Does Delayed-Time-Point Imaging Improve 18F-FDG-PET in Patients With MALT Lymphoma?

被引:15
作者
Mayerhoefer, Marius E. [1 ]
Giraudo, Chiara [1 ]
Senn, Daniela [1 ]
Hartenbach, Markus [1 ]
Weber, Michael [1 ]
Rausch, Ivo [2 ]
Kiesewetter, Barbara [3 ]
Herold, Christian J. [1 ]
Hacker, Marcus [1 ]
Pones, Matthias [1 ]
Simonitsch-Klupp, Ingrid [4 ]
Muellauer, Leonhard [4 ]
Dolak, Werner [5 ]
Lukas, Julius [6 ]
Raderer, Markus [3 ]
机构
[1] Med Univ Vienna, Dept Biomed Imaging & Image Guided Therapy, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[2] Med Univ Vienna, Ctr Med Phys & Biomed Engn, Vienna, Austria
[3] Med Univ Vienna, Dept Internal Med 1, Vienna, Austria
[4] Med Univ Vienna, Inst Pathol, Vienna, Austria
[5] Med Univ Vienna, Dept Internal Med 3, Vienna, Austria
[6] Med Univ Vienna, Dept Ophthalmol & Optometry, Vienna, Austria
基金
奥地利科学基金会;
关键词
lymphoma; 2-F-18-fluoro-2-deoxy-D-glucose; positron emission tomography; magnetic resonance imaging; computed tomography; DIFFUSION-WEIGHTED MRI; NON-HODGKIN-LYMPHOMA; FDG PET/CT; LESIONS; REPRODUCIBILITY;
D O I
10.1097/RLU.0000000000001005
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To determine whether in patients with extranodal marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue lymphoma (MALT), delayed-time-point 2-F-18-fluoro-2-deoxy-D-glucose-positron emission tomography (F-18-FDG-PET) performs better than standard-time-point F-18-FDG-PET. Materials and Methods: Patients with untreated histologically verified MALT lymphoma, who were undergoing pretherapeutic F-18-FDG-PET/computed tomography (CT) and consecutive F-18-FDG-PET/magnetic resonance imaging (MRI), using a single F-18-FDG injection, in the course of a larger-scale prospective trial, were included. Region-based sensitivity and specificity, and patient-based sensitivity of the respective F-18-FDG-PET scans at time points 1 (45-60 minutes after tracer injection, TP1) and 2 (100-150 minutes after tracer injection, TP2), relative to the reference standard, were calculated. Lesion-to-liver and lesion-to-blood SUVmax (maximum standardized uptake values) ratios were also assessed. Results: F-18-FDG-PET at TP1 was true positive in 15 o f 23 involved regions, and F-18-FDG-PET at TP2 was true-positive in 20 of 23 involved regions; no false-positive regions were noted. Accordingly, region-based sensitivities and specificities were 65.2% (confidence interval [CI], 45.73%-84.67%) and 100% (CI, 100%-100%) for F-18-FDG-PET at TP1; and 87.0% (CI, 73.26%-100%) and 100% (CI, 100%-100%) for F-18-FDG-PET at TP2, respectively. FDG-PET at TP1 detected lymphoma in at least one nodal or extranodal region in 7 of 13 patients, and F-18-FDG-PET at TP2 in 10 of 13 patients; accordingly, patient-based sensitivity was 53.8% (CI, 26.7%-80.9%) for F-18-FDG-PET at TP1, and 76.9% (CI, 54.0%-99.8%) for 18F-FDG-PET at TP2. Lesion-to-liver and lesion-to-blood maximum standardized uptake value ratios were significantly lower at TP1 (ratios, 1.05 +/- 0.40 and 1.52 +/- 0.62) than at TP2 (ratios, 1.67 +/- 0.74 and 2.56 +/- 1.10; P = 0.003 and P = 0.001). Conclusions: Delayed-time-point imaging may improve F-18-FDG-PET in MALT lymphoma.
引用
收藏
页码:101 / 105
页数:5
相关论文
共 16 条
  • [1] Staging non-Hodgkin lymphoma
    Armitage, JO
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2005, 55 (06) : 368 - 376
  • [2] Cheng G, 2014, CLIN NUCL MED, V39, P147, DOI 10.1097/RLU.0000000000000313
  • [3] When should we recommend use of dual time-point and delayed time-point imaging techniques in FDG PET?
    Cheng, Gang
    Torigian, Drew A.
    Zhuang, Hongming
    Alavi, Abass
    [J]. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2013, 40 (05) : 779 - 787
  • [4] Recommendations for Initial Evaluation, Staging, and Response Assessment of Hodgkin and Non-Hodgkin Lymphoma: The Lugano Classification
    Cheson, Bruce D.
    Fisher, Richard I.
    Barrington, Sally F.
    Cavalli, Franco
    Schwartz, Lawrence H.
    Zucca, Emanuele
    Lister, T. Andrew
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (27) : 3059 - +
  • [5] Chirindel A, 2015, CLIN NUCL MED, V40, pE17, DOI 10.1097/RLU.0000000000000446
  • [6] The Clinical Value of Dual-Time Point 18F-FDG PET/CT for Differentiating Extrahepatic Cholangiocarcinoma From Benign Disease
    Choi, Eun Kyoung
    Yoo, Ie Ryung
    Kim, Sung Hoon
    Hyun, Joo O.
    Choi, Woo Hee
    Na, Sae Jung
    Park, Sonya Youngju
    [J]. CLINICAL NUCLEAR MEDICINE, 2013, 38 (03) : E106 - E111
  • [7] Performance of Whole-Body Integrated 18F-FDG PET/MR in Comparison to PET/CT for Evaluation of Malignant Bone Lesions
    Eiber, Matthias
    Takei, Toshiki
    Souvatzoglou, Michael
    Mayerhoefer, Marius E.
    Fuerst, Sebastian
    Gaertner, Florian C.
    Loeffelbein, Denys J.
    Rummeny, Ernst J.
    Ziegler, Sibylle I.
    Schwaiger, Markus
    Beer, Ambros J.
    [J]. JOURNAL OF NUCLEAR MEDICINE, 2014, 55 (02) : 191 - 197
  • [8] Thoracic Staging in Lung Cancer: Prospective Comparison of 18F-FDG PET/MR Imaging and 18F-FDG PET/CT
    Heusch, Philipp
    Buchbender, Christian
    Koehler, Jens
    Nensa, Felix
    Gauler, Thomas
    Gomez, Benedikt
    Reiss, Henning
    Stamatis, Georgios
    Kuehl, Hilmar
    Hartung, Verena
    Heusner, Till A.
    [J]. JOURNAL OF NUCLEAR MEDICINE, 2014, 55 (03) : 373 - 378
  • [9] Evaluation of Dixon Sequence on Hybrid PET/MR Compared with Contrast-Enhanced PET/CT for PET-Positive Lesions
    Jeong J.H.
    Cho I.H.
    Kong E.J.
    Chun K.A.
    [J]. Nuclear Medicine and Molecular Imaging, 2014, 48 (1) : 26 - 32
  • [10] Quantitative liver ADC measurements using diffusion-weighted MRI at 3 Tesla: evaluation of reproducibility and perfusion dependence using different techniques for respiratory compensation
    Larsen, Nis Elbrond
    Haack, Soren
    Larsen, Lars Peter Skovgaard
    Pedersen, Erik Morre
    [J]. MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE, 2013, 26 (05) : 431 - 442