Literature DB >> 18374589

Prognostic value of FDG uptake in early stage non-small cell lung cancer.

François-Xavier Hanin1, Max Lonneux, Julien Cornet, Philippe Noirhomme, Corinne Coulon, Julien Distexhe, Alain J Poncelet.   

Abstract

BACKGROUND: Non-small cell lung cancer (NSCLC) has a poor prognosis even for early stages of the disease (stage I and II). We studied the prognostic value of PET FDG in patients with completely resected stage I and II NSCLC.
METHODS: Retrospective study of 96 patients with NSCLC whose staging included 18F-FDG PET (fluoro deoxy glucose positron emission tomography). Histopathological stage was either stage I (75) or stage II (n=21). FDG uptake was measured as maximal standardized uptake value for body weight (SUVmax). Mean follow-up was 45+/-30 months (1-142 months). Overall and cancer-free survival rates were recorded.
RESULTS: SUVmax were higher for stage II than for stage I (10.5+/-4.5 vs 8.5+/-5, p=0.04). Mean tumor volumes were equivalent for both stages (33 cm3, p=0.18), excluding a partial volume effect. The median SUVmax in the whole study population was 7.8. The median survival was significantly longer in patients with a lower (SUVmax<or=7.8) FDG uptake (127 months vs 69 months, p=0.001). For stage I tumors (n=75), high FDG uptake was significantly associated with reduced median survival: 127 months if SUVmax<or=7.8 and 69 months if SUVmax>7.8 (p=0.001). For stage II tumors (n=21), no statistical difference was observed: 72 months vs 40 months for SUVmax<or=7.8 and for SUVmax>7.8, respectively (p=0.11), although there was a clear trend towards reduced survival for highly metabolic tumors. Disease-free survival was also significantly better for lower metabolic tumors: 96.1 months vs 87.7 months (p=0.01).
CONCLUSION: High FDG uptake is associated with reduced overall survival and disease-free survival of patients with completely resected stage I-II NSCLC. Whether patients with highly metabolic tumors should undergo a closer postoperative surveillance or adjuvant chemotherapy has to be addressed in a properly designed prospective trial.

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Year:  2008        PMID: 18374589     DOI: 10.1016/j.ejcts.2008.02.005

Source DB:  PubMed          Journal:  Eur J Cardiothorac Surg        ISSN: 1010-7940            Impact factor:   4.191


  18 in total

1.  Impact of partial-volume effect correction on the predictive and prognostic value of baseline 18F-FDG PET images in esophageal cancer.

Authors:  Mathieu Hatt; Adrien Le Pogam; Dimitris Visvikis; Olivier Pradier; Catherine Cheze Le Rest
Journal:  J Nucl Med       Date:  2012-01       Impact factor: 10.057

2.  Independent prognostic value of whole-body metabolic tumor burden from FDG-PET in non-small cell lung cancer.

Authors:  Hao Zhang; Kristen Wroblewski; Daniel Appelbaum; Yonglin Pu
Journal:  Int J Comput Assist Radiol Surg       Date:  2012-05-30       Impact factor: 2.924

3.  Value of ¹⁸F-FDG uptake on PET/CT and CEA level to predict epidermal growth factor receptor mutations in pulmonary adenocarcinoma.

Authors:  Kai-Hsiung Ko; Hsian-He Hsu; Tsai-Wang Huang; Hong-Wei Gao; Daniel H Y Shen; Wei-Chou Chang; Yi-Chih Hsu; Tsun-Hou Chang; Chi-Ming Chu; Ching-Liang Ho; Hung Chang
Journal:  Eur J Nucl Med Mol Imaging       Date:  2014-05-23       Impact factor: 9.236

4.  FDG-PET maximum standardized uptake value is prognostic for recurrence and survival after stereotactic body radiotherapy for non-small cell lung cancer.

Authors:  Zachary A Kohutek; Abraham J Wu; Zhigang Zhang; Amanda Foster; Shaun U Din; Ellen D Yorke; Robert Downey; Kenneth E Rosenzweig; Wolfgang A Weber; Andreas Rimner
Journal:  Lung Cancer       Date:  2015-05-28       Impact factor: 5.705

5.  The association of 18F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (SLC2A1) and hypoxia-related genes (HIF1A, VEGFA, APEX1) in non-small cell lung cancer. SLC2A1 polymorphisms and FDG-PET in NSCLC patients.

Authors:  Seong-Jang Kim; Sang-Hyun Hwang; In Joo Kim; Min Ki Lee; Chang Hun Lee; Sang-Yull Lee; Eun Yup Lee
Journal:  J Exp Clin Cancer Res       Date:  2010-06-12

6.  Combined evaluation of preoperative FDG uptake on PET, ground-glass opacity area on CT, and serum CEA level: identification of both low and high risk of recurrence in patients with resected T1 lung adenocarcinoma.

Authors:  Kotaro Higashi; Tsutomu Sakuma; Kengo Ito; Seiji Niho; Yoshimichi Ueda; Takeshi Kobayashi; Ryuzo Sekiguchi; Tomoko Takahashi; Takashi Kato; Hisao Tonami
Journal:  Eur J Nucl Med Mol Imaging       Date:  2008-10-18       Impact factor: 9.236

7.  Revisiting the prognostic value of preoperative (18)F-fluoro-2-deoxyglucose ( (18)F-FDG) positron emission tomography (PET) in early-stage (I & II) non-small cell lung cancers (NSCLC).

Authors:  Mohit Agarwal; Govinda Brahmanday; Sunil K Bajaj; K P Ravikrishnan; Ching-Yee Oliver Wong
Journal:  Eur J Nucl Med Mol Imaging       Date:  2009-11-14       Impact factor: 9.236

8.  Serum C-reactive protein and procalcitonin levels in non-small cell lung cancer patients.

Authors:  Baykal Tulek; Habibe Koylu; Fikret Kanat; Ugur Arslan; Faruk Ozer
Journal:  Contemp Oncol (Pozn)       Date:  2013-03-15

9.  Prediction of 2 years-survival in patients with stage I and II non-small cell lung cancer utilizing (18)F-FDG PET/CT SUV quantification.

Authors:  Angelina Cistaro; Natale Quartuccio; Alireza Mojtahedi; Piercarlo Fania; Pier Luigi Filosso; Alfredo Campenni; Umberto Ficola; Sergio Baldari
Journal:  Radiol Oncol       Date:  2013-07-30       Impact factor: 2.991

10.  The maximum standardized FDG uptake on PET-CT in patients with non-small cell lung cancer.

Authors:  Mehmet Akif Ozgül; Gamze Kirkil; Ekrem Cengiz Seyhan; Erdoğan Cetinkaya; Güler Ozgül; Mahmut Yüksel
Journal:  Multidiscip Respir Med       Date:  2013-10-22
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