Positron emission tomography with 18F-FDG to detect residual disease after therapy for malignant lymphoma

被引:106
作者
Cremerius, U [1 ]
Fabry, U [1 ]
Neuerburg, J [1 ]
Zimny, M [1 ]
Osieka, R [1 ]
Buell, U [1 ]
机构
[1] Rhein Westfal TH Aachen, Univ Hosp, Dept Nucl Med, Aachen, Germany
关键词
D O I
10.1097/00006231-199811000-00005
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
We retrospectively evaluated the use of F-18-FDG PET for assessment of residual disease in 27 patients after therapy for malignant lymphoma. The images were evaluated qualitatively and quantitatively using standardized uptake values (SUV). All findings were validated either by biopsy or by clinical follow-up and compared with corresponding CT findings. The impact of blood glucose concentration, body weight, body surface area, lesion diameter and the time between injection and imaging on the SUVs were analysed. All 15 patients with biopsy-proven residual disease or relapse during follow-up and 11 of 12 patients who remained relapse-free were correctly identified by qualitative interpretation of the PET images. A case of pneumonitis after radiotherapy/chemotherapy accounted for the only false-positive finding. Compared with CT imaging, PET had a significantly higher specificity (P < 0.01), accuracy (P < 0.05) and positive predictive value (P < 0.05). The mean and maximum SUV of the tumour lesions were positively correlated to lesion diameter (P < 0.01) and imaging time post-injection (P < 0.01). Standardized uptake values corrected for the partial volume effect and normalized to a standardized imaging time (SUVBPT) were significantly higher (P < 0.05) in high-grade than in low-grade non-Hodgkin's lymphoma. In conclusion F-18-FDG PET may help in the identification of patients who need additional treatment after the completion of conventional therapy. Qualitative image interpretation appears sufficient for this purpose. ((C) 1998 Lippincott Williams & Wilkins).
引用
收藏
页码:1055 / 1063
页数:9
相关论文
共 31 条
  • [1] F-18 FLUORODEOXYGLUCOSE PET IN-VIVO EVALUATION OF PANCREATIC GLUCOSE-METABOLISM FOR DETECTION OF PANCREATIC-CANCER
    BARES, R
    KLEVER, P
    HAUPTMANN, S
    HELLWIG, D
    FASS, J
    CREMERIUS, U
    SCHUMPELICK, V
    MITTERMAYER, C
    BULL, U
    [J]. RADIOLOGY, 1994, 192 (01) : 79 - 86
  • [2] Bartold SP, 1997, J NUCL MED, V38, P990
  • [3] Bogart JA, 1998, CANCER-AM CANCER SOC, V82, P754, DOI 10.1002/(SICI)1097-0142(19980215)82:4<754::AID-CNCR19>3.0.CO
  • [4] 2-X
  • [5] CABANILLAS F, 1992, BLOOD, V79, P1024
  • [6] RESIDUAL MASS IN LYMPHOMA MAY NOT BE RESIDUAL DISEASE
    CANELLOS, GP
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (06) : 931 - 933
  • [7] Whole-body positron emission tomography (PET) for diagnosis of residual mass in patients with lymphoma
    deWit, M
    Bumann, D
    Beyer, W
    Herbst, K
    Clausen, M
    Hossfeld, DK
    [J]. ANNALS OF ONCOLOGY, 1997, 8 : 57 - 60
  • [8] EVALUATION OF TUMOR METABOLISM AND MULTIDRUG-RESISTANCE IN PATIENTS WITH TREATED MALIGNANT-LYMPHOMAS
    DIMITRAKOPOULOUSTRAUSS, A
    STRAUSS, LG
    GOLDSCHMIDT, H
    LORENZ, WJ
    MAIERBORST, W
    VANKAICK, G
    [J]. EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1995, 22 (05): : 434 - 442
  • [9] HAMBERG LM, 1994, J NUCL MED, V35, P1308
  • [10] HOEKSTRA OS, 1993, J NUCL MED, V34, P1706