Predictive value of metabolic 18FDG-PET response on outcomes in patients with locally advanced pancreatic carcinoma treated with definitive concurrent chemoradiotherapy

被引:51
|
作者
Topkan, Erkan [1 ]
Parlak, Cem [1 ]
Kotek, Ayse [1 ]
Yapar, Ali Fuat [2 ]
Pehlivan, Berrin [3 ]
机构
[1] Baskent Univ, Adana Med Fac, Dept Radiat Oncol, Adana, Turkey
[2] Baskent Univ, Adana Med Fac, Dept Nucl Med, Adana, Turkey
[3] Akdeniz Univ, Fac Med, Dept Radiat Oncol, TR-07058 Antalya, Turkey
关键词
Concurrent chemoradiotherapy; locally advanced pancreas cancer; positron emission tomography; metabolic response; clinical outcome prediction; POSITRON-EMISSION-TOMOGRAPHY; F-18; FLUORODEOXYGLUCOSE; FDG-PET; STEREOTACTIC RADIOSURGERY; DIFFERENTIAL-DIAGNOSIS; COMPUTED-TOMOGRAPHY; RADIATION-THERAPY; LUNG-CANCER; GEMCITABINE; CT;
D O I
10.1186/1471-230X-11-123
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: We aimed to study the predictive value of combined 18F-fluoro-deoxy-D-glucose positron emission tomography and computerized tomography (FDG-PET-CT), on outcomes in locally advanced pancreatic carcinoma (LAPC) patients treated with concurrent chemoradiotherapy (C-CRT). Methods: Thirty-two unresectable LAPC patients received 50.4 Gy (1.8 Gy/fr) of RT and concurrent 5-FU followed by 4 to 6 cycles of gemcitabine consolidation. Response was evaluated by FDG-PET-CT at post-C-CRT 12-week. Patients were stratified into two groups according to the median difference between pre- and post-treatment maximum standard uptake values (SUVmax) as an indicator of response for comparative analysis. Results: At a median follow-up of 16.1 months, 16 (50.0%) patients experienced local/regional failures, 6 of which were detected on the first follow-up FDG-PET-CT. There were no marginal or isolated regional failures. Median pre- and post-treatment SUVmax and median difference were 14.5, 3.9, and -63.7%, respectively. Median overall survival (OS), progression-free survival (PFS), and local-regional progression-free survival (LRPFS) were 14.5, 7.3, and 10.3 months, respectively. Median OS, PFS, and LRPFS for those with greater (N = 16) versus lesser (N = 16) SUVmax change were 17.0 versus 9.8 (p = 0.001), 8.4 versus 3.8 (p = 0.005), and 12.3 versus 6.9 months (p = 0.02), respectively. On multivariate analysis, SUVmax difference was predictive of OS, PFS, and LRPFS, independent of existing covariates. Conclusions: Significantly higher OS, PFS, and LRPFS in patients with greater SUVmax difference suggest that FDG-PET-CT-based metabolic response assessment is an independent predictor of clinical outcomes in LAPC patients treated with definitive C-CRT.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] The predictive value of MRI and 18F-FDG-PET/CT for assessing pathological response in locally advanced rectal cancer after neoadjuvant chemoradiotherapy
    Avci, G. Guler
    Aral, I.
    LEUKEMIA RESEARCH, 2019, 85 : S35 - S35
  • [42] Overview of the predictive value of quantitative 18 FDG PET in head and neck cancer treated with chemoradiotherapy
    Castelli, J.
    De Bari, B.
    Depeursinge, A.
    Simon, A.
    Devillers, A.
    Jimenez, G. Roman
    Prior, J.
    Ozsahin, M.
    de Crevoisier, R.
    Bourhis, J.
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2016, 108 : 40 - 51
  • [43] Role of Radiomics Applied to Baseline 18F-FDG PET/CT in Locally Advanced Cervical Carcinoma Patients Treated with Combined Chemoradiotherapy
    Mathoux, G.
    Monaco, L.
    De Bernardi, E.
    Di Martino, G.
    Crivellaro, C.
    Elisei, F.
    Musarra, M.
    Bazzano, L.
    Landoni, C.
    Guerra, L.
    Messa, C.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2023, 50 (SUPPL 1) : S557 - S557
  • [44] Predictive Value of Maximum Standardized Uptake Value (SUVmax) on 18F-FDG PET/CT in Patients With Locally Advanced or Metastatic Pancreatic Cancer
    Moon, Soo Young
    Joo, Kwang Ro
    So, Ye Ri
    Lim, Jun Uk
    Cha, Jae Myung
    Shin, Hyun Phil
    Yang, You-Jung
    CLINICAL NUCLEAR MEDICINE, 2013, 38 (10) : 778 - 783
  • [45] Baseline nutritional status is predictive of response to treatment and survival in patients treated by definitive chemoradiotherapy for a locally advanced esophageal cancer
    Di Fiore, Fredric
    Lecleire, Stephane
    Pop, Daniela
    Rigal, Olivier
    Hamidou, Hadji
    Paillot, Bernard
    Ducrotte, Philippe
    Lerebours, Eric
    Michel, Pierre
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (11): : 2557 - 2563
  • [46] Effectiveness of image-guided radiotherapy for locally advanced esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy
    Kuo, Yao-Hung
    Fang, Hsin-Yuan
    Lin, Yu-Sen
    Lein, Ming-Yu
    Yang, Chi-Ying
    Ho, Shih-Chi
    Li, Chia-Chin
    Chien, Chun-Ru
    THORACIC CANCER, 2020, 11 (01) : 113 - 119
  • [47] Comparing Mri And 18fdg-Pet/Ct As Response Evaluation Tools In Locally Advanced Cervical Cancer
    Garrido Botella, M. I.
    Rodriguez Roldan, M.
    Teja Ubach, M.
    Gonzalez Cantero, M.
    Rodriguez Rodriguez, I.
    Gonzalez Del Portillo, E.
    Belinchon Olmeda, B.
    Morera, R.
    RADIOTHERAPY AND ONCOLOGY, 2022, 170 : S1139 - S1140
  • [48] Predictive value of the early response in locally advanced non-small cell lung cancer treated with concurrent chemoradiotherapy by 18F-alfatide RGD PET/CT.
    Gao, Song
    Wei, Yuchun
    Liu, Ning
    Hu, Xudong
    Huang, Yong
    Zhao, Wei
    Hou, Wenhong
    Yuan, Shuanghu
    JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
  • [49] Predictive Value of Neutrophils Count for Local Tumor Control After Chemoradiotherapy in Patients With Locally Advanced Pancreatic Carcinoma
    Schernberg, Antoine
    Vernerey, Dewi
    Goldstein, David
    van Laethem, Jean-Luc
    Glimelius, Bengt
    van Houtte, Paul
    Bonnetain, Franck
    Louvet, Christophe
    Hammel, Pascal
    Huguet, Florence
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2021, 110 (04): : 1022 - 1031
  • [50] Outcomes and prognostic factors in patients with locally advanced cervical cancer treated with concurrent chemoradiotherapy
    Jing Liu
    Guyu Tang
    Qin Zhou
    Weilu Kuang
    Radiation Oncology, 17