High metabolic heterogeneity on baseline 18FDG-PET/CT scan as a poor prognostic factor for newly diagnosed diffuse large B-cell lymphoma

Author:

Senjo Hajime1ORCID,Hirata Kenji2ORCID,Izumiyama Koh3,Minauchi Koichiro4,Tsukamoto Eriko5,Itoh Kazuo6,Kanaya Minoru3ORCID,Mori Akio3,Ota Shuichi4ORCID,Hashimoto Daigo1ORCID,Teshima Takanori1ORCID,

Affiliation:

1. Department of Hematology, Faculty of Medicine, and

2. Department of Diagnostic Imaging, Graduate School of Medicine, Hokkaido University, Sapporo, Japan;

3. Blood Disorders Center, Aiiku Hospital, Sapporo, Japan;

4. Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan;

5. Department of Radiology, Central CI Clinic, Sapporo, Japan; and

6. Department of Radiology, Keiyukai Sapporo Hospital, Sapporo, Japan

Abstract

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.

Publisher

American Society of Hematology

Subject

Hematology

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