FDG-PET after two to three cycles of chemotherapy predicts progression-free and overall survival in high-grade non-Hodgkin lymphoma

被引:319
作者
Mikhaeel, NG
Hutchings, M
Fields, PA
O'Doherty, MJ
Timothy, AR
机构
[1] Guys & St Thomas Hosp, Dept Clin Oncol, London SE1 9RT, England
[2] Guys & St Thomas Hosp, Dept Haematol, London SE1 9RT, England
[3] Guys & St Thomas Hosp, Clin PET Ctr, London SE1 9RT, England
关键词
fluorodeoxyglucose F18; non-Hodgkin lymphoma; positron emission tomography; prognosis;
D O I
10.1093/annonc/mdi272
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Less than 50% of all high-grade non-Hodgkin lymphoma (NHL) patients experience lasting disease-free survival. Risk-adapted treatment strategies require better tools for prediction of outcome. This investigation aimed to assess the value of positron emission tomography with 2-[18F]fluoro-2-deoxy-D-glucose (FDG-PET) after two to three cycles of chemotherapy for prediction of progression-free survival (PFS) and overall survival (OS). Patients and methods: One hundred and twenty-one patients with high-grade NHL underwent FDG-PET. The therapy response on FDG-PET was correlated to PFS and OS using Kaplan-Meier survival analysis. Cox regression analyses were employed to test for independence of known pretreatment prognostic factors. Results: Fifty FDG-PET scans were negative, 19 scans showed minimal residual uptake (MRU), and 52 scans were positive. The estimated 5 year PFS was 88.8% for the PET-negative group, 59.3% for the MRU group, and 16.2% for the PET-positive group. Kaplan-Meier analyses showed strong associations between FDG-PET results and PFS (P < 0.0001) and OS (P < 0.01). Early interim FDG-PET was independent of the other prognostic factors. Conclusions: Early interim FDG-PET is an accurate and independent predictor of PFS and OS. An early assessment of chemotherapy response with FDG-PET could provide the basis for selection of patients for alternative therapeutic strategies.
引用
收藏
页码:1514 / 1523
页数:10
相关论文
共 29 条
  • [1] CHEMOTHERAPY FOR DIFFUSE LARGE-CELL LYMPHOMA - RAPIDLY RESPONDING PATIENTS HAVE MORE DURABLE REMISSIONS
    ARMITAGE, JO
    WEISENBURGER, DD
    HUTCHINS, M
    MORAVEC, DF
    DOWLING, M
    SORENSEN, S
    MAILLIARD, J
    OKERBLOOM, J
    JOHNSON, PS
    HOWE, D
    BASCOM, GK
    CASEY, J
    LINDER, J
    PURTILO, DT
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (02) : 160 - 164
  • [2] Germinal center phenotype and bcl-2 expression combined with the International Prognostic Index improves patient risk stratification in diffuse large B-cell lymphoma
    Barrans, SL
    Carter, I
    Owen, RG
    Davies, FE
    Patmore, RD
    Haynes, AP
    Morgan, GJ
    Jack, AS
    [J]. BLOOD, 2002, 99 (04) : 1136 - 1143
  • [3] Bartold SP, 1997, J NUCL MED, V38, P990
  • [4] Belhocine T, 2002, CLIN CANCER RES, V8, P2766
  • [5] RESIDUAL MASS IN LYMPHOMA MAY NOT BE RESIDUAL DISEASE
    CANELLOS, GP
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (06) : 931 - 933
  • [7] Early response to chemotherapy:: a surrogate for final outcome of Hodgkin's disease patients that should influence initial treatment length and intensity?
    Carde, P
    Koscielny, S
    Franklin, J
    Axdorph, U
    Raemaekers, J
    Diehl, V
    Aleman, B
    Brosteanu, O
    Hasenclever, D
    Oberlin, O
    Bonvin, N
    Björkholm, M
    [J]. ANNALS OF ONCOLOGY, 2002, 13 : 86 - 91
  • [8] CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma.
    Coiffier, B
    Lepage, E
    Brière, J
    Herbrecht, R
    Tilly, H
    Bouabdallah, R
    Morel, P
    Van den Neste, E
    Salles, G
    Gaulard, P
    Reyes, F
    Gisselbrecht, C
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) : 235 - 242
  • [9] Collett D, 2015, Modelling Survival Data in Medical Research
  • [10] Everitt, 2004, A Handbook of Statistical Analyses using SPSS