[68Ga]Ga-Pentixafor PET/MRI for CXCR4 Imaging of Chronic Lymphocytic Leukemia

医学 核医学 慢性淋巴细胞白血病 病理 骨髓 标准摄取值 淋巴瘤 白血病 正电子发射断层摄影术 内科学
作者
Marius E. Mayerhoefer,Ulrich Jaeger,Philipp B. Staber,Markus Raderer,Wolfgang Wadsak,Sarah Pfaff,Christoph Kornauth,Dietrich Beitzke,Michael Weber,Hans‐Juergen Wester,Cathrin Skrabs,Alexander Haug
出处
期刊:Investigative Radiology [Lippincott Williams & Wilkins]
卷期号:53 (7): 403-408 被引量:49
标识
DOI:10.1097/rli.0000000000000469
摘要

Objectives This prospective proof-of-principle study aimed to determine whether [ 68 Ga]Ga-Pentixafor uptake, which reflects CXCR4 expression, is higher in the bone marrow of chronic lymphocytic leukemia (CLL) than in other oncological diseases without bone marrow infiltration and can therefore be used for CLL imaging. Materials and Methods Thirteen CLL patients and 20 controls (10 with pancreatic adenocarcinoma and 10 with mucosa-associated lymphoid tissue lymphoma) with histologically proven cancer underwent [ 68 Ga]Ga-Pentixafor positron emission tomography/magnetic resonance imaging. Standardized [ 68 Ga]Ga-Pentixafor uptake values (SUV max , SUV mean ) were measured in the bone marrow of the pelvis, the lumbar vertebra L4, and the bony structure with the visually highest tracer uptake (“hottest lesion”). Mean apparent diffusion coefficient values were also measured in the pelvis. Serum leukocyte count (gram per liter), lymphocyte percentage (percent), lactate dehydrogenase (unit per liter), β2-microglobulin (milligram per deciliter), and C-reactive protein (milligram per deciliter) were measured. Statistical analyses comprised analysis of variance with Games-Howell post hoc tests and Spearman correlation coefficients. Results SUV max and SUV mean differed significantly between CLL and pancreatic adenocarcinoma in the pelvis ( P = 0.032 and P = 0.008) and lumbar vertebra L4 (both P < 0.001). SUV mean also differed in the pelvis ( P = 0.020) and L4 ( P = 0.041), and SUV max in L4 ( P = 0.019), between CLL and mucosa-associated lymphoid tissue lymphoma. Receiver operating characteristic–based areas under the curve for separation of CLL from the control groups were greatest for the SUV max of the bony structure with the strongest [ 68 Ga]Ga-Pentixafor uptake (0.94) and the SUV max of L4 (0.92). There was no significant correlation between [ 68 Ga]Ga-Pentixafor uptake and pelvic apparent diffusion coefficients or serum parameters. Conclusions [ 68 Ga]Ga-Pentixafor positron emission tomography/magnetic resonance imaging may possibly be useful for CXCR4-based CLL imaging.

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