A comparison of FLT to FDG PET/CT in the early assessment of chemotherapy response in stages IB-IIIA resectable NSCLC

被引:17
作者
Crandall, John P. [1 ]
Tahari, Abdel K. [2 ]
Juergens, Rosalyn A. [3 ]
Brahmer, Julie R. [4 ]
Rudin, Charles M. [5 ,6 ]
Esposito, Giuseppe [7 ]
Subramaniam, Deepa S. [8 ]
Knopp, Michael V. [9 ]
Hall, Nathan C. [10 ]
Gajwani, Prateek [11 ]
Leal, Jeffrey P. [12 ]
Lodge, Martin A. [12 ]
Joo, H. O. [13 ]
Gabrielson, Edward W. [14 ]
Shankar, Lalitha K. [15 ]
Wahl, Richard L. [1 ,12 ]
机构
[1] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, 510 S Kingshighway Blvd,Campus Box 8131, St Louis, MO 63110 USA
[2] King Fahad Specialist Hosp, Dept Med Imaging, POB 15215, Dammam 3144434, Saudi Arabia
[3] McMaster Univ, Juravinski Canc Ctr, 699 Concess St, Hamilton, ON L8V 5C2, Canada
[4] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, 1650 Orleans St,CRB 1 Room G-94, Baltimore, MD 21287 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, Thorac Oncol Serv, 633 3rd Ave, New York, NY 10017 USA
[6] Weill Cornell Med Coll, 633 3rd Ave, New York, NY 10017 USA
[7] Georgetown Univ Hosp, Dept Radiol, 3800 Reservoir Rd NW CCC Bldg, Washington, DC 20007 USA
[8] Georgetown Univ Hosp, Dept Med, 3800 Reservoir Rd NW LCCC Bldg,Second Floor Pod B, Washington, DC 20007 USA
[9] Ohio State Univ, Wexner Med Ctr, Dept Radiol, 395 W 12th Ave,Room 430, Columbus, OH 43210 USA
[10] Univ Penn, Perelman Sch Med, Dept Radiol, 116 Donner,HUP 3400 Spruce St, Philadelphia, PA 19104 USA
[11] Johns Hopkins Univ, Sch Med, Johns Hopkins Wilmer Eye Inst, 600 N Wolfe St, Baltimore, MD 21287 USA
[12] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol, Nelson B1-160,600 N Wolfe St, Baltimore, MD 21287 USA
[13] Catholic Med Ctr, Seoul St Marys Hosp, Dept Nucl Med, Banpo Daero 222, Seoul 06591, South Korea
[14] Johns Hopkins Univ, Sch Med, Dept Pathol, 1550 Orleans St,304 CRB 2, Baltimore, MD 21287 USA
[15] Natl Canc Inst, 6130 Execut Blvd,MSC 7412, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
FDG PET/CT; FLT PET/CT; Non-small cell lung cancer; Early treatment response monitoring; CELL LUNG-CANCER; POSITRON-EMISSION-TOMOGRAPHY; F-18-FDG PET; IMAGING PROLIFERATION; TUMOR RESPONSE; IN-VIVO; KI-67; IMMUNOHISTOCHEMISTRY; EARLY PREDICTION; BREAST-CANCER; CHEMORADIOTHERAPY;
D O I
10.1186/s13550-017-0258-3
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
Background: The aim of this study was to compare the percentage change in F-18-fluorothymidine (FLT) standard uptake value (SUV) between baseline and after one cycle of chemotherapy in patients categorized by RECIST 1.1 computed tomography (CT) as responders or non-responders after two cycles of therapy. Change in F-18-fluorodeoxyglucose (FDG) uptake was also compared between these time points. Nine patients with newly diagnosed, operable, non-small cell lung cancer (NSCLC) were imaged with FDG positron emission tomography/CT (PET), FLT PET/CT, and CT at baseline, following one cycle of neoadjuvant therapy (75 mg/m(2) docetaxel + 75 mg/m(2) cisplatin), and again after the second cycle of therapy. All patients had a biopsy prior to enrollment and underwent surgical resection within 4 weeks of post-cycle 2 imaging. Results: Between baseline and post-cycle 1, non-responders had mean SULmax (maximum standard uptake value adjusted for lean body mass) increases of 7.0 and 3.4% for FDG and FLT, respectively. Responders had mean decreases of 44.8 and 32.0% in FDG and FLT SULmax, respectively, between baseline and post-cycle 1 imaging. On post-cycle 1 imaging, primary tumor FDG SUL values were significantly lower in responders than in non-responders (P = 0.016). Primary tumor FLT SUL values did not differ significantly between these groups. Using the change from baseline to post-cycle 1, receiver-operating characteristic (ROC) analysis showed an area under the curve (AUC) of 0.94 for FDG and 0.78 for FLT in predicting anatomic tumor response after the second cycle of therapy. Conclusions: Fractional decrease in FDG SULmax from baseline to post-cycle 1 imaging was significantly different between anatomic responders and non-responders, while percentage changes in FLT SULmax were not significantly different between these groups over the same period of time.
引用
收藏
页数:10
相关论文
共 33 条
[1]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[2]  
[Anonymous], NCCN CLIN PRACT GUID
[3]   Is 18F-FDG PET/CT Useful for the Early Prediction of Histopathologic Response to Neoadjuvant Erlotinib in Patients with Non-Small Cell Lung Cancer? [J].
Aukema, Tjeerd S. ;
Kappers, Ingrid ;
Olmos, Renato A. Valdes ;
Codrington, Henk E. ;
van Tinteren, Harm ;
van Pel, Renee ;
Klomp, Houke M. .
JOURNAL OF NUCLEAR MEDICINE, 2010, 51 (09) :1344-1348
[4]  
Bhoil A, 2014, HELL J NUCL MED, V17, P90, DOI 10.1967/s002449910136
[5]  
Buck AK, 2003, J NUCL MED, V44, P1426
[6]   Preoperative chemotherapy for non-small-cell lung cancer: a systematic review and meta-analysis of individual participant data [J].
Burdett, Sarah ;
Rydzewska, Larysa H. M. ;
Tierney, Jayne F. ;
Auperin, Anne ;
Le Pechoux, Cecile ;
Le Chevalier, Thierry ;
Pignon, Jean-Pierre .
LANCET, 2014, 383 (9928) :1561-1571
[7]   Correlation between Ki-67 immunohistochemistry and 18F-Fluorothymidine uptake in patients with cancer: A systematic review and meta-analysis [J].
Chalkidou, A. ;
Landau, D. B. ;
Odell, E. W. ;
Cornelius, V. R. ;
O'Doherty, M. J. ;
Marsden, P. K. .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (18) :3499-3513
[8]  
Chen W, 2005, J NUCL MED, V46, P945
[9]   Complete metabolic tumour response, assessed by 18-fluorodeoxyglucose positron emission tomography (18FDG-PET), after induction chemotherapy predicts a favourable outcome in patients with locally advanced non-small cell lung cancer (NSCLC) [J].
Decoster, L. ;
Schallier, D. ;
Everaert, H. ;
Nieboer, K. ;
Meysman, M. ;
Neyns, B. ;
De Mey, J. ;
De Greve, J. .
LUNG CANCER, 2008, 62 (01) :55-61
[10]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247