Intensity of 18fluorodeoxyglucose uptake in positron emission tomography distinguishes between indolent and aggressive non-Hodgkin's lymphoma

被引:385
作者
Schöder, H
Noy, A
Gönen, M
Weng, LJ
Green, D
Erdi, YE
Larson, SM
Yeung, HWD
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, Nucl Med Serv, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Lymphoma Serv, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
关键词
D O I
10.1200/JCO.2005.12.072
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose (18)Fluorodeoxyglucose positron emission tomography (FDG PET) is widely used for the staging of lymphoma. We investigated whether the intensity of tumor FDG uptake could differentiate between indolent and aggressive disease. Materials and Methods PET studies of 97 patients with non-Hodgkin's lymphoma who were untreated or had relapsed and/or persistent disease and had not received treatment within the last 6 months were analyzed, and the highest standardized uptake value (SUV) per study was recorded. Correlations were made with histopathology. Results FDG uptake was lower in indolent than in aggressive lymphoma for patients with new (SUV, 7.0 +/- 3.1 v 19.6 +/- 9.3; P <.01) and relapsed (SUV, 6.3 +/- 2.7 v 18.1 +/- 10.9; P =.04) disease. Despite overlap between indolent and aggressive disease in the low SUV range (indolent, 2.3 to 13.0; aggressive, 3.2 to 43.0), all cases of indolent lymphoma had an SUV <= 13. A receiver operating characteristic (ROC) analysis demonstrated that the SUV distinguished reasonably well between aggressive and indolent disease (area under ROC curve, 84.7%), and an SUV > 10 excluded indolent lymphoma with a specificity of 81%. With a higher cutoff for the SUV, the specificity would have been higher. Conclusion FDG uptake is lower in indolent than in aggressive lymphoma. Patients with NHL and SUV > 10 have a high likelihood for aggressive disease. This information may be helpful if there is discordance between biopsy and clinical behavior.
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页码:4643 / 4651
页数:9
相关论文
共 37 条
  • [11] Filmont JE, 2002, J NUCL MED, V43, p79P
  • [12] Fukunaga T, 1998, J NUCL MED, V39, P1002
  • [13] World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee Meeting - Airlie House, Virginia, November 1997
    Harris, NL
    Jaffe, ES
    Diebold, J
    Flandrin, G
    Muller-Hermelink, HK
    Vardiman, J
    Lister, TA
    Bloomfield, CD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (12) : 3835 - 3849
  • [14] Lymphoma classification - from controversy to consensus: The REAL and WHO Classification of lymphoid neoplasms
    Harris, NL
    Jaffe, ES
    Diebold, J
    Flandrin, G
    Muller-Hermelink, HK
    Vardiman, J
    [J]. ANNALS OF ONCOLOGY, 2000, 11 : 3 - 10
  • [15] 18F-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) for staging and follow-up of marginal zone B-cell lymphoma
    Hoffmann, M
    Kletter, K
    Becherer, A
    Jäger, U
    Chott, A
    Raderer, M
    [J]. ONCOLOGY, 2003, 64 (04) : 336 - 340
  • [16] Hoh CK, 1997, J NUCL MED, V38, P343
  • [17] Huang SC, 2000, NUCL MED BIOL, V27, P643
  • [18] Whole-body positron emission tomography using 18F-fluorodeoxyglucose for posttreatment evaluation in Hodgkin's disease and non-Hodgkin's lymphoma has higher diagnostic and prognostic value than classical computed tomography scan imaging
    Jerusalem, G
    Beguin, Y
    Fassotte, MF
    Najjar, F
    Paulus, P
    Rigo, P
    Fillet, G
    [J]. BLOOD, 1999, 94 (02) : 429 - 433
  • [19] Positron emission tomography (PET) with 18F-fluorodeoxyglucose (18F-FDG) for the staging of low-grade non-Hodgkin's lymphoma (NHL)
    Jerusalem, G
    Beguin, Y
    Najjar, F
    Hustinx, R
    Fassotte, MF
    Rigo, P
    Fillet, G
    [J]. ANNALS OF ONCOLOGY, 2001, 12 (06) : 825 - 830
  • [20] INCREASED GLUCOSE-METABOLISM IN UNTREATED NON-HODGKINS-LYMPHOMA - A STUDY WITH POSITRON EMISSION TOMOGRAPHY AND FLUORINE-18-FLUORODEOXYGLUCOSE
    LAPELA, M
    LESKINEN, S
    MINN, HRI
    LINDHOLM, P
    KLEMI, PJ
    SODERSTROM, KO
    BERGMAN, J
    HAAPARANTA, M
    RUOTSALAINEN, U
    SOLIN, O
    JOENSUU, H
    [J]. BLOOD, 1995, 86 (09) : 3522 - 3527