| Literature DB >> 32453838 |
Hajime Senjo1, Kenji Hirata2, Koh Izumiyama3, Koichiro Minauchi4, Eriko Tsukamoto5, Kazuo Itoh6, Minoru Kanaya3, Akio Mori3, Shuichi Ota4, Daigo Hashimoto1, Takanori Teshima1.
Abstract
Metabolic heterogeneity (MH) can be measured using 18F-fluorodeoxyglucose (18FDG) positron emission tomography/computed tomography (PET/CT), and it indicates an inhomogeneous tumor microenvironment. High MH has been shown to predict a worse prognosis for primary mediastinal B-cell lymphoma, whereas its prognostic value in diffuse large B-cell lymphoma (DLBCL) remains to be determined. In the current study, we investigated the prognostic values of MH evaluated in newly diagnosed DLBCL. In the training cohort, 86 patients treated with cyclophosphamide, doxorubicin, vincristine, and prednisone-like chemotherapies were divided into low-MH and high-MH groups using receiver operating characteristic analysis. MH was not correlated with metabolic tumor volume of the corresponding lesion, indicating that MH was independent of tumor burden. At 5 years, overall survivals were 89.5% vs 61.2% (P = .0122) and event-free survivals were 73.1% vs 51.1% (P = .0327) in the low- and high-MH groups, respectively. A multivariate Cox-regression analysis showed that MH was an independent predictive factor for overall survival. The adverse prognostic impacts of high MH were confirmed in an independent validation cohort with 64 patients. In conclusion, MH on baseline 18FDG-PET/CT scan predicts treatment outcomes for patients with newly diagnosed DLBCL.Entities:
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Year: 2020 PMID: 32453838 PMCID: PMC7252551 DOI: 10.1182/bloodadvances.2020001816
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529