Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, South Korea.
- 키워드
- Biomarker; Fluorine-18 fluorodeoxyglucose positron-emission tomography; Metastatic colorectal cancer; Regorafenib
- 덧글달기
- 이전글 [J Nucl Med.] 18F-FDG PET/CT Can Predict Survival of Advanced Hepatocellular Carcinoma Patients: A Multicenter Retrospective Cohort Study.
- 다음글 [Clin Nucl Med.] Prognostic Value of Pretreatment Metabolic Tumor Volume and Total Lesion Glycolysis Using 18F-FDG PET/CT in Patients With Metastatic Renal Cell Carcinoma Treated With Anti-Vascular Endothelial Growth Factor-Targeted Agents.