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KMID : 1148920180520050342
Nuclear Medicine and Molecular Imaging
2018 Volume.52 No. 5 p.342 ~ p.349
Application of Quantitative Indexes of FDG PET to Treatment Response Evaluation in Indolent Lymphoma
Kim Hyun-Joo

Lee Ree-Ree
Choi Hong-Yoon
Paeng Jin-Chul
Cheon Gi-Jeong
Lee Dong-Soo
Chung June-Key
Kang Keon-Wook
Abstract
Purpose: Although 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) is a standard imaging modality for response evaluation in FDG-avid lymphoma, there is a controversy using FDG PET in indolent lymphoma. The purpose of this study was to investigate the effectiveness of quantitative indexes on FDG PET in response evaluation of the indolent lymphoma.

Methods: Fifty-seven indolent lymphoma patients who completed chemotherapy were retrospectively enrolled. FDG PET/computed tomography (CT) scans were performed at baseline, interim, and end of treatment (EOT). Response was determined by Lugano classification, and progression-free survival (PFS) by follow-up data. Maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were measured in the single hottest lesion (target A) or five hottest lesions (target B). Their efficacies regarding response evaluation and PFS prediction were evaluated.

Results: On EOT PET, SUVmax, and MTV of both targets were well associated with visual analysis. Changes between initial and EOT PET were not significantly different between CR and non-CR groups. On interim PET, SUVmax, and %¥ÄSUVmax in both targets were significantly different between CR and non-CR groups. For prediction of PFS, most tested indexes were significant on EOT and interim PET, with SUVmax being the most significant prognostic factor.

Conclusion: Quantitative indexes of FDG PET are well associated with Lugano classification in indolent lymphoma. SUVmax measured in the single hottest lesion can be effective in response evaluation and prognosis prediction on interim and EOT PET.
KEYWORD
Indolent lymphoma, 18F-Fluorodeoxyglucose (FDG) positron emission tomography (PET), Response evaluation
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