See editorial on pages 1129–31, this issue.
Original Article
Total lesion glycolysis in positron emission tomography is a better predictor of outcome than the International Prognostic Index for patients with diffuse large B cell lymphoma†
Article first published online: 4 DEC 2012
DOI: 10.1002/cncr.27855
Copyright © 2012 American Cancer Society
Additional Information
How to Cite
Kim, T. M., Paeng, J. C., Chun, I. K., Keam, B., Jeon, Y. K., Lee, S.-H., Kim, D.-W., Lee, D. S., Kim, C. W., Chung, J.-K., Kim, I. H. and Heo, D. S. (2013), Total lesion glycolysis in positron emission tomography is a better predictor of outcome than the International Prognostic Index for patients with diffuse large B cell lymphoma. Cancer, 119: 1195–1202. doi: 10.1002/cncr.27855
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See editorial on pages 1129–31, this issue.
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The first 2 authors contributed equally to this work.
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Publication History
- Issue published online: 4 MAR 2013
- Article first published online: 4 DEC 2012
- Manuscript Accepted: 7 JUN 2012
- Manuscript Revised: 2 MAY 2012
- Manuscript Received: 18 MAR 2012
- Abstract
- Article
- References
- Cited By
Keywords:
- diffuse large B cell lymphoma;
- positron emission tomography;
- total lesion glycolysis;
- Ann Arbor stage;
- International Prognostic Index
Abstract
BACKGROUND:
This study was undertaken to evaluate the prognostic value of quantitative metabolic parameters in [18F]2-fluoro-2-deoxyglucose (FDG)-positron emission tomography (PET) for diffuse large B cell lymphoma (DLBCL).
METHODS:
A total of 140 DLBCL patients underwent FDG-PET scans before rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) chemotherapy. The maximal standardized uptake value (SUVmax) and total lesion glycolysis (TLG) were calculated, with the margin thresholds as 25%, 50%, and 75% of SUVmax of all lesions. Treatment outcomes were compared between groups according to metabolic parameters and the International Prognostic Index (IPI).
RESULTS:
After a median follow-up of 28.5 months (range, 5-81 months), the 2-year progression-free survival (PFS) and overall survival (OS) were 83% and 87%, respectively. Among metabolic parameters, TLG at the threshold of 50% (TLG50) was significantly associated with treatment outcomes. High TLG50 values (>415.5) were associated with reduced survivals compared with low TLG50 values (≤415.5) (2-year PFS of 73% versus 92%, P = .007; and 2-year OS of 81% versus 93%, P = .031). High IPI score (≥3) significantly reduced OS (2-year OS of 79% versus 90%, P = .049). Ann Arbor stage III/IV adversely affected PFS (P = .013). However, high IPI score and Ann Arbor stage of III/V did not significantly shorten PFS (P = .200) and OS (P = .921), respectively. High TLG50 values independently predicted survivals by multivariate analysis (hazard ratio = 4.4; 95% confidence interval = 1.5-13.1; P = .008 for PFS and hazard ratio = 3.1; 95% confidence interval = 1.0-9.6; P = .049 for OS).
CONCLUSIONS:
Combined assessment of volume and metabolism (ie, TLG) is predictive of survivals in DLBCL patients who are treated with R-CHOP. Cancer 2013. © 2012 American Cancer Society.

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