TY - JOUR
T1 - Pretreatment 18F-FDG PET standardized uptake value of primary tumor and neck lymph nodes as a predictor of distant metastasis for patients with nasopharyngeal carcinoma
AU - Hung, Tsung Min
AU - Wang, Hung Ming
AU - Kang, Chung Jan
AU - Huang, Shiang Fu
AU - Liao, Chun Ta
AU - Chan, Sheng Chieh
AU - Ng, Shu Hang
AU - Chen, I. How
AU - Lin, Chien Yu
AU - Fan, Kang Hsing
AU - Chang, Joseph Tung Chieh
PY - 2013/2
Y1 - 2013/2
N2 - Objectives: To evaluate the prognostic value of maximum standardized uptake value (SUVmax) measured in [18F]-fluorodeoxyglucose positron emission tomography (18F-FDG PET) for patients with non-disseminated nasopharyngeal carcinoma (NPC). Materials and methods: From January 2002 to July 2008, 371 NPC patients who underwent 18F-FDG-PET before radical intensity-modulated radiotherapy (IMRT) were recruited. The SUVmax was recorded for the primary tumor (SUVmax-T) and neck lymph nodes (SUVmax-N). Results: The median follow-up was 64 months. The optimal cutoff value was 9.3 for SUVmax-T and 7.4 for SUVmax-N. Patients with a lower SUVmax-T or SUVmax-N had a significantly better 5-year distant metastasis-free survival (DMFS), but showed no significant difference in local control or regional control. Patients were divided into four groups by SUVmax, as follows: (a) both lower SUVmax-T and SUVmax-N, (b) higher SUVmax-T only, (c) higher SUVmax-N only, and d) both higher SUVmax-T and SUVmax-N. There were significant differences between these four groups in 5-year DMFS: (a) 95.5%, (b) 90.0%, (c) 83.3%, and (d) 79.9%, respectively (p = 0.004). When looking at the stage of disease, the 5-year DMFSs in group a, b, c, d were 96.9%, 94.6%, 97.4%, and 84.3%, respectively in stage I-III patients (p = 0.037) and were 91.6%, 82.9%, 68.5%, and 76.7% in stage IVA-B patients (p = 0.145). Using multivariate analysis, the SUVmax grouping, gender, and stage were independent factors for DMFS. Conclusion: The SUVmax of the primary tumor and neck lymph nodes were independent prognostic factors for DMFS in NPC patients treated with IMRT.
AB - Objectives: To evaluate the prognostic value of maximum standardized uptake value (SUVmax) measured in [18F]-fluorodeoxyglucose positron emission tomography (18F-FDG PET) for patients with non-disseminated nasopharyngeal carcinoma (NPC). Materials and methods: From January 2002 to July 2008, 371 NPC patients who underwent 18F-FDG-PET before radical intensity-modulated radiotherapy (IMRT) were recruited. The SUVmax was recorded for the primary tumor (SUVmax-T) and neck lymph nodes (SUVmax-N). Results: The median follow-up was 64 months. The optimal cutoff value was 9.3 for SUVmax-T and 7.4 for SUVmax-N. Patients with a lower SUVmax-T or SUVmax-N had a significantly better 5-year distant metastasis-free survival (DMFS), but showed no significant difference in local control or regional control. Patients were divided into four groups by SUVmax, as follows: (a) both lower SUVmax-T and SUVmax-N, (b) higher SUVmax-T only, (c) higher SUVmax-N only, and d) both higher SUVmax-T and SUVmax-N. There were significant differences between these four groups in 5-year DMFS: (a) 95.5%, (b) 90.0%, (c) 83.3%, and (d) 79.9%, respectively (p = 0.004). When looking at the stage of disease, the 5-year DMFSs in group a, b, c, d were 96.9%, 94.6%, 97.4%, and 84.3%, respectively in stage I-III patients (p = 0.037) and were 91.6%, 82.9%, 68.5%, and 76.7% in stage IVA-B patients (p = 0.145). Using multivariate analysis, the SUVmax grouping, gender, and stage were independent factors for DMFS. Conclusion: The SUVmax of the primary tumor and neck lymph nodes were independent prognostic factors for DMFS in NPC patients treated with IMRT.
KW - Distant metastasis
KW - F-fluorodeoxyglucose positron emission tomography
KW - Intensity-modulated radiotherapy
KW - Nasopharyngeal carcinoma
KW - Prognosis
UR - http://www.scopus.com/inward/record.url?scp=84872288171&partnerID=8YFLogxK
U2 - 10.1016/j.oraloncology.2012.08.011
DO - 10.1016/j.oraloncology.2012.08.011
M3 - 文章
C2 - 23063613
AN - SCOPUS:84872288171
SN - 1368-8375
VL - 49
SP - 169
EP - 174
JO - Oral Oncology
JF - Oral Oncology
IS - 2
ER -